Photonic Sensor Chip, Packaged Photonic Sensor Device and Arrangement
20200200972 ยท 2020-06-25
Inventors
- Patrick STEGLICH (Frankfurt (Oder), DE)
- Andreas MAI (Frankfurt (Oder), DE)
- Christian MAI (Frankfurt (Oder), DE)
Cpc classification
G01N33/54373
PHYSICS
G01N15/1456
PHYSICS
G02B6/12021
PHYSICS
G02B6/1225
PHYSICS
International classification
Abstract
The invention relates to a photonic sensor chip comprising a semiconductor substrate with a cavity extending from a back side through an entire depth of the semiconductor substrate, a photonic plane located on the front side of the semiconductor substrate. The chip includes a photonic particle sensor element with an active-surface element having an exposed active surface facing towards the back side of the semiconductor substrate, for capturing selected particles from at least one fluid or gas to which the active surface is exposable. The cavity provides access to the active surface from the back side. The photonic particle sensor element receives an optical input wave via the photonic plane, to expose captured particles on the active-surface element to interaction with the optical input wave and to provide a resulting optical output wave having a spectral component indicative of the interaction between the optical input wave and captured particles.
Claims
1. A photonic sensor chip comprising: a semiconductor substrate having a front side and a back side; at least one cavity extending from the back side through an entire depth of the semiconductor substrate; a photonic plane located on the front side of the semiconductor substrate and including at least one photonic particle sensor element with an active-surface element having an exposed active surface facing towards the back side of the semiconductor substrate and configured for capturing selected particles from at least one fluid or gas to which the active surface is exposable, wherein the least one cavity provides access to the active surface from the back side of the semiconductor substrate; and wherein the photonic particle sensor element is configured to receive an optical input wave via the photonic plane, to expose particles captured by the active-surface element to interact with the optical input wave and to provide a resulting optical output wave having a spectral component indicative of the interaction between the optical input wave and the captured particles; and a waveguide arranged in the photonic plane for guiding the optical input wave to the active-surface element and for guiding the resulting optical output wave from the active-surface element to a light detector of the photonic particle sensor element, which is configured to generate an output signal in response to receiving the optical output wave; the photonic sensor chip further comprising an electrically drivable phase shifter element, which is configured to set and maintain a predetermined phase shift to be effected by the active-surface element alone.
2. The photonic sensor chip according to claim 1, further comprising a control unit, which receives the output signal of the light detector and is configured to drive operation of the at least one photonic particle sensor element; wherein the control unit is configured to drive operation of the phase shifter element in dependence on the received output signal of the light detector in order to set and maintain a predetermined phase shift to be effected by the active-surface element alone.
3. The photonic sensor chip according to claim 1, wherein the electrically drivable phase shifter element comprises an electrically drivable heating element embedded in the electrical interconnect stack, or an electrically drivable doped waveguide.
4. The photonic sensor chip according to claim 2, a data acquisition unit configured to sample an output signal of the light detector; and an electrical interconnect stack, which is arranged on top of the photonic plane and comprises electrical interconnects for conducting electrical operating power and to conduct electronic signals to and from the control unit and the data acquisition unit.
5. The photonic sensor chip according to claim 1, wherein a microfluidic substrate is connected to the back side of the semiconductor substrate and comprises at least one microfluidic channel connecting an inlet for the fluid and an outlet for the fluid with the cavity.
6. The photonic sensor chip according to claim 5, wherein the microfluidic substrate is made of a plastic, glass or semiconductor.
7. The photonic sensor chip according to claim 1, wherein the active-surface element comprises a waveguide section of the waveguide, wherein the waveguide section comprises at least one functionalized surface section configured for capturing the selected particles by selective interaction, and has an optical path length that depends on an amount of particles captured by the active surface.
8. The photonic sensor chip according to claim 7, wherein the photonic particle sensor element comprises a plurality of active-surface elements optically arranged in a series connection and upstream of the light detector.
9. The photonic sensor chip according to claim 1, wherein the functionalized surface section is functionalized chemically.
10. The photonic sensor chip according to claim 1, wherein the functionalized surface section is functionalized physically.
11. The photonic sensor chip according to claim 1, wherein the waveguide is substantially made of silicon, silicon nitride, silicon oxynitride or germanium.
12. The photonic sensor chip according to claim 1, further comprising at least one light source connected to the waveguide and configured to generate and emit the optical input wave.
13. A packaged photonic sensor device, comprising: a photonic sensor chip according to claim 1; an electronic control chip electrically connected to the photonic sensor chip arranged on a carrier and comprising a control unit, which is configured to drive operation of the at least one photonic particle sensor element on the photonic sensor chip and a data acquisition unit configured to sample an output signal of the light detector; a package enclosing the photonic sensor chip and the electronic control chip and having an opening to ambient atmosphere facing the back side of the semiconductor substrate of the photonic sensor chip for providing access to the exposed active surface of the at least one photonic particle sensor element for the at least one fluid.
14. A photonic sensor arrangement, comprising: a packaged photonic sensor device according to claim 13, and a light source for generating the optical input wave, and an optical coupling element for coupling the optical input wave into the photonic plane of the photonic sensor chip.
15. The photonic sensor arrangement of claim 14, further comprising on the printed circuit board a data transmission unit configured to receive the output signal from the data acquisition unit and to transmit the output signal to an external device; and an interface unit configured to receive the output signal from the data acquisition unit and to indicate an amount of particles captured by the active surface.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0052] In the following, further embodiments will be described with reference to the enclosed drawings. In the drawings:
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DETAILED DESCRIPTION
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[0067] On the front side 114 of the semiconductor substrate 112 of the photonic sensor chip 100, electro-optical and electronic components 126 are arranged, and an electrical interconnect stack 130 is provided on top of the photonic plane 124. The electrical interconnect stack 130 comprises electrical interconnects 132 for conducting electrical operating power to the electro-optical and electronic components, including the light detector, and to conduct electronic signals to and from the electro-optical and electronic components to their respective destinations on chip or to an interface to external circuits. The opto-electronic and electronic components are fabricated using known front-end-of-line (FEOL) such as NMOS, PMOS, CMOS or BiCMOS, or a photodiode as light detector and the interconnect stack 132 can be fabricated using standard back-end-of-line (BEOL) technologies. The electronic components 126 can for instance form a circuit section or a complete circuit of a control unit, a data acquisition unit or other electrical circuitry.
[0068] The shown photonic sensor chip 100 makes sure that, in operation, a fluid or gas which transports particles to be detected at the active-surface element 122 in the cavity 118 will not get in contact with the front side 114 of the semiconductor substrate 112. In this example, the measuring solution is applied directly to the sensor surface as a drop. Thus, potential exposure of the photonic sensor chip 100 to a fluid or gas or to chemical reactions is restricted to the back side 116 of the semiconductor substrate 112.
[0069] The combination of photonic components with state-of-the-art silicon-based microtechnology is forms key to development of a biosensors according to embodiments of the present invention.
[0070] Thus, while prior art photonic devices are etched from the wafer surface and subsequently functionalized and electronic circuits located on the individual metal levels cannot be integrated, the innovative approach exemplified by the embodiment of
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[0072] The connection of the microfluidic substrate 210 to the semiconductor substrate 212 can be realized by wafer bonding for many of the materials mentioned. The ability to use a wafer bonding technique thus forms an additional advantage of the of the structure of the photonic sensor chip 200 which substantially simplifies the fabrication process.
[0073] The integration of microfluidic system 210 on the back side 216 of the semiconductor substrate 212 allows at least one fluid or gas to contact the active surface of the active-surface element 222 for allowing a detection of particles contained in the fluid or gas. Further, the use of microfluidics can increase the sensitivity of the measurement.
[0074] A biosensor resulting from this design can implement a laboratory diagnostic procedure integrated on a chip (lab-on-a-chip) and, in contrast to conventional on-site diagnostic procedures, is characterized by its miniaturization, sensitivity, parallelization and diversification possibilities. The advantage of the photonic measurement method proposed here over other label-free technologies that have already been developed is, on the one hand, the high inherent sensitivity of the measurement principle, the independence of the measurement signal from the amount of bound water and the possibility of producing cost-effective disposable chips. This approach combines the advantages of optical sensor technology (as with SPR) with the possibilities of chip production (as with SAW). In this way, components are provided that are suitable for practical use in bioanalytics.
[0075] As mentioned different waveguide types can be used in different embodiments of a photonic sensor chip.
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[0077] Examples of biosensor designs are photonic devices that allow the conversion of a refractive index change into an evaluable signal. Examples of such transducer components are Mach-Zehnder interferometers, ring resonators and Fabry-Perot resonators.
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[0079] Label-free detection of biomolecules is thus enabled by integrating a photonic resonator or interferometer structure into the chip along with other photonic and electronic components. In order to realize a selective interaction with the analyte, the silicon-based waveguide 710, 720 of the photonic device is functionalized with specific antibodies. When the analyte interacts with the antibody, the propagation of the light wave is influenced, the resonance condition changes and the resonance wavelength is shifted. The magnitude of the wavelength shift provides information about the amount of adsorbed analytes and thus about its concentration in the solution to be analysed.
[0080] With an ordinary silicon channel waveguide, the optical input wave is guided in the silicon waveguide and interacts only through an evanescent field with the captured specific particles. In comparison, silicon slit waveguides ensure a significantly increased interaction between the guided optical input wave and the captured specific particle, as a large part of the optical input wave up to 75% is guided in the slit and in the vicinity of the silicon webs where the captured specific particle is located. Thus, slot waveguides show a 3.5-fold greater light-particle interaction compared to channel waveguides.
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[0082] The photonic biosensor allows the selective and label-free detection of proteins or substances in general for which a specific capture molecule exists. Such evidence is relevant in many areas. Examples are the detection of proteins in food, toxins in the environment as well as the detection of substances in various body fluids in medical diagnostics or therapy monitoring. In addition, the sensor can also be used as a sensor without functionalizing the silicon surface. For example, it can be used as a gas sensor in which a change in refractive index is measured. An application for temperature measurement is also conceivable.
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[0084] On the front side 1014 of the semiconductor substrate 1012 of the photonic sensor chip 1000, electronic components 1030 are arranged, which are fabricated using known front-end-of-line (FEOL) and the interconnect stack can be fabricated using standard back-end-of-line (BEOL) technologies. In this example, the FEOL fabrication involves manufacturing NMOS devices, PMOS devices and SiGe:C HBTs. The FEOL fabrication also involves manufacturing of the Ge-photodiode. The electronic components can for instance form a circuit section or a complete circuit of a control unit, a data acquisition unit or other electrical circuitry. The photonic sensor chip 1000 is thus a SiGe BiCMOS device 1036. A thermal heating element 1032 is arranged in a metal layer of an interconnect stack 1035 located above the functionalized surface section of the active-surface element. Locating the thermal heating element 1032 above the functionalized surface section of the active-surface element allows calibrating the resonance condition of the photonic particle sensor element 1020 and stabilizing the temperature during measurements at the same time. For calibration the optical resonance of the photonic particle sensor element is shifted such that, the optical input wave received by the photonic particle sensor element lies on the resonance flank or the resonance peak. Stabilization of the temperature during the measurement is essential due to very specific binding affinities of biomolecules, which shall be captured by the photonic particle sensor element 1020. The electrical interconnect stack 1035 comprises electrical interconnects 1038 for conducting electrical operating power to the mentioned electro-optical and electronic components and to conduct electronic signals to and from the electro-optical and electronic components to their respective destinations on chip or to an interface to external circuits. In this embodiment, the waveguide in the photonic plane 1024 is arranged on a local island-like silicon-on-insulator (SOI) structure 1040 that is embedded in the bulk of the silicon substrate 1012. The SiGe BiCMOS 1036 is located next to the local island SOI 1040 on the bulk of silicon substrate 1012.
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[0086] For packaging, state of the art solutions can be used, including fabrication of a hole for providing access to the active-surface element of the particle sensor element of the photonic sensor chip 1110A.
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[0090] The signal-to-noise ratio of an optical output wave to be transformed into a corresponding electrical signal received by the light detector, can be increased by using a series connection of active-surface elements.
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[0092] As an application example of the photonic sensor chip, allergens in food (such as peanuts) or toxins (e.g. snake venom, toxic insects, scorpions, spiders, blue-green algae, mould poisons or poisonous fungi) can be investigated. Further applications of the photonic sensor chip are listed Table 1 below and can be followed or applied on the basis of the results obtained. The left column of the following table lists different analytes, and the right column list possible occurrences of the respective analytes.
TABLE-US-00001 TABLE 1 Application cases of the photonic sensor chip analyte Occurrence toxins aflatoxins nuts, corn, milk ergot alkaloids cereals fusarium toxins cereals, maize patulin Apples, pears ochratoxin Cereals, beer, wine, coffee, nuts, spices bacteria Salmonella (zoonoses) eggs, poultry, water Escherichia coli raw milk, vegetables, water, minced beef, sprouts campylobacter Raw poultry meat shigella toxin food viruses Influenza A birds, pig virus H1N1 allergens gluten food antibiotics penicillins Waste water Meat Milk hormones Water
[0093] An important application potential is currently seen in the detection of contaminations such as antibiotics in raw milk.
[0094] A cow is milked at least twice a day. The fresh raw milk is automatically piped into the cooling tank of the production plant. In principle, the raw milk is collected every one to two days from the producer in the milk collection truck. Depending on the vehicle type, this can hold between 10,000 and 25,000 litres. Once the smell, colour and temperature of the raw milk have been checked, it is pumped from the cooling tank into the milk collection truck. Milk samples are automatically taken and analysed in an independent laboratory or in the dairy. Once it arrives at the dairy, the raw milk is subjected to microbiological and chemical-physical checks for cleanliness, smell, taste, appearance, purity, fat content, acidity, germ content and weight. The milk is then pumped into large storage tanks. Seamless quality assurance from the producer to the refrigerated shelf is a matter of course for the German dairy industry. In order to further improve product safety, many dairies are developing additional quality assurance systems that go beyond the legal requirements. The close cooperation of all stakeholders within the value chain is crucial to ensure the production of safe and high quality products. The developed hybrid waveguide ring resonator can make a major contribution to this. In addition to fast on-site analysis, the sensor also enables digital evaluation and creation of databases without intermediate steps.
[0095] In summary, the solution proposed here considerably simplifies the development of a connection technique and the handling of the sensor, since the sensor surface is separated from the electronics and the light injection. This allows an analyte to interact with the sensor from the rear and does not interfere with further chip build-up. It is thus possible to manufacture the chip from the front with all the usual process steps, which also allows monolithic integration of the sensor. In monolithic integration, the photonic sensor is manufactured together with optoelectronic components (e.g. photodiodes) and electronic components (e.g. heating element). The bioanalytic part is accessible through the rear opening in the form of a cavity connecting to the optical sensor. For this purpose, a wafer, on which the photonic components are located, is etched from the reverse side in such a way that the areas with the sensor surfaces are exposed and can be functionalized with antibodies.
[0096] This also allows the integration of microfluidics on the back of the chip. Since the back of the chip consists of a planar silicon surface, the integration of microfluidics is considerably simplified compared to frontal integration.
[0097] The solution proposed has the following advantages: [0098] Decentralized diagnostics without laboratory diagnostic prior knowledge [0099] A mobile sensor platform enables fast on-site diagnostics [0100] Measurement of several biological substances and parameters in parallel and in short time can be enabled [0101] Functionalized surfaces with customized properties for bioanalytics [0102] The optical biosensor can be used for almost any requirements in medicine and industry due to its adaptable and functional optical waveguides [0103] Compatibility of photonic with electronic components on one chip without additional process steps (integration with separation of electrical and biosensory environment) [0104] Low-cost in terms of manufacturing and disposal costs (due to the CMOS technology used and the avoidance of complex and very expensive flow cells) [0105] Suitable for mass production, as the manufacturing and process technology is designed at wafer level [0106] Low power requirements and extremely high compactness (this offers the possibility of sensor arrays on a small area and the realization of mobile, battery-powered devices)