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Electrocatalytic and Solar‐Driven CO 2 Reduction to CO with a Molecular Manganese Catalyst Immobilized on Mesoporous TiO 2
Author(s) -
Rosser Timothy E.,
Windle Christopher D.,
Reisner Erwin
Publication year - 2016
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201601038
Subject(s) - mesoporous material , catalysis , electrode , electrolysis , materials science , electrocatalyst , manganese , cathode , bipyridine , dimer , inorganic chemistry , artificial photosynthesis , chemistry , photochemistry , photocatalysis , electrochemistry , organic chemistry , crystal structure , electrolyte , metallurgy
Electrocatalytic CO 2 reduction to CO was achieved with a novel Mn complex, fac ‐[MnBr(4,4′‐bis(phosphonic acid)‐2,2′‐bipyridine)(CO) 3 ] ( MnP ), immobilized on a mesoporous TiO 2 electrode. A benchmark turnover number of 112±17 was attained with these TiO 2 | MnP electrodes after 2 h electrolysis. Post‐catalysis IR spectroscopy demonstrated that the molecular structure of the MnP catalyst was retained. UV/vis spectroscopy confirmed that an active Mn–Mn dimer was formed during catalysis on the TiO 2 electrode, showing the dynamic formation of a catalytically active dimer on an electrode surface. Finally, we combined the light‐protected TiO 2 | MnP cathode with a CdS‐sensitized photoanode to enable solar‐light‐driven CO 2 reduction with the light‐sensitive MnP catalyst.