U.S. patent application number 15/547186 was filed with the patent office on 2018-01-25 for solar cell employing phosphorescent materials.
The applicant listed for this patent is Rensselaer Polytechnic Institute. Invention is credited to Vidhya Chakrapani.
Application Number | 20180025849 15/547186 |
Document ID | / |
Family ID | 56614802 |
Filed Date | 2018-01-25 |
United States Patent
Application |
20180025849 |
Kind Code |
A1 |
Chakrapani; Vidhya |
January 25, 2018 |
SOLAR CELL EMPLOYING PHOSPHORESCENT MATERIALS
Abstract
A solar cell device having a solid state light absorber region
that incorporates a donor-acceptor particle structure. The particle
structure includes acceptor particles that generate a flow of
electrons in the solid state light absorber region in response to
absorbed photons; and donor particles comprising a phosphorescent
material, wherein each donor particle is coupled to a group of
acceptor particles, and wherein the phosphorescent material absorbs
high energy photons and emits lower energy photons that are
absorbed by the acceptor particles.
Inventors: |
Chakrapani; Vidhya; (Clifton
Park, NY) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Rensselaer Polytechnic Institute |
Troy |
NY |
US |
|
|
Family ID: |
56614802 |
Appl. No.: |
15/547186 |
Filed: |
February 11, 2016 |
PCT Filed: |
February 11, 2016 |
PCT NO: |
PCT/US16/17482 |
371 Date: |
July 28, 2017 |
Related U.S. Patent Documents
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
|
|
62115667 |
Feb 13, 2015 |
|
|
|
Current U.S.
Class: |
136/257 |
Current CPC
Class: |
H01G 9/2031 20130101;
H01G 9/2063 20130101; Y02E 10/542 20130101; H01G 9/2022 20130101;
Y02E 10/52 20130101; H01G 9/0032 20130101; H01G 9/2013 20130101;
H01L 31/055 20130101 |
International
Class: |
H01G 9/20 20060101
H01G009/20; H01G 9/00 20060101 H01G009/00 |
Claims
1. A solar cell device, comprising: a solid state light absorber
region that includes a donor-acceptor particle structure having:
acceptor particles adsorbed on an inert nanoparticles current
collector, which results in a flow of electrons in the solid state
light absorber region in response to absorbed photons; and donor
panicles comprising a phosphorescent material, wherein each donor
particle is coupled to a group of acceptor particles, and wherein
the phosphorescent material absorbs high energy photons and emits
lower energy photons that are absorbed by the acceptor
particles.
2. The solar cell device of claim 1, wherein the acceptor particles
comprise an absorber adsorbed on an inert TiO.sub.2 nanoparticles
current collector.
3. The solar cell device of claim 1, wherein the donor particles
includes a coating that provides a spacer between each donor
particle and group of acceptor particles.
4. The solar cell device of claim 3, wherein the spacer comprises
TiO.sub.2.
5. The solar cell device of claim 1, wherein an emission spectrum
of the donor particles overlaps with an absorption spectrum of the
acceptor particles.
6. The solar cell device of claim 1, wherein the solid state light
absorber region forms, an electrode.
7. The solar cell device of claim 1 that comprises a device
selected from a group consisting of: a dye sensitive solar cell, a
quantum dot solar cell, a polymer solar cell, and a thin film solar
cell.
8. A dye sensitive solar cell (DSSC) device, comprising: a counter
electrode; an electrolyte region; a transparent back contact; and a
transparent electrode disposed between the electrolyte region and
transparent back content, wherein the transparent electrode
includes a donor-acceptor particle structure having: acceptor
particles adsorbed on an inert nanoparticles current collector,
which upon absorption of photons, results in a flow of free
electrons in the acceptor particles, injection of electrons into
the inert nanoparticles current collector, and transport of
injected electrons by the inert nanoparticles can collector to the
transparent back contact; and donor particles comprising a
phosphorescent material, wherein each donor particle is coupled to
a group of acceptor particles, and wherein the phosphorescent
material absorbs high energy photons and emits lower energy photons
that are absorbed by the acceptor particles.
9. The DSSC device of claim 8, wherein the acceptor particles
comprise a dye, quantum dot or other absorber material anchored on
TiO.sub.2 nanoparticles.
10. The DSSC device of claim 8, wherein the donor particles include
a coating that provides a spacer between each donor particle and
group of acceptor particles.
11. The DSSC of claim 10, wherein the spacer comprises
TiO.sub.2.
12. The DSSC of claim 8, wherein an emission spectrum of the donor
particles overlaps with an absorption spectrum of the acceptor
particles.
13. The DSSC of claim 8, wherein a volumetric ratio of acceptor
particles to donor particles is approximately 10:1.
14. The DSSC of claim 9, wherein the donor-acceptor particle
structure and TiO.sub.2 nanoparticles are coated onto a
substrate.
15. A method of forming a dye sensitive solar cell (DSSC) device,
comprising: providing a first and a second transparent back
contact; forming a transparent electrode on the first transparent
back contact, wherein the transparent electrode includes a
donor-acceptor particle structure having: acceptor particles
adsorbed on an inert nanoparticles current collector; and donor
particles comprising a phosphorescent material, wherein each donor
panicle is coupled to a group of acceptor particles, and wherein
the phosphorescent material absorbs high energy photons and emits
lower energy photons that are absorbed by the acceptor particles;
forming a counter electrode on the second transparent back contact;
and forming an electrolyte region between the counter electrode and
transparent electrode; wherein the transparent electrode forms a
light absorption region, which upon absorption of photons results
in a flow of free electrons in the acceptor particles, injection of
electrons into the inert nanoparticles current collector and
transport of injected electrons by the inert nanoparticles current
collector to the first transparent back contact.
16. The method of claim 15, wherein the acceptor particles comprise
a dye adsorbed on a TiO.sub.2 nanoparticles current collector.
17. The method of claim 15, wherein the donor panicles include a
coating that provides a spacer between each donor particle and
group of acceptor particles.
18. The method of claim 17, wherein the spacer comprises
TiO.sub.2.
19. The method of claim 15, wherein an emission spectrum of the
donor particles overlaps with an absorption spectrum of the
acceptor particles.
20. The method of claim 15, wherein a volumetric ratio of acceptor
particles to donor particles is approximately 10:1.
Description
PRIORITY CLAIM
[0001] This application claims priority to co-pending U.S.
provisional patent application "Solar Cell Employing Phosphorescent
Materials," Ser. No. 62/115,667 filed on Feb. 13, 2015, the content
of which is hereby incorporated by reference.
TECHNICAL FIELD
[0002] The subject matter of this invention relates to solar cells
employing phosphorescent materials, and more particularly to solar
cells having a solid state absorber region that integrates phosphor
particles with light acceptor particles.
BACKGROUND
[0003] Converting solar energy to electricity is the one of the
cleanest methods of producing useable energy. Among the various
renewable energy technologies available, solar cells hold
significant promise. One major drawback of this technology is the
lack of flexibility, e.g., solar cells only have the ability to
generate power during daylight hours and thus cannot provide an
uninterrupted power supply without incorporating additional
components. Another drawback is the relatively low efficiency of
known devices. Hence, a solar cell with improved efficiency that
can generate power during non-daylight hours and/or that enables
efficient storage of energy generated during daylight hours is
desirable.
SUMMARY
[0004] The disclosed solution describes a solar cell device that
has improved efficiency in converting light to electrical energy
and the ability to output power in the dark after a period of
excitation in light The device incorporates a phosphorescent
material, within controlled proximity of the light absorber used in
solar cells. The phosphorescent material is designed and
synthesized so as to match its emission wavelength with the
absorption spectrum of the light absorber.
[0005] The aforementioned phosphorescent material comprises a donor
chromophore (donor particles) that absorbs high energy photons of
solar light and emits light of low energy photons over extended
time periods. The transfer of energy from the phosphorescent
material to the absorber acceptor particles) results in the
generation of additional electron-hole pairs to the solar cell as
compared to those produced in the absence of the phosphorescent
material, and leads to an improvement in the efficiency of the
solar cell. A device comprising the energy transfer system
described herein can be adapted for Various solar cell
technologies.
[0006] A solid state light absorber region is provided that
includes a donor-acceptor particle structure having acceptor
particles adsorbed on a large surface area of inert nanoparticles
that serve as current collectors. Upon excitation, a generation, in
and flow of electrons in the solid state light absorber region
results ifs response to absorbed photons. Donor particles are
provided comprising a phosphorescent material that are coupled to
groups of acceptor particles such that the phosphorescent material
absorbs high energy photons and emits lower energy photons that are
absorbed b the acceptor panicles.
[0007] In a first aspect, the invention provides a solar cell
device, comprising: a solid state light absorber region that
includes a donor-acceptor particle structure having: acceptor
panicles adsorbed on an inert nanoparticles current collector,
which causes a flow of electrons in the solid state light absorber
region in response to absorbed photons; and donor particles
comprising a phosphorescent material, wherein each donor particle
is coupled to a group of acceptor particles, and wherein the
phosphorescent material absorbs high energy photons and emits lower
energy photons that are absorbed by the acceptor particles.
[0008] In a second aspect, the invention provides a dye sensitive
solar cell (DSSC) device, comprising: a counter electrode; an
electrolyte region; a transparent back contact; and a transparent
electrode disposed between the electrolyte region and transparent
back content, wherein the transparent electrode includes a donor
acceptor particle structure having: acceptor particles adsorbed on
an inert nanoparticles current collector, which upon absorption of
photons, results in a flow of free electrons in the acceptor
particles, injection of electrons into the inert nanoparticles
current collector, and transport of injected electrons by the inert
nanoparticles current collector to the transparent back contact;
and donor particles comprising a phosphorescent material, wherein
each donor particle is coupled to a group of acceptor particles,
and wherein the phosphorescent material absorbs high energy photons
and emits lower energy photons that are absorbed by the acceptor
particles.
[0009] In a third aspect, the invention provides a method of
forming a dye sensitive solar cell (DSSC) device, comprising:
providing a first and a second transparent back contact; forming a
transparent electrode on the first transparent back contact wherein
the transparent electrode includes a donor-acceptor particle
structure having: acceptor particles adsorbed on an inert
nanoparticles current collector; and donor particles comprising a
phosphorescent material, wherein each donor particle is coupled to
a group of acceptor particles, and wherein the phosphorescent
material absorbs high energy photons and emits lower energy photons
that are absorbed by the acceptor particles; forming a counter
electrode on the second transparent back contact; and forming an
electrolyte region between the counter electrode and transparent
electrode; wherein the transparent electrode forms a light
absorption region, which upon absorption of photons results in a
flow of free electrons in the acceptor particles, injection of
electrons into the inert nanoparticles current collector and
transport of injected electrons by the inert nanoparticles current
collector to the first transparent back contact.
BRIEF DESCRIPTION OF THE DRAWINGS
[0010] These and other features of this invention will be more
readily understood from the following detailed description of the
various aspects of the invention taken in conjunction with the
accompanying drawings in which:
[0011] FIG. 1 depicts a donor-acceptor particle Structure according
to embodiments.
[0012] FIG. 2 depicts a dye sensitive solar cell according to
embodiments.
[0013] FIG. 3 depicts a graph showing spectral matching of donor
and acceptor particles according to embodiments.
[0014] The drawings are not necessarily to scale. The drawings are
merely schematic representations, not intended to portray specific
parameters of the invention. The drawings are intended to depict
only typical embodiments of the invention, and therefore should not
be considered as limiting the scope of the invention. In the
drawings, like numbering represents like elements.
DETAILED DESCRIPTION
[0015] A solar cell device and associated method for forming the
device are disclosed having a solid state light absorber region or
chromophore that includes coated phosphor "donor" particles placed
in close proximity to associated "acceptor" particles. While both
types of particles act as chromophores (light absorbers), the donor
particles include a phosphorescent material that absorbs high
energy photons of solar light and emits light of low energy photons
over extended time periods. The phosphorescent material is selected
so as to enable spectral overlap of its emission wavelength with
the absorption spectrum of the acceptor particles. The transfer of
energy from the phosphorescent material to the acceptor particles
results in the generation of additional electron-hole pairs in the
absorber chromophore as compared to those produced in the absence
of the phosphorescent material, and leads to the improvement in the
efficiency of the solar cell. In addition, because the
phosphorescent material continues to emit low energy photons even
after the removal of an excitation light source (e.g., the sun in
the present case), the resulting solar cell device has the ability
to output power in the dark after a period of excitation in
light.
[0016] In an illustrative embodiment, the donor-acceptor particle
structure is implemented in a solid state form with inorganic
phosphor particles having a very high phosphorescence efficiency in
which the distance between each donor particle and associated
acceptor particles is carefully controlled to optimize energy
transfer between the two. The use of inorganic phosphorescent
materials allows emission of radiation for many hours in darkened
conditions, which can he used to power a solar cell device in the
absence of light. Experimental results in a dye sensitive solar
cell application show approximately a 60% improvement in the solar
cell device's efficiency under illumination using simulated
sunlight and 300 times improvement in the dark. Because the energy
transfer is achieved in a solid state, the present approach is not
restricted to organic phosphors embedded in liquid electrolytes,
such as photoelectrochemical (PEC) solar cells, but can instead be
adapted for a wide variety of known solar cells.
[0017] Referring now to the drawings, FIG. 1 depicts a
donor-acceptor panicle structure 10 that includes a phosphor
(donor) particle 16 having a coating or spacer 14 coupled to a
group of acceptor particles 12. The acceptor particles 12 are
adsorbed on inert nanoparticles that serve as current collectors,
the structure generally being referred to as an "inert
nanoparticles current collector" 15. When incorporated into a solar
cell device, the phosphorescent material that makes up the phosphor
particle 16 is excited by high energy photons of sunlight, which is
transferred to the acceptor particles 12 to both enhance efficiency
during lighted conditions and allow for extended periods of use
(e.g., several hours) in darkened conditions.
[0018] FIG. 2 depicts an illustrative embodiment of a dye
sensitized solar cell (DSSC) device 20 that employs the
abovementioned donor-acceptor particle structure 10. Device 20
generally includes a first transparent back contact 22, a top
electrode 24 (i.e., anode) that incorporates the donor-acceptor
particle structure 10 and inert nanoparticles current collector 15
to forma solid state light, absorbing region, an electrolyte 26, a
counter electrode 28 (cathode) and a second transparent back
contact 30. The illustrative solar cell device 20 is generally
implemented using a standard dye sensitized solar cell (DSSC)
architecture, with the additional phosphor material incorporated
with the acceptor particles in the top electrode 24.
[0019] In the illustrative DSSC embodiment 20, phosphor particles
16 may for example comprise SrAl.sub.2O.sub.4 coated with a thin
layer of polycrystalline TiO.sub.2 film that forms the spacer 14.
Acceptor particles 12 may for example be comprised of an absorber
such as dye or quantum dot. material adsorbed on a TiO.sub.2
nanoparticle current collector, The TiO.sub.2 film (i.e., spacer
14) prevents the direct contact of the phosphor material 16 with
die electrolyte 26, thus preventing the quenching of phosphorescent
signals by the iodide/triiodide or other redox couples. The spacer
14 also serves as a barrier against direct charge transfer between
the phosphor particle 16 and the acceptor particles 12, and serves
as an electrical conduit for injected electrons from the excited
dye to the back contact 30 of the solar cell. TiO.sub.2 is
transparent to the visible light (e.g., .lamda.=520 nm) emitted by
the phosphor particles 16. In one illustrative embodiment, the
thickness of the TiO.sub.2 spacer may be in the range of 8-10
nm.
[0020] DSSC device 20 generally includes a solid dye structure
formed within the top electrode 24 for catching photons of incoming
light, which convert the energy into excited electrons. The excited
electrons are then injected into a conduction band of the TiO.sub.2
nanoparticles in the electrode 24, and conducted away (upward in
FIG. 2) to the first transparent back contact 22 by the layer's
TiO.sub.2 nanoparticles current collector 15 (FIG. 1). Electrolyte
26 closes the circuit 32 allowing the electrons to return to the
dye within electrode layer 24. The movement of the electrons
through the electrical circuit 32 can be used to run electrical
devices and thus produce usable work. By incorporating the
donor-acceptor particle structure 10 into the top electrode 24, the
number of electron hole pairs is increased, thus improving
efficiency. Furthermore, because the phosphorescent material
continues to emit energy for many hours after excitation, the
device will continue to output electricity in darkened
conditions.
[0021] Although described in a DSSC embodiment, the described
donor-acceptor particle structure 10 may likewise be incorporated
into other types of devices, such as quantum dot solar cells,
polymer solar cells and thin film solar cells.
[0022] In the case of a DSSC device, the following illustrative
fabrication process may he utilized, with reference to FIGS. 1 and
2. First, a light emitting phosphor 16 is selected, such as a green
(Sr.sub.0.95Eu.sub.0.02Dy.sub.0.03Al.sub.2O.sub.4) or blue
(Sr.sub.2.90Eu.sub.0.03Dy.sub.0.07Al.sub.4SiO.sub.11) emitting
phosphor having particle diameters of approximately 230 mesh and
300 mesh respectively. Next the phosphor panicles 16 are coated
with a film (i.e., spacer) 14. This may for example be done by
repeatedly spraying a mixture of 0.1 M titanium (IV) isopropoxide
and 1.2 M acetylacetonate in ethanol on the phosphor particles 16
dispersed on a silicon wafer maintained at 400.degree. C. After the
deposition, the particles may be annealed at 500.degree. C for 30
minutes to remove trace organics. The thickness of the coating may
be in range of 8-10 nm, which may be accomplished with 40
deposition cycles.
[0023] TiO.sub.2 nanoparticles may be prepared as a transparent
TiO.sub.2 paste with hydrothermal synthesis using titanium (IV)
isopropoxide as the precursor. For example, the procedure may
utilize the drop wise addition of 3.7 mL of the precursor to a
beaker containing a mixture of 1 mL of 2-propanol, 8 ml of acetic
acid, and 25 mL distilled water kept over an ice bath.
[0024] The mixture can then be heated at 80.degree. C. for 25
minutes. The entire contents can then be transferred to an
autoclave and heated to a temperature of 250.degree. C. for
approximately 13 hours. The resulting particles are repeatedly
washed with distilled water, centrifuged, and finally suspended in
ethanol until further use. Particles obtained by this procedure
comprise pure anatase phase of with an average particles size of
.about.20 nm. Scattering TiO.sub.2 nanoparticles may be prepared by
dispersing 10 grams of P25 (Degussa) powder in 30 mL of ethanol.
The mixture may then be sonicated for 30 minutes.
[0025] The top electrode 24 may be fabricated as follows. First, a
fluorine-doped tin oxide coated glass (FTO substrate--i.e., first
transparent back contact 22) is coated with a transparent blocking
layer of TiO.sub.2, such as the provided by SOLARONIX.RTM., and
annealed in a furnace at 500.degree. C. for 30 minutes, which is
then followed with a deposition of thick transparent TiO.sub.2
nanoparticles. The film is then dried and coated with 150 .mu.m of
paste containing scattering TiO.sub.2 nanoparticles and TiO.sub.2
coated SrAl.sub.2O.sub.4. The volumetric ratio of TiO.sub.2 to
phosphor particles may for example be in the range of approximately
10:1. The film is then annealed at 500.degree. C. for 60 minutes to
achieve a total film thickness of approximately 100 microns. Before
sensitization with ruthenium dye (e.g., N719, SIGMA ALDRICH.RTM.),
the substrate is immersed in 0.02M TiCl.sub.4 solution for 10
minutes, and annealed again at 450.degree. C. for 60 minutes. The
resulting substrate is then immersed in a 0.5 mM N719 dye dissolved
in 1:1 (v/v) ratio of acetonitrile and tert-butyl alcohol at
4.degree. C. to form top electrode 24.
[0026] A platinum counter electrode 28 may be prepared by applying
a thin coating of chloroplatinic acid on a second FTO substrate
(i.e., second transparent back contact 30), followed by annealing
at 500.degree. C. for 1 hour.
[0027] The electrodes 24, 28 may be assembled using a 200
.mu.m-thick hot-melt film (Surlyn 1702, SOLARNIX.RTM.) as spacer
between the transparent electrode 24 and counter electrode 28. An
electrolyte 26, e.g., consisting of 0.6 M PMII, 0.05 M I.sub.2,
0.05M tertbutyl pyridine (0.04 M) and 0.025M guanidinium
thiocyanate in 4:1 (v/v) ratio of acetonitrile and valeronitrile,
may be injected through a small, predrilled hole in the counter
electrode 28.
[0028] As noted herein, the emission spectra of the donor particles
should be selected to overlap the absorption spectra of the
acceptor particle to maximize efficiency of the device. FIG. 3, for
example, shows the absorption and emission spectra of N719 dye
dissolved in tert-butyl alcohol along with the emission spectra of
SrAl.sub.2O.sub.4 (dispersed on a copper foil) recorded at room
temperature at an excitation wavelength of 373 nm. The absorption
spectrum of N719 dye shows an absorption peak at 520 nm and has a
good spectral overlap with the emission range of SrAl.sub.2O.sub.4,
which is necessary for efficient excitation energy transfer.
SrAl.sub.2O.sub.4 has a broad excitation spectrum from 460-250 nm,
and thus can be excited by solar radiation. The phosphor exhibits a
broad band photoluminescence (PL) with maximum intensity occurring
at 520 nm.
[0029] The foregoing description of various aspects of the
invention has been presented for purposes of illustration and
description. It is not intended to be exhaustive or to limit the
invention to the precise form disclosed, and obviously, many
modifications and variations are possible. Such modifications and
variations that may be apparent to an individual in the art are
included within the scope, of the invention as defined by the
accompanying claims.
* * * * *