Ag/AgCl/Ag2MoO4 composites for visible-light-driven photocatalysis

被引:67
作者
Jiao, Zhongyi [1 ]
Zhang, Junlei [1 ]
Liu, Zhendong [1 ]
Ma, Zhen [1 ,2 ]
机构
[1] Fudan Univ, Dept Environm Sci & Engn, Shanghai Key Lab Atmospher Particle Pollut & Prev, Shanghai 200433, Peoples R China
[2] Shanghai Inst Pollut Control & Ecol Secur, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金;
关键词
AgCl; Ag2MoO4; Photocatalysis; Degradation; Dyes; HIGH-EFFICIENCY; BETA-AG2MOO4/G-C3N4; HETEROJUNCTION; PLASMONIC PHOTOCATALYSTS; HYDROTHERMAL SYNTHESIS; FACILE SYNTHESIS; SILVER CHROMATE; AG2MO4; M; DEGRADATION; PERFORMANCE; NANOSTRUCTURES;
D O I
10.1016/j.jphotochem.2018.11.003
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ag2MoO4 shows low photocatalytic activity under visible light. It would be interesting to develop Ag2MoO4-based composite/heterojunction photocatalysts working efficiently under visible light. Herein, novel Ag/AgCl/Ag2MoO4 composites were obtained via photoreduction of AgCl/Ag2MoO4 composites prepared by sequential precipitation. The composition, morphologies, and optical properties of the samples were studied via various characterization techniques. Photocatalytic degradation of rhodamine B (RhB), methylene blue (MB), methyl orange (MO), norfloxacin (NOF), and tetracycline hydrochloride (TC) solutions was conducted under visible-light irradiation. An optimal Ag/AgCl/Ag2MoO4 catalyst showed much higher photocatalytic activity than Ag2MoO4, and it also showed reasonably fine recyclability. Through radical-capturing experiments, photo-generated holes (h(+)) were determined to be the main active species whereas hydroxyl radicals ((OH)-O-center dot) were found to play a secondary role in photocatalysis. Possible photocatalytic mechanisms were proposed.
引用
收藏
页码:67 / 75
页数:9
相关论文
共 76 条
[1]   In situ anion exchange synthesis of β-Ag2MoO4/AgBr heterojunctions with enhanced photocatalytic activity and stability [J].
Abulizi, Abulikemu ;
Kadeer, Kuerbangnisha ;
Zhou, Li ;
Tursun, Yalkunjan ;
Dilinuer, Talifu .
JOURNAL OF THE TAIWAN INSTITUTE OF CHEMICAL ENGINEERS, 2018, 88 :243-251
[2]   Plasmonic silver incorporated silver halides for efficient photocatalysis [J].
An, Changhua ;
Wang, Shutao ;
Sun, Yugang ;
Zhang, Qinhui ;
Zhang, Jun ;
Wang, Chenyu ;
Fang, Jiye .
JOURNAL OF MATERIALS CHEMISTRY A, 2016, 4 (12) :4336-4352
[3]   Effective quantum yield and reaction rate model for evaluation of photocatalytic degradation of water contaminants in heterogeneous pilot-scale solar photoreactors [J].
Angel Mueses, Miguel ;
Machuca-Martinez, Fiderman ;
Li Puma, Gianluca .
CHEMICAL ENGINEERING JOURNAL, 2013, 215 :937-947
[4]   A New Complementary Catalyst and Catalytic Mechanism: Ag2MoO4/Ag/AgBr/GO Heterostructure [J].
Bai, Yu-Yang ;
Wang, Feng-Rui ;
Liu, Jin-Ku .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2016, 55 (37) :9873-9879
[5]   An efficient photocatalyst for degradation of various organic dyes: Ag@Ag2MoO4-AgBr composite [J].
Bai, Yu-Yang ;
Lu, Yi ;
Liu, Jin-Ku .
JOURNAL OF HAZARDOUS MATERIALS, 2016, 307 :26-35
[6]   Silver molybdate nanoparticles, nanowires, and nanorods embedded in glass nanocomposites [J].
Bhattacharya, S. ;
Ghosh, A. .
PHYSICAL REVIEW B, 2007, 75 (09)
[7]   Two-dimensional dendritic Ag3PO4 nanostructures and their photocatalytic properties [J].
Bi, Yingpu ;
Hu, Hongyan ;
Jiao, Zhengbo ;
Yu, Hongchao ;
Lu, Gongxuan ;
Ye, Jinhua .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2012, 14 (42) :14486-14488
[8]   Visible-light-driven Ag2MoO4/Ag3PO4 composites with enhanced photocatalytic activity [J].
Cao, Wenrong ;
An, Yanting ;
Chen, Lifang ;
Qi, Zhiwen .
JOURNAL OF ALLOYS AND COMPOUNDS, 2017, 701 :350-357
[9]   Photoswitches of One-Dimensional Ag2MO4 (M = Cr, Mo, and W) [J].
Cheng, Liang ;
Shao, Qi ;
Shao, Mingwang ;
Wei, Xianwen ;
Wu, Zhengcui .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (05) :1764-1768
[10]   In-situ preparation of Z-scheme AgI/Bi5O7I hybrid and its excellent photocatalytic activity [J].
Cui, Min ;
Yu, Jingxiong ;
Lin, Hongjun ;
Wu, Ying ;
Zhao, Leihong ;
He, Yiming .
APPLIED SURFACE SCIENCE, 2016, 387 :912-920