Catalytic Membrane with Copper Single-Atom Catalysts for Effective Hydrogen Peroxide Activation and Pollutant Destruction

被引:68
作者
Ma, Wen [1 ,2 ]
Sun, Meng [5 ]
Huang, Dahong [1 ]
Chu, Chiheng [3 ]
Hedtke, Tayler [1 ]
Wang, Xiaoxiong [1 ]
Zhao, Yumeng [4 ]
Kim, Jae-Hong [1 ]
Elimelech, Menachem [1 ]
机构
[1] Yale Univ, Dept Chem & Environm Engn, New Haven, CT 06520 USA
[2] Univ Sherbrooke, Dept Chem & Biotechnol Engn, Sherbrooke, PQ J1K 2R1, Canada
[3] Zhejiang Univ, Fac Agr Life & Environm Sci, Hangzhou 310058, Peoples R China
[4] Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China
[5] Tsinghua Univ, Sch Environm, Ctr Water & Ecol, State Key Joint Lab Environm Simulat & Pollut Con, Beijing 100084, Peoples R China
基金
加拿大自然科学与工程研究理事会; 美国国家科学基金会;
关键词
single-atom catalysts; catalytic membrane; reactive membrane; membrane filtration; water-treatment membranes; Fenton-like catalysts; DISULFIDE-REDUCING AGENT; WATER-TREATMENT; WASTE-WATER; OXIDATION; DESALINATION; MECHANISMS; FENTON; FUTURE; EVOLUTION; DITHIOLS;
D O I
10.1021/acs.est.1c08937
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The superior catalytic property of single-atom catalysts (SACS) renders them highly desirable in the energy and environmental fields. However, using SACs for water decontamination is hindered by their limited spatial distribution and density on engineered surfaces and low stability in complex aqueous environments. Herein, we present copper SACs (Cu-1) anchored on a thiol-doped reactive membrane for water purification. We demonstrate that the fabricated Cu-1 features a Cu-S-2 coordination-one copper atom is bridged by two thiolate sulfur atoms, resulting in high-density Cu-SACs on the membrane (2.1 +/- 0.3 Cu atoms per nm(2)). The Cu-SACs activate peroxide to generate hydroxyl radicals, exhibiting fast kinetics, which are 40-fold higher than those of nanoparticulate Cu catalysts. The Cu-1- functionalized membrane oxidatively removes organic pollutants from feedwater in the presence of peroxide, achieving efficient water purification. We provide evidence that a dual-site cascade mechanism is responsible for in situ regeneration of Cu-1. Specifically, one of the two linked sulfur atoms detaches the oxidized Cu-1 while donating one electron, and an adjacent free thiol rebinds the reduced Cu(I)-S pair, retrieving the Cu-S-2 coordination on the reactive membrane. This work presents a universal, facile approach for engineering robust SACs on water-treatment membranes and broadens the application of SACs to real-world environmental problems.
引用
收藏
页码:8733 / 8745
页数:13
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