4.7 Article

Ag/Bi2MoO6-x with enhanced visible-light-responsive photocatalytic activities via the synergistic effect of surface oxygen vacancies and surface plasmon

期刊

APPLIED SURFACE SCIENCE
卷 436, 期 -, 页码 536-547

出版社

ELSEVIER
DOI: 10.1016/j.apsusc.2017.12.002

关键词

Heterostructured Ag/Bi2MoO6-x; Surface oxygen vacancy; Surface plasmonic Ag; Synergistic effect; Photocatalysis

资金

  1. National Natural Science Foundation of China [21666039, 21663030]
  2. Project of Science & Technology Office of Shaanxi Province [20155F291, 2013K11-08, 2013SZS20-P01]
  3. Natural Science Program of the Education Department of Shaanxi Province [15J5119]

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In this study, a heterostructured Ag/Bi2MoO6-x photocatalyst was rationally designed and successfully fabricated via the deposition of plasmonic silver nanoparticles onto the surface of Bi2MoO6 with surface oxygen vacancy (denoted as Bi2MoO6-x). Bi2MoO6-x (Abbr. BMO6-x was first synthesized via a solvothermal synthesis and calcination process. The plasmonic silver nanoparticles were then loaded onto the surface of BMO6-x using a simple photoreduction process to form Ag/BMO6-x composite. Surface oxygen vacancies (SOVs) in BMO6-x were confirmed by electron paramagnetic resonance (EPR) spectrum. The structures of BMO6-x and Ag/BiMoO6-x) were characterized using high-resolution transmission electron microscopy, powder X-ray diffraction, and X-ray photoelectron spectroscopy. Under visible light irradiation, sample Ag/BMO6-x exhibits a highest visible-light-responsive photocatalytic performance compared to those of pure-Bi2MoO6 (BMO), BMO6-x and Ag/BMO for the degradation of rhodamine B (RhB), which is attributed predominantly to the synergistic effect of SOVs and Ag surface plasmonic resonance (SPR) on the surface of Bi2MoO6-x leading to the efficient separation and migration of photogenerated electrons/holes and hence broadening light responsive region. The significant improvement of the migration and separation of photogenerated electrons/holes in the Ag/BMO6-x was evidenced by photoluminescence spectra, time-resolved fluorescence decay, photocurrent, and electrochemical impedance spectrum. The ESR with spin-trap technique and reactive species trapping experiments confirm that the mainly active species O-2(-) and h(+) are playing key roles in the RhB photodegradation process over Ag/BMO6-x. This study not only provides an understandable synergistic effect of SOVs and SPR Ag but also pioneers a new approach for fabricating a series of highly catalytically active metal-semiconductor photocatalysts with surface atom defects. (C) 2017 Elsevier B.V. All rights reserved.

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