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CoP nanoparticles embedded in P and N co-doped carbon as efficient bifunctional electrocatalyst for water splitting 被引量:6

CoP nanoparticles embedded in P and N co-doped carbon as efficient bifunctional electrocatalyst for water splitting
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摘要 Noble-metal-free hydrogen/oxygen evolution reaction(HER/OER) electrocatalysts, especially bifunctional electrocatalysts, are essential for overall water splitting, but their performance is impeded by many factors like poor electrical conductivity. Herein, we fabricated cobalt phosphide(Co P) nanoparticles embedded in P and N co-doped carbon(PNC) matrix(Co P@PNC) to fully realize the high activity of Co P by maximizing its conductivity. Simply a carbonization coupled phosphidation approach was utilized where Co ions and organic ligands of Co-MOF were transferred into Co P and P and N co-doped carbon. The synthesized material shows an ideal electrical conductivity, excellent HER(overpotential of-84 m V and-120 m V @10 m A cmin acidic and alkaline medias, respectively) and OER(overpotential of 330 m V@10 m A cmin alkaline media) performances. Further, Co P@PNC acts as a superior catalyst for both anode and cathode to catalyze overall water splitting and only requires an voltage of 1.52 V to deliver a current density of 10 m A cm, superior to the noble-metal catalysts system(Pt/C//IrO) and the reported noble-metal-free bifunctional electrocatalysts. Noble-metal-free hydrogen/oxygen evolution reaction(HER/OER) electrocatalysts, especially bifunctional electrocatalysts, are essential for overall water splitting, but their performance is impeded by many factors like poor electrical conductivity. Herein, we fabricated cobalt phosphide(Co P) nanoparticles embedded in P and N co-doped carbon(PNC) matrix(Co P@PNC) to fully realize the high activity of Co P by maximizing its conductivity. Simply a carbonization coupled phosphidation approach was utilized where Co ions and organic ligands of Co-MOF were transferred into Co P and P and N co-doped carbon. The synthesized material shows an ideal electrical conductivity, excellent HER(overpotential of-84 m V and-120 m V @10 m A cm^(-2) in acidic and alkaline medias, respectively) and OER(overpotential of 330 m V@10 m A cm^(-2) in alkaline media) performances. Further, Co P@PNC acts as a superior catalyst for both anode and cathode to catalyze overall water splitting and only requires an voltage of 1.52 V to deliver a current density of 10 m A cm^(-2), superior to the noble-metal catalysts system(Pt/C//IrO_2) and the reported noble-metal-free bifunctional electrocatalysts.
出处 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2017年第6期1223-1230,共8页 能源化学(英文版)
基金 support from the National Natural Science Foundation of China(51661145026,21676193,21506156) the Tianjin Municipal Natural Science Foundation(15JCZDJC37300)
关键词 Cobalt phosphide ELECTROCATALYST Hydrogen evolution reaction Oxygen evolution reaction Water splitting Cobalt phosphide Electrocatalyst Hydrogen evolution reaction Oxygen evolution reaction Water splitting
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