催化作用
双金属片
拉曼光谱
化学
原位
X射线光电子能谱
吸附
纳米颗粒
反应中间体
氢
化学工程
光化学
纳米技术
无机化学
材料科学
物理化学
有机化学
物理
光学
工程类
作者
Xiu‐Mei Lin,Xiaoting Wang,Yong-Liang Deng,Xing Chen,Hao‐Ning Chen,Petar M. Radjenovic,Xia‐Guang Zhang,Yaohui Wang,Jin‐Chao Dong,Tian Zhang,Jian‐Feng Li
出处
期刊:Nano Letters
[American Chemical Society]
日期:2022-06-14
卷期号:22 (13): 5544-5552
被引量:32
标识
DOI:10.1021/acs.nanolett.2c01744
摘要
In situ monitoring of the evolution of intermediates and catalysts during hydrogen oxidation reaction (HOR) processes and elucidating the reaction mechanism are crucial in catalysis and energy science. However, spectroscopic information on trace intermediates on catalyst surfaces is challenging to obtain due to the complexity of interfacial environments and lack of in situ techniques. Herein, core-shell nanoparticle-enhanced Raman spectroscopy was employed to probe alkaline HOR processes on representative PtRu surfaces. Direct spectroscopic evidence of an OHad intermediate and RuOx (Ru(+3)/Ru(+4)) surface oxides is simultaneously obtained, verifying that Ru doping onto Pt promotes OHad adsorption on the RuOx surface to react with Had adsorption on the Pt surface to form H2O. In situ Raman, XPS, and DFT results reveal that RuOx coverage tunes the electronic structure of PtRuOx to optimize the adsorption energy of OHad on catalyst surfaces, leading to an improvement in HOR activity. Our findings provide mechanistic guidelines for the rational design of HOR catalysts with high activity.
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