催化作用
甲烷
成核
氧化物
金属
化学工程
材料科学
水溶液中的金属离子
甲烷厌氧氧化
背景(考古学)
纳米技术
温室气体
化学
冶金
有机化学
工程类
古生物学
生物
生态学
作者
Haifeng Xiong,Deepak Kunwar,Dong Jiang,Carlos Garcia Vargas,Hengyu Li,Congcong Du,Griffin Canning,Xavier Isidro Pereira Hernández,Qiang Wan,Sen Lin,Stephen C. Purdy,Jeffrey T. Miller,Kevin Leung,Stanley S. Chou,Hidde H. Brongersma,Rik ter Veen,Jianyu Huang,Hua Guo,Yong Wang,Abhaya K. Datye
出处
期刊:Nature Catalysis
[Springer Nature]
日期:2021-10-18
卷期号:4 (10): 830-839
被引量:119
标识
DOI:10.1038/s41929-021-00680-4
摘要
The treatment of emissions from natural gas engines is an important area of research since methane is a potent greenhouse gas. The benchmark catalysts, based on Pd, still face challenges such as water poisoning and long-term stability. Here we report an approach for catalyst synthesis that relies on the trapping of metal single atoms on the support surface, in thermally stable form, to modify the nature of further deposited metal/metal oxide. By anchoring Pt ions on a catalyst support we can tailor the morphology of the deposited phase. In particular, two-dimensional (2D) rafts of PdOx are formed, resulting in higher reaction rates and improved water tolerance during methane oxidation. The results show that modifying the support by trapping single atoms could provide an important addition to the toolkit of catalyst designers for controlling the nucleation and growth of metal and metal oxide clusters in heterogeneous catalysts. Despite its importance in the context of natural gas engines emissions treatment, methane oxidation remains challenging. Now, the authors introduce an approach to stabilize PdOx rafts on ceria by trapping Pt single atoms in the support resulting in a superior catalyst for this transformation.
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