揭开反应驱动的聚合和原子分散Pt催化剂在体支上的碎片化的起源
Haodong Wang1, Hyuk Choi2, Ryuichi Shimogawa1,3
1Department of Materials Science and Chemical Engineering, Stony Brook University, Stony Brook, NY 11794, USA. anatoly.frenkel@stonybrook.edu.
Nanoscale
|June 3, 2024
概括
在ceria上的原子分散催化剂在高温下经历聚合,并在反应期间冷却后碎片化. 这种由一氧化碳和影响的动态结构变化会影响催化剂的稳定性和活性.
科学领域:
- 催化剂是一种催化剂.
- 材料科学 材料科学 材料科学
- 表面化学 表面化学
背景情况:
- 金属支相互作用对原子分散金属催化剂的稳定性和活性至关重要.
- 在反应条件下,活性位点的动态结构转变可以显著改变催化剂性能.
研究的目的:
- 在反应条件下,研究原子在基支上的结构演变.
- 阐明白金原子聚合和碎片化背后的机制.
- 了解吸附剂在这些转换中的作用和支持相互作用.
主要方法:
- 采用了多模式的"现场"特征化技术.
- 理论模拟被用来建模聚合和碎片化机制.
主要成果:
- 在逆水气转移反应中,在高温下观察到原子的聚合.
- 在冷却时观察到集群的碎片化成单个原子.
- 理论模拟揭示了一氧化碳结合和覆盖对这些过程的影响.
结论:
- Pt/ceria催化剂的结构转化是复杂的,并受到吸附剂-支持相互作用的影响.
- 了解这些动态变化对于设计稳定和活跃的单原子催化剂至关重要.
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