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立方氧化铈的表面再刻面机制

Surface Refaceting Mechanism on Cubic Ceria.

作者信息

Yang Chengwu, Capdevila-Cortada Marçal, Dong Chunyan, Zhou Yan, Wang Junjun, Yu Xiaojuan, Nefedov Alexei, Heißler Stefan, López Núria, Shen Wenjie, Wöll Christof, Wang Yuemin

机构信息

Beijing Key Laboratory of Bio-inspired Energy Materials and Devices, School of Space and Environment, Beihang University, Beijing 102206, China.

Institute of Functional Interfaces (IFG), Karlsruhe Institute of Technology (KIT), 76344 Eggenstein-Leopoldshafen, Germany.

出版信息

J Phys Chem Lett. 2020 Sep 17;11(18):7925-7931. doi: 10.1021/acs.jpclett.0c02409. Epub 2020 Sep 8.

Abstract

Polar surfaces of solid oxides are intrinsically unstable and tend to reconstruct due to the diverging electrostatic energy and thus often exhibit unique physical and chemical properties. However, a quantitative description of the restructuring mechanism of these polar surfaces remains challenging. Here we provide an atomic-level picture of the refaceting process that governs the surface polarity compensation of cubic ceria nanoparticles based on the accurate reference data acquired from the well-defined model systems. The combined results from advanced infrared spectroscopy, atomic-resolved transmission electron microscopy, and density functional theory calculations identify a two-step scenario where an initial O-terminated (2 × 2) reconstruction is followed by a severe refaceting via massive mass transport at elevated temperatures to yield {111}-dominated nanopyramids. This significant surface restructuring promotes the redox properties of ceria nanocubes, which account for the enhanced catalytic activity for CO oxidation.

摘要

固体氧化物的极性表面本质上是不稳定的,由于静电能发散往往会发生重构,因此常常展现出独特的物理和化学性质。然而,对这些极性表面重构机制进行定量描述仍然具有挑战性。在此,我们基于从明确的模型体系获得的精确参考数据,提供了一幅关于控制立方氧化铈纳米颗粒表面极性补偿的再刻面过程的原子级图像。先进的红外光谱、原子分辨透射电子显微镜和密度泛函理论计算的综合结果确定了一个两步过程,即最初的O端接(2×2)重构之后,在高温下通过大量的质量传输进行严重的再刻面,以产生{111}主导的纳米金字塔。这种显著的表面重构促进了氧化铈纳米立方体的氧化还原性质,这解释了其对CO氧化催化活性的增强。

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