Issue 5, 2018

Broadband photoresponse based on a synergistic effect of surface ions and plasmon polaritons

Abstract

New RbAg4I5-on-Au ionic–electronic conductors with a composite nanostructure were fabricated by coating a superionic conductor RbAg4I5 film on an electronic conductor Au thin film by thermal evaporation. Through a synergistic effect of surface ions and plasmon polaritons, this composite nanostructure displays a broadband photoresponse from ultraviolet (375 nm) to near-infrared (1064 nm). Our experimental results indicate that a photocatalytic solid-state electrochemical reaction occurred at the interface of the composite nanostructure. Under ultraviolet or visible light illumination, Au atoms at the interface can be rapidly ionized into electrons and Au+ ions, in which the two components will recombine spontaneously under dark conditions. The formation of Au+ ions has a significant influence on the transportation channel of electrons in the Au thin film. The ionization and recombination of electrons and Au+ ions are responsible for the dynamic process of negative photoconductivity. In addition, we observed a significant negative photoconductivity induced by the excited surface plasmon polaritons in the broadband spectral region from ultraviolet to near-infrared. These results pave the way for exploiting high-performance photodetectors based on ionic–electronic conductors with composite nanostructures. Moreover, the photocatalytic solid-state electrochemical reaction provides a better understanding about the interaction between metals and superionic conductors.

Graphical abstract: Broadband photoresponse based on a synergistic effect of surface ions and plasmon polaritons

Supplementary files

Article information

Article type
Paper
Submitted
29 Oct 2017
Accepted
06 Jan 2018
First published
08 Jan 2018

J. Mater. Chem. C, 2018,6, 1199-1205

Broadband photoresponse based on a synergistic effect of surface ions and plasmon polaritons

Y. Liu, J. Yin, P. Wang, J. Zhu, W. Ma, Z. Dong and J. Sun, J. Mater. Chem. C, 2018, 6, 1199 DOI: 10.1039/C7TC04923D

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