A Molecular Silane-Derivatized Ru(II) Catalyst for Photoelectrochemical Water Oxidation
Author(s) -
Lei Wu,
Michael S. Eberhart,
Animesh Nayak,
M. Kyle Brennaman,
Bing Shan,
Thomas J. Meyer
Publication year - 2018
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.8b10132
Subject(s) - chemistry , silane , catalysis , photoelectrochemistry , photochemistry , electrochemistry , organic chemistry , electrode
Photoanodes in dye-sensitized photoelectrosynthesis cells integrate molecular chromophore/catalyst assemblies on mesoporous n-type metal oxide electrodes for light-driven water oxidation. One limitation for sustainable photoanodes is the stability of chromophore/catalyst assembly on electrode surfaces for long periods. Progress has been made in stabilizing chromophores based on atomic layer deposition, polymer dip coating, C-C cross-coupling by electropolymerization, and silane surface binding, but little progress has been made on catalyst stabilization. We report here the silane-derivatized catalyst, Ru(bda)(L) 2 (bda = 2,2'-bipyridine-6,6'-dicarboxylate, L = 4-(6-(triethoxysilyl)hexyl)pyridine), catalyst 1, which is stabilized on metal oxide electrode surfaces over an extended pH range. A surface stabilization study shows that it maintains its reactivity on the electrode surface toward electrochemical oxidation over a wide range of conditions. Its electrochemical stability on electrode surfaces has been systematically evaluated, and its role as a catalyst for water oxidation has been explored. On surfaces of mesoporous nanostructured core/shell SnO 2 /TiO 2 , with a TiO 2 stabilized inner layer of the Ru(II) polypyridyl chromophore, [Ru(4,4'-(PO 3 H 2 ) 2 bpy)(bpy) 2 ] 2+ (RuP 2+ ; bpy = 2,2'-bipyridine), highly efficient photoelectrochemical water oxidation catalysis occurs to produce O 2 with a maximum efficiency of ∼1.25 mA/cm 2 . Long-term loss of catalytic activity occurs with time owing to catalyst loss from the electrode surface by axial ligand dissociation in the high oxidation states of the catalyst.
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