催化作用
钌
氧化物
吸附
金属
解吸
氢
无机化学
化学
化学物理
光化学
物理化学
有机化学
作者
Yuanyuan Zhou,Zhenyang Xie,Jinxia Jiang,Jian Wang,Xiaoyun Song,Qian He,Wei Ding,Zidong Wei
出处
期刊:Nature Catalysis
[Nature Portfolio]
日期:2020-04-27
卷期号:3 (5): 454-462
被引量:395
标识
DOI:10.1038/s41929-020-0446-9
摘要
An efficient catalyst for the hydrogen oxidation reaction (HOR) must maintain an oxide-free metal surface in a relatively high potential range. This requirement automatically excludes ruthenium because it is susceptible to oxidation in the hydrogen adsorption/desorption potential region. Herein we report Ru clusters partially confined in the lattice of urchin-like TiO2 crystals (Ru@TiO2) that can effectively catalyse the HOR up to a potential of 0.9 VRHE with a mass activity higher than that of a PtRu catalyst under both acidic and basic conditions. Moreover, the HOR activity of this Ru@TiO2 catalyst is not affected by 1,000 ppm CO impurity. Even at a high CO content of 10 vol%, Ru@TiO2 still selectively catalyses the HOR. Confined Ru clusters grow along the lattice of TiO2 with abundant Ru–Ti bond formation. Such atomically connected co-crystals offer efficient electron penetration from electron-rich TiO2 to Ru metal, leading to sluggish CO adsorption kinetics during the HOR. Efficient hydrogen oxidation catalysts must maintain an oxide-free metal surface in a relatively high potential range. Now, a catalyst consisting of Ru clusters partially confined in the lattice of urchin-like TiO2 crystals is shown to catalyse the reaction up to a potential of 0.9 VRHE with high mass activity and CO tolerance under both acidic and basic conditions.
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