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Enhanced Hydrogen Evolution Activity of Phosphorus‐Rich Tungsten Phosphide by Cobalt Doping: A Comprehensive Study of the Active Sites and Electronic Structure
Author(s) -
Yang Yixuan,
Feng Xiaoyu,
Liu Zhizhong,
Zhang Xuming,
Song Hao,
Pi Chaoran,
Gao Biao,
K Chu Paul,
Huo Kaifu
Publication year - 2021
Publication title -
chemelectrochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.182
H-Index - 59
ISSN - 2196-0216
DOI - 10.1002/celc.202100384
Subject(s) - phosphide , dopant , cobalt , tungsten , transition metal , catalysis , inorganic chemistry , hydrogen , tungsten compounds , materials science , doping , dissociation (chemistry) , electrochemistry , desorption , chemical engineering , adsorption , metal , chemistry , electrode , metallurgy , organic chemistry , engineering , optoelectronics
Abstract Phosphorus‐rich transition metal phosphides (TMPs) are considered efficient electrocatalysts for the hydrogen evolution reaction (HER). However, the actual activity of P‐rich TMPs is not as good as expected because of the undesirable electronic structure. Transition metal doping has been shown to be effective in improving the HER activity of TMPs in both acid and alkaline media, but the underlying mechanism is ambiguous, especially for P‐rich TMPs. Herein, cobalt‐doped and phosphorus‐rich tungsten phosphide nanowire arrays (Co/WP 2 NWs/CC) are synthesized and the electrochemical properties and mechanism are determined by both experiments and theoretical calculation. The results reveal that Co dopants serve as inert catalytic sites and do not participate in HER process, but the Co/WP 2 NWs/CC exhibits enhanced electrocatalytic activity as a result of the lower water dissociation barrier and hydrogen adsorption/desorption free energy on W or P sites and improved conductivity by strong electron‐donating effects of Co dopants, thereby boosting the catalytic activity and kinetics.