Surface-Plasmon-Mediated Hydrogenation of Carbonyls Catalyzed by Silver Nanocubes under Visible Light

被引:92
作者
Landry, Michael J. [1 ]
Gelle, Alexandra [1 ]
Meng, Beryl Y. [1 ]
Barrett, Christopher J. [1 ]
Moores, Audrey [1 ]
机构
[1] McGill Univ, Dept Chem, 801 Sherbrooke St West, Montreal, PQ H3A 0B8, Canada
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
photocatalysis; silver nanoparticles; hydrogenation; plasmonic catalysis; surface plasmon resonance; NOBLE-METAL NANOPARTICLES; AG-AT-AGCL; GOLD NANOPARTICLES; SELECTIVE HYDROGENATION; AEROBIC OXIDATION; HIGHLY EFFICIENT; INDUCED DISSOCIATION; ALLOY NANOPARTICLES; SOLAR-CELL; RESONANCE;
D O I
10.1021/acscatal.7b02128
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
Plasmonic nanoparticles are exciting and promising candidates for light-activated catalysis. We report herein the use of plasmonic nanocubes for the activation of molecular hydrogen and the hydrogenation of ketones and aldehydes via visible light irradiation at 405 nm, corresponding to the position of the plasmon band of the nanocubes, at 80 degrees C. Only I atm of molecular hydrogen is required to access, using catalytic amounts of silver, primary, and secondary alcohols, with complete chemoselectivty for C=O over C=C reduction. The resulting catalytic system was studied over a scope of 12 compounds. Exposure to other wavelengths, or absence of light failed to provide activity, thus proving a direct positive impact of the plasmonic excitation to the catalytic activity. By varying the irradiation intensity, we studied the relationship between plasmon band excitation and catalytic activity and propose a potential reaction mechanism involving plasmon-activated hot electrons. This study expands the scope of reactions catalyzed by free-standing plasmonic particles and sheds light on H-2 activation by silver surfaces.
引用
收藏
页码:6128 / 6133
页数:6
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