析氧
分解水
催化作用
过电位
双功能
电催化剂
铱
无机化学
氧化物
化学
化学工程
材料科学
电化学
光催化
物理化学
电极
工程类
生物化学
有机化学
作者
Xiaoping Ma,Xiaoman Zhang,Jiamin Huang,Jiawei Zhang,Xue Liu,Yi He,Yu Xin
标识
DOI:10.1016/j.apsusc.2023.158558
摘要
Iridium oxide (IrO2) has been intensively investigated as an efficient and stable anode catalyst for the oxygen evolution reaction (OER) in water splitting system. However, the overall water splitting performance of IrO2 is rarely studied because of its strong adsorption of hydrogen intermediates during the hydrogen evolution reaction (HER) process. Herein, a facile Ar/H2 plasma reduction strategy is developed to activate the HER performance of self-supported IrO2 by constructing a novel metal/oxide heterostructure. The in-situ synthesized Ir/IrO2 composite possesses excellent electrical interconnection and abundant catalytic active sites. Meanwhile, dual active sites induced by the strong interface effect between metallic Ir and IrO2 could optimize the adsorption energy and reaction path for both HER and OER. The optimized Ir–IrO2/Ti@Ar–H2 exhibits remarkable activities with a small overpotential of 58 and 211 mV toward HER and OER, respectively. Besides, Ir–IrO2/Ti@Ar–H2||Ir–IrO2/Ti@Ar–H2 electrolyzer only requires an operational voltage of 1.48 V to afford a current density of 10 mA cm−2, much lower than that of commercial Pt/C||IrO2 (1.61 V).
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