Multi-radicals mediated one-step conversion of methane to acetic acid via photocatalysis

被引:15
作者
Wang, Juxue [1 ,2 ]
Zhang, Ling [1 ,2 ]
Zeng, Di [1 ,2 ]
Wang, Wenjing [1 ]
Li, Ruofan [1 ,2 ]
Jia, Taikang [1 ,2 ]
Cui, Bingkun [1 ,2 ]
Chu, Hongxiang [1 ,3 ]
Wang, Wenzhong [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine M, 1295 Dingxi Rd, Shanghai 200050, Peoples R China
[2] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
[3] Univ Chinese Acad Sci, Hangzhou Inst Adv Study, Sch Chem & Mat Sci, 1 Sub Lane Xiangshan, Hangzhou 310024, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2023年 / 337卷
基金
中国国家自然科学基金;
关键词
Photocatalysis; Oxidative coupling of methane; Acetic acid; Chlorine radical; CO2; REDUCTION; OXIDATION; CH4; ACTIVATION; ENERGY; OXIDE;
D O I
10.1016/j.apcatb.2023.122983
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
One-step photocatalytic methane conversion to acetic acid possesses high economic and academic value, and carbonyl species (CO, CO2) are usually necessary to be introduced into the reaction system to realize the carboncarbon coupling reaction, which requires high energy input. In this work, a composite photocatalyst (Ag/AgCl-WO3-x) was constructed to successfully realize the one-step photocatalytic conversion of CH4 to CH3COOH without addition of carbonyl species. Chlorine radicals and hydroxyl radicals could be produced simultaneously under light irradiation over Ag/AgCl. Specifically, CH4 could undergo the hydrogen atom transfer reaction with chlorine radicals to produce methyl species, and hydroxyl radicals could mineralize CH4 to produce carbonyl species. After further combining WO3-x, carbon-carbon coupling reaction between carbonyl and methyl species occurred to effectively produce CH3COOH (188.5 mu mol center dot g(cat)(-1)center dot h(-1)). This work provides a new prospect of designing photocatalytic system to realize CH4 conversion to C-2 products.
引用
收藏
页数:9
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