热解
材料科学
化学工程
介孔材料
氧还原反应
石墨
电子转移
碳纤维
电化学
多孔性
活性炭
原位
电极
纳米技术
化学
催化作用
无机化学
光化学
冶金
有机化学
吸附
物理化学
复合材料
复合数
工程类
作者
Wenan Deng,Tianxiang Huang,Chuan Li,Lifu Zhang,Zhaodi Huang,Jianpeng Sun,Zhenpeng Hu,Fangna Dai
标识
DOI:10.1016/j.electacta.2021.138918
摘要
It is intriguing but still challenging to develop non-noble electrocatalysts with efficient catalytic centers to replace Pt-based ones for oxygen reduction reaction (ORR) in both alkaline and acidic conditions. Herein, newly C-S-Zn coordination-structured catalytic centers, originating from the strong interactions between autogenous ZnS and S-C defects, are constructed on Enteromorpha-based porous carbon by a simple pyrolysis and in-situ binding method. The experimental and computational results demonstrate that the C-S-Zn structures produce affluent defect sites and transfer more active electrons from Zn atom to graphite layer to capture and reduce O2, thus enhancing the ORR activities in both alkaline and acidic conditions. The in-situ assembly of C-S-Zn structures, micro/mesoporous architecture, and N/S-self-doped biocarbon represents an upgrading approach for the facile preparation of highly active ORR electrocatalysts from natural biomass.
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