The influence of carbon surface chemistry on supported palladium nanoparticles in heterogeneous reactions

被引:15
|
作者
Ding, Yuxiao [1 ,2 ]
Zhang, Liyun [1 ]
Wu, Kuang-Hsu [1 ]
Feng, Zhenbao [1 ]
Shi, Wen [1 ]
Gao, Qiang [2 ]
Zhang, Bingsen [1 ]
Su, Dang Sheng [1 ]
机构
[1] Chinese Acad Sci, Inst Met Res, Shenyang 110016, Peoples R China
[2] Max Planck Inst Chem Energy Convers, D-101365 Mulheim, Germany
关键词
Pd nanoparticles; Reduced graphene oxide; Surface chemistry; Ionic liquid; Heterogeneous catalysis; OXYGEN REDUCTION REACTION; LOW-TEMPERATURE OXIDATION; DOPED CARBON; CATALYTIC-ACTIVITY; COUPLING REACTIONS; PD NANOPARTICLES; SUZUKI-MIYAURA; IONIC LIQUIDS; PHENOL HYDROGENATION; MESOPOROUS CARBONS;
D O I
10.1016/j.jcis.2016.07.018
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
The surface chemistry of nanocarbon support can tailor chemical properties of precious metal nanoparticle/nanocarbon hybrid catalyst in heterogeneous reactions. We report on modified reduced graphene oxide (rGO) support with ionic liquid-derived carbonaceous surface for palladium nanoparticle (Pd NPs) decoration and their actions in different heterogeneous reactions. The surface chemistry of support materials was characterized in detail, and the influence of which on the formation and distribution of metal particles was further investigated. Three different types of reactions including Suzuki-Miyaura coupling reaction, CO oxidation and phenol reduction were examined in terms of reactivity and selectivity. The roles of substituted nitrogen in graphitic lattice and grafted groups on the carbon surface were exploited. Nitrogen-doping can give rise to changes in electronic properties of supported metals, and the Lewis basicity of the doped nitrogen atoms can favor the adsorption of acidic reactants in phenol reduction. The grafted groups derived a negative impact to the Suzuki-Miyaura coupling reaction, due to the involvement of larger reactant molecules, despite that they could prevent significant sintering of Pd NPs in the CO oxidation. (C) 2016 Published by Elsevier Inc.
引用
收藏
页码:175 / 183
页数:9
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