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催化反应过程中的单合金纳米颗粒X射线成像。

Single alloy nanoparticle x-ray imaging during a catalytic reaction.

作者信息

Kim Young Yong, Keller Thomas F, Goncalves Tiago J, Abuin Manuel, Runge Henning, Gelisio Luca, Carnis Jerome, Vonk Vedran, Plessow Philipp N, Vartaniants Ivan A, Stierle Andreas

机构信息

Deutsches Elektronen-Synchrotron (DESY), D-22607 Hamburg, Germany.

University of Hamburg, Physics Department, D-20355 Hamburg, Germany.

出版信息

Sci Adv. 2021 Oct;7(40):eabh0757. doi: 10.1126/sciadv.abh0757. Epub 2021 Oct 1.

Abstract

The imaging of active nanoparticles represents a milestone in decoding heterogeneous catalysts’ dynamics. We report the facet-resolved, surface strain state of a single PtRh alloy nanoparticle on SrTiO determined by coherent x-ray diffraction imaging under catalytic reaction conditions. Density functional theory calculations allow us to correlate the facet surface strain state to its reaction environment–dependent chemical composition. We find that the initially Pt-terminated nanoparticle surface gets Rh-enriched under CO oxidation reaction conditions. The local composition is facet orientation dependent, and the Rh enrichment is nonreversible under subsequent CO reduction. Tracking facet-resolved strain and composition under operando conditions is crucial for a rational design of more efficient heterogeneous catalysts with tailored activity, selectivity, and lifetime.

摘要

活性纳米粒子的成像代表了解码多相催化剂动力学的一个里程碑。我们报告了在催化反应条件下,通过相干X射线衍射成像确定的单个PtRh合金纳米粒子在SrTiO上的晶面分辨表面应变状态。密度泛函理论计算使我们能够将晶面表面应变状态与其依赖于反应环境的化学成分相关联。我们发现,最初以Pt为终止面的纳米粒子表面在CO氧化反应条件下会富集Rh。局部组成取决于晶面取向,并且在随后的CO还原过程中Rh的富集是不可逆的。在操作条件下跟踪晶面分辨的应变和组成对于合理设计具有定制活性、选择性和寿命的更高效多相催化剂至关重要。

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