Reaction Pathway Dependence in Plasmonic Catalysis: Hydrogenation as a Model Molecular Transformation

被引:40
作者
Barbosa, Eduardo C. M. [1 ]
Fiorio, Jhonatan L. [1 ]
Mou, Tong [2 ,3 ]
Wang, Bin [2 ,3 ]
Rossi, Liane M. [1 ]
Camargo, Pedro H. C. [1 ]
机构
[1] Univ Sao Paulo, Inst Quim, Dept Quim Fundamental, Av Prof Lineu Prestes 748, BR-05508000 Sao Paulo, SP, Brazil
[2] Univ Oklahoma, Ctr Interfacial React Engn, Norman, OK 73019 USA
[3] Univ Oklahoma, Sch Chem Biol & Mat Engn, Gallogly Coll Engn, Norman, OK 73019 USA
基金
巴西圣保罗研究基金会;
关键词
gold; hydrogenation; nanocatalysis; nanoparticles; surface plasmon resonance; AROMATIC NITRO-COMPOUNDS; GOLD NANOPARTICLES; CHEMOSELECTIVE HYDROGENATION; INDUCED DISSOCIATION; PHOTOSENSITIZER-FREE; ALLOY NANOPARTICLES; SODIUM-BOROHYDRIDE; AEROBIC OXIDATION; SOLAR-ENERGY; EFFICIENT;
D O I
10.1002/chem.201705749
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The localized surface plasmon resonance (LSPR) excitation in plasmonic nanoparticles can enhance or mediate chemical transformations. Increased reaction rates for several reactions have been reported due to this phenomenon; however, the fundamental understanding of mechanisms and factors that affect activities remains limited. Here, by investigating hydrogenation reactions as a model transformation and employing different reducing agents, H-2 and NaBH4, which led to different hydrogenation reaction pathways, we observed that plasmonic excitation of Au nanoparticle catalysts can lead to negative effects over the activities. The underlying physical reason was explored using density functional theory calculations. We observed that positive versus negative effects on the plasmonic catalytic activity is reaction-pathway dependent. These results shed important insights on our current understanding of plasmonic catalysis, demonstrating reaction pathways must be taken into account for the design of plasmonic nanocatalysts.
引用
收藏
页码:12330 / 12339
页数:10
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