Anchoring single atom cobalt on two-dimensional MXene for activation of peroxymonosulfate

被引:169
作者
Song, Haoran [1 ]
Du, Rong [2 ,3 ]
Wang, Yuwei [1 ]
Zu, Daoyuan [1 ]
Zhou, Rui [1 ]
Cai, Yang [1 ]
Wang, Fangxian [1 ]
Li, Zhuo [4 ]
Shen, Yongming [5 ]
Li, Changping [1 ]
机构
[1] Dongguan Univ Technol, Res Ctr Ecoenvironm Engn, Dongguan 523808, Guangdong, Peoples R China
[2] Chinese Acad Sci, Inst High Energy Phys, Beijing 100049, Peoples R China
[3] Spallat Neutron Source Sci Ctr, Dongguan 523808, Guangdong, Peoples R China
[4] Dongguan Univ Technol, Sch Environm & Civil Engn, Dongguan 523808, Guangdong, Peoples R China
[5] Guangdong Univ Technol, Inst Environm & Ecol Engn, Guangzhou 510006, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Single atom cobalt; Peroxymonosulfate; MXene; Molten metal salts;
D O I
10.1016/j.apcatb.2021.119898
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
A simple and general vacancy defects anchoring strategy was developed for the synthesis of single atom metals, which exhibited excellent performance for peroxymonosulfate (PMS) activation. Production of Ti vacancy defects, conversion of metal ions to metal atoms, anchoring of single atom metals and construction of two-dimensional (2D) MXene structure on the eco-friendly Ti2AlN ceramic substrate were accomplished in one step using the molten transition metal salts. Complete removal of model pollutants including carbamazepine (CBZ), sulfamethoxazole (SMX) and 2,4-dichlomphen (2,4-DCP) was achieved within less than 2 min in PMS/ single atom Co process. Hydroxyl radical ((OH)-O-center dot), sulfate radical (SO4-(center dot)) and nonradical oxidation jointly contributed to pollutants degradation. More importantly, the exposed Ti atoms with strong reducibility of MXene substrate triggered the Co(III)/Co(II) cycle and thus accelerated PMS activation. The single atom Co catalyst exhibited excellent performance even under alkaline condition or in actual river water.
引用
收藏
页数:9
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