In situ recombination for durable photoelectrocatalytic degradation of organic dye in wastewater

被引:9
|
作者
Zhang, Xiaoyan [1 ,2 ]
Liang, Xian [2 ]
Xu, Mai [2 ]
Wang, Jin [2 ]
Wang, Fengwu [2 ]
Chen, Minggong [1 ]
机构
[1] Anhui Univ Sci & Technol, Sch Earth & Environm, Huainan 232001, Anhui, Peoples R China
[2] Huainan Normal Univ, Sch Chem & Mat Engn, Huainan 232001, Anhui, Peoples R China
关键词
Photoelectrocatalysis; Electrode; Degradation; Recombination; Wastewater; TIO2 NANOTUBE ARRAYS; PHOTOCATALYTIC ACTIVITY; FILM ELECTRODE; OXIDATION; PHOTOANODES; PERFORMANCE; HETEROJUNCTION; 4-CHLOROPHENOL; POLLUTANTS; GENERATION;
D O I
10.1016/j.chemosphere.2022.137237
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Photoelectrocatalysis (PEC) can effectively degrade organic pollutants by using photoelectrodes without secondary pollution. However, significant mass transport resistance and decreased catalytic activity caused by the shedding of active components remain a barrier to achieving the photocatalytic system with a high degradation rate and long-term durability. Here, an in situ recombination concept is presented to overcome this challenge. The bionic coral-like electrode, obtained by in situ assembly of UIO-66 around TiO2 nanoflowers (TNF) on Tifoam substrate, is employed as the photoanode in PEC. Ex situ evaluation of photoelectrochemical activity demonstrates that the UIO-66@TNF/Ti-foam (U@T/T) design significantly improves the light-propagation, lightabsorption and charge transfer. In Situ degradation evaluations also shows that the interesting design promotes rapid and stable degradation of organic dye (e.g. Rhodamine B (RhB)). At 2.0 V of bias potential and pH 7.0 in 5 mg L-1 RhB, under the action of active species such as center dot O-2(-) and center dot OH (proved by the degradation mechanism experiments), the removal rate of RhB can reach 96.1% at 120 min and almost complete removal at 200 min (99.1%).
引用
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页数:11
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