Synthesis of Monodispersed VO2@Au Core-shell Nanoparticles and Their Switchable Optical Properties

Author(s):  
Jianfeng Zhu ◽  
Renwen Huang ◽  
Mingyi Ji ◽  
Guangxu Su ◽  
Peng Zhan ◽  
...  

Monodispersed VO2 core/Au semishell nanoparticles have been synthesized and optically characterized. Compared to standard noble metal particles, the Au@VO2 core-shell nanoparticles exhibit an additional reversible and tunable localized surface plasmon...

2014 ◽  
Vol 87 (2) ◽  
pp. 43-49
Author(s):  
Takashi KANDA ◽  
Kanjiro TORIGOE ◽  
Hirobumi SHIBATA ◽  
Masahiko ABE ◽  
Hideki SAKAI

MRS Advances ◽  
2019 ◽  
Vol 4 (33-34) ◽  
pp. 1877-1886 ◽  
Author(s):  
Jonathan Boltersdorf ◽  
Asher C. Leff ◽  
Gregory T. Forcherio ◽  
Joshua P. McClure ◽  
Cynthia A. Lundgren

AbstractColloidal 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.


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