Electronic synergism of pyridinic- and graphitic-nitrogen on N-doped carbons for the oxygen reduction reaction

被引:212
作者
Ning, Xiaomei [1 ,2 ]
Li, Yuhang [1 ]
Ming, Jingyan [1 ]
Wang, Qiang [3 ]
Wang, Hongjuan [1 ]
Cao, Yonghai [1 ]
Peng, Feng [4 ]
Yang, Yanhui [3 ]
Yu, Hao [1 ]
机构
[1] South China Univ Technol, Guangdong Prov Key Lab Green Chem Prod Technol, Sch Chem & Chem Engn, Guangzhou 510640, Guangdong, Peoples R China
[2] Lingnan Normal Univ, Sch Chem & Chem Engn, Zhanjiang 524048, Peoples R China
[3] Nanjing Tech Univ, Sch Chem & Mol Engn, Jiangsu Natl Synerget Innovat Ctr Adv Mat, Inst Adv Synth, Nanjing 211816, Jiangsu, Peoples R China
[4] Guangzhou Univ, Sch Chem & Chem Engn, Guangzhou 510006, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
HIGH ELECTROCATALYTIC ACTIVITY; METAL-FREE ELECTROCATALYSTS; GRAPHENE-BASED CATALYSTS; ACTIVE-SITES; AEROBIC OXIDATION; CHARGE-TRANSFER; NANOTUBES; PERFORMANCE; FUNCTIONALITIES; TRANSFORMATION;
D O I
10.1039/c8sc04596h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nitrogen-doped carbon materials (NCs) are extensively studied for the oxygen reduction reaction (ORR). However, the nature of active sites of pyridinic nitrogen (N-P) or graphitic nitrogen (N-G) on NCs is still under debate. Herein, we demonstrated that the ORR activity of NCs in alkaline media depended on the electronic synergism between N-P and N-G, rather than any single type of N. We measured the transferable electrons of NCs by absorption spectroscopy using 7'7'8'8-tetracyanoquinodimethane as an electron acceptor. The transferable electron amount of NCs is relevant to either N-P or N-G, leading to the [N-P]:[N-G] ratio as an electron transfer descriptor of NCs in a reverse volcano curve manner across nineteen NCs. The similar dependence of ORR activity on the [N-P]:[N-G] ratio of NCs was also discovered, demonstrating the synergistic effect of N-P and N-G. These results provide a new angle to understand the nature of ORR activity of NCs and optimize the ORR catalyst.
引用
收藏
页码:1589 / 1596
页数:8
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