Surface Plasmon Resonant Gold-Palladium Bimetallic Nanoparticles for Promoting Catalytic Oxidation

被引:6
|
作者
Boltersdorf, Jonathan [1 ]
Leff, Asher C. [1 ,2 ]
Forcherio, Gregory [1 ]
McClure, Joshua P. [1 ]
Lundgren, Cynthia A. [1 ]
机构
[1] US Army, Res Lab, Sensors & Electron Devices Directorate, Adelphi, MD 20783 USA
[2] Gen Tech Serv, Adelphi, MD 20783 USA
关键词
nanostructure; plasmonic; catalytic; ethanol; SINGLE-PARTICLE; AU NANORODS; ETHANOL; DEHYDROGENATION;
D O I
10.1557/adv.2019.222
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Colloidal gold-palladium (Au-Pd) bimetallic nanoparticles were used as catalysts to study the ethanol (EtOH) photo-oxidation cycle, with an emphasis towards driving carbon-carbon (C-C) bond cleavage at low temperatures. Au-Pd bimetallic alloy and core-shell nanoparticles were prepared to synergistically couple a plasmonic absorber (Au) with a catalytic metal (Pd) with composite optical and catalytic properties tailored towards promoting photocatalytic oxidation. Catalysts utilizing metals that exhibit localized surface plasmon resonance (SPR) can be harnessed for light-driven enhancement for small molecule oxidation via augmented photocarrier generation/separation and photothermal conversion. The coupling of Au to Pd in an alloy or core-shell nanostructure maintains SPR-induced charge separation, mitigates the poisoning effects on Pd, and allows for improved EtOH oxidation. The Au-Pd nanoparticles were coupled to semiconducting titanium dioxide photocatalysts to probe their effects on plasmonically-assisted photocatalytic oxidation of EtOH. Complete oxidation of EtOH to CO2 under solar simulated-light irradiation was confirmed by monitoring the yield of gaseous products. Bimetallics provide a pathway for driving desired photocatalytic and photoelectrochemical reactions with superior catalytic activity and selectivity.
引用
收藏
页码:1877 / 1886
页数:10
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