Cobalt porphyrin electrode films for electrocatalytic water oxidation

被引:58
|
作者
Han, Ali [1 ]
Jia, Hongxing [1 ]
Ma, Hao [1 ]
Ye, Shifan [1 ]
Wu, Haotian [1 ]
Lei, Haitao [2 ]
Han, Yongzhen [2 ]
Cao, Rui [2 ]
Du, Pingwu [1 ]
机构
[1] Univ Sci & Technol China, Dept Chem, Dept Mat Sci & Engn, CAS Key Lab Mat Energy Convers, Hefei 230026, Peoples R China
[2] Renmin Univ China, Dept Chem, Beijing 100872, Peoples R China
基金
中国国家自然科学基金;
关键词
OXYGEN-EVOLVING CATALYST; PHOTOSYSTEM-II; HOMOGENEOUS CATALYSTS; HYDROGEN-PRODUCTION; DIOXYGEN EVOLUTION; COMPLEXES; EFFICIENT; METAL; CHALLENGES; PHOSPHATE;
D O I
10.1039/c4cp00523f
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
Catalysts play very important roles in artificial photosynthesis for solar energy conversion. In this present study, two water-insoluble cobalt porphyrin complexes, cobalt(II) meso-tetraphenylporphyrin (CoP-1) and cobalt(II) 5,10,15,20-tetrakis-(4-bromophenyl) porphyrin (CoP-2), were synthesized and coated as thin films on the FTO working electrode. The films showed good activities for electrocatalytic water oxidation in aqueous solutions at pH 9.2. The Faradaic efficiencies of both films approached to similar to 100%, measured using a fluorescence-based oxygen sensor. The turnover frequencies were close to 0.50 s(-1) and 0.40 s(-1) for CoP-1 and CoP-2, respectively, under an applied anodic potential of 1.3 V (vs. Ag/AgCl) at pH 9.2. Importantly, no cobalt oxide particles were observed on the working electrode after catalysis. The stability of the catalyst films was further evaluated by UV-vis spectroscopy, inhibition measurements, mass spectrometry, scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX). The pH dependence of water oxidation on CoP-1 and CoP-2 suggested a proton-coupled electron transfer (PCET) mechanism. The catalyst films could be recycled and showed almost unchanged catalytic activities when they were reused in new electrocatalytic studies of water oxidation.
引用
收藏
页码:11209 / 11217
页数:9
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