Prof Henry Snaith FRS

Abstract:

Solid-state dye-sensitized solar cells offer the possibility of high-power conversion efficiencies due to theoretically lower fundamental losses in dye regeneration. Despite continuous progress, limitations in charge diffusion through the mesoporous photoanode still constrain the device thickness and hence result in reduced light absorption with the most common sensitizers. Here we examine block copolymer-assembled photoanodes with similar surface area and morphology but a large variation in crystal size. We observe that the crystal size has a profound effect on the electron transport, which is not explicable by considering solely the ratio between free and trapped electrons. Our results are consistent with the long-range mobility of conduction band electrons being strongly influenced by grain boundaries. Therefore, maximizing the crystal size while maintaining high enough surface area will be an important route forward. © 2013 American Chemical Society.

Abstract:

Lithium salts have been shown to dramatically increase the conductivity in a broad range of polymeric and small molecule organic semiconductors (OSs). Here we demonstrate and identify the mechanism by which Li(+) p-dopes OSs in the presence of oxygen. After we established the lithium doping mechanism, we re-evaluate the role of lithium bis(trifluoromethylsulfonyl)-imide (Li-TFSI) in 2,2',7,7'-tetrakis(N,N-di-p-methoxyphenyl-amine)9,9'-Spirobifluorene (Spiro-OMeTAD) based solid-state dye-sensitized solar cells (ss-DSSCs). The doping mechanism consumes Li(+) during the device operation, which poses a problem, since the lithium salt is required at the dye-sensitized heterojunction to enhance charge generation. This compromise highlights that new additives are required to maximize the performance and the long-term stability of ss-DSSCs.

Abstract:

We present an investigation on the optimisation of solid-state dye sensitized solar cells (SDSCs) comprising mesoporous tin oxide photoanodes infiltrated with poly(3-hexylthiophene-2,5-diyl) (P3HT) hole conductor and sensitized with an organic dye. We chose both the SnO(2) and P3HT for their high charge carrier mobilities and conductivities, but as a result preclude conventional device configurations because of high leakage current and low shunt-resistance. To minimize the "hole leakage current" through the FTO anode, we employed a double compact layer structure, and to minimize "electron leakage current" at the silver cathode, we developed a protocol for depositing an optimal P3HT "capping layer". After optimisation of cell fabrication, the electron lifetime is increased considerably and the solar cells exhibited simulated AM1.5 full sun solar power conversion efficiencies in excess of 1%.

Abstract:

There has been phenomenal effort synthesizing new low-band gap polymer hole-conductors which absorb into the near-infrared (NIR), leading to >10% efficient all-organic solar cells. However, organic light absorbers have relatively narrow bandwidths, making it challenging to obtain panchromatic absorption in a single organic semiconductor. Here, we demonstrate that (poly[2,6-(4,4-bis-(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b0]dithiophene)-alt-4, 7-(2,1,3-benzothiadia-zole)] (PCPDTBT) can be "photo-sensitized" across the whole visible spectrum by "doping" with a visible absorbing dye, the (2,2,7,7-tetrakis(3-hexyl-5-(7-(4-hexylthiophen-2-yl)benzo[c][1,2,5] thiadiazol-4-yl)thiophen-2-yl)-9,9-spirobifluorene) (spiro-TBT). Through a comprehensive sub-12 femtosecond-nanosecond spectroscopic study, we demonstrate that extremely efficient and fast energy transfer occurs from the photoexcited spiro-TBT to the PCPDTBT, and ultrafast charge injection happens when the system is interfaced with ZnO as a prototypal electron-acceptor compound. The visible photosensitization can be effectively exploited and gives panchromatic photoresponse in prototype polymer/oxide bilayer photovoltaic diodes. This concept can be successfully adopted for tuning and optimizing the light absorption and photoresponse in a broad range of polymeric and hybrid solar cells. © 2013 American Chemical Society.