Photoelectrochemical production of useful fuels from carbon dioxide on a polypyrrole-coated p-ZnTe photocathode under visible light irradiation

被引:67
作者
Won, Da Hye [1 ]
Chung, Jaehoon [1 ]
Park, Sung Hyeon [1 ]
Kim, Eun-Hee [3 ]
Woo, Seong Ihl [1 ,2 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Taejon 305701, South Korea
[2] Korea Adv Inst Sci & Technol, Grad Sch EEWS, Taejon 305701, South Korea
[3] Korea Basic Sci Inst, Div Magnet Resonance Res, Cheongjoo 363883, South Korea
关键词
ELECTROCHEMICAL REDUCTION; CO2; REDUCTION; HIGH-PRESSURE; THIN-FILMS; CONVERSION; CATALYST; ELECTRODEPOSITION; SEMICONDUCTOR; METHANOL;
D O I
10.1039/c4ta05901h
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
To achieve high performance photoelectrochemical CO2 reduction, a polypyrrole-coated p-ZnTe electrode (PPy/ZnTe) was fabricated as a new photocathode material and its catalytic activities were investigated. The PPy deposited on the p-ZnTe electrode improved the photoelectrochemical CO2 reduction activity as a surface modifying catalyst. Under the irradiation of visible light, the PPy/ZnTe showed a prominent performance with a 51.0% of Faradaic efficiency at -0.2 V (vs. RHE) without any significant overpotential loss. The ultraviolet photoelectron spectroscopy (UPS) and electrochemical impedance spectroscopy (EIS) implied that the enhanced catalytic performances were primarily attributed to the enhanced conversion efficiency of photoenergy on the PPy/ZnTe. It was suggested that the PPy/ZnTe electrode improved the generation of photo-induced electron-hole pairs, and the different work functions of ZnTe and PPy introduced an electron pathway from ZnTe to PPy and then to the reactants.
引用
收藏
页码:1089 / 1095
页数:7
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