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Photoelectrochemical Hydrogen Production in Alkaline Solutions Using Cu 2 O Coated with Earth‐Abundant Hydrogen Evolution Catalysts
Author(s) -
MoralesGuio Carlos G.,
Liardet Laurent,
Mayer Matthew T.,
Tilley S. David,
Grätzel Michael,
Hu Xile
Publication year - 2015
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201410569
Subject(s) - catalysis , oxygen evolution , hydrogen production , water splitting , inorganic chemistry , hydrogen , photocathode , chemistry , alkaline earth metal , oxide , amorphous solid , molybdenum , hydrogen sulfide , electrochemistry , metal , sulfur , photocatalysis , electrode , organic chemistry , physics , quantum mechanics , electron
The splitting of water into hydrogen and oxygen molecules using sunlight is an attractive method for solar energy storage. Until now, photoelectrochemical hydrogen evolution is mostly studied in acidic solutions, in which the hydrogen evolution is more facile than in alkaline solutions. Herein, we report photoelectrochemical hydrogen production in alkaline solutions, which are more favorable than acidic solutions for the complementary oxygen evolution half‐reaction. We show for the first time that amorphous molybdenum sulfide is a highly active hydrogen evolution catalyst in basic medium. The amorphous molybdenum sulfide catalyst and a Ni–Mo catalyst are then deposited on surface‐protected cuprous oxide photocathodes to catalyze sunlight‐driven hydrogen production in 1 M KOH. The photocathodes give photocurrents of −6.3 mA cm −2 at the reversible hydrogen evolution potential, the highest yet reported for a metal oxide photocathode using an earth‐abundant hydrogen evolution reaction catalyst.