碳纤维
热解
氮气
催化作用
多孔性
比表面积
化学工程
材料科学
无机化学
电催化剂
熔盐
吸收(声学)
化学
透射电子显微镜
纳米技术
有机化学
复合数
电极
电化学
复合材料
物理化学
工程类
作者
Danyang Wu,Jinwen Hu,Chao Zhu,Jiangwei Zhang,Hongyu Jing,Ce Hao,Yantao Shi
标识
DOI:10.1016/j.jcis.2020.10.115
摘要
Abstract Carbon-supported single-atom catalysts (C-SACs) demonstrate great potential in various key electrochemical reactions. Nevertheless, the development of facile and economical strategies is highly appealing yet challenging given that the commonly used pyrolysis method has strict requirements on the structure and composition of precursors. Here, we demonstrate for the first time a facile and low-cost pyrolysis strategy assisted by molten salts at high temperature for preparing porous C-SACs with well-dispersed Co-N4 sites directly from a Chlorella precursor. Based on the X-ray absorption fine structure results and aberration-corrected scanning transmission electron microscopy images, we show that single atom Co-N4 moieties are anchored on a carbon matrix. A porous structure with a large specific surface area (2907 m2 g−1) and atomically dispersed active sites of Co provide the as-prepared Co-N/C-SAC with excellent electrocatalytic activity and stability for the ORR. The electrochemical measurements show that the half-wave potential and limited current density of this material are 0.83 V vs. RHE and 5.5 mA cm−2, respectively, which are comparable to those of commercial Pt/C.
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