No abstract

We report all solid-state nanostructured inorganic-organic heterojunction solar cells fabricated by depositing Sb(2)S(3) and poly(3-hexylthiophene) (P3HT) on the surface of a mesoporous TiO(2) layer, where Sb(2)S(3) acts as an absorbing semiconductor and P3HT acts as both a hole conductor and light absorber. These inorganic-organic light harvesters perform remarkably well with a maximum incident-photon-to-current efficiency (IPCE) of 80% and power conversion efficiency of 5.13% under air-mass 1.5 global (AM 1.5G) illumination with the intensity of 100 mW cm(-2). These devices are highly stable under room light in air, even without encapsulation. The present findings offer novel directions for achieving high-efficiency solid-state solar cells by hybridization of inorganic-organic light harvesters and hole transporters.

Sb(2)S(3)-sensitized mesoporous-TiO(2) solar cells using several conjugated polymers as hole-transporting materials (HTMs) are fabricated. We found that the cell performance was strongly correlated with the chemical interaction at the interface of Sb(2)S(3) as sensitizer and the HTMs through the thiophene moieties, which led to a higher fill factor (FF), open-circuit voltage (V(oc)), and short-circuit current density (J(sc)). With the application of PCPDTBT (poly(2,6-(4,4-bis-(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b']dithiophene)-alt-4,7(2,1,3-benzothiadiazole)) as a HTM in a Sb(2)S(3)-sensitized solar cell, overall power conversion efficiencies of 6.18, 6.57, and 6.53% at 100, 50, and 10% solar irradiation, respectively, were achieved with a metal mask.

Additional photon-harvesting by hole transporting materials in Sb(2)S(3)-sensitized solar cell is demonstrated through the formation of electron channels in the hole transporter such as P3HT (poly(3-hexylthiophene)) and PCPDTBT(poly(2,6-(4,4-bis-(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b']dithiophene)-alt-4,7(2,1,3-benzothiadiazole)) that can act as both a hole conductor and light absorber. As a result, the short-circuit current density is improved with an increment in overall efficiency. These findings provide new insights into use of light-absorbing conjugated polymers as a hole conductor in the inorganic-organic heterojunction sensitized solar cells.

TiO 2 colloids are very useful photocatalytic systems, capable of converting solar energy to chemical or electrical energy and environmental cleaning. The key step in enhancing photocatalytic efficiency is improving photoinduced interfacial electron transfer like plant photosynthesis. It remains difficult to modify TiO 2 particles as a real analogue of the photosynthetic reaction centers of green plants. We attempted to incorporate a photoreactive heteropoly acid (HPA) such as H 3 PW 12 O 40 into TiO 2 colloids in aqueous polyvinyl alcohol (PVA) (0.1%) solution, and found that two light reactions appear to operate in a series. Upon illumination of the HPA/TiO 2 system with near-UV light (300-375 nm), interfacial electron transfer takes place from the conduction band of TiO 2 to the incorporated HPA, which is also excited to catalyze photoreduction of Methyl Orange. The extent of the photoinduced reduction of the HPA adsorbed on TiO 2 particles depends on the concentration ratio of the HPA and TiO 2 colloids, irradiation wavelength, and intensity of radiation. It is found that the interfacial electron-transfer mechanism of HPA/TiO 2 is quite analogous to the "Z-scheme" mechanism for plant photosynthetic systems. The photoinduced charge-carrier generation at the heterojunction is very efficient, and the photoreduction of Methyl Orange has been observed to be synergistically enhanced upon illumination of the HPA-incorporated TiO 2 with visible light as well as near-UV light.