Affiliation:
1. State Key Laboratory for Hubei New Textile Materials and Advanced Processing Technology School of Materials Science and Engineering Wuhan Textile University Wuhan 430200 China
2. Hydrogen Energy Technology Innovation Center of Hubei Province Faculty of Materials Science and Chemistry China University of Geosciences Wuhan Wuhan 430074 China
Abstract
AbstractThe commercialization of water‐splitting technology strongly relies on the stable and high‐performance electrocatalyst for hydrogen and oxygen evolution reactions (HER‐OER). In this work, the nickel dopants in IrRu alloyed electrocatalyst for acidic water splitting activity are investigated. The incorporation of nickel dopants induces more oxygen atoms coordinating with Ir/Ru facilitating the formation of *OOH species via nucleophilic attack by H2O. Additionally, a fast surface reconstruction is achieved due to the electrochemical dissolution of Ni dopants; as a result, more oxygen species are incorporated, evidenced by in situ Raman spectroscopy and electrochemical impedance spectroscopy. Therefore, the mass activity for Ni@IrRu is enhanced by threefold than commercial IrO2 in acidic OER catalysis. Moreover, the nickel dopants balance the hydrogen binding strength; as a result, only 609 mV overpotential is demanded to reach 1 A cm−2 in acidic HER catalysis. The polymer electrolyte membrane water electrolyzer (PEMWE) test indicates only 1.87 V is required to attain 2 A cm−2, 160 mV lower than Pt/C‐IrO2 revealing its potential application in PEMWE.
Funder
National Natural Science Foundation of China
Kementerian Pendidikan
Jianghan University