Nitrogen-doped hollow mesoporous carbon spheres for efficient oxygen reduction

被引:0
|
作者
Wang, Hao [1 ,2 ,3 ]
Zheng, Caixia [1 ,2 ,3 ]
Huang, Bing [2 ,3 ]
Jiang, Nannan [2 ,3 ]
Li, Yaoxin [1 ,2 ,3 ]
Wang, Minghao [2 ,3 ]
Wu, Qirui [1 ,2 ,3 ]
Wang, Huiying [1 ,2 ,3 ]
Guan, Lunhui [1 ,2 ,3 ]
机构
[1] Fuzhou Univ, Coll Chem, Fuzhou 350108, Peoples R China
[2] Chinese Acad Sci, Fujian Inst Res Struct Matter, CAS Key Lab Design & Assembly Funct Nanostruct, Fuzhou 350002, Fujian, Peoples R China
[3] Chinese Acad Sci, Fujian Inst Res Struct Matter, Fujian Prov Key Lab Nanomat, Fuzhou 350002, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
oxygen reduction reaction; nitrogen-doped carbon catalyst; hollow structure; energy conversion; ELECTROCATALYSTS; GRAPHENE; ALLOY;
D O I
10.1088/1361-6528/acf3f4
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Extensive investigations have been devoted to nitrogen-doped carbon materials as catalysts for the oxygen reduction reaction (ORR) in various conversion technologies. In this study, we introduce nitrogen-doped carbon materials with hollow spherical structures. These materials demonstrate significant potential in ORR activity within alkaline media, showing a half-wave potential of 0.87 V versus the reversible hydrogen electrode (RHE). Nitrogen-doped hollow carbon spheres (N-CHS) exhibit unique characteristics such as a thin carbon shell layer, hollow structure, large surface area, and distinct pore features. These features collectively create an optimal environment for facilitating the diffusion of reactants, thereby enhancing the exposure of active sites and improving catalytic performance. Building upon the promising qualities of N-CHS as a catalyst support, we employ heme chloride (1 wt%) as the source of iron for Fe doping. Through the carbonization process, Fe-N active sites are effectively formed, displaying a half-wave potential of 0.9 V versus RHE. Notably, when implemented as a cathode catalyst in zinc-air batteries, this catalyst exhibits an impressive power density of 162.6 mW cm-2.
引用
收藏
页数:9
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