Docampo, P and Ivaturi, A and Gunning, R and Diefenbach, S and Kirkpatrick, J and Palumbiny, CM and Sivaram, V and Geaney, H and Schmidt-Mende, L and Welland, ME and Snaith, HJ (2013) The influence of 1D, meso- and crystal structures on charge transport and recombination in solid-state dye-sensitized solar cells. Journal of Materials Chemistry A, 1. pp. 12088-12095. ISSN 2050-7488Full text not available from this repository.
We have prepared single crystalline SnO2 and ZnO nanowires and polycrystalline TiO2 nanotubes (1D networks) as well as nanoparticle-based films (3D networks) from the same materials to be used as photoanodes for solid-state dye-sensitized solar cells. In general, superior photovoltaic performance can be achieved from devices based on 3-dimensional networks, mostly due to their higher short circuit currents. To further characterize the fabricated devices, the electronic properties of the different networks were measured via the transient photocurrent and photovoltage decay techniques. Nanowire-based devices exhibit extremely high, light independent electron transport rates while recombination dynamics remain unchanged. This indicates, contrary to expectations, a decoupling of transport and recombination dynamics. For typical nanoparticle-based photoanodes, the devices are usually considered electron-limited due to the poor electron transport through nanocrystalline titania networks. In the case of the nanowire-based devices, the system becomes limited by the organic hole transporter used. In the case of polycrystalline TiO2 nanotube-based devices, we observe lower transport rates and higher recombination dynamics than their nanoparticle-based counterparts, suggesting that in order to improve the electron transport properties of solid-state dye-sensitized solar cells, single crystalline structures should be used. These findings should aid future design of photoanodes based on nanowires or porous semiconductors with extended crystallinity to be used in dye-sensitized solar cells. © 2013 The Royal Society of Chemistry.
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|Date Deposited:||04 Feb 2015 22:05|
|Last Modified:||01 May 2015 19:07|