SG190317A1 - A photovoltaic device and method for the production of a photovoltaic device - Google Patents
A photovoltaic device and method for the production of a photovoltaic device Download PDFInfo
- Publication number
- SG190317A1 SG190317A1 SG2013037965A SG2013037965A SG190317A1 SG 190317 A1 SG190317 A1 SG 190317A1 SG 2013037965 A SG2013037965 A SG 2013037965A SG 2013037965 A SG2013037965 A SG 2013037965A SG 190317 A1 SG190317 A1 SG 190317A1
- Authority
- SG
- Singapore
- Prior art keywords
- nanowires
- metallic electrode
- electrode
- photovoltaic device
- sub
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 48
- 238000004519 manufacturing process Methods 0.000 title claims description 17
- 239000002070 nanowire Substances 0.000 claims abstract description 206
- 239000000758 substrate Substances 0.000 claims abstract description 45
- 239000011149 active material Substances 0.000 claims abstract description 42
- 239000000463 material Substances 0.000 claims abstract description 33
- 230000003287 optical effect Effects 0.000 claims abstract description 10
- 239000003792 electrolyte Substances 0.000 claims description 23
- 238000000151 deposition Methods 0.000 claims description 10
- 239000011248 coating agent Substances 0.000 claims description 8
- 238000000576 coating method Methods 0.000 claims description 8
- 238000001523 electrospinning Methods 0.000 claims description 4
- 239000007921 spray Substances 0.000 claims description 4
- 238000004544 sputter deposition Methods 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 3
- 238000004528 spin coating Methods 0.000 claims description 3
- 238000007641 inkjet printing Methods 0.000 claims description 2
- 238000007639 printing Methods 0.000 claims description 2
- 238000007650 screen-printing Methods 0.000 claims description 2
- 239000000975 dye Substances 0.000 description 21
- 239000010410 layer Substances 0.000 description 15
- -1 Poly(3-hexylthiophene) Polymers 0.000 description 10
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 6
- 229910052707 ruthenium Inorganic materials 0.000 description 6
- 239000004065 semiconductor Substances 0.000 description 6
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 235000010210 aluminium Nutrition 0.000 description 4
- 238000000149 argon plasma sintering Methods 0.000 description 4
- 229920000301 poly(3-hexylthiophene-2,5-diyl) polymer Polymers 0.000 description 4
- 239000010409 thin film Substances 0.000 description 4
- 229910001887 tin oxide Inorganic materials 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 229910052787 antimony Inorganic materials 0.000 description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 3
- 229910052737 gold Inorganic materials 0.000 description 3
- 239000010931 gold Substances 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 239000002105 nanoparticle Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- YBNMDCCMCLUHBL-UHFFFAOYSA-N (2,5-dioxopyrrolidin-1-yl) 4-pyren-1-ylbutanoate Chemical compound C=1C=C(C2=C34)C=CC3=CC=CC4=CC=C2C=1CCCC(=O)ON1C(=O)CCC1=O YBNMDCCMCLUHBL-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910004613 CdTe Inorganic materials 0.000 description 2
- 229910004611 CdZnTe Inorganic materials 0.000 description 2
- 239000002033 PVDF binder Substances 0.000 description 2
- 229910002665 PbTe Inorganic materials 0.000 description 2
- 229910007709 ZnTe Inorganic materials 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 239000004411 aluminium Substances 0.000 description 2
- UHYPYGJEEGLRJD-UHFFFAOYSA-N cadmium(2+);selenium(2-) Chemical compound [Se-2].[Cd+2] UHYPYGJEEGLRJD-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000003306 harvesting Methods 0.000 description 2
- 239000002096 quantum dot Substances 0.000 description 2
- SBIBMFFZSBJNJF-UHFFFAOYSA-N selenium;zinc Chemical compound [Se]=[Zn] SBIBMFFZSBJNJF-UHFFFAOYSA-N 0.000 description 2
- OCGWQDWYSQAFTO-UHFFFAOYSA-N tellanylidenelead Chemical compound [Pb]=[Te] OCGWQDWYSQAFTO-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- SFPQDYSOPQHZAQ-UHFFFAOYSA-N 2-methoxypropanenitrile Chemical compound COC(C)C#N SFPQDYSOPQHZAQ-UHFFFAOYSA-N 0.000 description 1
- 229920003026 Acene Polymers 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 229920000144 PEDOT:PSS Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- RFFFKMOABOFIDF-UHFFFAOYSA-N Pentanenitrile Chemical compound CCCCC#N RFFFKMOABOFIDF-UHFFFAOYSA-N 0.000 description 1
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- MCEWYIDBDVPMES-UHFFFAOYSA-N [60]pcbm Chemical compound C123C(C4=C5C6=C7C8=C9C%10=C%11C%12=C%13C%14=C%15C%16=C%17C%18=C(C=%19C=%20C%18=C%18C%16=C%13C%13=C%11C9=C9C7=C(C=%20C9=C%13%18)C(C7=%19)=C96)C6=C%11C%17=C%15C%13=C%15C%14=C%12C%12=C%10C%10=C85)=C9C7=C6C2=C%11C%13=C2C%15=C%12C%10=C4C23C1(CCCC(=O)OC)C1=CC=CC=C1 MCEWYIDBDVPMES-UHFFFAOYSA-N 0.000 description 1
- JLQGBYLRJLXNCG-UHFFFAOYSA-L [I-].C(CC)[N+]1=CN(C=C1)C.[I-].C(CC)[N+]1=CN(C=C1)C Chemical compound [I-].C(CC)[N+]1=CN(C=C1)C.[I-].C(CC)[N+]1=CN(C=C1)C JLQGBYLRJLXNCG-UHFFFAOYSA-L 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical class C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 150000001716 carbazoles Chemical class 0.000 description 1
- 239000002717 carbon nanostructure Substances 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229960000956 coumarin Drugs 0.000 description 1
- 235000001671 coumarin Nutrition 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 239000002001 electrolyte material Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 125000001810 isothiocyanato group Chemical group *N=C=S 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000002086 nanomaterial Substances 0.000 description 1
- 239000002071 nanotube Substances 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- SLIUAWYAILUBJU-UHFFFAOYSA-N pentacene Chemical compound C1=CC=CC2=CC3=CC4=CC5=CC=CC=C5C=C4C=C3C=C21 SLIUAWYAILUBJU-UHFFFAOYSA-N 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920000172 poly(styrenesulfonic acid) Polymers 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 229920000447 polyanionic polymer Polymers 0.000 description 1
- 229920000867 polyelectrolyte Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229940005642 polystyrene sulfonic acid Drugs 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 150000004032 porphyrins Chemical class 0.000 description 1
- 238000009417 prefabrication Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 150000003303 ruthenium Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 229910001251 solid state electrolyte alloy Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 150000003577 thiophenes Chemical class 0.000 description 1
- 230000007723 transport mechanism Effects 0.000 description 1
- ZTWTYVWXUKTLCP-UHFFFAOYSA-N vinylphosphonic acid Chemical compound OP(O)(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
- H10K30/80—Constructional details
- H10K30/81—Electrodes
- H10K30/82—Transparent electrodes, e.g. indium tin oxide [ITO] electrodes
- H10K30/821—Transparent electrodes, e.g. indium tin oxide [ITO] electrodes comprising carbon nanotubes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/20—Light-sensitive devices
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/549—Organic PV cells
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Landscapes
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Nanotechnology (AREA)
- Physics & Mathematics (AREA)
- Electromagnetism (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Photovoltaic Devices (AREA)
Abstract
A photovoltaic device (1; 14; 17), comprising a substrate (2) comprising a major surface (3) and a material that is transparent at optical wavelengths, a first metallic electrode (6) arranged on the major surface (3), a second metallic electrode (11) spaced apart from the first electrode (6), a first plurality of nanowires (7) comprising a longitudinal outer surface and end faces and at least one photovoltaically active material (10; 23). The plurality of nanowires extends generally parallel to the major surface of the substrate and comprises semiconductive material. The plurality of first nanowires (7) and the photovoltaically active material (10; 23) are arranged between the first metallic electrode (6) and the second metallic electrode (11). The longitudinal outer surface (9) of opposing ends of the plurality of first nanowires (7) is embedded in the first metallic electrode (6).
Description
A PHOTOVOLTAIC DEVICE AND METHOD FOR THE PRODUCTION OF A PHOTOVOLTAIC
DEVICE
The application relates to a photovoltaic device, such as a solar cell, and methods for the production of a photovoltaic device.
Nanowires have the potential to facilitate a whole new generation of electronic devices. US 7,339,184 B2 discloses methods of harvesting, integrating and exploiting nano-materials, in particu- lar, elongated nanowire materials. Nanowires may be grown by successive growth on a surface to form nanowires which are orientated generally vertically with respect to the surface. Nanowires may then be harvested from this surface by selectively etching a sacrificial layer placed on a nanowire growth substrate in order to remove the nanowires. The harvested nanowires may be integrated into electronic devices such as transistors and photovoltaic devices such as solar cells.
US 7,339,184 B2 also discloses a method in which an outer surface of a cylinder is placed in contact with a fluid suspension of nanowires so that nanowires adhere to the outer surface of the cylinder and can then be deposited onto a device surface by rolling the nanowire coated cylinder onto the device surface. The nanowires are arranged laterally and parallel to the device surface.
However, further device arrangements as well as methods for nanowire harvesting and integration that facilitate mass production, yield consistent nanowire performance characteristics and generate improved device performance are desirable.
A photovoltaic device is provided that comprises a substrate comprising a major surface and a mate- rial that is transparent at optical wavelengths. The photovoltaic device further comprises a first metal- lic electrode arranged on the major surface and a second metallic electrode spaced apart from the first electrode. A first plurality of semiconductive nanowires comprising a longitudinal outer surface and end faces are provided. The plurality of nanowires extends generally parallel to the major sur- face of the substrate. The photovoltaic device also comprises at least one photovoltaically active material. The plurality of first semiconductive nanowires and the photovoltaically active material are arranged between the first metallic electrode and the second metallic electrode. The longitudinal outer surface of opposing ends of the plurality of first nanowires is embedded in the first metallic electrode.
The nanowires are generally elongated in form and are defined by the longitudinal outer surface that extends orthogonally from and between two opposing end faces. The longitudinal outer surface at regions of opposing ends of the nanowires is embedded within the first metallic electrode. This ar- 40 rangement is in contrast to an arrangement in which only the end face is in contact with the metallic electrode as would be the case if the nanowire were grown upwards vertically on the surface of the metallic electrode.
Since the longitudinal outer surface of opposing ends of the plurality of first nanowires is embedded in the first metallic electrode of the photovoltaic device, charge produced in the photovoltaically ac- tive material can be conducted along the first nanowires directly into the first metallic electrode. This avoids charge hopping between nanowires as a mechanism for charge conduction within the photo- voltaic device and increases the efficiency of charge transfer to the first metallic electrode.
The nanowires comprise a semiconductive material such as ZnO, SnO, or Sb-doped SnO,. The first metallic electrode and the second metallic electrode may comprise the same or different metals or alloys. Suitable metals are aluminum, silver, and gold.
The first metallic electrode and the second metallic electrode of the photovoltaic cell may have dif- ferent arrangements with respect to one another.
In the first group of embodiments, the second metallic electrode is spaced vertically apart from the first metallic electrode. In this sense vertical is used to define a direction perpendicular to the major surface of the substrate. Such an arrangement of the first metallic electrode and the second metallic electrode enables the photovoltaic device to be build up in a layered fashion on the first major sur- face of the substrate.
One or more of the first metallic electrode and the second metallic electrode may comprise a ring portion. Ring-shaped electrodes enable the cross-sectional area of the electrode to be increased so as to reduce the contact resistance and increase efficiency of the photovoltaic device.
The area of the photovoltaic device confined by the ring-shaped electrode remains uncovered by metal and is transparent to impinging photons. The photovoltaically active material and the nan- owires used to conduct the generated charge are arranged in this region. If both the first metallic electrode and the second metallic electrode are ring-shaped the photovoltaic device may be illumi- nated from two opposing sides.
In an embodiment, a portion of the longitudinal outer surface at opposing ends of the nanowires is embedded in opposing portions of the ring portion of the first metallic electrode. This provides a short conduction path for the generated charges along the nanowires to the first metallic electrode thus reducing resistance and loss of energy.
The photovoltaic device may further comprise an electrolyte extending between the photovoltaically active material and at least the second electrode. The first plurality of nanowires may comprise a 40 material comprising a first conductivity type and the electrolyte may comprise a material comprising a second conductivity type which opposes the first conductivity type. For example, the first plurality of nanowires may conduct electrons and the electrolyte may conduct holes or vice versa. The electro- lyte can be used to increase the collection and transfer efficiency of the second conductivity type charges within the photovoltaic device. The electrolyte may be a solid and may also have a material in the form of nanoparticles, nanowires, or carbon nanostructures.
In a second group of embodiments, the second metallic electrode is spaced laterally apart from the first metallic electrode. In this sense, laterally is used to denote a plane that is generally parallel to the first major surface. Both the first metallic electrode and the second metallic electrode may be in direct contact with the first major surface of the substrate. Such an arrangement can be used to re- duce the height of the photovoltaic device compared with embodiments in which the second metallic electrode is spaced vertically above the first metallic electrode.
In a particular embodiment of the second group of embodiments, the photovoltaic device further comprises a second plurality of nanowires. The second plurality of nanowires are arranged generally parallel to the major surface of the substrate and at an angle 6 with respect to the first plurality of nanowires, wherein 0° < 6 < 90°. The second plurality of nanowires may be generally orthogonally orientated with respect to the first plurality of nanowires, i.e. 6 = 90°.
In an embodiment, the first metallic electrode comprises at least two sub-electrodes spaced laterally apart from one another and the second metallic electrode comprises sub-electrodes spaced laterally apart from one another. The first plurality of nanowires extends between a first sub-electrode and a second sub-electrode providing the first metallic electrode and the second plurality of nanowires extend between a third sub-electrode and a fourth sub-electrode providing the second metallic elec- trode.
This arrangement of the sub-electrodes allows charge to be conducted along the first plurality of nanowires to a portion of the first metallic electrode arranged at opposing ends of the first plurality of nanowires and likewise for charge to be conducted along the second plurality of nanowires to a por- tion of the second metallic electrode arranged at opposing ends of the second plurality of nanowires.
Therefore, the area over which charge can be created by the photovoltaically active material and collected by the nanowires can be increased whilst still enabling the conduction of the charge along the length of the nanowires to the sub-electrodes to avoid a charge-hopping mechanism between nanowires as the conduction mechanism.
The photovoltaically active material may be provided in different forms. The photovoltaically active material may be provided as a coating on the plurality of first nanowires and the second plurality of nanowires, if present. The photovoltaically active material may have the form of a layer that is ar- ranged between the first plurality of nanowires and the second plurality of nanowires. The layer may 40 be a deposited layer or may be self-supporting in the form of a foil, for example. The photovoltaically active material may be a dye or a low band gap semiconductor.
A method for producing a photovoltaic device is provided that comprises providing a substrate hav- ing a major surface. The substrate comprises a material, which is transparent at optical wavelengths.
A plurality of nanowires is provided. Each nanowire comprises a longitudinal outer surface and end faces. The plurality of nanowires is arranged on the major surface of the substrate so that the nan- owires extend generally parallel to the major surface of the substrate and a photovoltaically active material is deposited onto the nanowires. A first metallic electrode and a second metallic electrode are deposited on portions of the plurality of nanowires so that a portion of the longitudinal outer sur- face of opposing ends of the plurality of nanowires is embedded in the first metallic electrode.
This method enables pre-fabricated nanowires to be applied to a major surface of a substrate and the metallic electrodes to be subsequently deposited onto the nanowires so as to embed opposing end portions of the nanowires in the first metallic electrode and provide an electrical connection be- tween the nanowires and the first metallic electrode. This method enables the production of nan- owires to be performed separately from the production of the metallic electrodes and enables each production step to be separately optimized. This may lead to a reduction in production costs as lower cost production methods may be used. For example, the nanowires may be pre-fabricated using a lower cost electro-spinning technique rather than a more expensive solid-vapor production tech- nique. Also, the material of the first metallic electrode can be selected to optimize its performance as an electrode as it does not have the dual purpose of acting as a growth surface for the nanowires as is the case for in-situ grown nanowires, for example. This enables lower cost metals such as alumi- num to be used for the metallic electrodes. Nanowires may be fabricated by a vapour-liquid-solid technique or electrospinning, for example.
An electrolyte may be deposited onto the first plurality of nanowires if it is desired that the photo- voltaic device has a further electrolyte to improve conduction of the charges generated in the photo- voltaically active material. The electrolyte may be deposited by coating the nanowires, for example by dip coating or spraying, with a suitable material before application of the nanowires onto the first major surface of the substrate. The electrolyte may also be deposited onto the nanowires after they have been applied to the substrate. The electrolyte may be deposited by a vapour deposition tech- nique, a sputtering technique, a doctor blade process, a spray process, a spin-coating technique, a screen-printing technique or an ink-jet printing technique.
If an electrolyte is provided, the second metallic electrode may be deposited onto the electrolyte and the first metallic electrode may be deposited so as to embed opposing ends of the first plurality of nanowires in the first metallic electrode.
The method may also comprise depositing a second plurality of nanowires onto the first plurality of 40 nanowires so that the second plurality of nanowires are arranged generally parallel to the major sur-
face of the substrate and at and angle 8 with respect to the first plurality of nanowires, wherein 0° < 86 < 90°. The second plurality of nanowires may be pre-fabricated and may comprise the same or a different material. For example, the first plurality of nanowires may comprise material that conducts a first charge type, for example, electrons, and the second plurality of nanowires may comprise mate- 5 rial that conducts a second charge type, for example holes, that is opposite to the first charge type.
If two pluralities of nanowires are deposited, the photovoltaically active material may be deposited onto the first plurality of nanowires and the second plurality of the nanowires deposited onto the pho- tovoltaically active material to create a layered structure in which the photovoltaically active material is sandwiched between the first plurality of nanowires and the second plurality of nanowires. This arrangement allows the charge generated in the photovoltaically active material to be transferred over a small distance to the first plurality of nanowires and the second plurality of nanowires where it is conducted directly along the nanowires to the first metallic electrode and second metallic elec- trode, respectively.
The position of the first metallic electrode and the second metallic electrode including sub- electrodes, if present, may be performed by selective deposition of the metal or alloy through a struc- tured mask. In an embodiment, a first sub-electrode is deposited onto first ends of the first plurality of nanowires, a second sub-electrode is deposited onto opposing ends of the first plurality of nan- owires, a third sub-electrode is deposited onto first ends of the second plurality of nanowires and a fourth sub-electrode is deposited onto opposing ends of the second plurality of nanowires.
One or more of the first electrode and the second electrode may be deposited by a vapour deposi- tion technique, a sputtering technique, a doctor blade process, a spray process or a solution-based printing technique.
In addition to the materials disclosed above, the following materials may also be used in the photo- voltaic device.
The photovoltaically active material may also be described as a conversion material or an absorber.
Different classes of material may be used for the photovoltaically active material such as inorganic thin films, organic thin films, dye molecules and quantum dots.
An inorganic thin film may comprise CdS, PbS, ZnS, SnS,, Ag,S, FeS;, SnS, SnS;, Cu,S, Cus,
Sb,S;, CZTS, Sh,Se;, CIS, CIGS, CdSe, PbSe, ZnSe, SnSe, Ag,Se, Sb,Te;, CdTe, CdZnTe, PbTe,
ZnTe, Ag,Te, or In Tes.
An organic thin film may comprise Poly(3-hexylthiophene) (P3HT) and other thiophenes, Poly[[9-(1- octylnonyl)-9H-carbazole-2,7-diyl]-2,5-thiophenediyl-2,1,3-benzothiadiazole-4,7-diyl-2,5- 40 thiophenediyl] (PCDTBT) and other carbazoles, Pentacene and other acenes, PCBM and other C60 derivatives, vinazenes, Poly[2,1,3-benzothiadiazole-4,7-diyl[4,4-bis(2-ethylhexyl)-4H-cyclopenta[2,1- b:3,4-b'ldithiophene-2,6-diyl]] (PCPDTBT).
A dye molecule may comprise metal center dyes including but not limited to cis-
Bis(isothiocyanato)(2,2’-bipyridyl-4,4’-dicarboxylato)(4,4’-di-nonyl-2’-bipyridyl)ruthenium(ll), Di- tetrabutylammonium cis-bis(isothiocyanato)bis(2,2’-bipyridyl-4,4’-dicarboxylato)ruthenium(ll), metal free dyes such as indoline dyes, perylene derivatives, coumarin dyes, porphyrin dyes and cyanine or merocyanine dyes.
Quantum dots may comprise CdS, PbS,ZnS,SnS; ,Ag,S,FeS,,5nS,5nS,,Cu,S,CuS,Sb,S3,CZTS,
Sb,Se;, CIS,CIGS, CdSe, PbSe, ZnSe, SnSe Ag,Se, Sb, Tes, CdTe, CdZnTe,PbTe,ZnTe,Ag,Te, In Tes.
If an electrolyte in the form of a hole conductor is provided it may comprise lodide salts dissolves in appropriate solvents including acetonitrile, valeronitrile, methoxypropionitrile and liquid organic iodide salt 1-propyl-3-methylimidazolium iodide, Spiro-OMTAD, P3HT, PEDOT:PSS and other conductive polymers, solid state electrolytes formed by dissolving lithium,chloride, phosphate and iodide ions in polymers such as PVA,PEO,PVDF and other polymer matrices or polyelectrolyte comprising a single component organic materials including but not limited to Polystyrene sulfonic acid (PSSH) or random copolymer of vinyl phosphonic acid and acrylic acid P(VPAAA) or other groups of polyanions or poly- cations with appropriate counterions including and not limited to I, Cl, OH, Li.
Embodiments will now be described with reference to the accompanying drawings.
Figure 1 illustrates a cross-sectional view of a photovoltaic device according to a first embodiment,
Figure 2 illustrates a further cross-sectional view of the photovoltaic device according to the first embodiment,
Figure 3 illustrates a top view of the photovoltaic device according to the first embodi- ment,
Figure 4 illustrates a photovoltaic device according to a second embodiment,
Figure 5 illustrates a top view of a photovoltaic cell according to a third embodiment,
Figure 6 illustrates a cross-sectional view of the photovoltaic cell according to the third embodiment, 40 Figure 7 illustrates a graph of IV-characteristics obtained from dye decorated SnO,
nanowires,
Figure 8 illustrates a graph of IV-characteristics obtained from dye decorated TiO, nanowires, and
Figure 9 illustrates a table of device performances inferred from figure 8.
Figure 1 illustrates a schematic cross-sectional view of a photovoltaic device 1 according to a first embodiment. The photovoltaic device 1 comprises a substrate 2 which comprises a major surface 3 on which the active components of the photovoltaic device 1 are positioned. The substrate 2 com- prises a material that is transparent at optical wavelengths, for example glass. The substrate 2 com- prises a second major surface 4 which opposes the first major surface 3. The second major surface 4 may provide the surface of the photovoltaic device 1 on which light impinges as schematically illus- trated by the arrows 5.
The photovoltaic device 1 comprises a first metallic electrode 6 positioned on the first major surface 3 of the substrate 2. In this embodiment, the first metallic electrode 6 has a ring shape, as illustrated in the top view of Figure 3, which may be also thought of as a rectangular frame. The photovoltaic device 1 comprises a plurality of nanowires 7, of which only one is illustrated in the cross-sectional view of figure 1, which are arranged generally parallel to the first major surface 3 of the substrate 2.
Each nanowire 7 has a generally elongated form comprising end faces 8 and a longitudinal outer surface 9 extending orthogonally from and between the end faces 8. The nanowire may have any shape (e.g. hexagonal, square, etc) cross-section and core can be hollow. Each of the nanowires 7 comprises a semiconductor material such as an oxide or a nitride, for example ZnO, SnO, or Sb- doped SnO, and nanotube.
The plurality of nanowires 7 extend between opposing portions of the ring shaped first metallic elec- trode 6 so that the outer longitudinal surface 9 of the opposing ends of the plurality of nanowires 7 is embedded within portions of the ring-shaped first metallic electrode 6 that oppose one another.
Each of the plurality of nanowires 7 is coated with a layer of a photovoltaically active material 10. As used herein, a photovoltaically active material is a material that generates a charged pair that is an electron-hole pair when light having energy bigger than the energy band gap impinges the photovol- taically active material, thus converting optical energy to electrical energy. In this embodiment, the photovoltaic active material 10 is a dye such as a Ruthenium-based dye or a low band-gap semicon- ductor.
The photovoltaic device 1 further comprises a second metallic electrode 11 which is arranged 40 spaced vertically apart from the first metallic electrode 6. The first metallic electrode 6 may comprise aluminium and the second metallic electrode 11 may comprise gold.
The photovoltaic device 1 further comprises an electrolyte 12 which extends between the second metallic electrode 11 and the first plurality of nanowires 7. In this embodiment, the plurality of nan- owires 7 comprises a semiconductor material such as tin oxide or antimony-doped tin oxide which is able to conduct electrons. The electrolyte 12 comprises a material which conducts holes such as poly (3, 4-ethylenedioxythiophene), polyaniline, poly(3-hexylthiophene), or ion-doped PVDF (polyvi- nylidene fluoride).
When light impinges the photovoltaic device 1 and the photovoltaically active material 10, an elec- tron-hole pair is formed in the photovoltaically active material 10. The electrons formed within the photovoltaic active coating 10 of the plurality of nanowires 7 are able to be conducted along the length of the nanowires 7 to the first metallic electrode 6 so that charge hopping between nanowires can be avoided, thus increasing efficiency of conduction.
The holes generated in the photovoltaically active coating 10 can be conducted through the electro- lyte 12 to the second metallic electrode 11 to produce a voltage between the first metallic electrode 6 and the second metallic electrode 11 and convert optical energy to electrical energy.
Figure 2 illustrates a second cross-sectional view of the photovoltaic device 1 illustrated in figure 1.
In the cross-sectional view of figure 2, the plurality of nanowires 7 are illustrated. In this embodiment, only a single layer of nanowires is illustrated. However, the plurality of nanowires may be arranged in several layers and may not necessarily be arranged exactly parallel to one another but also at angles of up to 90° with respect to one another.
Figure 3 illustrates a top view of the photovoltaic device 1 illustrated in figures 1 and 2. In figure 3, the rectangular ring form of the first metallic electrode 6 and of the second metallic electrode 11 can be seen. The plurality of nanowires 7 extend between two opposing sides of the rectangular ring form of the first metallic electrode 6. The first metallic electrode 6 further includes a protruding por- tion 13 which extends from one side of the first metallic electrode 6 along the major surface 3 of the substrate 2. This extended portion 13 can be used as a contact area for the first metallic electrode 6.
The second metallic electrode 11 is arranged vertically above the plurality of nanowires 7. The first metallic electrode 6 may be electrically contacted by means of a bondwire, for example. In further non-illustrated embodiment, the second metallic electrode 11 may also have a protrusion similar to portion 13 for electrical contact.
Figure 4 illustrates a photovoltaic device 14 according to a second embodiment. Similar parts are indicated with the same number as in the first embodiment.
The photovoltaic device 14 of the second embodiment also includes a ring shaped first electrode 6 positioned on a substrate 2 that is optically transparent and a first plurality of nanowires 7 extending between opposing portions of the first metallic electrode 6. Again, the plurality of nanowires 7 is coated with a photovoltaically active material 10 in the form of a ruthenium-based dye or low band gap semiconductor. The plurality of nanowires 7 is embedded in an electrolyte material 12 which has the opposing conductivity as that of the material of the plurality of nanowires 7. Alternatively, the plurality of nanowires 7 itself may absorb the light and play the role of the photovoltaically active material 10.
In the second embodiment, the photovoltaic device 14 further comprises a light scattering layer 15 comprising a second plurality of nanowires 16. A ring shaped second metallic electrode 11 is posi- tioned on the light scattering layer 15, which can comprise nanoparticles so that the second metallic electrode 11 is spaced apart from the first metallic electrode 6.
The light scattering layer 15 serves to prevent shorting between the first metallic electrode 6 and the second metallic electrode 11 and may also provide light scattering so as to reflect light back towards the photovoltaically active material 10 coating the plurality of nanowires 7. This can help to increase the efficiency of the conversion of the optical energy into electrical energy.
Figure 5 illustrates a top view of a photovoltaic cell 17 according to a third embodiment. Figure 6 illustrates a cross-sectional view along the line A-A of the photovoltaic cell 17 of Figure 5. The photo- voltaic device 17 comprises a substrate 2 that is optically transparent as in the first and second em- bodiments. The photovoltaic device 17 comprises, in addition to a first plurality of nanowires 7, a second plurality of nanowires 18 which also extend generally parallel to the major surface 3 of the substrate 2 but generally orthogonally to the first plurality of nanowires 7. The second plurality of nanowires 18 is positioned vertically above or can be intermixed (e.g. like in textiles or clothing) with the first plurality of nanowires 7.
In contrast to the previous embodiments, the first metallic electrode 6 and a second metallic elec- trode 11 are laterally spaced apart from one another and are both positioned on the major surface 3 of the substrate 2 rather than being vertically spaced apart from one another as is illustrated in the cross-sectional view of figure 6.
Each of the first metallic electrode 6 and the second metallic electrode 11 comprises two sub- electrodes which are spaced apart from one another so that each sub-electrode embeds opposing ends of the respective plurality of nanowires. The photovoltaic device 17 comprises four sub- electrodes, each spaced apart from one another.
A first sub-electrode 19 and a second sub-electrode 20 provide the first metallic electrode 6 and are 40 arranged so as to embed opposing ends of the first plurality of nanowires 7. A third sub-electrode 21 and a fourth sub-electrode 22 provide the second metallic electrode 11 and are arranged so as to embed opposing end portions of the second plurality of nanowires 18. Therefore, the first sub- electrode 19 and second sub-electrode 20 together form the anode and the third sub-electrode 21 and the fourth sub-electrode 22 together form the cathode of the photovoltaic device 17.
A photovoltaically active material is provided in the form of a layer 23 that is positioned between the first plurality of nanowires 7 and the second plurality of nanowires 18.
The material of the first plurality of nanowires 7 and of the second plurality of nanowires 18 is chosen so that the first plurality of nanowires 7 has a complimentary conduction type to that of the second plurality of nanowires 18. For example, the first plurality of nanowires 7 may conduct electrons and the second plurality of nanowires 18 may conduct holes, or vice versa.
When light impinges the lower surface 4 of the substrate 2, or, in the case of discontinuous elec- trodes, also from the opposing side of the photovoltaic device 17, it passes into the photovoltaically device 17 generating electron-hole pairs in the photovoltaic active layer 23. The electrons are con- ducted by means of the first plurality of nanowires 7 to the first sub-electrode 19 and to the second sub-electrode 20 which form the anode and the holes generated are conducted by the second plural- ity of nanowires 18 to the third sub-electrode 21 and to the fourth sub-electrode 22 which form the cathode of the photovoltaic device 17.
The photovoltaically active layer 23 not only generates electron hole pairs under the illumination but can also be used to prevent recombination of the electrons and holes at the junctions where the first plurality of nanowires 7 and the second plurality of nanowires 18 cross. This arrangement of the two pluralities of nanowires also allows for elimination of the photovoltaically active layer 23 from both sides whilst avoiding the use of transparent conductive oxides.
In further embodiments, the photovoltaically active layer 23 can be replaced by a photovoltaically active coating of both the first plurality of nanowires 7 and of the second plurality of nanowires 18.
In further embodiments, the use of additional photoactive layer 23 and of photovoltaically active ma- terial in the form of a coating can be avoided by either making the first plurality of the nanowires 7 or the second plurality of nanowires 18 photovoltaically active.
In all of the previously described embodiments, the nanowires are used to collect charges produced in the photovoltaically active material of the photovoltaic device and conduct them directly to the respective metallic electrode or sub-electrode. This avoids the use of charge hopping between sepa- rate nano-sized particles as a charge transport mechanism and increases the efficiency of the de- vice.
The nanowires may be configured so as to optimize the efficiency of the device. For example, the density of the nanowires may be optimized. The use of a low-density nanowires results in larger charge collection lengths and lower collection efficiency. However, increasing the nanowire network density above a threshold-level resulted in reduced light transmission since the nanowires them- selves are not transparent at optical wavelengths. Therefore, an optimum density of nanowires is required. The density of nanowires is also dependent on the length and in particular the diameter, as well as the electrical resistivity of the nanowires. By using long nanowires of high-quality, that is low electrical resistance, the density of the nanowires may be reduced whilst obtaining sufficient charge collection.
In the embodiments described above, the photovoltaic active material is described as a dye and, in particular, a ruthenium-based dye. However, this dye can be replaced by compounds such as a low bandgap polymer or other inorganic semiconductors.
The photovoltaic devices may be fabricated using pre-fabricated nanowires which are then arranged on the major surface of the device substrate so that they are aligned generally parallel to the major surface of the device substrate. The photovoltaically active material may then be deposited onto the nanowires or the nanowires may be pre-coated with the photovoltaically active material before they are applied to the device substrate. The metallic electrodes and the electrolyte may them be depos- ited onto the nanowires to build up the device structure. This method enables the photovoltaic device to be fabricated using a wide variety of fabrication techniques and allows different fabrication tech- niques to be combined. For example, the electrolyte may be deposited using spin-coating and the metallic electrode deposited by evaporation. The method is flexible so that the device structure can be better optimized and the production methods optimized so as to reduce costs.
The photovoltaic devices described above may be fabricated using pre-fabrication nanowires. These pre-fabricated nanowires may be produced using the following methods.
In an embodiment, tin oxide nanowires are synthesised on a silicon (100) substrate comprising a 2 nm thick gold film as a catalyst using a vacuum vapour transport approach. A mixture of tin oxide (SnO,) and active graphite powder, both having a 99% purity, in a molar ratio of 2 to 1, are used as a source and are loaded in to the centre of quartz tube arranged in a furnace. The temperature is rap- idly increased to 900° C and the silicon substrate is placed downstream of the tin oxide and graphite powder source materials in a temperature zone at around 780°C. The peak temperature is held for 15 minutes using argon carrier gas at a flow rate of 120 standard cubic centimetres per minute under pressure of 6.107" Torr. The system is then cooled to room temperature in vacuum. Tin oxide nan- owires grow generally vertically from the silicon substrate. The tin oxide nanowires may also be doped with 5% antimony to increase the conductivity of the nanowires.
In further embodiments, the tin oxide nanowires may also be fabricated by electro-spinning. What- ever, the fabrication method, the prefabricated nanowires are coated with a ruthenium-based dye which acts as the photovoltaically active material.
The pre-fabricated tin oxide nanowires are then transferred to a device substrate, such as a glass substrate, using a contact method so that laterally aligned tin oxide nanowires are formed on the major surface of the device substrate. The nanowires lie parallel to the major surface of the device substrate rather than vertically. The first and second electrodes may be formed by selectively evapo- rating aluminium using a mask to form electrodes having a thickness of around 100 nm. The shape of mask is chosen so as to provide the desired arrangement of the electrodes with respect to the nanowires.
Figure 7 illustrates a graph of Current-Voltage (IV) characteristics measured for dye decorated SnO, nanowire networks under photoillumination. The overall thickness of the nanowire networks was around 100nm. The insert of Figure 7 illustrates a strip electrode used to collect the charges.
Figure 8 illustrates a graph of IV-characteristics measured for dye decorated TiO, nanowire networks under photoillumination. The overall thickness of the nanowire networks was around 1 um (micron).
The device performances inferred from figure 8 are summarized in table 1 of figure 9.
The results illustrated in Figures 7 and 8 demonstrate that dye decorated semiconductive and, in particular, oxide nanowires can be successfully used in the production of photovoltaically active de- vices, such as solar cells.
Claims (20)
1. A photovoltaic device (1; 14; 17), comprising: a substrate (2) comprising a major surface (3) and a material that is transparent at optical wave- lengths, a first metallic electrode (6) arranged on the major surface (3), a second metallic electrode (11) spaced apart from the first electrode (6), a first plurality of nanowires (7) comprising a longitudinal outer surface and end faces, the plu- rality of nanowires extending generally parallel to the major surface of the substrate and com- prising semiconductive material, and at least one photovoltaically active material (10; 23), the plurality of first nanowires (7) and the photovoltaically active material (10; 23) being arranged between the first metallic electrode (6) and the second metallic electrode (11), the longitudinal outer surface (9) of opposing ends of the plurality of first nanowires (7) being embedded in the first metallic electrode (6).
2. The photovoltaic device (1; 14) according to claim 1, wherein the second metallic electrode (11) is spaced vertically apart from the first metallic electrode (6).
3. The photovoltaic device (1; 14) according to claim 1 or claim 2, wherein one or more of the first metallic electrode (6) and the second metallic electrode (11) comprises a ring portion.
4. The photovoltaic device (1; 14) according to claim 2, wherein a portion of the longitudinal outer surface (9) at opposing ends of the first plurality of nanowires (7) is embedded in opposing por- tions of the ring portion of the first metallic electrode (6).
5. The photovoltaic device (1; 14) according to one of claims 1 to 4, further comprising an electro- lyte (12) extending between the photovoltaically active material (10) and at least the second electrode (11), wherein the first plurality of nanowires (7) comprise a material comprising a first conductivity type and the electrolyte (12) comprises a material comprising a second conductivity type which opposes the first conductivity type.
6. The photovoltaic device (17) according to claim 1, wherein the second metallic electrode (11) is spaced laterally apart from the first metallic electrode (6).
7. The photovoltaic device (17) according to claim 6 further comprising a second plurality of nan- owires (18) , the second plurality of nanowires (18) being arranged generally parallel to the ma- jor surface (3) of the substrate (2) and at an angle 0 with respect to the first plurality of nan- owires (7), wherein 0° < 8 < 90°.
8. The photovoltaic device (17) according to claim 7, wherein the first metallic electrode (6) com- prises at least two sub-electrodes (19, 20) spaced laterally apart from one another and the sec- ond metallic electrode (11) comprises sub-electrodes (21, 22) spaced laterally apart from one another, wherein the first plurality of nanowires (7) extend between a first sub-electrode (19) and a second sub-electrode (20) providing the first metallic electrode (6) and the second plural- ity of nanowires (18) extend between a third sub-electrode (21) and a fourth sub-electrode (22) providing the second metallic electrode (11).
9. The photovoltaic device (17) according to claim 7 or claim 8, wherein the first plurality of nan- owires (7) comprise a material comprising a first conduction type and the second plurality of nanowires (18) comprise a material comprising a second conduction type that opposes the first conduction type.
10. The photovoltaically device (1; 14; 17) according to one of claims 1 to 9, wherein the photovol- taically active material (10) is provided as a coating on the plurality of first nanowires (7) and the second plurality of nanowires (18), if present.
11. The photovoltaic device (17) according to one of claims 6 to 9, wherein the photovoltaically active material (23) has the form of a layer and is arranged between the first plurality of nan- owires (7) and the second plurality of nanowires (18).
12. Method for producing a photovoltaic device (1; 14; 17) comprising: providing a substrate (2) having a major surface (3) that comprises a material that is transpar- ent at optical wavelengths, providing a plurality of nanowires (7) comprising a longitudinal outer surface (9) and end faces (8), arranging the plurality of nanowires (7) on the major surface (3) of the substrate (2) so that the plurality of nanowires (7) extend generally parallel to the major surface (3) of the substrate (2), depositing a photovoltaically active material (10) onto the plurality of nanowires (7), and depositing a first metallic electrode (6) and a second metallic electrode (11) on portions of the plurality of nanowires (7) so that a portion of the longitudinal outer surface (9) of opposing ends of the plurality of nanowires (7) is embedded in the first metallic electrode (6).
13. The method according to claim 12, wherein the plurality of nanowires (7) are fabricated by a vapour-liquid-solid technique or electrospinning.
14. The method according to claim 12 or claim 13 further comprising depositing an electrolyte (12) onto the first plurality of nanowires (7) .
15. The method according to claim 14, wherein the second metallic electrode (11) is deposited onto the electrolyte (10) and the first metallic electrode (6) is deposited so as to embed oppos- ing ends of the first plurality of nanowires (7) in the first metallic electrode (6).
16. The method according to one of claims 12 to 14 further comprising depositing a second plurality of nanowires (18) onto the first plurality of nanowires (7) so that the second plurality of nan- owires (18) are arranged generally parallel to the major surface (3) of the substrate (2) and at and angle 6 with respect to the first plurality of nanowires (7), wherein 0° <6 < 90°.
17. The method according to claim 16, wherein photovoltaically active material (23) is deposited onto the first plurality of nanowires (7) and the second plurality of the nanowires (18) is depos- ited onto the photovoltaically active material (23).
18. The method according to claim 17 or claim 18, wherein a first sub-electrode (19) is deposited onto first ends of the first plurality of nanowires (7), a second sub-electrode (20) is deposited onto opposing ends of the first plurality of nanowires (7), a third sub-electrode (21) is deposited onto first ends of the second plurality of nanowires (18) and a fourth sub-electrode (22) is de- posited onto opposing ends of the second plurality of nanowires (18).
19. The method according to one of claims 12 to 18, wherein one or more of the first metallic electrode (6) and the second metallic electrode (11) is depos- ited by a vapour deposition technique, a sputtering technique, a doctor blade process, a spray process or a solution-based printing technique.
20. The method according to one of claims 12 to 19, wherein the electrolyte (12) is deposited by a vapour deposition technique, a sputtering technique, a doctor blade process, a spray process, a spin-coating technique, a screen-printing technique or an ink-jet printing technique.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/IB2010/055256 WO2012066386A1 (en) | 2010-11-18 | 2010-11-18 | A photovoltaic device and method for the production of a photovoltaic device |
Publications (1)
Publication Number | Publication Date |
---|---|
SG190317A1 true SG190317A1 (en) | 2013-06-28 |
Family
ID=46083535
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG2013037965A SG190317A1 (en) | 2010-11-18 | 2010-11-18 | A photovoltaic device and method for the production of a photovoltaic device |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP2641273A1 (en) |
CN (1) | CN103299434A (en) |
SG (1) | SG190317A1 (en) |
WO (1) | WO2012066386A1 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101352861B1 (en) * | 2012-12-21 | 2014-02-18 | 한국에너지기술연구원 | Preparation method of a(c)igs-based thin film using core(se)-shell(ag2se) nanoparticles, a(c)igs-based thin film prepared by the same, and tandem solar cell containing the same |
CN108502933B (en) * | 2018-05-21 | 2019-07-12 | 中国科学院广州地球化学研究所 | Photovoltaic device, pyrite band gap modulator approach, photovoltaic material and preparation method thereof |
CN110846752B (en) * | 2019-11-21 | 2022-05-06 | 东华大学 | Device and method for preparing efficient light hot water evaporation material |
CN118299445B (en) * | 2024-06-06 | 2024-08-16 | 中北大学 | Self-powered photoelectric detection device with wide spectral response and preparation method thereof |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20070025745A (en) * | 2005-09-05 | 2007-03-08 | 삼성전자주식회사 | Photoelectrochemical device using carbonnanotube |
KR100659831B1 (en) * | 2005-10-19 | 2006-12-19 | 삼성전자주식회사 | Dye-sensitized photovoltaic cell and preparation method of electrode substrate for the photovoltaic cell |
KR100648273B1 (en) * | 2005-12-21 | 2006-11-27 | 고려대학교 산학협력단 | Dye-sensitized solar cell and manufacturing method thereof |
CN101411001A (en) * | 2006-02-16 | 2009-04-15 | 索莱赞特公司 | Nanoparticle sensitized nanostructured solar cells |
JP5127330B2 (en) * | 2007-07-12 | 2013-01-23 | 日立造船株式会社 | Photoelectric conversion element and manufacturing method thereof |
CN101971360A (en) * | 2008-02-08 | 2011-02-09 | 清洁电池国际股份有限公司 | Composite nanorod-based structures for generating electricity |
US8551558B2 (en) * | 2008-02-29 | 2013-10-08 | International Business Machines Corporation | Techniques for enhancing efficiency of photovoltaic devices using high-aspect-ratio nanostructures |
JP5746143B2 (en) * | 2009-04-09 | 2015-07-08 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | Three-dimensional dye-sensitized solar cell with nanoscale architecture |
-
2010
- 2010-11-18 WO PCT/IB2010/055256 patent/WO2012066386A1/en active Application Filing
- 2010-11-18 EP EP10859755.0A patent/EP2641273A1/en not_active Withdrawn
- 2010-11-18 SG SG2013037965A patent/SG190317A1/en unknown
- 2010-11-18 CN CN2010800702146A patent/CN103299434A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
EP2641273A1 (en) | 2013-09-25 |
WO2012066386A1 (en) | 2012-05-24 |
CN103299434A (en) | 2013-09-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR101172534B1 (en) | Inorganic-Organic Heterojunction Solar Cells with All-Solid State | |
KR101168227B1 (en) | Fabrication Method of Nanostructured Inorganic-Organic Heterojunction Solar Cells | |
US7462774B2 (en) | Photovoltaic devices fabricated from insulating nanostructured template | |
US20080230120A1 (en) | Photovoltaic device with nanostructured layers | |
US20100224252A1 (en) | Photovoltaic Cell Having Multiple Electron Donors | |
US10199590B2 (en) | Photovoltaic cell module | |
JP2002111031A (en) | Solid hetero junction and solid sensitization (photosensitive) photovoltaic cell | |
JP2009532851A (en) | Nanoparticle-sensitized nanostructure solar cell | |
JP4991126B2 (en) | Laminated organic solar cell and method for producing the same | |
US20140060639A1 (en) | Copper oxide core/shell nanocrystals for use in photovoltaic cells | |
US8742253B1 (en) | Device configurations for CIS based solar cells | |
WO2009005805A2 (en) | Distributed coax photovoltaic device | |
KR101543438B1 (en) | Perovskite solar cell and preparing method thereof | |
CN102142523A (en) | Solar cells with enhanced efficiency | |
SG190317A1 (en) | A photovoltaic device and method for the production of a photovoltaic device | |
TW201123583A (en) | Dye-sensitized solar cell and method forming the same | |
US20110247693A1 (en) | Composite photovoltaic materials | |
Li et al. | Flexible Optoelectronic Devices Based on Hybrid Perovskites | |
EP2538452A2 (en) | All-solid-state heterojunction solar cell | |
KR102135101B1 (en) | Semi-transparent/flexible solar cell and method for manufacturing thereof | |
KR101281566B1 (en) | Organic solar cell with high efficiency and manufacturing method thereof using carbon nonotubes | |
Duraisamy et al. | Fabrication of Metal Top Electrode via Solution‐based Printing Technique for Efficient Inverted Organic Solar Cells | |
KR101262258B1 (en) | Organic and inorganic hybrid solar cell with high efficiency and manufacturing method thereof using nanowires and carbon nonotubes | |
Sivasubramanian et al. | Silicon Nanowires for green energy applications | |
Zhu | Research on indoor applications of organic photovoltaics |