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CMP
Credit: Jack Hobhouse

Prof Henry Snaith FRS

Professor of Physics

Sub department

  • Condensed Matter Physics

Research groups

  • Snaith group
  • Advanced Device Concepts for Next-Generation Photovoltaics
Henry.Snaith@physics.ox.ac.uk
Robert Hooke Building, room G21
  • About
  • Publications

A new ion-coordinating ruthenium sensitizer for mesoscopic dye-sensitized solar cells

Inorganica Chimica Acta 361:3 (2008) 699-706

Authors:

D Kuang, C Klein, HJ Snaith, R Humphry-Baker, SM Zakeeruddin, M Grätzel

Abstract:

A new ion-coordinating ruthenium polypyridyl sensitizer, NaRu(4-carboxylic acid-4′-carboxylate)(4,4′-bis[(triethyleneglycolmethylether) heptylether]-2,2′-bipyridine)(NCS)2 (coded as K68), has been synthesized and characterized by 1H NMR, FTIR, UV-Vis absorption and emission spectroscopy. A power conversion efficiency of 6.6% was obtained for dye-sensitized solar cells (DSCs) based on the K68 dye and a newly developed binary ionic liquid electrolyte containing 1-propyl-3-methyl-imidazolium iodide (PMII) and 1-ethyl-3-methyl-imidazolium tetracyanoborate (EMIB(CN)4). For a non-volatile organic solvent based electrolyte, a photovoltaic power conversion efficiency of 7.7% was obtained under simulated full sun light and exhibited a good thermal stability during the accelerated test under 80 °C in the dark. Solid-state DSCs incorporating K68 also perform remarkably well, out-performing our previously best ruthenium complexes employed in this type of DSC. © 2007 Elsevier B.V. All rights reserved.
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Charge transport in mesoscopic hybrid solar cells

SPIE Newsroom SPIE, the international society for optics and photonics (2008)
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Electron and hole transport through mesoporous TiO2 infiltrated with spiro-MeOTAD

Advanced Materials 19:21 (2007) 3643-3647

Authors:

HJ Snaith, M Grätzel

Abstract:

In-plane 'hole-only' and 'electron-only' devices were fabricated and the the conductivity was selectively measured through the TiO2 and the Spiro-MeOTAD. The hole conductivity through the composite was approximately three times higher than the electron conductivity. The mobility of TiO 2 decreases as the illumination intensity was increased towards intensities comparable with full sunlight. The effective diffusion coefficient for electrons reduced considerably as the light intensity approached solar illumination intensities, with the diffusion length becoming shorter than the film thickness.
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Efficiency enhancements in solid-state hybrid solar cells via reduced charge recombination and increased light capture.

Nano Lett 7:11 (2007) 3372-3376

Authors:

Henry J Snaith, Adam J Moule, Cédric Klein, Klaus Meerholz, Richard H Friend, Michael Grätzel

Abstract:

We compare a series of molecular sensitizers in dye-sensitized solar cells containing the organic hole transporter 2,2',7,7'-tetrakis(N,N-di-p-methoxypheny-amine)-9,9'-spirobifluorene (spiro-MeOTAD). Charge recombination is reduced by the presence of "ion-coordinating" moieties on the dye, with the longest electron lifetime and highest solar cell efficiency achieved using a novel sensitizer with diblock alkoxy-alkane pendent groups. By further increasing the optical path length in the active layer, we achieve a power conversion efficiency of over 5% under simulated sun light.
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Advances in liquid-electrolyte and solid-state dye-sensitized solar cells

Advanced Materials 19:20 (2007) 3187-3200

Authors:

HJ Snaith, L Schmidt-Mende

Abstract:

This Progress Report highlights recent developments in dye-sensitized solar cells composed of both liquid electrolytes and solid-state hole transport materials. The authors discuss and review the present understanding of and recent developments in the operational processes, such as charge generation, transport, recombination, and charge collection. Also, the merits and challenges of alternative device approaches are discussed, including extremely thin absorber cells, device containing inorganic p-type hole-transporters and non-TiO2 mesoporous metal-oxide electrodes employed in dye-sensitized solar cells. © 2007 WILEY-VCH Verlag GmbH & Co. KGaA.
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