Noble Metal Modification of CdS-Covered CuInS2 Electrodes for Improved Photoelectrochemical Activity and Stability

被引:16
|
作者
Takashima, Toshihiro [1 ,2 ]
Fujishiro, Yukitaka [2 ]
Irie, Hiroshi [1 ,2 ]
机构
[1] Univ Yamanashi, Clean Energy Res Ctr, 4-3-11 Takeda, Kofu, Yamanashi 4008511, Japan
[2] Univ Yamanashi, Integrated Grad Sch Med Engn & Agr Sci, 4-3-11 Takeda, Kofu, Yamanashi 4008511, Japan
关键词
photoelectrochemistry; water splitting; hydrogen; photocathode; carbon dioxide; HYDROGEN-EVOLUTION; THIN-FILM; SILVER TANTALATE; SOLID-SOLUTION; CO2; REDUCTION; SOLAR-CELLS; WATER; PHOTOCATHODE; NANOPARTICLES; COCATALYST;
D O I
10.3390/catal10090949
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this paper, efficient and stable photoelectrochemical (PEC) hydrogen (H-2) evolution using copper indium sulfide (CuInS2) thin film electrodes was studied. Modification with a cadmium sulfide (CdS) layer led to improved charge separation at the interface between CuInS2 and CdS; however, the photocorrosive nature of CdS induced poor stability of the photocathode. Further surface coating with an electrodeposited Pt layer over the CdS-covered CuInS2 photocathode prevented the CdS layer from making contact with the electrolyte solution, and enabled efficient PEC H-2 evolution without appreciable degradation. This indicates that the Pt layer functioned not only as a reaction site for H-2 evolution, but also as a protection layer. In addition, it was found that surface protection using a noble metal layer was also effective for stable PEC carbon dioxide (CO2) reduction when appropriate noble metal cocatalysts were selected. When Au or Ag was used, carbon monoxide was obtained as a product of PEC CO2 reduction.
引用
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页数:12
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