4.8 Article

Rational Regulation of Co-N-C Coordination for High-Efficiency Generation of 1O2 toward Nearly 100% Selective Degradation of Organic Pollutants

期刊

ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 56, 期 12, 页码 8833-8843

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.2c00706

关键词

multiple pollutants; selective oxidation; singlet oxygen; peroxymonosulfate; Co-N-C catalysts

资金

  1. National Key Research and Development Program of China [2019YFC0408302]
  2. National Natural Science Foundation of China [51878352, BX20200167]
  3. China Postdoctoral Science Foundation [2020M680070]

向作者/读者索取更多资源

Single oxygen-based advanced oxidation processes show great promise in selectively degrading organic pollutants. However, achieving efficient production of O-1(2) through tailored catalyst design for selective oxidation of contaminants remains challenging.
Single oxygen-based advanced oxidation processes (O-1(2)-AOPs) exhibit great prospects in selective degradation of organic pollutants. However, efficient production of O-1(2) via tailored design of catalysts to achieve selective oxidation of contaminants remains challenging. Herein, we develop a simple strategy to regulate the components and coordination of Co-N-C catalysts at the atomic level by adjusting the Zn/Co ratio of bimetallic zeolitic imidazolate frameworks (ZnxCo1-ZIFs). Zn4Co1-C demonstrates 98% selective removal of phenol in the mixed phenol/benzoic acid (phenol/BA) solutions. Density functional theory calculations and experiments reveal that more active CoN4 sites are generated in Zn4Co1-C, which are beneficial to peroxymonosulfate activation to generate O-1(2). Furthermore, the correlation between the origin of selectivity and well-defined catalysts is systematically investigated by the electron paramagnetic resonance test and quenching experiments. This work may provide novel insights into selective removal of target pollutants in a complicated water matrix.

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