异质结
催化作用
材料科学
碳纤维
兴奋剂
锌
热解
氧气
氧还原反应
再分配(选举)
氧还原
化学工程
纳米技术
化学
光电子学
电极
复合数
物理化学
电化学
冶金
复合材料
有机化学
政治学
法学
生物化学
工程类
政治
作者
Jizhao Zou,Minhai Zheng,Hongliang Wu,Zhangjing Pan,Jingyou Xu,Xierong Zeng,Tongbin Lan,Yuechao Yao,Zhangjian Li
标识
DOI:10.1016/j.est.2023.107950
摘要
Constructing transition metal compounds (TMC) in carbon-based materials is a desirable strategy for developing efficient oxygen reduction reaction (ORR) electrocatalysts, while the lacked a feasible synthesis method and its unclear catalytic mechanism put a challenge. Here, we report a FeP/Fe2P heterojunction embedded in N, S, P-doped carbon (FeNSPC) catalyst by facile in-situ pyrolysis. Compared with the control sample FeP/Fe2P heterojunction embedded in N, P-doped carbon (FeNPC), the FeNSPC presents higher ORR activity. Furthermore, the S-doping strategy modulates the electronic structure of FeP/Fe2P heterojunction and carbon matrix (the charge distribution/spin density redistribution), thereby endowing a superior ORR activity of FeNSPC. Specifically, the FeNSPC1000 possesses a half-wave potential of 0.83 V. Meanwhile, the FeNSPC1000 only loses 14 mV of the half-wave potential after 3000 cycles, and the relative current of FeNSPC1000 remains 87.8 % after 8 h i-t-test. Moreover, the FeNSPC1000 assembled ZAB shows excellent performance with a specific capacity of 702 mA h g−1 and an energy density of 737 W h kg−1.
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