催化作用
电子转移
格子(音乐)
化学物理
氯
分子
电子
工作(物理)
金属
材料科学
纳米技术
化学
多相催化
氯原子
匹配(统计)
制作
过程(计算)
化学工程
晶格常数
费米能级
密度泛函理论
选择性
过渡金属
光电子学
结构稳定性
作者
Yu‐Chen Zhang,Songpei Zhang,Yuxue Yue,Mingyi Xiao,Guangyu Cheng,Yilun Pan,Shitong Liu,Chunfa Li,Jia Zhao,Xiao‐Nian Li
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-10-06
卷期号:15 (20): 17445-17455
被引量:2
标识
DOI:10.1021/acscatal.5c04277
摘要
The Deacon process is important and highly desired for chlorine recycling in the chlor-alkali industry. Ru-based catalysts have always attracted much attention in the Deacon reaction; however, they are very easy to deactivate. One of the most advanced methods for adjusting the electrical and geometrical configurations of metal centers is lattice strain engineering, which plays a key role in controlling the interactions between adsorbate molecules and catalytic surfaces. In this study, a catalyst was developed via lattice matching between the active site and the support to enhance d-electron density near the Fermi level and strengthen metal–support interactions. The resulting catalyst achieves sustained chlorine production with a conversion rate of 90% and maintains stability for over 200 h during the Deacon process. This work presents a strategy to inhibit the aggregation of RuO2 and a fresh platform for designing highly stable catalysts.
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