Bioinspired molecular co-catalysts bonded to a silicon photocathode for solar hydrogen evolution
Author(s) -
Yidong Hou,
Billie L. Abrams,
Peter C. K. Vesborg,
Mårten E. Björketun,
Konrad Herbst,
Lone Bech,
Alessandro M. Setti,
Christian Danvad Damsgaard,
Thomas Pedersen,
Ole Hansen,
Jan Rossmeisl,
Søren Dahl,
Jens K. Nørskov,
Ib Chorkendorff
Publication year - 2011
Publication title -
nature materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 14.344
H-Index - 483
eISSN - 1476-4660
pISSN - 1476-1122
DOI - 10.1038/nmat3008
Subject(s) - photocathode , solar fuel , hydrogen , hydrogen production , catalysis , materials science , platinum , water splitting , solar energy , silicon , density functional theory , hydrogen fuel , nanotechnology , chemical physics , chemical engineering , chemistry , optoelectronics , computational chemistry , photocatalysis , physics , organic chemistry , ecology , quantum mechanics , electron , biology , engineering
The production of fuels from sunlight represents one of the main challenges in the development of a sustainable energy system. Hydrogen is the simplest fuel to produce and although platinum and other noble metals are efficient catalysts for photoelectrochemical hydrogen evolution, earth-abundant alternatives are needed for large-scale use. We show that bioinspired molecular clusters based on molybdenum and sulphur evolve hydrogen at rates comparable to that of platinum. The incomplete cubane-like clusters (Mo(3)S(4)) efficiently catalyse the evolution of hydrogen when coupled to a p-type Si semiconductor that harvests red photons in the solar spectrum. The current densities at the reversible potential match the requirement of a photoelectrochemical hydrogen production system with a solar-to-hydrogen efficiency in excess of 10%. The experimental observations are supported by density functional theory calculations of the Mo(3)S(4) clusters adsorbed on the hydrogen-terminated Si(100) surface, providing insights into the nature of the active site.
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