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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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作者 Jing-Yi Xie zi-zhang liu +7 位作者 Jia Li Lei Feng Min Yang Yu Ma Da-Peng liu Lei Wang Yong-Ming Chai Bin Dong 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2020年第9期328-333,I0010,共7页
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... 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. 展开更多
关键词 Core-shell structure CoFe-PBA Cation exchange PHOSPHATING Oxygen evolution reaction
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