Enhancement of mineralization ability for phenol via synergetic effect of photoelectrocatalysis of g-C3N4 film

被引:171
作者
Liang, Fenfen [1 ]
Zhu, Yongfa [1 ]
机构
[1] Tsinghua Univ, Dept Chem, Beijng Key Lab Analyt Methods & Instrumentat, Beijing 100084, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENTAL | 2016年 / 180卷
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
Photoelectrocatalysis; Synergetic; g-C3N4; film; Mineralization phenol; CARBON NITRIDE SEMICONDUCTORS; HYDROGEN EVOLUTION; WASTE-WATER; METHYLENE-BLUE; RHODAMINE-B; TIO2; FILM; THIN-FILM; DEGRADATION; OXIDATION; PHOTOCATALYSTS;
D O I
10.1016/j.apcatb.2015.05.009
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
The enhancement of mineralization of phenol via photoelectrocatalytic (PEC) degradation of g-C3N4 film under visible light irradiation (lambda > 420 nm) was investigated. The phenol was degraded completely by the g-C3N4 with a 2.5V bias, and 89.3% of the total organic carbon (TOC) was removed, which was 2.4 times the amount achieved using photocatalytic degradation. The synergistic effect of photoelectrocatalysis was proposed to explain the dramatic enhancement. The visible light irradiation was not only able to eliminate the passivation of the g-C3N4 electrode for the phenol polymer film at potentials below 1.0V but also generated a promoting effect of electrocatalytic (EC) oxidation at potentials above 1.0V. The more active substances, such as OH and O-2(-), could be produced under light irradiation promoted the EC oxidation of phenol and the intermediate products. Simultaneously, the applied bias could reduce the recombination of the photogenerated electron-hole pairs, promote the separation of photogenerated charge carriers, and improve the photocatalytic oxidation efficiency of g-C3N4. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:324 / 329
页数:6
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