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Fe-doped CoP core–shell structure with open cages as efficient electrocatalyst for oxygen evolution 被引量:3

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摘要 Developing a facile approach based on transition metal-based Prussian blue(PB)and its analogues(PBAs)with core-shell nanostructure is a very promising choice for constructing cost-effective electrocatalysts for oxygen evolution reaction(OER).Herein,a bimetallic core-shell structure with open cages of Fe-doped CoP(Fe-CoP cage)has been synthesized using CoFe-PBA cage-4 as precursor through a facile hydrothermal method and following phosphating process.Interestingly,there is an open hole in each face center of Fe-CoP cage,which suggests the more exposure of active sites for OER.Electrochemical measurements show that Fe-CoP cage can afford a current density of 10 mA cm-2 at a low overpotential(300 mV),which is better than that of RuO2.The excellent performance can be attributed to Fe doping composition and unique open-cage core-shell structure.The synergistic effect derived from bimetallic active for OER has been discussed.And its great catalytic stability has been evaluated via 1000 cycles of CV and chronoamperometry measurement.This work provides a potential method to design multiple transitional metal-doping electrocatalysts with complex framework derived from PBAs for water splitting.
出处 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2020年第9期328-333,I0010,共7页 能源化学(英文版)
基金 financially supported by Shandong Provincial Natural Science Foundation(ZR2017MB059) the Fundamental Research Funds for the Central Universities(18CX05016A) Postgraduate Innovation Project of China University of Petroleum(YCX2019096)。
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