催化作用
电催化剂
析氧
色散(光学)
电解水
电解
质子交换膜燃料电池
化学工程
化学
制氢
电化学
氧气
无机化学
材料科学
电极
物理化学
电解质
工程类
物理
有机化学
光学
生物化学
作者
Abissaid Martinez-Séptimo,Miguel A. Valenzuela,P. Del Ángel,R. Huerta
标识
DOI:10.1016/j.ijhydene.2021.04.040
摘要
Proton Exchange Membrane Electrolysis of Water (PEMWE) stands out as a scalable, CO2-free process to produce H2 for energy delivery and industrial applications. Due to the limited Ir and Ru worldwide availability, one of the main challenges for the GW-scale PEMWE implementation is the loading reduction of these metals in the anodic catalytic layer. Here, Ir–Ru loading (5 wt%Ir-40 wt%Ru) was deposited through their impregnation over TiO2, followed by a thermal-oxidative treatment, obtaining IrRuOx/TiO2 catalyst. SEM-EDS and HR-TEM confirmed the homogeneous dispersion of IrRuOx on TiO2. The supported catalyst showed a 1.4-fold higher mass activity (85 mA/mg Ir–Ru) for the oxygen evolution reaction (OER) than a mechanical mixture of IrO2–RuO2 1:3 (54 mA/mgIr+Ru) in H2SO4 0.5 M, at 1.52 V/RHE. Furthermore, the supported catalyst retains 90% of its catalytic activity after 100 reaction cycles suggesting the RuO2 intermediate species stabilization by IrOx, which can avoid its irreversibly transform into hydrous RuOx.
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