An electroactive single-atom copper anchored MXene nanohybrid filter for ultrafast water decontamination

被引:60
作者
Jin, Limin [1 ]
You, Shijie [2 ]
Yao, Yuan [3 ]
Chen, Hong [4 ]
Wang, Yi [5 ]
Liu, Yanbiao [1 ]
机构
[1] Donghua Univ, Coll Environm Sci & Engn, Text Pollut Controlling Engn Ctr, Minist Environm Protect, Shanghai 201620, Peoples R China
[2] Harbin Inst Technol, Sch Environm, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China
[3] Harbin Inst Technol, Sch Chem & Chem Engn, MIIT Key Lab Crit Mat Technol New Energy Convers, Harbin 150080, Peoples R China
[4] Southern Univ Sci & Technol, Sch Environm Sci & Engn, Shenzhen 518055, Peoples R China
[5] State Key Lab NBC Protect Civilian, Beijing 102205, Peoples R China
基金
中国国家自然科学基金;
关键词
EFFICIENT CO2 ELECTROREDUCTION; HETEROGENEOUS ACTIVATION; PEROXYMONOSULFATE; DEGRADATION; CATALYSTS; MEMBRANE; RADICALS; KINETICS;
D O I
10.1039/d1ta07396f
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
Single-atom catalysts possess attractive electrocatalytic ability for degrading contaminants owing to their desirable characteristics compared with bulk counterparts. Herein, single Cu atoms anchored on Ti3C2Tx MXene (Cu-SA/Ti3C2Tx) have been demonstrated as a highly reactive and robust nanohybrid filter for ultrafast removal of micropollutants via electro-peroxymonosulfate (PMS) activation. Sulfamethoxazole, a typical antibiotic, is observed to fully degrade via a single-pass through the nanohybrid filter (<150 ms) at 1.5 mL min(-1). Both experimental and theoretical studies verified that the Cu-O-3 are the active sites for electro-PMS activation to produce O-1(2) and induce electron transfer for SMX degradation. As a result of the size effects, the HO radicals dominate the SMX degradation process when anchoring Cu nanoparticles to the Ti3C2Tx nanosheets. This study provides a proof-in-concept demonstration of the free-standing Cu-SA/Ti3C2Tx nanohybrid filter that may find important applications in addressing the global problem of water pollution.
引用
收藏
页码:25964 / 25973
页数:11
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