Photofunctional Construct That Interfaces Molecular Cobalt-Based Catalysts for H2 Production to a Visible-Light-Absorbing Semiconductor

被引:125
作者
Krawicz, Alexandra [1 ]
Yang, Jinhui [1 ]
Anzenberg, Eitan [1 ]
Yano, Junko [1 ]
Sharp, Ian D. [1 ]
Moore, Gary F. [1 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, JCAP, Berkeley, CA 94720 USA
关键词
ELECTROCATALYTIC HYDROGEN EVOLUTION; SOLAR FUEL PRODUCTION; POLYMER BRUSHES; PHOTOELECTROCHEMICAL CELL; ARTIFICIAL PHOTOSYNTHESIS; FUNCTIONAL MODELS; ELECTRON-TRANSFER; WATER REDUCTION; COBALOXIMES; ENERGY;
D O I
10.1021/ja404158r
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Molecular cobalt-containing hydrogen production catalysts are grafted to a visible-light-absorbing semiconductor. The attachment procedure exploits the UV-induced immobilization chemistry of vinylpyridine to p-type (100) gallium phosphide (GaP). Single step surface-initiated photopolymerization yields a covalently attached polymer with pendent pyridyl groups that provide attachment points for assembling cobaloxime catalysts. Successful attachment is characterized by grazing angle attenuated total reflection Fourier transform infrared spectroscopy (GATR-FTIR), which shows distinct vibrational modes associated with the catalyst, as well as X-ray photoelectron spectroscopy (XPS) and X-ray absorption near edge structure spectroscopy (XANES) that confirm the presence of intact Co-III complex on the surface. The Co-functionalized photocathode shows significantly enhanced photoelectrochemical (PEC) performance in aqueous conditions at neutral pH, compared to results obtained on GaP without attached cobalt complex PEC measurements, at 100 mW cm(-2) illumination, yield a 2.4 mA cm(-2) current density at a 310 mV underpotential.
引用
收藏
页码:11861 / 11868
页数:8
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