Optoelectronic device and fabrication method
AssigneeNanosolar, Inc.
InventorsBrian Sager, Martin Roscheisen, Klaus Petritsch, Greg Smestad, Jacqueline Fidanza, Gregory Miller, Dong Yu
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AssigneeNanosolar, Inc.
InventorsBrian Sager, Martin Roscheisen, Klaus Petritsch, Greg Smestad, Jacqueline Fidanza, Gregory Miller, Dong Yu
Estimating the term…
Charge-splitting networks, optoelectronic devices, methods for making optoelectronic devices, power generation systems utilizing such devices and method for making charge-splitting networks are disclosed. An optoelectronic device may include a porous nano-architected (e.g., surfactant-templated) film having interconnected pores that are accessible from both the underlying and overlying layers. A pore-filling material substantially fills the pores. The interconnected pores have diameters of about 1-100 nm and are distributed in a substantially uniform fashion with neighboring pores separated by a distance of about 1-100 nm. The nano-architected porous film and the pore-filling, material have complementary charge-transfer properties with respect to each other, i.e., one is an electron-acceptor and the other is a hole-acceptor. The nano-architected porous, film may be formed on a substrate by a surfactant temptation technique such as evaporation-induced self-assembly. A solar power generation system may include an array of such optoelectronic devices in the form of photovoltaic cells with one or more cells in the array having one or more porous charge-splitting networks disposed between an electron-accepting electrode and a hole-accepting electrode.
An optoelectronic device, comprising:
A method for making an optoelectronic device, the method comprising:
The method of claim 17 wherein the one or more alkoxides include titanium ethoxide or titanium isopropoxide, the one or more surfactants include p123, hexadecyl trimethylammonium bromide (CTAB), or F127, and the one or more condensation inhibitors include hydrochloric acid (HCl).
The method of claim 24 wherein the initial sol is prepared by refluxing the titanium tetra-isopropoxide, ethanol, water and HCl, at approximately 60° C.
The method of claim 29, wherein the inorganic material includes copper oxide or another metal oxide.
The method of claim 31, wherein the polymer is a chosen from the group of poly(phenylene) and derivatives thereof, poly(phenylene vinylene) and derivatives thereof (e.g., poly(2-methoxy-5-(2-ethyl-hexyloxy)-1,4-phenylene vinylene (MEH-PPV), poly(para-phenylene vinylene), (PPV)), poly(thiophene) and derivatives thereof (e.g., poly(3-octylthiophene-2,5,-diyl), regioregular, poly(3-octylthiophene2,5,-diyl), regiorandom, Poly(3-hexylthiophene-2,5-diyl), regioregular, Poly(3-hexylthiophene-2,5-diyl), regiorandom), poly(thienylenevinylene) and derivatives thereof, and poly(isothianaphthene) and derivatives thereof, organometallic polymers, polymers containing perylene units, poly(squaraines) and their derivatives.
The method of claim 32 wherein the polythiophene is poly 3-hexylthiophene (P3HT).
The method of claim 33, further comprising, after infiltrating the pores with the solution, incubating the surfactant-templated porous film at an infiltration temperature of about 200° C. for about 30 minutes.
A solar power generation system, comprising:
The system of claim 38, wherein each of the porous charge-splitting networks includes:
The system of claim 39, wherein two or more of the cells in the array are electrically connected to each other in series.
A method for making a charge-splitting network, the method comprising:
The method of claim 41, wherein the porous-nano-architected film is produced using one or more techniques selected from the following group:
Dependencies are inferred from the claim text.