Constructing single atom sites on bipyridine covalent organic frameworks for selective electrochemical production of H2O2

被引:18
作者
Huang, Shaoda [1 ,2 ]
Zhang, Bingyan [1 ]
Sun, Huimin [1 ]
Hu, Hongyin [1 ]
Wang, Jinyan [1 ]
Duan, Fang [1 ]
Zhu, Han [1 ]
Du, Mingliang [1 ]
Lu, Shuanglong [1 ]
机构
[1] Jiangnan Univ, Sch Chem & Mat Engn, Key Lab Synthet & Biol Colloids, Minist Educ, Wuxi 214122, Jiangsu, Peoples R China
[2] Nanyang Technol Univ, Sch Mat Sci & Engn, Nat Sci & Sci Educ Natl Inst Educ, Singapore 637616, Singapore
关键词
HYDROGEN-PEROXIDE;
D O I
10.1039/d3cc02948d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We developed a series of single atom catalysts (SACs) anchored on bipyridine-rich COFs. By tuning the active metal center, the optimal Py-Bpy-COF-Zn shows the highest selectivity of 99.1% and excellent stability toward H2O2 production via oxygen reduction, which can be attributed to the high *OOH dissociation barrier indicated by the theoretical calculations. As a proof of concept, it acts as a cathodic catalyst in a homemade Zn-air battery, together with efficient wastewater treatment.
引用
收藏
页码:10424 / 10427
页数:4
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