A novel visible-light responsive photocatalytic fuel cell with a heterostructured BiVO4/WO3 photoanode and a Pt/C air-breathing cathode

被引:37
作者
Xie, Shan [1 ,2 ]
Ouyang, Ke [1 ,2 ]
Ye, Xinyi [2 ]
机构
[1] Cent South Univ Forestry & Technol, Sch Environm Sci & Engn, Changsha 410004, Hunan, Peoples R China
[2] Wuyi Univ, Sch Chem & Environm Engn, Jiangmen 529020, Peoples R China
基金
中国国家自然科学基金;
关键词
BiVO4/WO3; photoanode; Pt/C air-breathing cathode; Photocatalytic fuel cell; Power production; Photoelectrocatalytic degradation; REFRACTORY ORGANIC-COMPOUNDS; WASTE-WATER TREATMENT; PHOTOELECTROCATALYTIC DEGRADATION; WO3/BIVO4; HETEROJUNCTION; WO3/FTO PHOTOANODE; CHARGE SEPARATION; PERFORMANCE; OXIDATION; ELECTRODE;
D O I
10.1016/j.jcis.2018.07.032
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
A series of heterostructured BiVO4/WO3 photoanodes were successfully prepared via a two-step method of hydrothermal deposition and impregnation. The optimized BiVO4/WO3 sample showed the highest photocurrent density of similar to 880 mu A/cm(2) at 0.8 V (vs Ag/AgCI) in 0.1 M KH2PO4 aqueous solution (pH 7) under simulated AM1.5 illumination. The optimized BiVO4/WO3 photoanode was coupled with a Pt/C air-breathing cathode to build up a visible-light responsive PFC system. The as-prepared PFC system showed outstanding photoelectrocatalytic performances in converting organics into electricity, and when glucose was used as the 'fuel', the maximum power density (P-max) and the short-circuit current density (I-sc) were 8.58 mu W/cm(2) and 91.8 mu A/cm(2), respectively. Degradation experiments showed that the removal rate of tetracycline hydrochloride in PFC with BiVO4/WO3 photoanode and Pt/C air-breathing cathode was similar to 87.2% in 8 h, which was much higher than photolysis and photocatalysis process. The mechanism responsible for the enhanced photoelectrocatalytic performance of the as-prepared PFC system was also discussed. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:758 / 766
页数:9
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