电催化剂
催化作用
电子转移
吸附
可逆氢电极
化学
密度泛函理论
无机化学
碳纤维
材料科学
化学工程
电极
物理化学
计算化学
电化学
复合材料
有机化学
工作电极
工程类
复合数
作者
Pianpian Zhang,Tingting Sun,Rong Jiang,Tianyu Zheng,Qingmei Xu,Ruanbo Hu,Xinxin Wang,Kang Wang,Lianbin Xu,Dingsheng Wang,Jianzhuang Jiang
标识
DOI:10.1016/j.apcatb.2023.123645
摘要
Herein, an asymmetric diatomic site oxygen reduction reaction (ORR) electrocatalyst with atomically dispersed Fe and Cu species co-anchored on porous nitrogen-doped polyhedra carbon was successfully prepared through a facile cooperation of post-adsorption and two-step pyrolysis method. Density functional theory (DFT) calculations reveal that the asymmetric FeCu dual atomic site experiences a symmetry destruction of electron transfer due to the existing Cu-N4 sites and thus results in the electron redistribution in FeSACuSA/NC, contributing significantly to the optimization of intermediates adsorption and acceleration of kinetics during ORR process. Attributed to the structural advantages of FeSA-N4&CuSA-N4 sites and highly porous carbon matrix, the FeSACuSA/NC catalyst exhibits excellent electrocatalytic ORR performance with half-wave potentials (E1/2) of 0.86 and 0.88 V versus reversible hydrogen electrode in 0.1 M HClO4 and 0.1 M KOH solutions as well as high durability. Moreover, FeSACuSA/NC-based H2/O2 fuel cell and zinc-air battery present superior performance with high peak power density.
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