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在钯纳米颗粒上生长的用于直接合成过氧化氢的具有催化活性的金层:晶格应变和电荷转移视角分析

Catalytically Active Au Layers Grown on Pd Nanoparticles for Direct Synthesis of HO: Lattice Strain and Charge-Transfer Perspective Analyses.

作者信息

Kim Jin-Soo, Kim Hong-Kyu, Kim Sung-Hoon, Kim Inho, Yu Taekyung, Han Geun-Ho, Lee Kwan-Young, Lee Jae-Chul, Ahn Jae-Pyoung

机构信息

Department of Materials Science and Engineering , Korea University , Seoul 02841 , South Korea.

Advanced Analysis Center , Korea Institute of Science and Technology , Seoul 02792 , South Korea.

出版信息

ACS Nano. 2019 Apr 23;13(4):4761-4770. doi: 10.1021/acsnano.9b01394. Epub 2019 Apr 5.

DOI:10.1021/acsnano.9b01394
PMID:30943005
Abstract

Despite its effectiveness in improving the properties of materials, strain engineering has not yet been employed to endow catalytic characteristics to apparently nonactive metals. This limitation can be overcome by controlling simultaneously lattice strains and charge transfer originated from the epitaxially prepared bimetallic core-shell structure. Here, we report the experimental results of the direct HO synthesis enabled by a strained Au layer grown on Pd nanoparticles. This system can benefit the individual catalytic properties of each involved material, and the heterostructured catalyst displays an improved productivity for the direct synthesis of HO by ∼100% relative to existing Pd catalysts. This is explained here by exploring the individual effects of lattice strain and charge transfer on the alteration of the electronic structure of ultrathin Au layers grown on Pd nanoparticles. The approach used in this study can be viewed as a means of designing catalysts with multiple catalytic functions.

摘要

尽管应变工程在改善材料性能方面具有有效性,但尚未被用于赋予明显无活性的金属催化特性。通过同时控制外延制备的双金属核壳结构产生的晶格应变和电荷转移,可以克服这一限制。在此,我们报告了在钯纳米颗粒上生长的应变金层实现直接合成过氧化氢的实验结果。该体系可使每种参与材料的催化性能得到提升,并且这种异质结构催化剂相对于现有的钯催化剂,在直接合成过氧化氢方面显示出约100%的生产率提高。通过探究晶格应变和电荷转移对钯纳米颗粒上生长的超薄金层电子结构变化的各自影响来对此进行解释。本研究中使用的方法可被视为设计具有多种催化功能催化剂的一种手段。

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