Journal
JOURNAL OF ENERGY CHEMISTRY
Volume 26, Issue 6, Pages 1223-1230Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.jechem.2017.07.021
Keywords
Cobalt phosphide; Electrocatalyst; Hydrogen evolution reaction; Oxygen evolution reaction; Water splitting
Funding
- National Natural Science Foundation of China [51661145026, 21676193, 21506156]
- Tianjin Municipal Natural Science Foundation [15JCZDJC37300]
Ask authors/readers for more resources
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 (CoP) nanoparticles embedded in P and N co-doped carbon (PNC) matrix (CoP@PNC) to fully realize the high activity of CoP by maximizing its conductivity. Simply a carbonization coupled phosphidation approach was utilized where Co ions and organic ligands of Co-MOF were transferred into CoP and P and N co-doped carbon. The synthesized material shows an ideal electrical conductivity, excellent HER (overpotential of -84 mV and -120 mV@10 mA cm(-2) in acidic and alkaline medias, respectively) and OER (overpotential of 330 mV@10 mA cm(-2) in alkaline media) performances. Further, CoP@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 mA cm(-2), superior to the noble-metal catalysts system (Pt/C//IrO2) and the reported noble-metal-free bifunctional electrocatalysts. (C) 2017 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available