US20120250716A1 - Flexible Microcavity Structure Made Of Organic Materials Using Spin-Coating Technique And Methods Of Making - Google Patents

Flexible Microcavity Structure Made Of Organic Materials Using Spin-Coating Technique And Methods Of Making Download PDF

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US20120250716A1
US20120250716A1 US13/397,958 US201213397958A US2012250716A1 US 20120250716 A1 US20120250716 A1 US 20120250716A1 US 201213397958 A US201213397958 A US 201213397958A US 2012250716 A1 US2012250716 A1 US 2012250716A1
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polymer
layer
pair
distributed bragg
reflecting mirrors
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Vinod M. Menon
Nikesh V. Valappil
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Research Foundation of City University of New York
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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01S—DEVICES USING THE PROCESS OF LIGHT AMPLIFICATION BY STIMULATED EMISSION OF RADIATION [LASER] TO AMPLIFY OR GENERATE LIGHT; DEVICES USING STIMULATED EMISSION OF ELECTROMAGNETIC RADIATION IN WAVE RANGES OTHER THAN OPTICAL
    • H01S3/00—Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range
    • H01S3/05—Construction or shape of optical resonators; Accommodation of active medium therein; Shape of active medium
    • H01S3/06—Construction or shape of active medium
    • H01S3/0602—Crystal lasers or glass lasers
    • H01S3/0604—Crystal lasers or glass lasers in the form of a plate or disc
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01S—DEVICES USING THE PROCESS OF LIGHT AMPLIFICATION BY STIMULATED EMISSION OF RADIATION [LASER] TO AMPLIFY OR GENERATE LIGHT; DEVICES USING STIMULATED EMISSION OF ELECTROMAGNETIC RADIATION IN WAVE RANGES OTHER THAN OPTICAL
    • H01S3/00—Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range
    • H01S3/05—Construction or shape of optical resonators; Accommodation of active medium therein; Shape of active medium
    • H01S3/06—Construction or shape of active medium
    • H01S3/0627—Construction or shape of active medium the resonator being monolithic, e.g. microlaser
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01S—DEVICES USING THE PROCESS OF LIGHT AMPLIFICATION BY STIMULATED EMISSION OF RADIATION [LASER] TO AMPLIFY OR GENERATE LIGHT; DEVICES USING STIMULATED EMISSION OF ELECTROMAGNETIC RADIATION IN WAVE RANGES OTHER THAN OPTICAL
    • H01S3/00—Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range
    • H01S3/14—Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range characterised by the material used as the active medium
    • H01S3/16—Solid materials
    • H01S3/169—Nanoparticles, e.g. doped nanoparticles acting as a gain material
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01S—DEVICES USING THE PROCESS OF LIGHT AMPLIFICATION BY STIMULATED EMISSION OF RADIATION [LASER] TO AMPLIFY OR GENERATE LIGHT; DEVICES USING STIMULATED EMISSION OF ELECTROMAGNETIC RADIATION IN WAVE RANGES OTHER THAN OPTICAL
    • H01S3/00—Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range
    • H01S3/14—Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range characterised by the material used as the active medium
    • H01S3/16—Solid materials
    • H01S3/17—Solid materials amorphous, e.g. glass
    • H01S3/178—Solid materials amorphous, e.g. glass plastic
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01S—DEVICES USING THE PROCESS OF LIGHT AMPLIFICATION BY STIMULATED EMISSION OF RADIATION [LASER] TO AMPLIFY OR GENERATE LIGHT; DEVICES USING STIMULATED EMISSION OF ELECTROMAGNETIC RADIATION IN WAVE RANGES OTHER THAN OPTICAL
    • H01S5/00—Semiconductor lasers
    • H01S5/10—Construction or shape of the optical resonator, e.g. extended or external cavity, coupled cavities, bent-guide, varying width, thickness or composition of the active region
    • H01S5/18—Surface-emitting [SE] lasers, e.g. having both horizontal and vertical cavities
    • H01S5/183—Surface-emitting [SE] lasers, e.g. having both horizontal and vertical cavities having only vertical cavities, e.g. vertical cavity surface-emitting lasers [VCSEL]
    • H01S5/18361—Structure of the reflectors, e.g. hybrid mirrors
    • H01S5/18369—Structure of the reflectors, e.g. hybrid mirrors based on dielectric materials
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01S—DEVICES USING THE PROCESS OF LIGHT AMPLIFICATION BY STIMULATED EMISSION OF RADIATION [LASER] TO AMPLIFY OR GENERATE LIGHT; DEVICES USING STIMULATED EMISSION OF ELECTROMAGNETIC RADIATION IN WAVE RANGES OTHER THAN OPTICAL
    • H01S5/00—Semiconductor lasers
    • H01S5/30—Structure or shape of the active region; Materials used for the active region
    • H01S5/36—Structure or shape of the active region; Materials used for the active region comprising organic materials

Definitions

  • the embodiments of the present invention relate to a flexible microcavity, and more particularly, the embodiments of the present invention relate to a flexible microcavity structure made of organic materials using spin-coating technique and method of making.
  • Microcavities helping confine electromagnetic radiation (light) is of utmost importance for realizing highly efficient lasers, single photon emitters, and displays. Indeed, efficient photonic devices, such as lasers, single photon sources, and novel displays have been realized using microcavities. Most of the microcavity structures were realized using techniques, such as molecular beam epitaxy, chemical vapor deposition, or sputtering. More recently a few groups have demonstrated microcavities using spin coating—a far simpler technique in comparison to the previous techniques. In the past, the inventors have shown enhanced spontaneous emission from quantum dots embedded in such microcavities.
  • an object of the embodiments of the present invention is to provide a flexible microcavity structure made of organic materials using spin-coating technique, which avoids the disadvantages of the prior art.
  • another object of the present invention is to provide a flexible microcavity structure made of organic materials using spin-coating technique for allowing large area structures using a roll-to-roll process.
  • the structure includes at least one first polymer layer, at least one second polymer layer, and a cavity layer.
  • the cavity layer has quantum dots embedded therein for realizing an electrically pumped microcavity emitter.
  • the at least one first polymer layer alternates with the at least one second polymer layer, respectively, to form a pair of distributed Bragg reflecting mirrors.
  • the cavity layer is sandwiched between the pair of distributed Bragg reflecting mirrors.
  • FIG. 1 is a schematic drawing of the solution processed polymer microcavity structure
  • FIG. 2 is a graph of reflectivity of the solution processed microcavity at various locations on a 1 cm ⁇ 1 cm sample
  • FIG. 3 is a graph of enhanced spontaneous emission observed from Qdots embedded the flexible microcavity, with the emission from bare Qdots shown for comparison;
  • FIG. 4 is a photograph of the flexible microcavity.
  • FIG. 1 is a schematic drawing of the solution processed polymer microcavity structure.
  • Alternating layers of two polymers having different refractive indices are spin-coated to fabricate distributed Bragg reflecting (DBR) mirrors. It is important to choose the polymers so that a solvent dissolving one does not affect the other one.
  • polyvinyl carbazole (PVK) and cellulose acetate (CA) are used for the two layers.
  • the refractive indices of PVK and CA are 1.683 and 1.475, respectively, at 650 nm.
  • a cavity layer including quantum dots embedded in PVK is sandwiched between two DBR mirrors. The thickness of the cavity layer must be equal to an integer multiple of half the wavelength of emission of the QDs.
  • the emission wavelength was 670 nm.
  • the microcavity structure includes the cavity layer between top and bottom DBRs having 5 and 10 periods, respectively. Lesser periods are used in the top mirror to have better light extraction from the top.
  • PVK Poly-vinyl carbazol
  • CA cellulose acetate
  • Alternating layers of the first layer and the second layer were spin-coated onto a glass substrate to create a pair of Distributed Bragg Reflecting (DBR) mirrors.
  • the pair of DBR mirrors showed excellent uniformity in their optical properties over a 1 cm ⁇ 1 cm sample.
  • Spin-coating involves dropping a small amount of each first layer and each second layer onto a glass substrate and spin at high speeds to create uniformly thick layers. Then the sample is placed on a hot plate to evaporate any remaining solvent,
  • a DBR mirror can be created with layers ⁇ /4n thick, where n is the index of refraction for the polymer and ⁇ is the wavelength of the quantum dot emission used in the cavity.
  • One set of alternating first and second layers constitutes a period. Ten periods are built onto the glass substrate using spin speeds of 3150 RPM for the first layers and 5000 RPM for the second layers. The first layers were placed on a hotplate at 80° C. and the second layers at 120° C., each for 15 minutes.
  • a ⁇ /2n thick defect layer containing InGaP Quantum Dots was formed above one of the pair of DBR mirrors, and an additional 5 periods of the other one of the pair of DBR mirrors were constructed and placed on the defect layer.
  • FIG. 2 is a graph of reflectivity of the solution processed microcavity at various locations on a 1 cm ⁇ 1 cm sample.
  • the emission from the QDs embedded in the microcavity structure showed enhanced spontaneous emission evidenced by a significant reduction in the spectral width and increased intensity in comparison to the bare QDs.
  • the emission from the microcavity also showed angle dependence as expected from any microcavity on a fiat surface.
  • FIG. 3 is a graph of enhanced spontaneous emission observed from Qdots embedded the flexible microcavity, with the emission from bare Qdots shown for comparison. More recently samples with similar uniformity over 2.5 cm ⁇ 2.5 cm have been demonstrated.
  • FIG. 4 is a photograph of the flexible microcavity.
  • the entire structure is fabricated using spin-coating. This allows the realization of large area structures using a roll-to-roll process.
  • the exact reflectivity and the cavity quality factors can be controlled by altering the layer thicknesses, and the number of periods and the type of polymer.
  • the choice of the polymer allows one to alter the stop band width of the Bragg mirror.

Abstract

A flexible microcavity structure made of organic materials using spin-coating technique for allowing large area structures using a roll-to-roll process. The structure includes at least one first polymer layer, at least one second polymer layer, and a cavity layer. The cavity layer has quantum dots embedded therein fir realizing an electrically pumped microcavity emitter. The at least one first polymer layer alternates with the at least one second polymer layer, respectively, to form a pair of distributed Bragg reflecting mirrors. The cavity layer is sandwiched between the pair of distributed Bragg reflecting mirrors.

Description

    BACKGROUND OF THE INVENTION
  • 1. Field of the Invention
  • The embodiments of the present invention relate to a flexible microcavity, and more particularly, the embodiments of the present invention relate to a flexible microcavity structure made of organic materials using spin-coating technique and method of making.
  • 2. Description of the Prior Art
  • Microcavities helping confine electromagnetic radiation (light) is of utmost importance for realizing highly efficient lasers, single photon emitters, and displays. Indeed, efficient photonic devices, such as lasers, single photon sources, and novel displays have been realized using microcavities. Most of the microcavity structures were realized using techniques, such as molecular beam epitaxy, chemical vapor deposition, or sputtering. More recently a few groups have demonstrated microcavities using spin coating—a far simpler technique in comparison to the previous techniques. In the past, the inventors have shown enhanced spontaneous emission from quantum dots embedded in such microcavities.
  • Flexible microcavity was previously demonstrated using a commercially available reflector film from 3M acting as the bottom mirror and a metal mirror as the top mirror.1 1“All-organic flexible polymer microcavity light-emitting diodes using 3M reflective multilayer polymer mirrors,” Appl. Phys. Lett. 87, 243504 (2005).
    • SUMMARY OF THE INVENTION
  • Thus, an object of the embodiments of the present invention is to provide a flexible microcavity structure made of organic materials using spin-coating technique, which avoids the disadvantages of the prior art.
  • Briefly stated, another object of the present invention is to provide a flexible microcavity structure made of organic materials using spin-coating technique for allowing large area structures using a roll-to-roll process. The structure includes at least one first polymer layer, at least one second polymer layer, and a cavity layer. The cavity layer has quantum dots embedded therein for realizing an electrically pumped microcavity emitter. The at least one first polymer layer alternates with the at least one second polymer layer, respectively, to form a pair of distributed Bragg reflecting mirrors. The cavity layer is sandwiched between the pair of distributed Bragg reflecting mirrors.
  • The novel features considered characteristic of the embodiments of the present invention are set forth in the appended claims. The embodiments of the present invention themselves, however, both as to their construction and their method of operation together with additional objects and advantages thereof will be best understood from the following description of the specific embodiments when read and understood in connection with the accompanying drawings.
    • BRIEF DESCRIPTION OF THE DRAWINGS
  • The figures of the drawings are briefly described as follows:
  • FIG. 1 is a schematic drawing of the solution processed polymer microcavity structure;
  • FIG. 2 is a graph of reflectivity of the solution processed microcavity at various locations on a 1 cm×1 cm sample;
  • FIG. 3 is a graph of enhanced spontaneous emission observed from Qdots embedded the flexible microcavity, with the emission from bare Qdots shown for comparison; and
  • FIG. 4 is a photograph of the flexible microcavity.
    •  DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS General
  • In the embodiments of the present invention, there is developed a technique whereby spin-coated microcavities are easily peeled off a substrate, thereby forming a flexible microcavity.
  • A schematic drawing of the microcavity structure of the embodiments of the present invention is shown generally in FIG. 1, which is a schematic drawing of the solution processed polymer microcavity structure.
  • Alternating layers of two polymers having different refractive indices are spin-coated to fabricate distributed Bragg reflecting (DBR) mirrors. It is important to choose the polymers so that a solvent dissolving one does not affect the other one. In the prototype demonstrated, polyvinyl carbazole (PVK) and cellulose acetate (CA) are used for the two layers. The refractive indices of PVK and CA are 1.683 and 1.475, respectively, at 650 nm. A cavity layer including quantum dots embedded in PVK is sandwiched between two DBR mirrors. The thickness of the cavity layer must be equal to an integer multiple of half the wavelength of emission of the QDs. In the embodiments of the present invention including InGaP QDs, the emission wavelength was 670 nm. The microcavity structure includes the cavity layer between top and bottom DBRs having 5 and 10 periods, respectively. Lesser periods are used in the top mirror to have better light extraction from the top.
    • Method of Making
  • Poly-vinyl carbazol (PVK) polymer, with an index of refraction of 1.683, was dissolved in chlorobenzene to form a first layer, and cellulose acetate (CA) polymer, with an index of refraction of 1.475, was dissolved in di-acetone alcohol to form a second layer.
  • Alternating layers of the first layer and the second layer were spin-coated onto a glass substrate to create a pair of Distributed Bragg Reflecting (DBR) mirrors. The pair of DBR mirrors showed excellent uniformity in their optical properties over a 1 cm×1 cm sample. Spin-coating involves dropping a small amount of each first layer and each second layer onto a glass substrate and spin at high speeds to create uniformly thick layers. Then the sample is placed on a hot plate to evaporate any remaining solvent, By spin-coating alternating layers of the first layer and the second layer, a DBR mirror can be created with layers λ/4n thick, where n is the index of refraction for the polymer and λ is the wavelength of the quantum dot emission used in the cavity. One set of alternating first and second layers constitutes a period. Ten periods are built onto the glass substrate using spin speeds of 3150 RPM for the first layers and 5000 RPM for the second layers. The first layers were placed on a hotplate at 80° C. and the second layers at 120° C., each for 15 minutes.
  • A λ/2n thick defect layer containing InGaP Quantum Dots was formed above one of the pair of DBR mirrors, and an additional 5 periods of the other one of the pair of DBR mirrors were constructed and placed on the defect layer.
  • Following the fabrication, the optical characteristics on the glass substrate were tested. The embodiments of the present invention demonstrated excellent uniformity in their optical properties over a 1 cm×1 cm sample, as shown in FIG. 2, which is a graph of reflectivity of the solution processed microcavity at various locations on a 1 cm×1 cm sample. The emission from the QDs embedded in the microcavity structure showed enhanced spontaneous emission evidenced by a significant reduction in the spectral width and increased intensity in comparison to the bare QDs. The emission from the microcavity also showed angle dependence as expected from any microcavity on a fiat surface. Spectral narrowing observed from this microcavity is shown in FIG. 3, which is a graph of enhanced spontaneous emission observed from Qdots embedded the flexible microcavity, with the emission from bare Qdots shown for comparison. More recently samples with similar uniformity over 2.5 cm×2.5 cm have been demonstrated.
  • Following the optical characterization of the microcavity of the glass substrate, the microcavity structure was peeled off the substrate using a sharp scalpel (sharp blade will work just as good). A photograph of the free standing microcavity structure is shown in FIG. 4, which is a photograph of the flexible microcavity.
    • Advantages
  • The entire structure is fabricated using spin-coating. This allows the realization of large area structures using a roll-to-roll process.
  • The exact reflectivity and the cavity quality factors can be controlled by altering the layer thicknesses, and the number of periods and the type of polymer.
  • The choice of the polymer allows one to alter the stop band width of the Bragg mirror.
  • It is also possible to realize an electrically pumped microcavity emitter with embedded Qdots.
    • Conclusion
  • It will be understood that each of the elements described above or two or more together may also find a useful application in other types of constructions differing from the types described above.
  • While the embodiments of the present invention have been illustrated and described as embodied in a flexible microcavity structure made of organic materials using spin-coating technique, however, they are not limited to the details shown, since it will be understood that various omissions, modifications, substitutions, and changes in the forms and details of the embodiments of the present invention illustrated and their operation can be made by those skilled in the art without departing in any way from the spirit of the embodiments of the present invention.
  • Without further analysis, the foregoing will so fully reveal the gist of the embodiments of the present invention that others can by applying current knowledge readily adapt it for various applications without omitting features that from the standpoint of prior art fairly constitute characteristics of the generic or specific aspects of the embodiments of the present invention.

Claims (9)

1. A flexible microcavity structure made of organic materials using spin-coating technique allowing large area structures using a roll-to-roll process, comprising:
a) at least one first polymer layer;
b) at least one second polymer layer; and
c) a cavity layer;
wherein said cavity layer has quantum dots embedded therein for realizing an electrically pumped microcavity emitter,
wherein each of said at least one first polymer layer alternates with said at least one second polymer layer to form a pair of distributed Bragg reflecting mirrors; and
wherein said cavity layer is sandwiched between said pair of distributed Bragg reflecting mirrors.
2. The structure of claim 1, wherein a first polymer chosen for said at least one first polymer layer and a second polymer chosen for said at least one second polymer layers are not dissolvable in the same solvent so as to prevent the solvent dissolving one polymer from dissolving the other polymer.
3. The structure of claim 1, wherein said first polymer used for said at least one first polymer layer is polyvinyl carbazole; and
wherein said second polymer used for said at least one second polymer layer is cellulose acetate.
4. The structure of claim 1, wherein said cavity layer is polyvinyl carbazole.
5. The structure of claim 4, wherein said cavity layer has a thickness;
wherein said quantum dots has an emission with a wavelength; and
wherein said thickness of said cavity layer is equal to an integer multiple of half said wavelength of said emission of said quantum dots.
6. The structure of claim 5, wherein said quantum dots include InGaP; and
wherein said wavelength of said emission of said InGaP is 670 nm.
7. The structure of claim 1, wherein a lower one of said pair of distributed Bragg reflecting mirrors has ten periods; and
wherein an upper one of said pair of distributed Bragg reflecting mirrors has five periods for better light extraction from said upper one of said pair of distributed Bragg reflecting mirrors.
8. The structure of claim 2, wherein each of said pair of distributed Bragg reflecting mirrors has a stop bandwidth; and
wherein said first polymer and said second polymer are chosen to allow alteration of said stop bandwidth of each of said pair of distributed Bragg reflecting mirrors.
9. The structure of claim 1, wherein exact reflectivity and quality factors of said cavity layer is controlled by altering one of layer thicknesses, number of periods, and type of polymer.
US13/397,958 2007-12-04 2012-02-16 Flexible Microcavity Structure Made Of Organic Materials Using Spin-Coating Technique And Methods Of Making Abandoned US20120250716A1 (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109950792A (en) * 2019-03-29 2019-06-28 钟祥博谦信息科技有限公司 The distributed bragg reflector mirror of gallium nitride and the preparation method of resonant cavity

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8610103B2 (en) * 2009-01-14 2013-12-17 Research Foundation Of The City University Of New York Flexible microcavities through spin coating
DE102014012981A1 (en) * 2014-09-02 2016-03-03 Karlsruher Institut für Technologie Fully polymeric microresonators
CN104831363A (en) * 2015-04-24 2015-08-12 中国科学技术大学先进技术研究院 Three-dimensional photonic crystals based on polymer thin film layer
CN106299066B (en) * 2016-08-31 2018-04-13 武汉光谷量子技术有限公司 A kind of quantum dot single-photon source and preparation method thereof

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5260957A (en) 1992-10-29 1993-11-09 The Charles Stark Draper Laboratory, Inc. Quantum dot Laser
US6160830A (en) 1998-03-04 2000-12-12 Motorola, Inc. Semiconductor laser device and method of manufacture
US6366017B1 (en) 1999-07-14 2002-04-02 Agilent Technologies, Inc/ Organic light emitting diodes with distributed bragg reflector
US6436613B1 (en) 1999-08-23 2002-08-20 The Arizona Board Of Regents Integrated hybrid optoelectronic devices
KR100319772B1 (en) * 1999-12-02 2002-01-09 오길록 Organic Micro-Cavity Laser
US20030031218A1 (en) 2001-08-13 2003-02-13 Jang-Hun Yeh VCSEL structure and method of making same
EP1430549A2 (en) * 2001-09-04 2004-06-23 Koninklijke Philips Electronics N.V. Electroluminescent device comprising quantum dots
US7132787B2 (en) * 2002-11-20 2006-11-07 The Regents Of The University Of California Multilayer polymer-quantum dot light emitting diodes and methods of making and using thereof
JP2005055543A (en) * 2003-08-07 2005-03-03 Super Technology Innovators Co Ltd Polymer optical multilayer film and manufacturing method of polymer optical multilayer film
US7411223B2 (en) * 2003-09-15 2008-08-12 General Electric Company Compound electrodes for electronic devices
US7732237B2 (en) * 2005-06-27 2010-06-08 The Regents Of The University Of California Quantum dot based optoelectronic device and method of making same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109950792A (en) * 2019-03-29 2019-06-28 钟祥博谦信息科技有限公司 The distributed bragg reflector mirror of gallium nitride and the preparation method of resonant cavity

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