Published September 2019 | Version v1
Journal article

Piezotronics enhanced photocatalytic activities of Ag-BaTiO3 plasmonic photocatalysts

  • 1. Beijing Institute of Nanoenergy and Nanosystems, Chinese Academy of Sciences, Beijing, 100083, PR (China)
  • 2. School of Advanced Materials and Nanotechnology, Xidian University, Xi'an, 710126 (China)
  • 3. State Key Laboratory of Information Photonics and Optical Communications, School of Science, Beijing University of Posts and Telecommunications, Beijing, 100876 (China)

Description

Ag-BaTiO3 piezo-photocatalysts were fabricated by precipitating Ag nanoparticles on BaTiO3 nano-piezoelectric through a photochemical reducing approach. The mechanism of piezo-photocatalysis and the effect of the size and distribution of Ag nanoparticles on the properties of the photocatalyst were investigated. The surface plasmon resonance (SPR) of Ag nanoparticles endows the catalyst an absorption in the visible light region. The piezoelectric field originated from the deformation of BaTiO3 can further enhance the separation of the photogenerated carriers of SPR and promote the formation of oxidizing radicals that could accelerate the degradation of organic dyes. The 1mAg-BaTiO3 showed an excellent photocatalytic performance of degrading 83% Rh B in 75 min under full-spectrum light irradiation with ultrasonic excitation. The piezoelectric charges on the surfaces of the BaTiO3 and formed piezoelectric potential in the nanocrystal have been confirmed to express an increment of the catalytic activity more than 20% (compared with the sole photocatalysis). This work provides an effective technology for environment purification and could be extended to other piezoelectric materials.

Additional details

Identifiers

DOI
10.1016/j.jallcom.2019.06.115;
PII
S0925838819321905;

Publishing Information

Journal Title
Journal of Alloys and Compounds
Journal Volume
801
Journal Page Range
p. 483-488
ISSN
0925-8388
CODEN
JALCEU

Optional Information

Copyright
Copyright (c) 2019 Elsevier B.V. All rights reserved.