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奥斯特瓦尔德熟化与单原子捕获:迈向理解铂颗粒烧结

Ostwald ripening versus single atom trapping: towards understanding platinum particle sintering.

作者信息

Wang Xing, van Bokhoven Jeroen A, Palagin Dennis

机构信息

Institute for Chemical and Bioengineering, ETH Zurich, Vladimir Prelog Weg 1, 8093 Zurich, Switzerland.

出版信息

Phys Chem Chem Phys. 2017 Nov 22;19(45):30513-30519. doi: 10.1039/c7cp05887j.

Abstract

Ostwald ripening is a leading cause of the degradation of platinum group catalysts at high temperature in an oxidizing atmosphere. Recent experiments suggested that volatile species can be trapped on ceria, forming atomically dispersed active catalytic sites instead of large nanoparticles. Here we present a comparative density functional theory study of the interaction of PtO(g), the most likely volatile species responsible for the process of Ostwald ripening, with various surfaces. Defect-free CeO(111) and AlO(100) surfaces have a very small binding energy towards PtO(g) compared to the platinum surface, indicative of particle growth. However, the stepped edge of the CeO(111) surface effectively traps the mobile species, generating atomically dispersed catalysts. Such trapped single-atom platinum-on-ceria catalysts are predicted to have a square-planar [PtO] structure, with the platinum atom strongly binding to the surface, preventing platinum atoms from aggregating into larger nanoparticles. These results provide an atomic insight into the single atom trapping and suggest a route for the development of sinter-resistant catalysts.

摘要

奥斯特瓦尔德熟化是铂族催化剂在氧化气氛中高温降解的主要原因。最近的实验表明,挥发性物质可以捕获在二氧化铈上,形成原子分散的活性催化位点,而不是大的纳米颗粒。在此,我们对铂(II)氧化物(PtO(g))(奥斯特瓦尔德熟化过程中最可能的挥发性物质)与各种表面的相互作用进行了比较密度泛函理论研究。与铂表面相比,无缺陷的CeO(111)和AlO(100)表面对PtO(g)的结合能非常小,这表明颗粒在生长。然而,CeO(111)表面的台阶边缘有效地捕获了移动物种,生成了原子分散的催化剂。这种捕获的二氧化铈负载单原子铂催化剂预计具有平面正方形[PtO]结构,铂原子与表面强烈结合,防止铂原子聚集成更大的纳米颗粒。这些结果为单原子捕获提供了原子层面的见解,并为开发抗烧结催化剂提供了一条途径。

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