Almost 100 % Peroxymonosulfate Conversion to Singlet Oxygen on Single-Atom CoN2+2 Sites

被引:565
作者
Mi, Xueyue [1 ]
Wang, Pengfei [2 ]
Xu, Shizhe [1 ]
Su, Lina [1 ]
Zhong, Hui [1 ]
Wang, Haitao [1 ]
Li, Yi [3 ]
Zhan, Sihui [1 ]
机构
[1] Nankai Univ, Coll Environm Sci & Engn, MOE Key Lab Pollut Proc & Environm Criteria, Tianjin Key Lab Environm Remediat & Pollut Contro, Tianjin 300350, Peoples R China
[2] Hebei Univ Technol, Sch Energy & Environm Engn, Tianjin Key Lab Clean Energy & Pollutant Control, Tianjin 300401, Peoples R China
[3] Tianjin Univ, Sch Sci, Dept Chem, Tianjin Key Lab Mol Optoelect Sci, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
advanced oxidation processes; CoN2+2 sites; peroxymonosulfate activation; reactive oxygen species; singlet oxygen; ADVANCED OXIDATION; CATALYSTS; REDUCTION; RADICALS; SULFATE;
D O I
10.1002/anie.202014472
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Single-atom CoN4 active sites have demonstrated excellent efficiency in peroxymonosulfate activation. However, the identification of CoN4 active sites and the detailed singlet oxygen generation mechanism in peroxymonosulfate activation remains ambiguous. We demonstrate a strategy to regulate the generation of reactive oxygen species by atomically dispersed cobalt anchored on nitrogen-doped carbon. As indicated by experiment and DFT calculations, CoN2+2 was the active site and singlet oxygen was the predominant reactive oxygen species with a proportion of 98.89 %. Spontaneous dissociation of adsorbed peroxymonosulfate on the CoN2+2 active sites was energetically unfavorable because of the weakly positive Co atoms and CoN2+2 coordination, which directed PMS oxidation by a non-radical pathway and with simultaneous singlet oxygen generation. The generated singlet oxygen degraded several organic pollutants with high efficiency across a broad pH range.
引用
收藏
页码:4588 / 4593
页数:6
相关论文
共 47 条
[1]  
[Anonymous], 2013, Angew. Chem
[2]  
Chen, 2019, ANGEW CHEM, V131, P8218, DOI DOI 10.1002/ANGE.201903531
[3]   Single-atom dispersed Co-N-C: A novel adsorption-catalysis bifunctional material for rapid removing bisphenol A [J].
Chen, Mantang ;
Wang, Nan ;
Zhu, Lihua .
CATALYSIS TODAY, 2020, 348 :187-193
[4]   Confining Free Radicals in Close Vicinity to Contaminants Enables Ultrafast Fenton-like Processes in the Interspacing of MoS2 Membranes [J].
Chen, Yu ;
Zhang, Gong ;
Liu, Huijuan ;
Qu, Jiuhui .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2019, 58 (24) :8134-8138
[5]   Single-Atom Catalysts: Synthetic Strategies and Electrochemical Applications [J].
Chen, Yuanjun ;
Ji, Shufang ;
Chen, Chen ;
Peng, Qing ;
Wang, Dingsheng ;
Li, Yadong .
JOULE, 2018, 2 (07) :1242-1264
[6]   Reactivity and role of SO5•- radical in aqueous medium chain oxidation of sulfite to sulfate and atmospheric sulfuric acid generation [J].
Das, TN .
JOURNAL OF PHYSICAL CHEMISTRY A, 2001, 105 (40) :9142-9155
[7]   Metal-Free Carbocatalysis in Advanced Oxidation Reactions [J].
Duan, Xiaoguang ;
Sun, Hongqi ;
Wang, Shaobin .
ACCOUNTS OF CHEMICAL RESEARCH, 2018, 51 (03) :678-687
[8]   Cascading of Molecular Logic Gates for Advanced Functions: A Self-Reporting, Activatable Photosensitizer [J].
Erbas-Cakmak, Sundus ;
Akkaya, Engin U. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (43) :11364-11368
[9]  
Fudickar W., 2018, ANGEW CHEM, V130, P13153
[10]   Release of Singlet Oxygen from Aromatic Endoperoxides by Chemical Triggers [J].
Fudickar, Werner ;
Linker, Torsten .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 57 (39) :12971-12975