Issue 40, 2017

Plasmonic enhanced photoelectrochemical and photocatalytic performances of 1D coaxial Ag@Ag2S hybrids

Abstract

Silver (Ag) as one of the most important plasmonic metals has attracted enormous attention due to its distinct surface plasmon resonance (SPR) absorption and high electrical conductivity. Here, we use Ag nanowires (NWs) as the starting material to prepare a series of core–shell structured Ag@Ag2S composites through an in situ controllable and spontaneous sulfidation process at room temperature. It has been found that the obtained coaxial Ag@Ag2S hybrid with an optimized ratio of Ag NWs exhibits enhanced photoelectrochemical and photocatalytic performances under visible light irradiation. The underlying contribution of Ag SPR to the enhancement of photoelectrochemical and photocatalytic activities of the Ag@Ag2S hybrids has been elucidated through wavelength-dependent experiments and transient absorption spectroscopy. The results indicate that the SPR phenomenon of Ag NWs has an influential effect on the photoelectrochemical and photocatalytic activities enhancement of Ag@Ag2S hybrids, which is often overlooked in the previous reports. An ultrafast electron transfer process (∼350 fs) from the Ag core to the Ag2S shell has been measured. This work provides a valuable insight into the role of the Ag component in improving the photoelectrochemical and photocatalytic performances of Ag–Ag2S hybrid nanosystems, which is expected to promote comprehensive understanding and better exploitation of plasmonic Ag in universal photophysical and photochemical systems.

Graphical abstract: Plasmonic enhanced photoelectrochemical and photocatalytic performances of 1D coaxial Ag@Ag2S hybrids

Supplementary files

Article information

Article type
Paper
Submitted
24 Jul 2017
Accepted
14 Sep 2017
First published
15 Sep 2017

J. Mater. Chem. A, 2017,5, 21570-21578

Plasmonic enhanced photoelectrochemical and photocatalytic performances of 1D coaxial Ag@Ag2S hybrids

N. Zhang, M. Li, C. F. Tan, C. K. Nuo Peh, T. C. Sum and G. W. Ho, J. Mater. Chem. A, 2017, 5, 21570 DOI: 10.1039/C7TA06473J

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