Energy conversion system
10727365 · 2020-07-28
Assignee
Inventors
Cpc classification
H01S3/09403
ELECTRICITY
H01L31/02168
ELECTRICITY
H01L31/055
ELECTRICITY
H01L31/0547
ELECTRICITY
Y02E10/52
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
H01S3/169
ELECTRICITY
H01S3/0408
ELECTRICITY
International classification
H01L31/055
ELECTRICITY
H01L31/054
ELECTRICITY
Abstract
A method of emitting photons at a desired wavelength, including: providing a material having a first region of high absorption of radiation at a first set of wavelength of radiation, contiguous with a second region of low absorption of radiation at a shorter set of wavelengths, and a third region of high emission at a further shorter set of wavelengths; applying energy to the material at the first region, such that most of an effective black body radiation of said material at a temperature of the material would fall within the second region and be configured to transfer energy to said third region and not overlap with the first region; and emitting energy from the material at the third region, powered by said applying energy.
Claims
1. A method for using an energy conversion apparatus to convert incoming radiation to electrical energy comprising: accepting incoming radiation from a radiation source external to an energy conversion apparatus; heating a photoluminescent material to a temperature T, where T >(Eg2-Eg1)/3Kb where Eg2 is a band-gap energy of a photovoltaic material, Eg1 is a band-gap energy of said photoluminescent material, and Kb is the Boltzmann constant; using insulation to maintain said temperature of said photoluminescent material; using said photoluminescent material to absorb a first photon from the incoming radiation; the absorbing the first photon and the heating causing said photoluminescent material to emit a second photon at a shorter wavelength than said first photon; and placing a photovoltaic cell comprising said photovoltaic material to absorb said second photon and generate electricity.
2. The method of claim 1, in which said heating said photoluminescent material comprises using the photoluminescent material to absorb radiation photons thereby to absorb heat.
3. The method of claim 2, in which said band-gap of said photovoltaic material for absorbing said radiation photons is larger than a band-gap of said photoluminescent material.
4. The method of claim 2 and further comprising using a first optical unit for concentrating said radiation photons on said photoluminescent material.
5. The method of claim 1 and further comprising using said photoluminescent material to absorb heat energy by convection.
6. The method of claim 2, in which using said photoluminescent material to absorb heat comprises using said photoluminescent material to absorb heat by absorbing heat radiation.
7. The method of claim 1 and further comprising using an optical element for coupling said photoluminescent radiation from said photoluminescent material to said photovoltaic material.
8. The method of claim 1, in which said photoluminescent material is absorptive at solar radiation wavelengths.
9. The method of claim 1 and further comprising providing a photon reflecting configuration to reflect stray radiation for reabsorbing by said photoluminescent material.
10. The method of claim 2 and further comprising using a light source coupled to provide said radiation photons to said photoluminescent material, at a wavelength longer than a wavelength corresponding to a band.sub.zgap of said photovoltaic material.
11. The method of claim 1, comprising using as said photoluminescent material a material which comprises a dopant selected from a group consisting of: quantum dots; nano-particles; gold nano-particles; rare earths; Ytterbium; Neodymium; Europium; Erbium; direct band-gap semiconductors; InGa; and CdTe.
12. The method of claim 1 in which: said using said photoluminescent material to absorb a first photon comprises absorbing the first photon at a wavelength in a range between 0.5 to 1.5 microns; and said causing said photoluminescent material to emit a second photon comprises emitting the second photon at a wavelength in a range approximately between 0.80 to 1.2 microns.
13. Apparatus for converting incoming radiation to electrical energy, comprising: a photoluminescent material for: absorbing heat and absorbing a first photon from incoming radiation; combining energy of said first photon with energy of said heat; and emitting a second photon at a shorter wavelength than said first photon; a photovoltaic cell comprising photovoltaic material for absorbing said second photon and generating electricity; and insulation placed between said photoluminescent material and said photovoltaic cell for maintaining temperature of said photoluminescent material, wherein: said apparatus is configured to expose said photoluminescent material to the incoming radiation at wavelengths corresponding to energies greater than a band-gap of said photovoltaic material, and said photoluminescent material is selected to have a luminescence peak emission at a wavelength which matches absorption of said photovoltaic material.
14. The apparatus of claim 13 in which: said photoluminescent material is selected to absorb said first photon at a wavelength in a range between 0.5 to 1.5 microns; and said photoluminescent material is selected to emit said second photon at a wavelength in a range approximately between 0.80 to 1.2 microns.
15. The apparatus of claim 13, in which said absorbing heat comprises absorbing heat and radiation photons.
16. The apparatus of claim 15, in which a band-gap for absorbing radiation photons of said photovoltaic material is larger than a band-gap of said photoluminescent material.
17. The apparatus of claim 15, and further comprising a first optical element for concentrating said radiation photons on said photoluminescent material.
18. The apparatus of claim 13, wherein said photoluminescent material further comprises a contact location for absorbing convective heat energy.
19. The apparatus of claim 13, in which said photoluminescent material is configured to absorb heat by absorbing heat radiation.
20. The apparatus of claim 15 and further comprising an optical element for coupling said photoluminescent radiation to said photovoltaic cell.
21. The apparatus of claim 13, in which said photoluminescent material is absorptive at solar radiation wavelengths.
22. The apparatus of claim 13, in which said photoluminescent material is absorptive at a wavelength of light generated in a chemical reaction.
23. The apparatus of claim 13 and further comprising a photon reflecting configuration to reflect stray radiation for reabsorbing by said photoluminescent material.
24. The apparatus of claim 15 and further comprising a light source at a wavelength longer than a wavelength corresponding to a band-gap of a photovoltaic material comprised in said photovoltaic cell and coupled to provide said radiation photons to said photoluminescent material.
25. The apparatus of claim 13, in which said photoluminescent material is selected from a group consisting of: quantum dots; nano-particles; gold nano-particles; rare earths; Ytterbium; Neodymium; Europium; Erbium; direct band-gap semiconductors; InGa; and CdTe.
26. The apparatus of claim 15, wherein said photoluminescent material is configured to absorb heat by absorbing said radiation photons.
27. The method of claim 1, in which said photoluminescent material emits photoluminescent radiation when said photoluminescent material is at a temperature above 600 Kelvin.
28. The apparatus of claim 13, in which said photoluminescent material is selected to emit photoluminescent radiation at a temperature above 600 Kelvin.
29. The apparatus of claim 13 in which said apparatus is configured with said photovoltaic cell placed behind said photoluminescent material relative to a direction of the incoming radiation.
30. The apparatus of claim 13, in which said insulation is configured to maintain said temperature of said photoluminescent material at a temperature equal to or greater than 600 Kelvin.
31. The method of claim 1 in which the temperature T is equal to or greater than 600 Kelvin.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.
(2) Some embodiments of the invention are herein described, by way of example only, with reference to the accompanying drawings. With specific reference now to the drawings in detail, it is stressed that the particulars shown are by way of example and for purposes of illustrative discussion of embodiments of the invention. In this regard, the description taken with the drawings makes apparent to those skilled in the art how embodiments of the invention may be practiced.
(3) In the drawings:
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DESCRIPTION OF SPECIFIC EMBODIMENTS OF THE INVENTION
(22) Overview
(23) The present invention, in some embodiments thereof, relates to an energy conversion system and, more particularly, but not exclusively, to a conversion system which up-converts energy from longer wavelengths to shorter wavelength.
(24) A broad aspect of some embodiments of the invention relates to energy conversion in which energy is coupled from one (or more) longer wavelength to a shorter wavelength using solid state energy coupling in a material. Optionally, the material has a low emissivity window between the one wavelength and the shorter wavelength, to reduce energy loss at that window. In an exemplary embodiment of the invention, the material is formed into a body which uses surface characteristics thereof (e.g., polaritons) to assist said energy transfer. In an exemplary embodiment of the invention, surface modes, rather than volume modes are used to transfer energy.
(25) In an exemplary embodiment of the invention, energy at said one wavelength is used to occupy energy states in non-radiative energy sates and then energy at these states is siphoned off using a high emissivity peak and/or a resonant cavity and/or surface structures, such as gratings or prisms.
(26) An aspect of some embodiments of the invention relates to a method of energy conversion in which energy is provided to a body at one wavelength and selectively emitted at another wavelength. In an exemplary embodiment of the invention, the provided energy fills energy states in the body using an entropy driven mechanism, which heats the body to a temperature where its black body emission is at shorter wavelength than the low entropy source photons. Optionally, the energy is emitted at a high-emissivity wavelength region which overlaps with said occupied energy states (as defined by the body temperature). In an exemplary embodiment of the invention, the high-emissivity wavelength region overlaps with the occupied energy states by less than 90%, 80%, 50%, 30%, 10% or intermediate or smaller overlap. Optionally or alternatively, the high-emissivity wavelength substantially overlaps only energy states occupied with energies at less than 90%, 80%, 50%, 30% or intermediate percentages of a peak occupied state. In an exemplary embodiment of the invention, the emission peak is at an effective temperature which is at least 30% (or at least 200%, or at least 1000% or intermediate percentages) higher than a temperature as defined by said energy states. In an exemplary embodiment of the invention, said body has a low emissivity over a range of wavelengths that covers at least 30%, at least 50%, at least 80%, at least 90% or intermediate percentages of wavelengths that would be emitted if the body were a black body with the occupied energy states. In some embodiments, the emission wavelength is longer than a wavelength of peak energy.
(27) In an exemplary embodiment of the invention, the emission at the low emissivity region comprises less than 90%, 80%, 50%, 5% or intermediate percentages of the total emission by said body. Optionally, this region is provided to avoid and/or reduce radiative loss.
(28) In an exemplary embodiment of the invention, the properties of the body are provided by two or three different materials, optionally not mixed together. For example, absorption may be provided by one material, which is coupled to a second material which provides the transparency and which is coupled to a third material (or the first material) to provide the emissions. Thus, in an exemplary embodiment of the invention, the second material serves as an energy reservoir to which incoming energy is coupled and from which energy is coupled to emission.
(29) In an exemplary embodiment of the invention, the emissivity of the emitting high emissivity region is greater by a factor of, for example, 10, 100, 1,000, 10,000, 100,000 or greater or intermediate factors from a low emissivity of the low emissivity wavelength range, or at least of 90% or 95% or more thereof. In one example, the high emissivity is between 0.5 and 1 and the low emissivity is less than 0.1.
(30) In an exemplary embodiment of the invention, a width of the low emissivity window is greater by a factor of 10, 100, 1000, or intermediate or greater factors than the width of the high emissivity window. It is noted that in some embodiments, the high emissivity window may be large, however.
(31) In an exemplary embodiment of the invention, the slope of the high emissivity window at the longer wavelength side is high, such that, for example, emissivity increases by a factor of at least 10, 100, 1000 or intermediate or greater factors, within a range of wavelengths, of, for example, 100 microns, 10, microns, 0.1 microns and/or smaller or intermediate or greater ranges.
(32) In an exemplary embodiment of the invention, the low emissivity region covers wavelengths containing at least 30%, at least 50%, at least 70%, at least 90% or intermediate or greater percentages of energy in radiative states.
(33) An aspect of some embodiments of the invention relates to an entropy driven laser, in which low energy coherent photons are used to drive a shorter wavelength lasing effect, for example, with an up-conversion of at least a factor of 2, 3, 4, 5, 6, 10 or intermediate or greater factors. In an exemplary embodiment of the invention, the efficiency of conversion (e.g., ignoring heat loss) is at least 0.5% 15, 3%, 5%, 10%, 20%, 30%, 50% or intermediate or greater efficiencies.
(34) In accordance with an exemplary embodiment of the invention, the inventors have realized that taking into account the complete thermodynamic picture work can also be achieved by a change in a system's entropy. Apparently, the temperature and entropy term, [T.Math.S] has never been used before as a pump and the inventors have realized that it offers an additional, independent route for new pump mechanisms. This route allows pumping with coherent photons at lower energy than the photoluminescence photons. Here the entropy, as defined by the pump coherence, governs the amount of up conversion that can be achieved. In particular, utilizing this change in entropy one can eliminate the need high chemical potential excitation photons and enable lasing with excitation of much lower chemical potential than is emitted.
(35) In an exemplary embodiment of the invention, a laser with an up-conversion of a factor of above 10 is provided, for example, a lasing at less than 1000 nm is provided (e.g., Ytterbium laser at 980 nm) using a pumping at more than 10 microns (e.g., CO2 laser at 10.6 microns).
(36) In an exemplary embodiment of the invention, a solar pumped laser is provided in which direct or optionally concentrated sunlight (e.g., by a factor of 2, 5, 10, 100, 1000, 10000 or intermediate or greater values) is used to pump a laser. Optionally, the laser has a wavelength shorter than the peak wavelength of radiation of the sun.
(37) In an exemplary embodiment of the invention, up-conversion is used to convert laser radiation at one wavelength to laser radiation at a shorter wavelength, for example, to provide UV or soft x-ray lasers. As an example the emitter can be one of known UV emitters. The phosphor typically used for a near 368 to 371 nanometer emission peak is either europium-doped strontium fluoroborate (SrB.sub.4O.sub.7F:Eu.sup.2+) or europium-doped strontium borate (SrB.sub.4O.sub.7:Eu.sup.2+), whereas the phosphor used to produce a peak around 350 to 353 nm is lead-doped barium silicate (BaSi.sub.2O.sub.5:Pb.sup.+). Also mercury can be modified to produce a UVA, UVB emission.
(38) In an exemplary embodiment of the invention, the body is in or forms a cavity or other resonant structure, to enhance emission at the wavelengths of the high-emission window. In one example, the body is spherical. In another example, the body is placed between reflective surfaces, which are optionally used also for preventing heat loss.
(39) In an exemplary embodiment of the invention, of a sphere coupled to a fiber, energy input and/or output is optionally via the fiber. In an alternative example, emission is in a plane which is shared with a ring on the body which defines the resonance. In an example of a body in a mirrored chamber, emission is optionally through a less reflecting part of the mirror.
(40) An aspect of some embodiments of the invention relates to a heat to electrical converter in which the converter converts energy at multiple wavelengths to energy at a single or small number of peaks and which utilizes a high efficiency photo-converter optimized for said peak or peaks.
(41) An aspect of some embodiments of the invention relates to an energy conversion system which utilizes surface phonon polaritons to enhance energy transfer between a set of low energy states and a set of high energy states, where the polaritons bridge a low or non-emissive region between the states and do not substantially emit at said low or non-emissive region.
(42) An aspect of some embodiments of the invention relates to up-conversion of a laser to a shorter wavelength laser emission by first coupling a longer wavelength laser to a body via surface phonon polaritons and then coupling these polaritons to emission at a narrow, shorter wavelength. In an exemplary embodiment of the invention, the second coupling uses a rare earth as a coupler. Optionally, energy loss is reduced by choosing a body made of a material which does not emit too much at wavelengths intermediate said shorter and said longer wavelengths.
(43) An aspect of some embodiments of the invention relates to providing a high effective temperature, as evidenced by emission wavelength without providing a real high temperature, as would be evidenced by black body radiation, on a body. In an exemplary embodiment of the invention, the lack of a real high temperature preventing melting and/or evaporation of the body. Optionally, the effective high temperature is used for energy storage, chemical reactions and/or photovoltaic output.
(44) An aspect of some embodiments of the invention relates to a method of producing electric power from radiation, in which radiation is provided to a first material body at one wavelength and emitted at another, shorter wavelength. The shorter wavelength is then optionally absorbed by a photovoltaic cell, and produces electricity.
(45) Before explaining at least one embodiment of the invention in detail, it is to be understood that the invention is not necessarily limited in its application to the details of construction and the arrangement of the components and/or methods set forth in the following description and/or illustrated in the drawings and/or the Examples. The invention is capable of other embodiments or of being practiced or carried out in various ways.
(46) Exemplary Scheme
(47) Referring now to the drawings,
(48) Referring first to
(49) At 204, the energy is used to populate energy levels at a low emission wavelength of body 304. This is now explained with reference to
(50) At 206, energy is sufficient to populate levels overlapping with an emission window 108. Optionally, this window is provided by coating body 304 with a suitable coating 306 or by doping all or part (e.g., a surface portion) of body 304. The doping may include, for example, rare earth materials, semi-conductor materials, organic materials, and/or any other material known to emit at a desired peak or region and/or which affects the body to affect at such a peak. The window may be, for example, sub nanometer full width half max narrow emission, as shown or above 1 full width half max emission width. Intermediate, greater or smaller widths may be provided as well. In some embodiments, the energy populates non-emitting levels that overlap emission window 108, but black body radiative states do not so overlap.
(51) At 208, emissions at a wavelength range 110 corresponding to an overlap between the energy states and the emission window are collected, for example, by a collector 308. Optionally, the emissions are used, for example, as a laser source or a narrow beam light source. Optionally, the collector comprises a converter to electrical energy used to power a load 310.
(52) Optionally, system 300 includes an insulation layer 307 to maintain the temperature of body 304. In an exemplary embodiment of the invention, insulation is provided by reflective mirrors 309, which also serve to define a resonant cavity for body 304. In some embodiments, body 304 is shaped in the form of a cavity, for example, a sphere.
(53) In an exemplary embodiment of the invention, a controller 312 is provided which may, for example, control energy provision via a control circuit 314 (e.g., add or decrease fuel in a chemical heat source). Optionally or alternatively, controller 312 uses a sensor 318 to determine if a desired emission is being achieved, optionally changing the energy provision in response. Optionally or alternatively, a sensor 316 receives a signal from, for example, collector 308 or load 310 indicating a total efficiency or amount of energy conversion.
(54) In a particular embodiment, described in more detail below, energy 109/source 302 is CO2 laser light at 10.6 microns, concentrated on a SiO2 body 304 and layer 306 is a doping of Ytterbium on a tip of a SiO2 fiber optic, melted to form a sphere, which acts as an optical cavity for lasing.
(55) Referring briefly to
(56) Possible Hypotheses
(57) Without being necessarily limited by one hypothesis or another, parameters for some embodiments of the invention may be more usefully optimized using a theoretical model, such as provided below. However, while these hypotheses can be used to define parameters for some embodiments of the invention, incorrectness of one or more of these hypotheses does not lead to invalidation of the description of particular embodiments of the invention.
(58) In a possible way to explain the thermodynamic reasons that allow low entropy to generate efficient extreme up-conversion and laser work, it may be constructive to consider the following process: Coherent beams can be considered as having an entropy approaching zero and thus temperature approaching infinity. This allows a CO2 laser beam to be focused to generate maximum photon flux that heats a SiO2 optical cavity to a temperature much above 3500 kelvin. At thermodynamic equilibrium, this body emits at all frequencies according to Plank's formula at the (same) body temperature. For temperatures above 3500 kelvin most of black body photons are at the visible and Near IR part of the spectrum. Therefore, a black body at 3500 kelvin can be used as a pump source for lasing at 1 micron by red shifting the pump photons in a conventional lasing media of three or four energy levels scheme. In such a description the efficiency of generating pump photons at the visible is similar to other heating through radiation processes such as solar thermal, which can approach unity.
(59) However, this description cannot be correct for the example of
(60) As shown by the experimental results, the actual emission by body 304 at wavelengths other than the lasing wavelengths resembles a black body emission at 600 kelvin reduced by low emissivity at those emission wavelengths. It is hypothesized that what is at work is the huge difference in emissivity between the SiO2 and Ytterbium. SiO2 is one of the most transparent materials between 0.4 micron and 2.4 micron wavelengths, which according to Kirchhoff's law of thermal radiation, is accompanied by negligible emissivity at that range. Ytterbium on the other hand, has emissivity approaches unity at 1 micron, which together with an optional Purcell effect of the cavity results in efficient Ytterbium emission. This interpretation can be tested, when comparing the Ytterbium emission without the cavity and black body emission at 600 Kelvin. By definition a black body has emissivity of one and therefore if Ytterbium emission is part of a system in thermodynamic equilibrium it must be lower than the black body emission. However, the experiments described below show emission at an amplitude greater than predicted by black body radiation by a factor greater than 2.
(61) One possible hypothesis is as follows. The coherent CO2 excitation excites single (or numerous) phonons, through vibration modes of body 304. That is, the non-equilibrium laser excitation is projected to a discrete phonon population at huge amplitude at effective high temperature. Since SiO2 is transparent between 400 nm and 2.4 microns wavelength, the possibility of multi phonon up-conversion as a result of phonon scattering in the SiO2 is weak. Ytterbium on the other hand has high emissivity at 1 micron and is known to convert thermal excitation to emission. Inventors hypothesize that direct conversion of the discrete excited phonons to photons are done at the YbO3 molecules used as a dopant in layer 306. The residual non-radiative energy is scattered to many phonons. As many modes are excited the system shift towards thermodynamic equilibrium and the temperature can be defined and set at 600 kelvin. In other words, because of the enhanced emissivity of Ytterbium compared to SiO2, the Ytterbium excitation rate is preferred over the SiO2 heating (scattering too many phonons).
(62) In an exemplary embodiment of the invention, what is done is using an energy source at low entropy so as to allow low energy photons (at long wavelength) to heat a body to such a high temperature where it's black body emission will be at wavelength much shorter than the energy source. If a body has a high absorption at the long wavelength and a high transparency at a shorter wavelength (e.g., the transparent window) the body, when heated to a high enough temperature, cannot efficiently emit the photons and therefore will store the energy. If a body with such transparent window has a strong emitter at a short wavelength the stored energy can only radiate from the body at the strong emitter wavelength. The effective outcome is conversion of long wavelength of the initial energy source to shorter wavelength of the heated body emitter, without electronic conversion or mechanical mechanism, but possibly using solid state physics.
(63) Another possible hypothesis to explain the efficient energy transfer to the Ytterbium is excitation through surface phonon polaritons. Conventionally, surface modes must be coupled to radiative excitations by a prism or grating in order to overcome the momentum mismatch. SiO.sub.2 absorption cross section at CO.sub.2 excitation is very high, result in excitation absorption at a length shorter than wavelength. At such short distances momentum mismatch between the photon and the excited phonon may be eliminated, which allows to couple surface phonons to free space radiation. SiO.sub.2 has high density of surface phonon polariton modes (SPhP) in the spectrum close to the CO.sub.2 emission, therefore it is expected that much of the energy is coupled to the SPhP. When using a spherical body 304 which also acts as a resonator, body 304 supports whispering-gallery modes at the sphere surface, which enhance the Ytterbium emission through the Purcell effect. The SPhP conservation of the energy at the surface, where the cavity modes are located, enhances the total energy transferred to Ytterbium emission. Possibly, under this interpretation, one cannot assign a temperature to this non-equilibrium Ytterbium emission, and it cannot be defined if emissivity is above unity, which indicates a gain process. Optionally, surface heating is by other means, for example, IR radiation, RF, ultrasound contact heating and/or convection heating.
(64) It is noted that Dye-Zone A. Chan [PhD thesis MIT 2007] have shown that the density of states near the surface of dielectric materials such as SiO.sub.2 and metals is much higher than remote from the surface by orders of magnitude due to surface modes. In polar materials such as SiO.sub.2 these modes are surface phonons polaritons, which directly enhance heat conductivity and heat capacity. As shown in the above thesis there is a 1000 fold enhancement of DoS on the surface. In other embodiments, a lesser enhancement (or none), such as a factor of 0.5, 1, 2, 10, 100, 300 or intermediate or smaller or greater factors, may be used, or a factor of more than 100, such as 200, 5000 or more may be provided. Such modes are generally not radiative unless coupled to the free space by prism or grating.
(65) As the propagation length of SPhP is, for example, in the order of 1 meter, which means that the SiO2 cavity at the size of sub millimeters supports whispering gallery phonons modes [Carmon, and Vahala, Phys. Rev. Lett. 98, 123901 (2007)]. Optionally, the cavity enhances SPhP amplitude by its Q factor. Optionally, a Direct coupling between the Ytterbium to the SPhP excite its 1 micron emission via a nonlinear process in the Ytterbium. In this case curve 112 can be ignored due to the up-conversion at the Ytterbium. Materials with other propagations lengths, for example, a factor of 2, 4, 6, 10, 500, 1000 or smaller or intermediate factors as a function of the size of the cavity/body, may be used.
(66) Exemplary Materials
(67) In an exemplary embodiment of the invention, body 304 is formed one or more materials so as to have the following properties: a region 104 of high emissivity (and energy absorption), one or more regions 106 of low emissivity, so that body 304 can be heated so most black body radiation overlaps with low emission and one or more regions of high emission 108, formed, for example, as a peak or as a wider emission window.
(68) In the example above, SiO2 doped with Ytterbium provides this desired mix.
(69) In an exemplary embodiment of the invention, region 104 is selected according to the desired input wavelengths and according to the operating temperature.
(70) Region 106 is selected so that most (e.g., at least 50%, at least 70%, at least 90%, at least 95% or intermediate percentages) of the black body emission overlaps with low emissivity wavelengths (e.g., emissivity less than 0.3, 0.2, 0.1, 0.04, 0.01 or intermediate emissivities).
(71) Region 108 is optionally selected according to a desired emission wavelength.
(72) As can be appreciated different combinations of materials and properties are useful for different situations of input energy, operating temperature and desired emission.
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(74) In an exemplary embodiment of the invention, body 304 is doped with or coated with a material which has a desired peak 108. In other embodiments an alloy or other formulation is selected according to its inherent emissivity curve 102. For example some rare earths, quantum dots, transition metals or metal nano-particles, semiconductor materials have high emissivity (and absorption) in the visible rang and low emissivity at longer wavelength. By adding small amount of these one can enhance visible light emissivity and absorption while maintaining transparency (and thus low emissivity) at the transparent window. Such addition can, for example, enhance the conversion of solar radiation to heat and thus to 1 micron emission (as described, for example, below).
(75) In some embodiments, it is desired to have sub-wavelength absorption in the surface, for example, for polariton-based designs. Optionally, body 304 is coated with, for example, plasmonic materials such as metals which absorb visible light at sub wavelength distance, and organic and quantum dots which also absorb at near wavelength distance.
(76) Some example dopants for absorption and/or emission include metals such as gold nano-particles at the size of tens of nanometers absorbs well in the visible and transparent at the Near IR (Nanoscape Volume 2, Issue 1, Spring 2005); Quantum dots such as CdSe/ZnS_core/shell_ Quantum Dots (QDs) at the size of a few nanometers are good absorbers at the visible and transparent at the Near IR (Applied Physics Letters 89, 191124 2006).
(77) Rare earths for the visible and Near IR emission include Tb3+, Ce3+:LaPO4, Eu:Y2O3, Nd3+, Yb;
(78) Other exemplary phosphors are listed in Shigeo Shionoya (1999). VI: Phosphors for cathode ray tubes. Phosphor handbook. Boca Raton, Fla.: CRC Press. ISBN 0-8493-7560-6 and Jankowiak, Patrick. Cathode Ray Tube Phosphors. Revision 20100226.1844.
(79) It should be noted that if peak 108 is gradual in the direction of black body radiation curve 112, there will be a relatively broad range of frequencies of emission, which may be less than optimal for some applications. For example for energy conversion to 1 wavelength, high emissivity at 1.2 may drain most of the energy to 1.2 emission.
(80) Similarly, if there is overlap between region 104 and curve 112, significant amounts of energy may be emitted at such longer wavelengths.
(81) Referring specifically to quantum dots, there are colloidal methods to produce many different semiconductors. Typical dots are made of or silicon binary alloys such as cadmium selenide, cadmium sulfide, indium arsenide, and indium phosphide. Their size is typically between 2 and 20 nm depending on their spectral activity (e.g., smaller size for shorter wavelength). Such quantum dots can be tuned by size to absorb the visible and emit at 1 micron and thus be used as a dopant for absorbing and/or for emitting and/or for coupling to an emitter.
(82) In addition, metal (such as gold, silver, copper) nano-particles at sizes between 2 and 100 nm can be absorptive at the visible and transfer the energy to Ytterbium via Forester Energy Transfer.
(83) Such nano-particles can be doped in the body to absorb solar spectrum or thermal radiation in the visible-near IR range, for example as described below.
(84) Exemplary Cavity and Body Shapes
(85) Body 304 can have various shapes, for example, to enhance energy application, energy emission and/or resonance. In an exemplary embodiment of the invention, a sphere is used. In an alternative embodiment, ring, round plate, a cylinder or ovoid shape is provided. In yet another embodiment, body 304 is, for example, rod or cube shaped and placed in a resonant cavity formed by mirrors. Examples of some body cavity design which may be used are described in text books such as optical electronics in modern communication and Quantum Electronics by Amnon Yariv.
(86) In an exemplary embodiment of the invention, a slab laser cavity can be constricted in a thickness of less than a millimeter made from one of the transparent materials in table 4. An emitter is optionally doped on one or more of the surfaces by, for example, coating, sputtering or implanting. Optionally, the excitation hits the slab on the surface where the emitter is and the cavity is designed to support lasing at that surface by for example two planar mirrors.
(87) Other cavities designs include spherical or fiber (e.g., at the circumference direction) which support surface modes. Additionally, a cavity made by a photonic band gap structure designed for surface modes can be used when coated by the emitter. Optionally, the mode volume is located on the surface and optionally has a depth of about the depth of the surface excited modes (of less than a millimeter).
(88) In one example, body 304 has a diameter of less than 10 mm, less than 5 mm, less than 2 mm, less than 1 mm.
(89) In another example, a slab with dimension of less than 200 mm, less than 30 mm and less than 10 mm is used.
(90) Other body designs may be used, for example, with a maximal dimension of about 1 mm, 10 mm, 20 mm, 40 mm, 100 mm, 200 mm or intermediate or larger maximal dimensions. Optionally or alternatively, such a body may have a minimal dimension of about 1 mm, 10 mm, 20 mm, 40 mm, 100 mm, 200 mm or smaller or intermediate or larger dimension.
(91) Down Conversion
(92) While
(93) Referring specifically to flowchart 500 in
(94) At 504, low emission wavelengths are populated by the energy application.
(95) At 506, also energy levels that overlap with the emission peak are populated.
(96) At 508 emission is provided and collected and/or otherwise utilized.
(97) Exemplary Solar and/or Entropy Pumped Laser
(98)
(99) Solar radiation from a sun 602 is optionally concentrated on a body 606 with a dopant layer 608, for example as described above. A resonant cavity 610 is optionally provided by a fully reflecting mirror 613 and a partially reflecting mirror 612. Laser light 614 is then emitted from mirror 612.
(100) In an exemplary embodiment of the invention, body 606 is adapted for use with solar radiation. In one example, body 606 is adapted to absorb visible radiation (e.g., possibly at shorter wavelength than the emitted wavelength) and convert the absorbed radiation to heat or polariton states. In one example, absorbers at solar (e.g., visible) wavelengths are added to body 606. This can be used to heat body 606 to a black body temperature which overlaps most of its radiative energy with the low emissivity region of body 606.
(101) In an alternative design, heat is used instead of sun 602 or the CO2 laser described below.
(102) As a generalized description of a pumped system, in an exemplary embodiment of the invention, body 606 is formed of a substrate which has a transparent wavelength range. At the (longer wavelength) end of the transparent window the pump can be absorbed. The pump may include, for example, solar radiation, laser emission, thermal source or any other excitation/heat source. The heating source is optionally used to heat body 606 to a temperature where its black body emission is arrested in the transparent window. That is black body emission is defined uniquely by the Temperature, but due to the transparent window and thus the low emissivity, minimal radiation will drain out from the device. Adding an emitter at 1 micron (or at a different desired wavelength) will drain the thermal (or other) excitation because of the high emissivity of the emitter, optionally with the help of cavity 610 which enhances the emitter emission due to Purcell effect, and thus enhance the conversion efficiency. Optionally, the ratio between the emissivity of the substrate and the emitter at the wavelength of the black body relevant wavelengths set the conversion efficiency. In an experiment described below, Silica is used as a substrate and Ytterbium as an emitter.
(103) As noted, an additional absorber at shorter wavelengths than the emitter may be added to the device in order to collect heat from the visible spectrum such as to convert visible solar radiation to heat. In an exemplary embodiment of the invention, it is desired to limit the transparency above the substrate transparency at the transparent window. Such absorbers can be metal nano-particles, quantum dots, rare earths, transition metals, and other materials. The high transparency at the transparent window usually demands that the pump absorption at the visible spectrum is low. This can be overcome by a cavity design for the visible spectrum, which enhances the propagation distance of the pump at the device.
(104)
(105) Exemplary PV Upconverter
(106) As a variation on a solar pumped laser, apparatus in accordance with an exemplary embodiment of the invention can be used to convert heat and light into radiation suitable for a photovoltaic (PV) converter and thereby electricity.
(107)
(108) Light from a sun 702 is optionally focused optics 704 on a body 706. As shown, body 706 is enclosed in cavity formed by reflectors 710 and includes, for example, a doped high emission area 708 (or all of body 706 may be so emitting).
(109) Body 706 is heated as described above and emits radiation at the high emissivity window of dopant 708, which, due to optional cavity 710, causes the emission of laser radiation. Such radiation is optionally collected by a PV converter 714 which is optimized for conversion at the wavelength of the laser radiation.
(110) In an exemplary embodiment of the invention, the process may be described as follows. Body 706 is configured to absorb of thermal radiation at a high emissivity region in the Near IR range. This causes heating of body 706 the cavity to a temperature associated with black body emission at the transparent region (in order to reduce losses). The thermal energy is emitted by an emitter matched to a band-gap of a photovoltaic cell (e.g., Silicon about 1 eV) via photoluminescence or lasing. Optionally, the photovoltaic cell is placed around the cavity (e.g., on all sides) to convert the band-gap emission into electricity.
(111) In an exemplary embodiment of the invention, the optimized conversion wavelength is at about 1 micron.
(112) It should be noted that the thermodynamic limit for the efficiency of single junction photovoltaic cells is at 30%. The state of the art Si cells reach 24% efficiency. Theoretically, maximal efficiency approaches unity could be achieved if the sun's light was harvested by an optical system that could emit it as monochromatic light at 1 micron, where Si PV have efficiency approaching unity. In an exemplary embodiment of the invention, this is provided or approached by the design described herein.
(113) Referring to the experiment described below, the CO2 pump, is replaced with solar radiation at the range between 2.4 micron and 10 micron where SiO2 absorbs. Adding absorbing materials such as metal nano-particles to absorb the visible spectrum can be used to enhance the power conversion as long as these materials are as transparent as SiO2 above 1 micron. It is noted that the converted wavelengths may be shorter than the emitted wavelengths.
(114) The SiO2 can be replaced with many transparent materials. One recipe for choosing a material is the requirement for a wide optical window where the material is transparent (e.g., as SiO2 is transparent between 0.4 and 2.4 microns). Optionally or alternatively, the Ytterbium can be replaced with other photoluminescence and/or phosphorescence materials depending on the desired wavelength to match the specific solar cell. For a silicon solar cell Neodymium can replace the Ytterbium, while for CIGS an Europium emitter may be preferred.
(115) Exemplary Solar Storage System
(116)
(117) A potential advantage of some embodiments of the invention is that high energy illumination can be provided by the methods described herein. Optionally, this is used for generating storage energy, for use, for example, at night or at other times with lower solar flux. Another potential advantage of some embodiments of the invention is that heat can be used to power a conversion process as described herein. System 800 shows both of these potential advantages by both using part of the solar radiation to create stored energy and by using that stored energy to generate electricity using the same process as described herein, thus potentially reducing material costs by reusing a same element both for solar conversion and for heat conversion.
(118) Referring to
(119) In a first type of conversion, the high energy emissions 804 are converted into chemical energy by the employment of a high temperature endothermic thermo-chemical response in oxides. This includes reactions such as the MgOMg redox reaction, where MgO is reduced at high temperatures to Mg, which is oxidized again by water to produce H.sub.2 gas fuel. High heat is optionally provided by concentrating emissions 804. In an alternative reaction, emissions 804 store energy by bond breaking, for example, splitting water, or splitting Ammonia splitting to Nitrogen and Hydrogen (or splitting a mixture of ammonia and water). In a further alternative reaction, emissions 804 are used to make high temperature.
(120) As noted with respect to the results of the experiment below, the output luminescence shows that energetic phonons are promoted as if ultra-high surface temperatures were provided. This can be used to derive such thermo-chemical reactions. Optionally, absorption at visible light wavelength is enhanced as described above or using transition metals. Optionally, the chemical reactants (e.g., the oxides) are provided in place of the emitter.
(121) In an exemplary embodiment of the invention, the effective temperature is increased by using Europium as an emitter.
Example Implementations
(122) The additional exemplary implementations described below provide example embodiments of the invention, and serve not only to limit but also to broaden the scope of the above description.
(123) Another example embodiment is a system which includes two conjugated active band gap materials.
(124) A first material is a fluorescent absorber/emitter of a band-gap named herein Eg.sub.1. The first material may optionally include a band-gap material such as Quantum Dots (QD), rare earths and direct band-gap semiconductors such as GaAs, InGa, as well as other materials, such as, for example, included in
(125) Radiation from the first material then optionally illuminates a solar cell which includes a second material having a band-gap named herein Eg.sub.2, where Eg.sub.2>Eg.sub.1. Temperature of the second material is optionally maintained at room temperature.
(126) The second material can be silicon and amorphous silicon with various dopings as well as other materials, such as, for example, included in
(127) At high quantum efficiency, meaning also low non-radiative losses, for nearly each solar-photon absorbed by the first material a photon is emitted, which encapsulates thermal energy and Eg.sub.1. Each emitted photon potentially has an average energy of Eg.sub.1+3KbT.sub.1, where T.sub.1 is a temperature of the emitter and Kb is the Boltzmann constant. The photons are absorbed by the solar cell of the second material when Eg.sub.2<Eg.sub.1+3KbT.sub.1. Since Eg.sub.2>Eg.sub.1, the voltage over the solar cell is greater than that which is expected of a single solar cell configuration at room temperature, and energy harvested by the above-described system is greater. The above-described system is an example embodiment of up-conversion of thermal radiation.
(128) Reference is now made to
(129)
(130) In some embodiments the light 1501 is optionally concentrated by a lens 1502 onto the first material 1503.
(131) The first material 1503 emits radiation 1505 onto a second material 1507, such as the second material having a band-gap Eg.sub.2 described above.
(132) In some embodiments, a gap 1506 exists between the first material 1503 and the second material 1507.
(133) In some embodiments, the gap 1506 is in a vacuum.
(134) In some embodiments, the second material 1507 includes a back reflector 1509, which potentially reflects radiation which may pass through the second material 1507 and potentially enables more of the radiation to be absorbed by the second material 1507.
(135) In some embodiments the second material 1507 is equivalent to a solar cell collector, and produces a voltage V 1511 across the solar cell, or, in other terms, produces a current J 1513.
(136) In some embodiments sub band-gap photons, having an energy E.sub.ph<Eg.sub.2, are optionally reflected back towards the first material 1503, potentially maintaining a high temperature through the back reflector 1509.
(137) In general terms, the embodiment depicted in
(138) For example, solar cells are limited at approximately 32% efficiency for most single band-gap materials, such as silicon, at room temperature.
(139) The example embodiment depicted in
(140) Reference is now made to
(141) The energy diagram 1529 depicts energy increasing along a vertical direction, and depicts a first region 1531 which corresponds to the first material of
(142) The energy diagram 1529 of
(143)
(144) An arrow 1541 represents an excitation from below the band-gap Eg1 to above the band-gap Eg.sub.1, and another arrow 1542 represents the excitation joining an energy distribution associated with a thermal distribution corresponding to a temperature T.sub.1 in the first material. Another depiction of the energy levels in the first material, not necessarily to scale, is a depiction of a lower Fermi level 1536 of a population of holes, and a higher Fermi level 1537 of an excited electron population. A gap between the lower Fermi level 1536 and the higher Fermi level 1537 is related to the amount of energy which may be produced from the excitation of the electron population in the first material. The amount of energy which may be produced from the excitation of the electron population in the first material depends on the first material, on the illumination rate and on the absorption of the second material.
(145) The first material radiates a portion of its energy toward the second material, as represented by an arrow 1543, and another arrow 1544 represents absorbed energy in the second material joining an energy distribution associated with a thermal distribution corresponding to a temperature T.sub.2 in the second material. Another depiction of the energy levels in the second material, not necessarily to scale, is a depiction of a lower Fermi level 1538 of a population of holes, and a higher Fermi level 1539 of an excited electron population. A gap between the lower Fermi level 1538 and the higher Fermi level 1539 is related to the amount of energy which may be produced from the excitation of the electron population in the second material. The amount of energy which may be produced from the excitation of the electron population in the second material depends on the second material, on the radiation rate and from the first material to the second material and on the absorption of the second material.
(146) In an example embodiment, such as the example embodiment of
(147) The second material acts as a solar collector, as described above with reference to
(148) Some radiation 1545 is radiated from the first material to the second material at energy levels which are not absorbed by the second material. At least some of such radiation 1545 is optionally reflected to the first material by the optional back reflector 1509 depicted in
(149) Exemplary Laser Up-Converter
(150)
(151) A laser source 902 illuminates a body 906 held in a cavity 910 (or forming one), having, for example, a fully reflecting mirror 911 (which is optionally transparent at the wavelength of source 902) and a partially reflecting mirror 912. A dopant 908, optionally provided as a layer, acts as an emitter. When stimulated, body 906 transfers energy to energy states which overlap with emission of emitter 908, generating a laser illumination 914.
(152) In an exemplary embodiment of the invention, the absorber (e.g., an added dopant) is matched to source 902. An emitter is optionally matched to the desired wavelength of laser illumination 914. The material of body 906 is optionally selected so as to be transparent at wavelengths below that of emitter 908 in a region wide enough to allow non-radiating energy states to store the incoming energy.
(153) In an exemplary embodiment of the invention, the emitter is a known UV emitters. The phosphor typically used for a near 368 to 371 nanometer emission peak is either europium-doped strontium fluoroborate (SrB.sub.4O.sub.7F:Eu.sup.2+) or europium-doped strontium borate (SrB.sub.4O.sub.7:Eu.sup.2+), whereas the phosphor used to produce a peak around 350 to 353 nm is lead-doped barium silicate (BaSi.sub.2O.sub.5:Pb.sup.+). Also mercury can be modified to produce a UVA, UVB emission.
(154) In an exemplary embodiment of the invention, the SiO2 used in some embodiments of the invention is replaced by a UV transparent glass/crystal to support lasing in the UV.
(155) In a conventional x-ray tube, X-rays are generated by accelerating electrons released by a hot cathode to collide with a metal target, the anode, creating the X-rays. In an exemplary embodiment of the invention, the hot cathode is replaced by an effective high temperature excitation as described herein (using an optically pumped electrode emitter and/or by placing an electron emitter on the emitter and/or using the high effective optical emission to heat an electron source). Optionally, the heat causes the electrons to accelerate so that when they hit a target (e.g., tungsten, optionally at a positive voltage), x-rays are emitted. Optionally, a system as described in U.S. Pat. No. 6,463,124, for converting laser light to x-ray radiation, is used.
(156) High Temperature Chemistry
(157) As noted above with respect to storage, the emitted illumination indicates effective high temperature, which may be used for chemical reactions. In one example, a chemical reactant or reactor is coupled to body 304 and/or to the emission radiation and uses this radiation to drive a reaction, such as bond splitting. In an exemplary embodiment of the invention, the emission radiation is selected to match a desired energy for bond breaking and/or ionization and/or for other photo-chemical and/or high temperature processes. Optionally or alternatively, the emission illumination is focused as used as a heat source.
(158) Chemical reactants may be provided and results carried away using flow systems as known in the art of photo-chemistry and chemical engineering, for example.
(159) In an exemplary embodiment of the invention, a chemical process includes, heating a body (or a cavity enclosing the body and/or formed thereof) to a temperature associated with black body emission at a transparent region of the body (in order to reduce losses) by means of thermal radiation or laser radiation. Then emitting the thermal energy using an emitter matched to a desired chemical process. Following this, or previously or simultaneously, an ingredient of the chemical process is placed in the vicinity of the lasing mode. Then, allowing the effective high temperature of the lasing mode to induce a relevant high temperature chemical process. At this time, the cavity can remain at low temperature as the average temperature of all the modes in the body and/or cavity is low.
(160) It is expected that during the life of a patent maturing from this application many relevant emitters and absorbers will be developed and the scope of these terms is intended to include all such new technologies a priori.
(161) As used herein the term about refers to 10%.
(162) The terms comprises, comprising, includes, including, having and their conjugates mean including but not limited to.
(163) The term consisting of means including and limited to.
(164) The term consisting essentially of means that the composition, method or structure may include additional ingredients, steps and/or parts, but only if the additional ingredients, steps and/or parts do not materially alter the basic and novel characteristics of the claimed composition, method or structure.
(165) As used herein, the singular form a, an and the include plural references unless the context clearly dictates otherwise. For example, the term a compound or at least one compound may include a plurality of compounds, including mixtures thereof.
(166) Throughout this application, various embodiments of this invention may be presented in a range format. It should be understood that the description in range format is merely for convenience and brevity and should not be construed as an inflexible limitation on the scope of the invention. Accordingly, the description of a range should be considered to have specifically disclosed all the possible subranges as well as individual numerical values within that range. For example, description of a range such as from 1 to 6 should be considered to have specifically disclosed subranges such as from 1 to 3, from 1 to 4, from 1 to 5, from 2 to 4, from 2 to 6, from 3 to 6 etc., as well as individual numbers within that range, for example, 1, 2, 3, 4, 5, and 6. This applies regardless of the breadth of the range.
(167) Whenever a numerical range is indicated herein, it is meant to include any cited numeral (fractional or integral) within the indicated range. The phrases ranging/ranges between a first indicate number and a second indicate number and ranging/ranges from a first indicate number to a second indicate number are used herein interchangeably and are meant to include the first and second indicated numbers and all the fractional and integral numerals therebetween.
(168) It is appreciated that certain features of the invention, which are, for clarity, described in the context of separate embodiments, may also be provided in combination in a single embodiment. Conversely, various features of the invention, which are, for brevity, described in the context of a single embodiment, may also be provided separately or in any suitable subcombination or as suitable in any other described embodiment of the invention. Certain features described in the context of various embodiments are not to be considered essential features of those embodiments, unless the embodiment is inoperative without those elements.
(169) Various embodiments and aspects of the present invention as delineated hereinabove and as claimed in the claims section below find experimental support in the following experiments.
Some Experiments and Exemplary Implementations
(170) Reference is now made to the following experimental setup in which several experiments were carried out and which together with the above descriptions illustrate some embodiments of the invention in a non limiting fashion.
(171) Referring now to
(172) In an exemplary implementation, a commercial, 125 micron diameter, SiO.sub.2 fiber tip was melted to form spherical cavities at diameters between 300 micron and 500 micron. The cavities were dipped in Yb.sub.2O.sub.3 micro crystals powder and melted again to form bodies 1004. A 2 W CO.sub.2 laser beam at 10.6 micron from a source 1002 was focused on the resonator inside an integrating sphere. Resonator emission between 400 nm and 11 micron were detected by a spectrograph 1008 and calibrated against a black body source 1010 at 1437 kelvin, which also was focused onto the integrating sphere, for calibration purposes.
(173)
(174) The broad power spectrum of doped and bare cavities, is shown at
(175) It is important to note that throughout the many excitation measurements the cavities remain stable with no evidence of melting or changing of their spectral response, this strongly suggests that the cavities, including their surfaces, did not melt and that the real temperature of the cavity and/or its surface was not at the emission temperature.
(176) Another interesting result is that experiments using YbO.sub.2 without SiO2 do not show strong emission at similar excitation levels. At very high excitation when the temperature reaches 1800 Kelvin YbO.sub.2 emission is known to be characterized by a typical black body shape with an additional peak at 980 nm.
(177) Another interesting result is the effect of removing the cavity structure. YbO.sub.2 doped SiO2 without cavity structure emits very weakly, which suggests that the use of a cavity for providing resonance may be important to enhance lasing effect or even to enhance emission efficiency. Possibly, the use of a cavity enhances emission by a factor of, for example, 2, 10, 50, 100 or greater or intermediate factors.
(178) According to measurements made, approximately 20% of the emitted photons were consistent with the high-emissivity window and 80% with black body radiation. Due to thermal losses, the total conversion efficiency appears to be about 5%, for a non-insulated system.
(179) Various variations were tried out, including using either Ytterbium or Erbium as emitter (both worked), various power levels (levels as low as 0.8 W CO2 beam power worked). In another experiment, indirect heating of the cavity as a bulk did not result in laser emission. Possibly, if the wavelength of the heating were to match the surface phonon polaritons in the cavity, emission would have resulted. Optionally or alternatively, efficiency was lower and results not detected and/or losses too high. In another embodiment, using solar radiation allows a coupling to surface phonons, as possible, for example, using a CO2 laser. In an exemplary embodiment of the invention, heating wavelengths are selected to match surface characteristics (e.g., phonons) of the cavity rather than volume.
(180)
Additional Experiments and Exemplary Implementations
(181) The additional experiments and exemplary implementations described below provide example embodiments of the invention, and serve not only to limit but also to broaden the scope of the above description.
(182) An entropy-driven tenfold up-conversion, from mid to near-infrared, at efficiency above 10% is experimentally demonstrated. This enables novel uses of thermal radiation.
(183) Introduction
(184) Frequency up-conversion of low-energy photons into a high-energy photon, greatly contributes to imaging, light sources, detection and other fields of research. However, to date, frequency up-conversion offered negligible efficiency when up-converting many photons. Thermodynamically, conventional incoherent up-conversion is driven by an internal energy of incoming photons. However, a system can also drive work through change in its collective properties, such as entropy. In the example implementation described below, an entropy-driven ten-fold up-conversion from 10.6 to 1 m at an internal efficiency above 27% and at a total efficiency above 10% is experimentally demonstrated. In addition, the emitted radiance at 1 m exceeds the Black-Body radiance of our device as expected according to its bulk temperature, indicating an emitter's effective-temperature which is considerably above the bulk-temperature. This example implementation opens the door for up-conversion of thermal-radiation, and high-temperature chemistry done at room-temperature.
(185) Traditional frequency up-conversion effects include coherent (second, third and parametric up-conversion and incoherent (two photon and multi-photon absorption) processes, yet they all offer negligible efficiency when converting many (by way of a non-limiting example 10) photons into a single high-energy photon.
(186) Some reasons for such low efficiency:
(187) i. A large frequency difference between the pump and the produced photon induces a large momentum mismatch, making phase-matching extremely challenging, while without phase-matching the nonlinear parametric up-conversion process becomes highly inefficient.
(188) ii. The nonlinear medium should be transparent at these two very different frequencies.
(189) iii. The high-order nonlinear optical susceptibility involved in a ten-fold up-conversion process is very weak, and requires long propagation distances, beyond the limit set by transparency and phase matching considerations.
(190) iv. The probability for simultaneous multi-photon interaction requires huge intensities.
(191) The above-mentioned problems are actually magnified when the radiation source is incoherent. For these reasons, the record efficiency of tenfold up-conversion to date is lower than 0.01%, which was achieved under pulse excitation at intensities of 10.sup.15 W/cm; many orders of magnitude higher than currently available continuous wave [CW] sources.
(192) To find efficient up-conversion mechanisms for partially-incoherent light, the work involved in the process of photon emission is compared to the work performed by a thermodynamic system. Here, the potential energy of each photon is defined by its chemical potential, . In such a view, absorption of an energetic photon followed by emission of a red shifted photon while releasing heat to the environment acts as an optical heat pump driven by a difference in the chemical potentials of the photons. This description is general to many light sources, and also includes the absorption of two or more pump photons to generate a single high energy photon (with lower chemical potential than the sum of the pump photons). However, in addition to this mechanism, which is energetically balanced at the single excitation-emission level, collective properties of the system can also drive work. The amount of work a system can produce is limited by the change in its Gibbs free energy, G: dG=d[PVTS+N]. Here P, V, T and S are collective properties of the system: P is pressure, V is volume, T is temperature, S is the entropy which is proportional to the number of populated states in the system, and N is the sum of the chemicals potentials.
(193) In many optical systems P and V are constant, thus the change in PV can be excluded from generating work. An exception to this general rule is the phenomenon of Sonoluminescence, where UV emission is generated as sound is converted into light through a drastic change in PV.
(194) To the best of the inventors' knowledge, the change in the temperature and entropy of a system, TS, has never been used for frequency up-conversion. Below it is shown how to utilize the change in TS for an efficient tenfold frequency up-conversion.
(195) For lasers, entropy relates to the spatial and temporal coherences. As the entropy is lower, the laser coherence is higher and the Gibbs free energy is higher, allowing higher light concentration. Such a radiation source has a high Brightness-temperature, which is defined as radiance in a specific wavelength which is equal to a Black-Body radiance at the same temperature and the same wavelength. The term radiance refers to the amount of radiation power per wavelength per solid-angle per area. Such a high brightness-temperature radiation, if absorbed under perfect conditions, can equate a target's temperature to the brightness-temperature.
(196) A thought experiment involving this concept is a use of a laser to heat a highly emissive body in order to increase its temperature, thereby enhancing its Black-Body radiation. Consider for example, a single-mode CO.sub.2 laser at 100 W of optical power heating a thermally-insulated emissive body to the temperature of the sun (5800K), resulting in thermal radiation similar to solar radiance. In such a temperature, most of the generated photons are in the visible and near-infrared wavelength range, which have more than tenfold enhancement in internal-energy compared to the pump CO.sub.2 photons at 10.6 wavelength. However, although this concept can be highly efficient up-conversion mechanism, it is challenging to realize because there are no materials that remain stable at the temperature of the sun. Also, the broad thermal emission of black body radiation is less attractive for many applications, such as communication and detection where information is frequency-dependent. A much better device should operate at a reasonable temperature, for example room temperature, and preferably emit spectrally narrow up-converted light.
(197) An example embodiment uses a high brightness-temperature source, such as a laser, to excite only specific modes to a high effective-temperature, while the bulk remains at a relatively low temperature. Although under such non-equilibrium conditions the term temperature is not well defined, Effective-temperature describes a population of a specific phonon-mode which corresponds to Boltzmann's thermal population at that temperature. An emitter which is coupled to these excited modes, shares their effective-temperature, and emits a spectrally narrow radiation at a high brightness-temperature, considerably higher than its bulk temperature. Thus far, utilizing such ideas for frequency conversion have not been explored.
(198) In photoluminescence, the absorption of an energetic photon is followed by heat dissipation, and emitting of a Stocks shifted photon. A reduction in internal-energy between the absorbed and emitted photos corresponds to the change in Gibbs free energy that drives the process. In the example embodiment described herein the high internal-energy of the incoming photon is replaced with high free-energy of the incoming photons, embedded in their entropy (high Brightness temperature) rather than their internal-energy. This allows a spontaneous process, a reduction in free-energy, to support up-conversion.
(199) Reference is now made to
(200)
(201) To experimentally demonstrate the concept illustrated by
(202) Reference is now made to
(203)
(204)
(205)
(206)
(207) The resonator's radiance is measured at the near-infrared [NIR] under excitation of 684 mW. The emission image is captured using a Si CCD camera, (detecting wavelengths shorter than 1.10 in order to gain information about the spatial distribution of the radiation, which is used for calculating the radiance.
(208) The power spectrum at the NIR region is measured using the calibrated integrating sphere. Normalizing the power spectrum with the emission area gives a minimal value for isotropic radiance. The measured radiance is compared with the Black-Body and Yb.sub.2O.sub.3 radiances at 1650 C, which is the melting point of SiO.sub.2, hence serving as an upper limit for the device stability.
(209) Results:
(210) Reference is now made to
(211)
(212)
(213)
(214)
(215)
(216)
(217)
(218)
(219)
(220) Furthermore, the emission at 980 nm contains 27% of the total emission power, and 1% of the total input power deposited into the system. Such efficiency is many orders of magnitude better than any existing art the inventors are aware of. In fact, more than an order of magnitude enhancement in Ytterbium emission under partial pressure of 300 mbar, measured through a vacuum chamber window is observed. This indicates a total conversion efficiency in excess of 10%.
(221) Discussion:
(222) Some evidence for high effective-temperature of the Yb.sub.2O.sub.3 is now described:
(223) i. At the infra-red wavelength (5-10) where silica is highly emissive, its thermal emission fits a Black-Body radiation at just below melting temperature, 1650 C. This evidence reflects a true temperature of the resonator near thermodynamic equilibrium, also evident by the stability of the device, which does not melt.
(224) ii. At this temperature, in thermodynamic equilibrium, most of the thermal energy is at wavelengths longer than 1 m. This doesn't appear in the example embodiment described above. The emission exhibits a sharp single peak.
(225) iii. The radiance of the Yb.sub.2O.sub.3 is four times the Black Body radiance at 1650 C, which is the maximal possible radiance under thermodynamic equilibrium.
(226) Without being limited to theory, the above three observations may be proof that Yb.sub.2O.sub.3 is at a considerably higher Brightness-temperature than the bulk.
(227) Some conditions which are suggested in order to reach high Yb.sub.2O.sub.3 brightness-temperature: i. Pump source at high brightness-temperature. This condition is easily matched, by way of a non-limiting example, with a CO.sub.2 laser, optionally operating at a single (or few) emission modes, at a brightness-temperature in the order of 10.sup.10 C.
(228) ii. The excitation rate to a set of modes preferably exceeds their dumping rate to other modes; This condition can be met by, for example, the high absorption cross-section of SiO.sub.2, which absorbs the 10.6 CO.sub.2 laser radiation within a depth of less than a wavelength from the surface, possibly through its vibronic-states.
(229) iii. The Yb.sub.2O.sub.3 is preferably efficiently coupled to vibronic-states. This condition is satisfied, by way of a non-limiting example, by rare-earths. Furthermore, Yb.sub.2O.sub.3 radiation is enhanced by Purcell's effect of the high-Q WGM.
(230) In some embodiments described herein, the target for absorbing radiation and up-converting the radiation was placed under vacuum.
(231) In some embodiments described herein, the target for absorbing radiation and up-converting the radiation was placed under partial vacuum, for example a partial pressure of 300 mBar as described above. In some embodiments the partial pressure values are 500 mBar and below.
(232) The inventors believe that placing the target under vacuum or partial pressure possibly reduces energy loss from the target, such as thermal losses.
(233) To summarize, the above example described a frequency up-conversion mechanism, and experimentally demonstrated an efficient tenfold frequency up-conversion driven by entropy.
(234) The example potentially opens new directions in various fields.
(235) In solar energy for example, an embodiment of the invention potentially opens efficient ways for up-converting sub-bandgap solar photons to wavelengths where photovoltaics are more efficient.
(236) In another example, the possibility to excite modes to a very high effective-temperature while the bulk remains at low temperature enables hot chemistry carried out at much lower temperatures such as room temperature. Examples of hot chemistry include conversion of sunlight into stored chemical energy, by employing a high temperature endothermic thermo-chemical response such as MgOMg redox, which exhibits energy recovery above 42%.
(237) Each of the above examples potentially revolutionizes the ability to harvest the sun's energy for humanity needs.
(238) Methods:
(239) 1. Sample Preparation:
(240) Commercial 125 fibers (Thorlabs) were positioned in the focus of a 20 W CO.sub.2 laser (Synrad). The fiber tip was melted and fed into the focal point until the formation of a sphere, as seen under a microscope. The Sphere was subsequently dip-coated in a methanol:Yb.sub.2O.sub.3 nano-crystal suspension (1 ml methanol:100 mg Yb.sub.2O.sub.3), and then melted again by a short laser exposure of about half a second to smooth the surface of the sphere. For smaller spheres fabrication, the fibers were etched in an HF solution until the desired diameter was reached, prior to the melting process.
(241) 2. Optical Measurements:
(242) A sample's radiance was measured by placing the sample in a white integrating sphere (LabSphere) for the NIR range and in a self-designed gold coated sphere for the IR range. A CO2 laser (Access lasers) at various intensities with stability of 2% was focused onto the sample by a gold parabolic mirror and ZnSe lens. In addition, a 1200 C calibrated black-body source (CI-systems) was focused inside the sphere for calibration purposes. The luminescence signals were chopped by an optical chopper (Stanford Research Systems) and amplified by a lock-in amplifier (Stanford Research Systems), after passing through a spectrograph equipped with appropriate gratings for the different spectral ranges (Oriel Instruments). In the NIR region signals were measured by a Ge detector (Judson Technologies), and an InGaAs camera (Andor Technology). In the IR region between 2 m and 10 m, the signal was detected using InSb and MCT (InfraRed Associates) detectors.
(243) For measurements under vacuum, samples were put in a Dewar with optical windows connected to a vacuum system. The laser was focused onto the sample through a ZnSe window. The luminescence signal was measured by imaging the sample through the Dewar window onto the spectrograph equipped with a spectroscopic InGaAs camera.
(244) General
(245) Although the invention has been described in conjunction with specific embodiments thereof, it is evident that many alternatives, modifications and variations will be apparent to those skilled in the art. Accordingly, it is intended to embrace all such alternatives, modifications and variations that fall within the spirit and broad scope of the appended claims.
(246) All publications, patents and patent applications mentioned in this specification are herein incorporated in their entirety by reference into the specification, to the same extent as if each individual publication, patent or patent application was specifically and individually indicated to be incorporated herein by reference. In addition, citation or identification of any reference in this application shall not be construed as an admission that such reference is available as prior art to the present invention. To the extent that section headings are used, they should not be construed as necessarily limiting.