Method for production of quantum rods with precisely controllable wavelength of emission

Abstract

A method for fabricating quantum rods includes: preparing a Cd-precursor; preparing a S-precursor and CdSe seeds; preparing a Zn-precursor; mixing the S-precursor and the CdSe seeds with the Cd-precursor in a reaction mixture; adding the Zn-precursor to the reaction mixture; stopping the reaction; and performing a purification process to obtain the quantum rods.

Claims

1. A method for fabricating quantum rods, comprising: preparing a Cd-precursor; preparing an S-precursor and CdSe seeds; preparing a Zn-precursor; mixing the S-precursor and the CdSe seeds with the Cd-precursor in a reaction mixture to initiate CdS shell growth over the CdSe seeds; after initiating the CdS shell growth, adding the Zn-precursor to the reaction mixture; stopping the reaction; and performing a purification process to obtain the quantum rods.

2. The method according to claim 1, wherein the method further comprises adding additional S-precursor to the reaction mixture after initiating the CdS shell growth.

3. The method according to claim 2, wherein adding the additional S-precursor to the reaction mixture is performed in multiple steps.

4. The method according to claim 1, wherein adding the Zn-precursor causes a blue shift of emission wavelength.

5. The method according to claim 4, Wherein the blue shift is in the range of 10 nm to 150 nm.

6. The method according to claim 1, wherein the turn rods have an emission wavelength of less than or equal to 530 nm.

7. The method according to claim 1, wherein the quantum rods have an emission wavelength of less than or equal to 470 nm.

8. The method according to claim 1, wherein the quantum rods have thermally stable integral intensity of emission in a 0-200 C. temperature range.

9. The method according to claim 1 wherein the S-precursor and the CdSe seeds are prepared as a combined stock solution.

10. The method according to claim 1, wherein the S-precursor and the CdSe seeds are prepared as separate stock solutions.

11. The method according to claim 1, wherein mixing the S-precursor and the CdSe seeds with the Cd-precursor comprises injecting the S-precursor and the CdSe seeds into a reaction mixture comprising the Cd-precursor to initiate a reaction between the Cd-precursor with the CdSe seeds and the S-precursor.

12. The method according to claim 11, wherein the reaction mixture comprises a solvent at a temperature greater than 300 C.

13. The method according to claim 1 wherein the Zn-precursor is of general formula Zn(RCOO).sub.2.

14. The method according to claim 13, Wherein R is alkyl group C.sub.nH.sub.2n+1 with n being in the range of 0 to 30 or wherein R is a branched alkyl or alkenyl group or a branched carbon chain of total length in the range of 5 to 22 carbon atoms comprising two or more double or triple bonds.

15. The method according to claim 1, wherein the Zn-precursor is an individual chemical compound or a mixture of organic compounds.

16. The method according to claim 1, wherein the Zn-precursor comprises zinc salt or zinc oleate.

17. The method according to claim 1, wherein adding the Zn-precursor to the reaction mixture comprises adding the Zn-precursor to the reaction mixture in multiple steps.

18. The method according to claim 1 wherein the purification process comprises one or more precipitation-redispersion sequences.

19. A method for fabricating blue-shifted quantum rods, comprising: preparing quantum rods comprising a CdSe seed and a CdS blue-shifting the emission wavelength of the prepared quantum rods by reacting the prepared quantum rods with a Zn-precursor and an S-precursor; stopping the reaction; and performing a purification process to obtain the blue-shifted quantum rods.

20. The method according to claim 19, wherein the blue-shifted quantum rods have an emission wavelength of less than or equal to 530 nm.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 depicts an exemplary general scheme for the fabrication of quantum rods with a high degree of control for the emission wavelength of the quantum rods.

(2) FIG. 2 depicts emission anisotropy of quantum rods having a rod-in-rod structure (top three curves) and quantum rods having a dot-in-rod structure (bottom three curves).

(3) FIG. 3 depicts an exemplary process for fabrication of Zn-doped quantum rods in accordance with an exemplary embodiment of the present invention.

(4) FIG. 4 depicts the evolution of emission spectra for quantum rods during synthesis in accordance with Example 1 (part a of FIG. 4) and Example 2 (part b of FIG. 4), corresponding to excitation by a 405 nm laser. The arrows indicate the blue shift of emission during the synthesis.

(5) FIG. 5 depicts the kinetics of emission spectra evolution in accordance with Example 1 (part a of FIG. 5), Example 2 (part b of FIG. 5) and Example 3 (part c of FIG. 5).

(6) FIG. 6 depicts transmission electron microscopy (TEM) images of quantum rods obtained from the purification of Pr3 of Example 1 (part a of FIG. 6), from the final product of Example 1 (part b of FIG. 6), from the final product of Example 2 (part c of FIG. 6), from the Pr2 of Example 3 (part d of FIG. 6), from the Pr11 of Example 3 (part e of FIG. 6), and from the final product of Example 3 (part f of FIG. 6)

(7) FIG. 7 depicts the size distribution of nanoparticles obtained from the purification of Pr3 of Example 1 (parts a-b of FIG. 7), from the final product of Example 1 (parts c-d of FIG. 7), and from the final product of Example 2 (parts e-f of FIG. 7).

(8) FIG. 8 depicts results of a thermogravimetrical analysis (TGA) performed with respect to a final purified product from Example 1. The 801 curve corresponds to mass lost, and the 802 curve corresponds to the mass loss derivative.

(9) FIG. 9 depicts a comparison of green QRs obtained without Zn-precursor (part a of FIG. 9) and with Zn-precursor (part b of FIG. 9).

(10) FIG. 10 depicts an exemplary laboratory installation for the synthesis of quantum rods. The laboratory installation includes an electronic thermocontroller (left), a heating source and a magnetic stirrer (bottom), a condenser trap with inert gas/vacuum supply (top), and a glass syringe with stainless steel needle (right).

(11) FIGS. 11A-11D depict the evolution of luminescence spectrum at different heat levels (FIGS. 11A-11B), temperature dependence of integrated emission intensity (FIG. 11C) and temperature dependence of FWHM (FIG. 11D) for quantum rods enriched with Zn (corresponding to Pr11 from Example 3) and enriched with Cd (corresponding to Pr3 from Example 3).

DETAILED DESCRIPTION

(12) Exemplary embodiments of the present invention provide a method to fabricate quantum rods, which is more reliable in terms of emission wavelength control than the current state of the art. Exemplary embodiments of the present invention further provide an efficient, detailed, convenient and reproducible method for production of quantum rods with precise control of emission wavelength in a broad range.

(13) In an exemplary embodiment, the present invention provides a method for production of core-shell semiconductor nanoparticles of an elongated shape (also called quantum rods), which are characterized by very large (e.g., up to 100 nm or more) blue shift of emission wavelength during synthesis, and wherein the synthesis is slow and gradual enough to stop the reaction precisely at a desired value of .sub.em within this shift. The method is convenient and reproducible, and the method provides very uniform quantum rods with low size distribution, high quantum yield and enhanced stability with respect to the environment (taking advantage of treatment with [Zn]). The method makes possible to synthesize truly green (<530 nm) and blue (<470 nm) emitting quantum rods which are highly desirable for display and LED applications.

(14) Exemplary embodiments of the present invention will be discussed herein in further detail, including, for example, amounts of reagents/solvents, composition, an addition method for a Zn-precursor, and quantum rod isolation/purification procedures. It will be appreciated that these exemplary embodiments are merely exemplary and non-limiting, and that one of ordinary skill in the art may derive other embodiments based thereon without departing from the inventive principles.

(15) In an exemplary embodiment, the present invention provides a method for production of quantum rods with precisely controllable emission wavelength. The method includes: preparation of a Cd-precursor for shell growth; preparation of stock solution(s) of S-precursor and of CdSe seeds either as one solution or as separate solutions; preparation of a Zn-precursor of general formula Zn(RCOO).sub.2; initiating a reaction by fast injection (e.g., continuous injection which is completed in less than a few seconds) of the combined mixture of S-precursor and the seeds or separately of the seeds solution followed by the S-precursor solution to a reaction mixture with the prepared Cd-precursor in an appropriate solvent (i.e., a solvent which dissolves the reactants) at a high temperature for initiation of the shell growth (e.g., >300 C. to initiate growth of CdS material); single or multiple addition(s) of the Zn-precursor of general formula Zn(RCOO).sub.2 (e.g., in solid form) or a solution of the same to the reaction mixture; further single or multiple addition(s) of S-precursor when large blue shift (>35 nm) and/or increased reaction rate is/are desired; stopping the reaction at a time when desired emission properties are reached; and performing a purification procedure.

(16) In a further exemplary embodiment, within the general formula for the Zn-precursor, R is alkyl group C.sub.nH.sub.2n1 with n being in the range of 0 to 30.

(17) In a further exemplary embodiment, within the general formula for the Zn-precursor, R is a carbon chain of total length in the range of 5 to 22 carbon atoms comprising two or more double or triple bonds. For example, R may be alkenyl group A-CHCHB wherein independently A is a hydrogen (H) atom or an alkyl group C.sub.nH.sub.2n1.sub. with n in the range of 0 to 16 and B is either absent or is an alkylene group (CH.sub.2).sub.n wherein n is in the range of 0 to 16.

(18) In a further exemplary embodiment, within the general formula for the Zn-precursor, R is a branched alkyl or alkenyl group or a branched carbon chain of total length in the range of 5 to 22 carbon atoms comprising two or more double or triple bonds.

(19) In a further exemplary embodiment, the Zn-precursor is an individual chemical compound.

(20) In a further exemplary embodiment, the Zn-precursor is a mixture of organic compounds.

(21) In a further exemplary embodiment, the Cd-precursor is prepared from Cd-containing derivatives and alkylphosphonic acids. For example, the Cd-precursor may be prepared from CdO and alkylphosphonic acids in a molar ratio wherein Cd to total phosphonic acids quantity is 1:2 in a solvent having a high boiling point (e.g., >300 C.). In another example, the Cd-precursor may be prepared from CdO and alkylphosphonic acids of general formula C.sub.nH.sub.2n+1PO.sub.3H.sub.2 wherein n is in the range of 6 to 18.

(22) In a further exemplary embodiment, the S-precursor is prepared separately by dissolving the elementary sulfur in appropriate solvents. In an example, the appropriate solvents may be heavy alkanes (C.sub.14-C.sub.22), 1-octadecene, trialkylphosphines, trialkylphosphinoxides, and glicerole trialkanoates individually or in different combinations thereof.

(23) In a further exemplary embodiment, the Zn-precursor is a solution of zinc salt or a mixture thereof with high boiling solvents. In an example, the high boiling solvents are heavy alkanes (C.sub.14-C.sub.22), 1-octadecene, trialkylphosphines, trialkylphosphinoxides, glicerole trialkanoates individually or in different combinations thereof.

(24) In a further exemplary embodiment, the Zn-precursor is a solution of zinc oleate in 1-octadecene.

(25) In a further exemplary embodiment, the Zn-precursor is added to the reaction mixture after initiating of CdS shell growth.

(26) In a further exemplary embodiment, the Zn-precursor is added to the reaction mixture in a range from 1 s to 1000 min after initiating of CdS shell growth.

(27) In a further exemplary embodiment, wherein after addition of the Zn-precursor, the reaction is allowed to proceed for a duration in a range from 1 min to 10,000 mins prior to terminating the reaction.

(28) In a further exemplary embodiment, a Zn/Cd feed ratio is in the range 0.1 to 10.

(29) In a further exemplary embodiment, the shift of emission wavelength of the resulting quantum rods to shorter wavelengths during the synthesis is in the range 10-150 nm.

(30) FIG. 1 depicts an exemplary general scheme for the fabrication of quantum rods having Cd.sub.xZn.sub.1xS shells (wherein x is in the range of 0 to 0.99) with a high degree of control for the emission wavelength of the quantum rods. In particular, FIG. 1 depicts exemplary processes for obtaining two types of core-shell quantum rods: dots in rods (top part) and rods in rods (bottom part). One of ordinary skill in the art will appreciate that the seeds for both types (dot and rods) can be obtained according to known methods, and that these seeds are covered with organic ligands (such as alkyl phosphoric acids, trioctylphosphine oxide, alkylamines, long-chain carboxylic acids, etc.) and can form stable colloids in non-polar organic solvents (e.g., toluene, chloroform, hexane, octadecene).

(31) With reference to FIG. 1: AlkPO.sub.3H.sub.2 is a single compound or a mixture of different alkylphosphoric acids. Alk is the alkyl group CH.sub.3(CH.sub.2).sub.n with n in the range of 2 to 20 (or from 3 to 18, or from 6 to 16). x is the atom index of [Cd] atoms in the stoichiometric formulas for the shell material and is in the range of 0 to 0.99 (or from 0.95 to 0.05, or from 0.75 to 0.25). Alk.sub.3PS and Alk.sub.3PSe are trialkylphosphine sulfide and trialkylphosphine selenide, respectively. L is an average length of the quantum rods and in the range of 10 to 100 nm (or from 15 to 80 nm, or from 20 to 50 nm). d is an average diameter of the quantum rods and in the range of 3 to 15 nm (or from 4 to 10 nm, or from 5 to 8 nm). The shape of the quantum rods is depicted schematically. It will be appreciated that different shapes are possible, such as an ellipsoid shape, a cylinder shape, etc. The shape satisfies the condition L>d. The Zn-precursor is a source of [Zn] atoms and may be a derivative of zinc carboxylates of general formulae Zn(RCOO).sub.2, wherein R is: alkyl group CH.sub.3(CH.sub.2).sub.n with n in the range of 0 to 30 (or from 0 to 18); alkenyl group A-CHCHB wherein independently A is a hydrogen (H) atom or an alkyl group CH.sub.3(CH.sub.2).sub.n with n in the range of 0 to 16 and B is absent or is an alkylene group (CH.sub.2).sub.n wherein n is in the range of 0 to 16; a carbon chain of a total length in the range of 5 to 22 carbon atoms comprising two or more double or triple bonds; or a branched alkyl or alkenyl group or a branched carbon chain of a total length in the range of 5 to 22 carbon atoms comprising two or more double or triple bonds. The Zn-precursor is an individual chemical compound or a mixture with other organic compounds (which may be low melting organic compounds, or which may be aliphatic, aromatic or long-chain alkenes and/or long chain alkylcarbxylic and/or alkenylcarboxylic acids).

(32) It will be appreciated that in the case where x=0, the CdZnS shell may be referred to as a ZnS shell.

(33) As depicted in FIG. 2, rods-in-rods nanoparticles show a higher degree of emission anisotropy relative to dots-in-rods nanoparticles.

(34) FIG. 3 depicts an exemplary process for fabrication of Zn-doped quantum rods in accordance with an exemplary embodiment of the present invention.

(35) At stage 301, a Cd-precursor for the shell growth is prepared. The Cd-precursor may be prepared, for example, from CdO and alkylphosphonic acids of appropriate length in a molar ratio Cd to total phosphoric acids quantity no less than 1:2 in a solvent having a high boiling point. For example, a coordinating high boiling solvent may be used, such as trioctylphosphine oxide.

(36) At stage 302, a stock solution of S-precursor and of CdSe seeds is prepared as one stock solution, or stock solutions of S-precursor and of CdSe seeds are prepared as separate solutions. A stock solution of S-precursor may be prepared by dissolving elementary sulfur in an appropriate high boiling solvent such as long-chain alkanes (C.sub.14-C.sub.22), 1-octadecene, or trioctylphosphine. In an exemplary implementation, trioctylphosphine may be preferred since the formed trioctylphosphine sulfide possesses an appropriate reactivity toward cadmium alkylphosphonates to form a CdS shell of elongated shape. The CdSe seeds can be either added to the stock solution of S-precursor or prepared separately by dissolving the CdSe seeds in an appropriate solvent.

(37) It will be appreciated that with respect to stages 301 and 302, the amounts of CdO, phosphonic acids, solvents, sulfur, and seeds can be varied while still achieving good results with respect to preparation of quantum rods in accordance with exemplary embodiments of the present invention (see, e.g., Examples 1-3 discussed below).

(38) At stage 303, a Zn-precursor is prepared. Zn-precursors can be prepared in different ways.

(39) In one exemplary embodiment, the Zn-precursor is a solution of zinc salt in an organic solvent. It can be prepared from ZnO and carboxylic acid by heating of both reactants in organic solvent at >300 C. for a few hours in an inert atmosphere. Examples of zinc salt and organic solvent are zinc oleate and 1-octadecene.

(40) In another exemplary embodiment, the Zn-precursor is zinc salt which is isolated from solution prepared from ZnO and carboxylic acid by heating of both reactants in organic solvent at >300 C. for a few hours in an inert atmosphere. The isolation step can be performed by filtration of reaction mixture at r.t. or by evaporation of organic solvent in a vacuum. The isolated zinc salt can be dissolved in organic solvent for use in synthesis of quantum rods or can be used as is in solid form.

(41) In yet another exemplary embodiment, the Zn-precursor is zinc salt obtained via an exchanged reaction between Zn salt of lower boiling carboxylic acid (e.g., zinc acetate) and higher boiling carboxylic acid (e.g., oleic acid or stearic acid).

(42) The concentration of Zn salt in a solution can be varied. An exemplary concentration of Zn salt in the solution may be 0.1-5.0 mmol/g, or may be 0.2-1.0 mmol/g.

(43) At stage 304, a fast injection is performed of the seeds and the S-precursor to the Cd-precursor at high temperature (>300 C.) for initiation of the growth of a CdS shell of elongated shape over the CdSe seeds. In the case where separate solutions of seeds and S-precursor are used, the seeds solution is injected first followed by injection of the S-precursor solution.

(44) At stage 305, the Zn-precursor is added to the reaction mixture after the injection of the seeds and the S-precursor. Additional S-precursor may also be added to the reaction at stage 305. The addition of Zn-precursor into the reaction mixture containing CdSe/CdS quantum rods may be performed in a single step or multiple steps. The addition of S-precursor into the reaction mixture containing CdSe/CdS quantum rods may also be performed in a single step or multiple steps.

(45) In one exemplary embodiment, the Zn-precursor is added to reaction mixture immediately after the injection of seeds and S-precursor. In another exemplary embodiment, the Zn-precursor is added some time after the injection (e.g., in the range of 1 s to 180 mins after the injection).

(46) The rate and duration for the addition of the Zn-precursor can be varied. A rate for the addition of the Zn-precursor which minimizes temperature deviations may be preferrede.g., the Zn-precursor may be added at a slow rate over a 1-20 min duration.

(47) The amount of Zn-precursor that is added at stage 305 can vary. However, it should noted that in accordance with exemplary embodiments of the present invention, a small amount of Zn may result in a significant blue shift of absorption. For instance, as demonstrated with respect to Examples 1-3 discussed below, a Zn/Cd molar ratio of 1.57 resulted in blue shifts of 24 nm and 27 nm, respectively. In case of synthesis of blue emitting quantum rods, a Zn/Cd molar ratio was about 4.57 which results in blue shift of 102 nm.

(48) Immediately after the injection of S-precursor and seeds at stage 304, emission wavelength begins shifting towards longer wavelengths at a fast rate. The shift towards longer wavelengths then slows down, and after a certain amount of Zn-precursor (around 1 equivalent to Cd) is added, the emission wavelength starts to slowly shift the other way towards shorter wavelengths. This shift towards shorter wavelengths (also referred to as a blue shift) may be large (e.g., 10-150 nm), and happens slowly enough for a probe to be taken to measure a luminescence wavelength and quench the reaction at stage 306 when the emission wavelength reaches the desired emission wavelength. The foregoing principles are demonstrated with respect to Examples 1-3 and depicted in FIGS. 4-5.

(49) The Zn-precursor can be added into the reaction mixture containing CdSe/CdS quantum rods in a single step or multiple steps. The single addition of Zn-precursor to the reaction mixture containing CdSe/CdS quantum rods provides blue shift of around 30-40 nm. Multiple addition of Zn-precursor results in further blue shift of the emission wavelength for more than 30 nm up to around 50 nm. Moreover, the addition of S-precursor enlarges the blue shift to around 100 nm (see Example 3 for multiple additions of Zn- and S-precursors). The addition(s) of Zn- or S-precursors can be performed in any combination.

(50) Utilizing the Zn-precursor during the synthesis of the quantum rods also results in an increase of luminescence quantum yield due to improvement of CdS shell crystallinity by reducing the amount of charge/exciton surface traps (as demonstrated in Example 1 discussed below).

(51) The size and shape of the particles do not change significantly during Zn addition (compare part a of FIG. 6 to part c of FIG. 6 and compare part d of FIG. 6 to parts e-f of FIG. 6, and compare parts a-b of FIG. 7 to parts c-d of FIG. 7), but a blue shift of emission occurs.

(52) At stage 306, after reaching the desired emission properties of the quantum rods, the reaction is quenched, for example, via cooling (e.g., by addition of a cold solvent to the reaction mixture and/or by removing the heating source).

(53) The timing for terminating the reaction may vary based on the desired properties for the final product. In one exemplary embodiment, the reaction is immediately terminated after addition of Zn-precursor. In other exemplary embodiments, after addition of Zn-precursor, the reaction is allowed to proceed with a further blue shift of emission wavelength to the desired emission wavelength. In another exemplary embodiment the reaction is terminated after multiple additions of Zn-precursor or after multiple additions of Zn- and S-precursors. The time of reaction may varyfor example, it may take 30-120 mins after addition of Zn-precursor to reach a desired blue shift of emission wavelength of 10-30 nm depending on the reaction conditions and seed size. In other exemplary embodiments a blue shift of up to around 450 nm can occur within 16-20 hours depending on reaction rate which can be controlled by amounts of Zn- and S-precursors added.

(54) At stage 307, purification of the final product (e.g., quantum rods) is performed via one or more precipitation-redispersion sequences. For precipitation, polar solvents (such as alcohols, ketones, etc.) may be used. The solvent used for precipitation should mix well with the reaction solvent and be able to dissolve organic impurities, starting materials, and other contaminations. For isolation of quantum rods from this mixture, centrifugation or filtration can be used. After isolation, the quantum rods are then dissolved in a weakly polar solvent (such as aromatic and aliphatic hydrocarbons, chlorinated alkanes, etc.), which results in a solution of quantum rods being obtained. The latter can be purified again (to remove contaminates that may still remain) by performing another precipitation procedure and another centrifugation (or filtration) procedure. Sonication may be used to speed up the process of dissolution of reaction product.

(55) The separation of the final quantum rods from the reaction mixture can be performed by a normal procedure of precipitation/dissolving. For example, the reaction mixture can be diluted by toluene or another appropriate weak-polar solvent (benzene, chlorobenzene, etc.), and a polar solvent (like methanol, ethanol, acetone) can be added for precipitation of quantum rods. The quantum rods can be collected either by filtration or centrifugation and can be also further washed with appropriate solvent (e.g., toluene, benzene, chlorobenzene, etc.) following by precipitation and collection of the precipitate of quantum rods.

(56) In another exemplary alternative embodiment, instead of adding Zn-precursor to a reaction mixture in stage 305, CdSe/CdS quantum rods can be separated from a reaction mixture after stage 304, dissolved in an appropriate high boiling solvent (e.g. TOPO, ODE, TOP) and further treated with Zn-precursor and S-precursor. The obtained CdSe/CdS quantum rods can be dissolved in a high boiling solvent, degassed via flushing with inert gas, heated to temperature above 270 C. (preferably above 300 C. or above 340 C.), and Zn-precursor can be added. To increase blue shift and/or reaction rate, S-precursor can be added either before or after addition of Zn-precursor. Multiple additions of Zn- and S-precursor can be performed.

(57) In alternative exemplary embodiments, already-prepared CdSe/CdS quantum rods obtained by any other methods can be treated with Zn-precursor and/or S-precursor for controllable blue shift of emission wavelength. In this case, the process would start with the already-prepared CdSe/CdS quantum rods being mixed with Zn-precursor (and extra S-precursor) in a reaction mixture and/or by injection(s) of Zn-precursor (and extra S-precursor) to the reaction mixture comprising CdSe/CdS quantum rods.

(58) The result of the process of FIG. 3 provides a final product of highly uniform quantum rods (see, e.g., FIGS. 6-7), stabilized with an organic ligand shell and almost free of impurities. The quantum rods can be dissolved in non-polar organic solvents.

(59) The methods disclosed herein provide high reproducibility in terms of emission wavelength, shape, and size of the fabricated quantum rods. Quantum rods in accordance with the foregoing exemplary embodiments have better thermal/chemical stability in comparison to quantum rods without doping with Zn. The method makes possible the synthesis of quantum rods with emission in entire visible spectral range, including fully blue and green regions, which is not achievable by other colloidal methods for fabrication of seeded highly bright luminescent quantum rods (i.e., those in the absence of Zn-precursor).

(60) Exemplary products achievable via the described methods include:

(61) 1. Quantum rods having a dot-in-rod structure with a Cd.sub.yZn.sub.1ySe seed and a Cd.sub.xZn.sub.1xS shell, wherein y is in the range from 0 to 1 and x is in the range from 0 to 0.99; and

(62) 2. Quantum rods having a rod-in-rod structure with a Cd.sub.yZn.sub.1ySe seed and a Cd.sub.xZn.sub.1xS shell, wherein y is in the range from 0 to 1 and x is in the range from 0 to 0.99.

(63) At the initial stage of Zn-precursor addition, only the shell is affected by the addition of Zn, resulting in gradual decrease of Cd and an increase of Zn in the shell composition, which corresponds to a gradual change of index x from 1 (no Zn in the shell) to 0 (all Cd is replaced with Zn). As the reaction progresses, the CdSe seed may also be affected by the addition of Zn, resulting in either a decrease of initial CdSe seed size or a decrease of Cd and an increase of Zn in the seed composition which corresponds to a gradual change of index y from 1 (no Zn in the seed) to 0 (all Cd is replaced with Zn in the seed).

(64) FIGS. 11A-11D shows enhanced thermal stability of the photoluminescence for Zn-doped quantum rods obtained by exemplary embodiments of the invention. It is clearly seen that the quantum rods treated with Zn-precursor, in comparison to quantum rods not treated with Zn-precursor, show stable PL properties up to 200 C., which is highly desired for LED applications (e.g., for on-chip architecture wherein the temperature can approach 150 C. or more). The obtained quantum rods are, in general, more homogeneous in terms of size and aspect ratio (see example in FIG. 9). Furthermore, the exchange of Cd with Zn is more favorable from an environmental perspective and a market perspective, in terms of lower toxicity of the obtained materials.

(65) The following examples (Examples 1-3) further illustrate exemplary implementations of the present invention and demonstrate exemplary advantages achieved thereby. It will be appreciated that the following examples are exemplary and should not be construed as limiting the scope of the present invention.

(66) As demonstrated in connection with Example 1 and FIG. 8, exemplary embodiments of the present invention are able to achieve a mass loss of no more than 20%, which is a typical mass fraction of organic ligands for CdSe/CdS quantum rods.

(67) It was further demonstrated in connection with Examples 1-2 that exemplary embodiments of the present invention are able to achieve a coefficient of variance (COV) (defined as COV=(standard deviation/average size)*100%) of less than 10%, which advantageously provides a narrow particle size distribution.

(68) It was also further demonstrated in connection with Examples 1-3 that, according to exemplary embodiments of the present invention, the quantity of Zn-precursor (the ratio Zn/Cd) needed for significant gradual blue shift of emission wavelength during synthesis can be relatively small. Increasing the amount of added Zn-precursor would increase the blue shift of the emission wavelength due to the larger degree of replacement of Cd with Zn atoms in the composition of the quantum rods.

(69) In addition to Examples 1-3, a control product was fabricated using the same reaction conditions for CdSe/CdS fabrication (including the ratios between reagents, temperature, the same seeds as in Example 1, concentrations, volumes, laboratory setup, etc.), but without the addition of Zn-precursor. In this synthesis, the reaction was terminated when the emission wavelength reached approximately the same value as for final product in example 1. As can be seen from the TEMs and plots in FIG. 9, the control QRs (part a of FIG. 9) had nearly the same emission wavelength as the QRs of Example 1 (part b of FIG. 9), had shorter size (13 nm on average vs. 26 nm on average), and large size distribution (12% COV vs. 8% COV). This demonstrates that the addition of the Zn-precursor allows for preparation of more uniform QRs with emission in green and blue spectral ranges.

Example 1

(70) Example 1 provides an example for synthesis of a Zn-precursor and controlled synthesis of core-shell quantum rods using the Zn-precursor.

(71) At a preliminary stage, the Zn-precursor was prepared as follows. A mixture of ZnO (Merger, 99%, 3.22 g, 123 mmol), oleic acid (Sigma, 85%, 71.1 g, 252 mmol) and 1-octadecene (Sigma, 90%, 100 ml) were degassed at reduced pressure (10-20 mbar) at 130 C. for 90 min with vigorous stirring, followed by five cycles of pumping out and filling with inert gas (nitrogen) sequence. The mixture was then heated up to 310 C. for 1 hour and allowed to cool to 95 C. At this temperature, the water formed during the reaction was removed from the reaction mixture under reduced pressure. During the evacuation, the mixture was slowly heated to 170 C. (1 hour) with vigorous stirring, followed by, again, five cycles of pumping out and filling with inert gas (nitrogen) sequence. The mixture was heated to 320 C. with vigorous stirring and the reaction was allowed to proceed until all the white solid was dissolved (8 hours). The solution (S1) was cooled to ambient temperature and used as is without further purification. The yield of the final mixture was 103.1 g, with the concentration of [Zn] being calculated to be 0.4 mmol/g, with density d 0.8 g/ml. The solution solidifies upon long storage at room temperature but melts upon slight heating 40 C.).

(72) CdSe seeds were synthesized according to a known protocol, for example, as described in U.S. Pat. No. 6,872,249. After injection of an Se-precursor, the synthesis was terminated in 5 seconds. After precipitation, the seeds from the reaction mixture with methanol (1:1 volume ratio of Tol:MeOH) were washed once by dissolution in toluene and precipitation with methanol (1:1 ratio). The precipitate was collected by centrifugation, dissolved in toluene, filtered through a 0.2 m polytetrafluoroethylene (PTFE) filter and the toluene was blown out by the steam of nitrogen. The yield of solid product was 134 mg. Emission spectra of the obtained nanoparticles are shown in part a of FIG. 4 (.sub.max=504 nm). The obtained solid product was dissolved in 6.6 ml of TOP to form a clear solution with 20.25 mg/ml concentration (S2). The solution was stored under nitrogen in a dark place.

(73) CdO (Meryer, 99%, 90 mg, 0.7 mmol), hexadecylphoshonic acid (99.95%, 265 mg, 0.86 mmol), hexylphosphonic acid (99.5%, 80 mg, 0.48 mmol) and trioctylphosphine oxide (Stream, 90%, 3.0 g, 7.8 mmol) were degassed in a similar manner as discussed above with respect to the synthesis of Zn precursor. Then, the suspension was heated to 340 C. with vigorous stirring, after which it became transparent colorless solution (S3). At this temperature trioctylphosphine (Stream, 97%, 1 ml) was swiftly injected. In a separate flask, sulfur (84 mg, 2.6 mmol) was dissolved in trioctylphosphine (1.6 ml) with vigorous stirring following by addition of solution S2 (400 mkl) to the obtained sulfur solution. The combined solution was swiftly injected to S3 at 375 C. to initiate the growth of elongated CdS shells around the CdSe seeds. This corresponds to the start of a reaction time counter.

(74) Probes were taken to measure emission wavelength of the nanoparticles at different times during the synthesis (see part a of FIG. 4 and Table 1 below). For example, as shown in part a of FIG. 4 and Table 1 below, a first probe is taken 2 minutes and 40 seconds after the start of the reaction time counter (Pr1: 160 sec.). Starting from 3 minutes after the start of the reaction time counter (when the temperature after injection has stabilized), solution S1 (3.5 g, 4.4 ml) was gradually added dropwise at the same temperature, 370 C., over a 30 minute duration. Second and third probes were taken at 18 minutes and 35 minutes (Pr2 and Pr3, respectively). A TEM image and a size distribution corresponding to the quantum rods corresponding to the third probe Pr3 are depicted in part a of FIG. 6 and parts a-b of FIG. 7. The dimensions of the quantum rods corresponding to the third probe Pr3 are as follows: 27.2 nm (SD=1.7 nm)5.3 nm (SD=0.45 nm); COVs are 6% and 8% for length and width, respectively; aspect ratio=5.1. The reaction was further allowed to proceed for 90 min. Fourth, fifth and sixth probes Pr4, Pr5 and Pr6 were taken at 68 minutes, 95 minutes, and 120 minutes, respectively. The obtained emission spectra for the probes are depicted in part a of FIG. 4.

(75) The synthesis was terminated by removing the heating source. Then, 10 ml of toluene were added at 180 C. After cooling to room temperature, the product was precipitated with 10 ml of ethanol, collected by centrifugation, and washed once by redispersion in toluene (8 ml, 10 min of ultrasonication) followed by precipitation with ethanol (8 ml, centrifugation). The obtained solid product was then redispersed in toluene (5 ml) and centrifuged (4000 rpm, 10 min). The solution was collected and filtered through a 0.2 m PTFE filter, and the solvent was blown out by nitrogen stream at 60 C.

(76) The yield was 120 mg. According to TGA data, the inorganic part of the product constitutes 82% of the product (see FIG. 8). The volatile part (18%) is consistent with the typical mass fraction of organic ligands on quantum rods surface. A TEM image and a size distribution corresponding to the resulting quantum rods are depicted in part b of FIG. 6 and parts c-d of FIG. 7, respectively. The dimensions of the resulting quantum rods were as follows: 26.1 nm (SD=2.1 nm)5.2 nm (SD=0.54 nm); COVs are 8% and 10% for length and width, respectively; aspect ratio=5.0. The quantum yield (measured using integration sphere) was 59%. For comparison, quantum rods corresponding to the second and third probes Pr2 and Pr3 were treated in the same way (precipitation, washing, redispersion, and drying) and quantum yield measured (52% and 56%, respectively).

(77) The evolution of emission wavelengths during the synthesis of Example 1 is also shown in Table 1 below and in part a of FIG. 5.

(78) TABLE-US-00001 TABLE 1 Probe Time, sec .sub.max, nm Pr1 160 558 Pr2 1080 567 Pr3 2100 573 Pr4 4080 558 Pr5 5700 554 Pr6 7200 549

Example 2

(79) Example 2 provides an example for controlled synthesis of core-shell quantum rods using a Zn-precursor wherein 25 nm blue shift occurs.

(80) CdSe quantum dot seeds were synthesized in a similar manner as discussed above with respect to Example 1, except that the reaction was terminated immediately after the injection of the Se-precursor. The CdSe seeds were purified in the same way and a solution with concentration 20.25 mg/ml was prepared (S4). The photoluminescence spectra of the obtained nanoparticles have an emission maximum, .sub.max, at 473 nm.

(81) The controlled synthesis of the quantum rods was performed in a similar manner as discussed above with respect to Example 1 using 200 L of S4 instead of S3. With respect to Example 2, the mixture of S4 and S-precursor were used for initiation of CdS shell growth in a similar manner as discussed above with respect to Example 1. Then, starting from the fifth minute after starting the reaction, S1 was gradually added in over a duration of 25 minutes.

(82) Probes were taken to measure emission wavelength of the nanoparticles formed at different points during the synthesis (Pr1: 2 mins., Pr2: 8 mins., Pr3: 20 mins., Pr4: 36 mins., Pry: 75 mins.), the results of which are shown in Table 2 below and in part b of FIG. 4 and in part b of FIG. 5. The reaction was terminated at 76 minutes, and the product was isolated in a similar manner as discussed above with respect to Example 1.

(83) The yield was 115 mg. A TEM photo and a size distribution of the resulting quantum rods are depicted in part c of FIG. 6 and in parts e-f of FIG. 7, respectively. The dimensions of the quantum rods were as follows: 79.4 nm (SD=4.7 nm)5.3 nm (SD=0.55 nm); COVs were 6% and 10% for length and width, respectively; aspect ratio=15.0.

(84) The evolution of emission wavelengths during the synthesis of Example 2 is also shown in Table 2 below and in part b of FIG. 5.

(85) TABLE-US-00002 TABLE 2 Probe Time, sec .sub.max, nm Pr1 120 542 Pr2 480 556 Pr3 1200 548 Pr4 4080 537 Pr5 5700 527

Example 3

(86) Example 3 provides an example for controlled synthesis of core-shell quantum rods emitting in blue spectral range using multiple injections of Zn-precursor and additional injections of S-precursor with large (>100 nm) blue shift.

(87) CdSe quantum dot seeds were synthesized in a similar manner as discussed above with respect to Example 1, except that the reaction was terminated 15 seconds after the injection of the Se-precursor. The CdSe seeds were purified in the same way and a solution with concentration 16.52 mg/ml was prepared (S5). The photoluminescence spectra of the obtained nanoparticles have an emission maximum, .sub.max, at 519 nm.

(88) The controlled synthesis of the quantum rods was performed in a similar manner as discussed above with respect to Example 1 using 350 L of S5 instead of S3. With respect to Example 3, the mixture of S5 and S-precursor was used for initiation of CdS shell growth in a similar manner as discussed above with respect to Example 1. Then, starting from the fifth minute after starting the reaction, S1 was gradually added in over a duration of 20 minutes. The following additions of Zn-precursor were performed at 32 min (1 ml), 38 min (0.5 ml), 46 min (0.5 ml), 52 min (0.5 ml), 70 min (0.5 ml), 93 min (1 ml), 125 min (1 ml), 18 min (0.5 ml), 210 min (0.5 ml), 300 min (2 ml), 690 min (1 ml), 845 min (1 ml). The following additions of S-precursor (S1) were performed at 300 min (0.4 ml), 465 min (0.2 ml), 580 min (0.2 ml), 780 min (0.2 ml), 870 min (0.2 ml). Each addition means injection of solution with an average rate 0.2 ml/min. Probes were taken to measure emission wavelength of the nanoparticles formed at different points during the synthesis (Pr1: 3 min., Pr2: 13 min., Pr3: 24 min., Pr4: 38 min., Pr5: 51 min, Pr6: 95 min., Pr7: 120 min., Pr8: 167 min., Pr9: 222 min., Pr10: 268 min., Pr11: 298 min., Pr12: 350 min., Pr13: 394 min., Pr14: 454 min., Pr15: 520 min, Pr16: 570 min., Pr17: 685 min., Pr18: 745 min., Pr19: 835 min., Pr20: 950 min), the results of which are shown in Table 3 below and in part c of FIG. 5. The reaction was terminated at 950 minutes, and the product was isolated in a similar manner as discussed above with respect to Example 1. The yield was 100 mg. A TEM photo of the resulting quantum rods as well as the quantum rods isolated from Pr3 and Pr11 are depicted in part f, part d and part e of FIG. 6, respectively. The temperature dependence of photoluminescence intensity and FWHM for the quantum rods isolated from Pr11 (enriched with Zn) in comparison to ones isolated from Pr3 (enriched with Cd) are depicted in FIGS. 11A-11D.

(89) TABLE-US-00003 TABLE 3 Probe Time, min .sub.max, nm Pr1 3 558 Pr2 13 569 Pr3 24 569 Pr4 38 566 Pr5 51 562 Pr6 95 546 Pr7 120 542 Pr8 167 538 Pr9 222 531 Pr10 268 527 Pr11 298 524 Pr12 350 513 Pr13 394 499 Pr14 454 497 Pr15 520 491 Pr16 570 488 Pr17 685 483 Pr18 745 480 Pr19 835 474 Pr20 950 467

(90) All references, including publications, patent applications, and patents, cited herein are hereby incorporated by reference to the same extent as if each reference were individually and specifically indicated to be incorporated by reference and were set forth in its entirety herein.

(91) The use of the terms a and an and the and at least one and similar referents in the context of describing the invention (especially in the context of the following claims) are to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. The use of the term at least one followed by a list of one or more items (for example, at least one of A and B) is to be construed to mean one item selected from the listed items (A or B) or any combination of two or more of the listed items (A and B), unless otherwise indicated herein or clearly contradicted by context. The terms comprising, having, including, and containing are to be construed as open-ended terms (i.e., meaning including, but not limited to,) unless otherwise noted. Recitation of ranges of values herein are merely intended to serve as a shorthand method of referring individually to each separate value falling within the range, unless otherwise indicated herein, and each separate value is incorporated into the specification as if it were individually recited herein. All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. The use of any and all examples, or exemplary language (e.g., such as) provided herein, is intended merely to better illuminate the invention and does not pose a limitation on the scope of the invention unless otherwise claimed. No language in the specification should be construed as indicating any non-claimed element as essential to the practice of the invention.

(92) Preferred embodiments of this invention are described herein, including the best mode known to the inventors for carrying out the invention. Variations of those preferred embodiments may become apparent to those of ordinary skill in the art upon reading the foregoing description. The inventors expect skilled artisans to employ such variations as appropriate, and the inventors intend for the invention to be practiced otherwise than as specifically described herein. Accordingly, this invention includes all modifications and equivalents of the subject matter recited in the claims appended hereto as permitted by applicable law. Moreover, any combination of the above-described elements in all possible variations thereof is encompassed by the invention unless otherwise indicated herein or otherwise clearly contradicted by context.