The relationship between the high-frequency performance of supercapacitors and the type of doped nitrogen in the carbon electrode

被引:1
作者
Fan, Ya-feng [1 ,2 ]
Yi, Zong-lin [1 ]
Zhou, Yi [3 ]
Xie, Li-jing [1 ]
Sun, Guo-hua [1 ]
Wang, Zhen-bing [1 ]
Huang, Xian-hong [1 ]
Su, Fang-yuan [1 ]
Chen, Cheng-meng [1 ,4 ]
机构
[1] Chinese Acad Sci, Inst Coal Chem, CAS Key Lab Carbon Mat, Taiyuan 030001, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Taiyuan Univ Technol, Coll Biomed Engn, Taiyuan 030024, Peoples R China
[4] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
High-frequency supercapacitors; Carbon electrodes; Doped nitrogen species; Adsorption energy; Descriptor; DOUBLE-LAYER CAPACITOR; ORIENTED GRAPHENE; ELECTROCHEMICAL CAPACITORS; FILMS; NANOSHEETS; MECHANISM;
D O I
10.1016/S1872-5805(24)60849-8
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Nitrogen doping has been widely used to improve the performance of carbon electrodes in supercapacitors, particularly in terms of their high-frequency response. However, the charge storage and electrolyte ion response mechanisms of different nitrogen dopants at high frequencies are still unclear. In this study, melamine foam carbons with different configurations of surface-doped N were formed by gradient carbonization, and the effects of the configurations on the high-frequency response behavior of the supercapacitors were analyzed. Using a combination of experiments and first-principle calculations, we found that pyrrolic N, characterized by a higher adsorption energy, increases the charge storage capacity of the electrode at high frequencies. On the other hand, graphitic N, with a lower adsorption energy, increases the speed of ion response. We propose the use of adsorption energy as a practical descriptor for electrode/electrolyte design in high-frequency applications, offering a more universal approach for improving the performance of N-doped carbon materials in supercapacitors
引用
收藏
页码:1015 / 1026
页数:10
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