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Journal ArticleDOI

Photodriven heterogeneous charge transfer with transition-metal compounds anchored to TiO2 semiconductor surfaces

Shane Ardo, +1 more
- 01 Jan 2009 - 
- Vol. 38, Iss: 1, pp 115-164
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TLDR
A critical review of light-driven interfacial charge-transfer reactions of transition-metal compounds anchored to mesoporous, nanocrystalline TiO2 (anatase) thin films is described.
Abstract
A critical review of light-driven interfacial charge-transfer reactions of transition-metal compounds anchored to mesoporous, nanocrystalline TiO2 (anatase) thin films is described. The review highlights molecular insights into metal-to-ligand charge transfer (MLCT) excited states, mechanisms of interfacial charge separation, inter- and intra-molecular electron transfer, and interfacial charge-recombination processes that have been garnered through various spectroscopic and electrochemical techniques. The relevance of these processes to optimization of solar-energy-conversion efficiencies is discussed (483 references).

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Citations
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Dye-Sensitized Solar Cells

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Graphitic Carbon Nitride (g-C3N4)-Based Photocatalysts for Artificial Photosynthesis and Environmental Remediation: Are We a Step Closer To Achieving Sustainability?

TL;DR: It is anticipated that this review can stimulate a new research doorway to facilitate the next generation of g-C3N4-based photocatalysts with ameliorated performances by harnessing the outstanding structural, electronic, and optical properties for the development of a sustainable future without environmental detriment.
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Semiconductor-mediated photodegradation of pollutants under visible-light irradiation

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Artificial photosynthesis for solar water-splitting

TL;DR: In this paper, a vision for a future sustainable hydrogen fuel community based on artificial photosynthesis is outlined and current progress towards artificial photosynthetic devices is reviewed, with particular focus on visible light active nanostructures.
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Spatial separation of photogenerated electrons and holes among {010} and {110} crystal facets of BiVO4

TL;DR: The results show that the photogenrated electrons and holes can be separated between the different facets of semiconductor crystals, which may be useful in semiconductor physics and chemistry to construct highly efficient solar energy conversion systems.
References
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Journal ArticleDOI

Excited State Electron Transfer from Ru(II) Polypyridyl Complexes Anchored to Nanocrystalline TiO2 through Rigid-Rod Linkers

TL;DR: In this paper, rigid-rod linkers varying in length were used to bind Ru(II) polypyridyl complexes to the surface of TiO2 (anatase) and of ZrO2 nanoparticle thin films.
Journal ArticleDOI

Evidence for multiple-state emission from ruthenium(II) complexes

TL;DR: In this article, the lifetime of decay and the quantum yield of luminescence for tris(2,2′-bipyridine)ruthenium(II) cation were measured for each individual level and group theoretical symmetry assignments were made on the basis of a proposed electronic coupling model.
Journal ArticleDOI

Using spectroscopy to probe the band energetics of transparent nanocrystalline semiconductor films

TL;DR: In this article, the flatband potential of a photoelectrochemical cell based on polycrystalline semiconductor films is derived from the measured relationship between free electron absorbance or the Burstein shift, and the applied potential at different pHs.
Journal ArticleDOI

Determination of exciton hopping rates in ruthenium(II) tris(bipyridine) complexes by picosecond polarized absorption spectroscopy

TL;DR: In this paper, the depolarization ratio exhibits a biexponential decay, consisting of 75 ps and 2.4 ns components, and the two components of the decay are assigned to exciton hopping and to rotational diffusion.
Journal ArticleDOI

Synthesis and electron transfer studies of ruthenium-terpyridine-based dyads attached to nanostructured TiO2.

TL;DR: A series of bis(terpyridine)RuII complexes have been prepared, where one of the terpyridines is functionalized in the 4'-position by a phosphonic or carboxylic acid group for attachment to TiO2, followed by secondary electron transfer from the donor to the photogenerated RuIII.
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