Fe, N, S-codoped carbon frameworks derived from nanocrystal superlattices towards enhanced oxygen reduction activity

被引:24
作者
Zou, Jinxiang [1 ,2 ]
Wang, Biwei [1 ,2 ]
Zhu, Baixu [3 ,4 ]
Yang, Yuchi [3 ,4 ]
Han, Wendian [1 ,2 ]
Dong, Angang [1 ,2 ]
机构
[1] Fudan Univ, iChem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
[2] Fudan Univ, Dept Chem, Shanghai 200433, Peoples R China
[3] Fudan Univ, State Key Lab Mol Engn Polymers, Shanghai 200433, Peoples R China
[4] Fudan Univ, Dept Macromol Sci, Shanghai 200433, Peoples R China
关键词
Self-assembly; Nanocrystals; Heteroatom doping; Single atom; Oxygen reduction reaction; ELECTROCATALYSTS; PERFORMANCE; IRON; CATALYSTS; NANOPARTICLES; EVOLUTION;
D O I
10.1186/s40580-019-0174-5
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Recently, iron, nitrogen and sulfur codoped carbon-based materials have gained increasing attention for their synergistic effect towards superior electrocatalytic oxygen reduction performance. To gain insight into the contributions of the heteroatoms, we developed a facile and reproducible method for constructing Fe, N, S-codoped carbon frameworks derived from self-assembled Fe3O4 nanocrystal superlattices. The material constructed by the suggested method exhibited excellent ORR activity with more positive half-wave potential (similar to 0.869V, vs RHE), higher diffusion-limiting current density (similar to 5.88mA/cm(2)) and smaller Tafel slope (45mV/dec) compared with Fe, N-codoped carbon frameworks and Pt/C. Notably, Fe3O4 nanocrystals served as both the building blocks for constructing carbon frameworks and the source of Fe residues leaving in the frameworks at the same time. By artificially tailoring the doping type and level as well as the homogeneousness of heteroatoms, the results discussed herein prove the importance of each kind of heteroatom in boosting ORR activity.
引用
收藏
页数:10
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