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一种构建用于氧还原反应的高效铜 - 氮活性位点的简便方法。

A Facile Route for Constructing Effective Cu-N Active Sites for Oxygen Reduction Reaction.

作者信息

Li Jingjing, Xia Wei, Wang Tao, Zheng Lirong, Lai Yue, Pan Junjie, Jiang Cheng, Song Li, Wang Mengyu, Zhang Huting, Chen Na, Chen Guang, He Jianping

机构信息

College of Materials Science and Technology, Jiangsu Key Laboratory of, Electrochemical Energy Storage Technologies, Nanjing University of, Aeronautics and Astronautics, 210016, Nanjing, P. R. China.

Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing, 100049, P. R. China.

出版信息

Chemistry. 2020 Mar 26;26(18):4070-4079. doi: 10.1002/chem.201903822. Epub 2019 Dec 6.

Abstract

The coordination number between copper and nitrogen in copper/nitrogen-based electrocatalysts is important for boosting the oxygen reduction reaction (ORR). However, it is difficult to control unsaturated copper/nitrogen constructions as well as to compare their ORR performances in similar carbon matrices in a simple yet efficient manner. In this study, we have easily attained two types of Cu -N and Cu -N constructions simply by etching pyrolyzed Cu-doped zeolitic imidazolate framework nanoleaves (Cu-ZIF-L) with sulfuric acid or nitric acid, respectively. X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) spectra were recorded to further confirm the different copper/nitrogen constructions after the different acid treatments. Electrochemical studies have demonstrated that Cu -N sites are more active in boosting the ORR performance than Cu -N sites. Furthermore, Cu-N/C-H SO , used as an air cathode in a zinc-air battery, exhibited excellent performance and stability.

摘要

铜/氮基电催化剂中铜与氮之间的配位数对于促进氧还原反应(ORR)至关重要。然而,以简单而有效的方式控制不饱和铜/氮结构以及比较它们在类似碳基质中的ORR性能是困难的。在本研究中,我们分别通过用硫酸或硝酸蚀刻热解的铜掺杂沸石咪唑酯骨架纳米片(Cu-ZIF-L),轻松获得了两种类型的Cu-N和Cu-N结构。记录了X射线吸收近边结构(XANES)和扩展X射线吸收精细结构(EXAFS)光谱,以进一步确认不同酸处理后不同的铜/氮结构。电化学研究表明,Cu-N位点在促进ORR性能方面比Cu-N位点更具活性。此外,用作锌空气电池空气阴极的Cu-N/C-H SO表现出优异的性能和稳定性。

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