Anisotropic growth of Pt on Pd nanocube promotes direct synthesis of hydrogen peroxide

被引:24
作者
Kim, Min-Cheol [1 ]
Han, Geun-Ho [1 ]
Xiao, Xiangyun [3 ]
Song, Joseph [4 ]
Hong, Jaeyoung [4 ]
Jung, Euiyoung [3 ,5 ]
Kim, Hong-Kyu [4 ]
Ahn, Jae-Pyoung [4 ]
Han, Sang Soo [1 ]
Lee, Kwan-Young [2 ]
Yu, Taekyung [3 ]
机构
[1] Korea Inst Sci & Technol, Computat Sci Res Ctr, Seoul 02792, South Korea
[2] Korea Univ, Dept Chem & Biol Engn, 145 Anam Ro, Seoul 02841, South Korea
[3] Kyung Hee Univ, Dept Chem Engn, Yongin 17104, South Korea
[4] Korea Inst Sci & Technol, Adv Anal Ctr, Seoul 02792, South Korea
[5] Ewha Womans Univ, Dept Chem & Nano Sci, Seoul 120750, South Korea
基金
新加坡国家研究基金会;
关键词
Anisotropic growth; Catalytic activity; Core@shell nanocrystal; Density functional theory; Hydrogen peroxide direct synthesis; Selectivity; ACTIVE THERMOCHEMICAL TABLES; SHAPE-CONTROLLED SYNTHESIS; DENSITY-FUNCTIONAL THEORY; CATALYTIC-ACTIVITY; PARTICLE-SIZE; NANOPARTICLES; PALLADIUM; H2O2; H-2; OXYGEN;
D O I
10.1016/j.apsusc.2021.150031
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
As a joint investigation principle using experimental and theoretical approaches, we report that the anisotropic growth of Pt on Pd nanocubes significantly promotes the direct synthesis of hydrogen peroxide (H2O2) from hydrogen (H-2) and oxygen (O-2). The superior H2O2 productivity of the anisotropic Pd@Pt core@shell nanocrystals results from the enhanced H-2 conversion and the H2O2 selectivity compared to Pd and Pt. From the joint investigation, during the anisotropic growth of the Pd@Pt nanocrystals, high-index facets such as (210) are generated, and they provide numerous active sites for hydrogen dissociation. Notably, even the nano-catalyst is enclosed by Pt shell, the high-index facets are favorable for opening a new route for hydrogen dissolution into the Pd bulk lattices of the Pd@Pt nanocrystals, in which the dissolved hydrogen can react with chemisorbed O-2 over the nanocrystals to form H2O2. This mechanism is suggested by a hydrogen temperature programmed reduction (H-2-TPR) analysis, in situ transmission electron microscopy (TEM), and density functional theory (DFT) calculations. This study provides another option to improve the catalytic performance of core@shell nanocrystals via the generation of high-index facets through anisotropic growth of nanocrystals, in addition to the well-known strain and charge transfer effects. We expect that the anisotropic growth approach could be extended to other catalytic reactions.
引用
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页数:9
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