Issue 3, 2017

An Au/AgBr–Ag heterostructure plasmonic photocatalyst with enhanced catalytic activity under visible light

Abstract

This study reports an easy synthesis protocol of a novel bimetallic silver halide (Au/AgBr–Ag) plasmonic heterostructure as a visible light induced photocatalyst. In this process, first CTAB capped Au NPs were coated with AgBr, and then Ag nanoparticles were formed on the surface of AgBr by photoreduction, while exposing to daylight at room temperature. The presence of Au and Ag improves the visible absorption ability of NPs and avoids charge recombination of the semiconductor AgBr during photoexcitation, which in turn enhances 16 and 8.9 fold the photocatalytic efficiency of Rhodamine B dye degradation under visible light irradiation compared to that of pure AgBr and AgBr/Ag, respectively. The recycling tests of the photocatalyst show only ∼8.7% decrease in efficiency after the 5th cycle of reuse without changing the morphology. During the photocatalytic process, active superoxide radicals (O2˙) play a major role, proved through scavenger trapping and photoluminescence experiments. The presence of two plasmonic metals (Au and Ag) in the heterostructure helps to improve visible light absorption as well as avoid charge recombination of the semiconductor AgBr to act as a better photocatalyst. Since this heteronanostructure can be easily synthesized by a one-step method, this study could provide a new approach for the development of efficient bimetallic/semiconductor halide plasmonic photocatalysts with enhanced visible absorption and better charge separation.

Graphical abstract: An Au/AgBr–Ag heterostructure plasmonic photocatalyst with enhanced catalytic activity under visible light

Supplementary files

Article information

Article type
Paper
Submitted
25 Sep 2016
Accepted
14 Dec 2016
First published
15 Dec 2016

Dalton Trans., 2017,46, 890-898

An Au/AgBr–Ag heterostructure plasmonic photocatalyst with enhanced catalytic activity under visible light

R. Purbia and S. Paria, Dalton Trans., 2017, 46, 890 DOI: 10.1039/C6DT03723B

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