析氧
材料科学
催化作用
氧气
持续时间(音乐)
化学工程
电化学
结晶学
化学物理
纳米技术
化学
物理化学
有机化学
电极
工程类
艺术
文学类
作者
Shangheng Liu,Huang Tan,Yucheng Huang,Qiaobao Zhang,Haiping Lin,Ling Li,Zhiwei Hu,Wei‐Hsiang Huang,Chih‐Wen Pao,Jyh‐Fu Lee,Qingyu Kong,Qi Shao,Yong Xu,Xiaoqing Huang
标识
DOI:10.1002/adma.202305659
摘要
Abstract Oxygen evolution reaction (OER) plays a key role in proton exchange membrane water electrolysis (PEMWE), yet the electrocatalysts still suffer from the disadvantages of low activity and poor stability in acidic conditions. Here, a new class of CdRu 2 IrO x nanoframes with distorted structure for acidic OER is successfully fabricated. Impressively, CdRu 2 IrO x displays an ultralow overpotential of 189 mV and an ultralong stability of 1500 h at 10 mA cm⁻ 2 toward OER in 0.5 M H 2 SO 4 . Moreover, a PEMWE using the distorted CdRu 2 IrO x can be steadily operated at 0.1 A cm⁻ 2 for 90 h. Microstructural analyses and X‐ray absorption spectroscopy (XAS) demonstrate that the synergy between Ru and Ir in CdRu 2 IrO x induces the distortion of Ru−O, Ir−O, and Ru−M (M = Ru, Ir) bonds. In situ XAS indicates that the applied potential leads to the deformation octahedral structure of RuO x /IrO x and the formation of stable Ru 5+ species for OER. Theoretical calculations also reveal that the distorted structures can reduce the energy barrier of rate‐limiting step during OER. This work provides an efficient strategy for constructing structural distortion to achieve significant enhancement on the activity and stability of OER catalysts.
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