杂原子
材料科学
电催化剂
催化作用
硫黄
金属
碳纤维
化学工程
露天
对偶(语法数字)
吸附
纳米技术
Atom(片上系统)
物理化学
电极
化学
戒指(化学)
有机化学
电化学
冶金
复合材料
复合数
建筑工程
嵌入式系统
艺术
计算机科学
文学类
工程类
作者
Yunyan Wu,Caichao Ye,Lei Yu,Yifan Liu,Jing‐Fang Huang,Jiabao Bi,Liang Xue,Jing‐Wen Sun,Juan Yang,Wenqing Zhang,Xin Wang,Pan Xiong,Junwu Zhu
标识
DOI:10.1016/j.ensm.2021.12.029
摘要
Dual single-atom catalysts (DSACs) with maximized atomic utilization efficiency largely depend on stabilization of dual-metallic single atoms on ideal supports, such as those two-dimensional (2D) atomic layers with open double-sided surfaces. However, the modulation of metal-2D support interactions is critical for enhancing the catalytic performance of DSACs, which has rarely been achieved by routine 2D atomic nanosheets. Here we report a soft template-directed interlayer confinement route for the synthesis of a Fe-Co DSAC. Fe and Co single atoms are stabilized separately on 2D carbon nanosheets via coordination with nitrogen (N) and sulfur (S) heteroatoms to form a FeN4S1/CoN4S1 configuration. The synergistic effect of Fe-Co dual metal centers can optimize the adsorption/desorption features and decrease the reaction barriers for enhanced oxygen reduction reaction (ORR) activities. The Fe-Co DSAC exhibits outstanding electrocatalytic activities of ORR with a half-wave potential of 0.86 V and Zn-air batteries with a maximum power density of 152.8 mW cm−2, outperforming the monometallic Fe and Co SACs. This work paves a new avenue for synthesis of effective DSACs for high-performance electrocatalysis.
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