Fabrication of ZnO, ZnS, Ag-ZnS, and Au-ZnS microspheres for photocatalytic activities, CO oxidation and 2-hydroxyterephthalic acid synthesis

被引:81
作者
Choi, Young In [1 ]
Lee, Seungwon [1 ]
Kim, Seog K. [1 ]
Kim, Young-Il [1 ]
Cho, Dae Won [1 ]
Khan, Mohammad Mansoob [2 ]
Sohn, Youngku [1 ]
机构
[1] Yeungnam Univ, Sch Chem & Biochem, Gyongsan 38541, South Korea
[2] Univ Brunei Darussalam, Fac Sci, Chem Sci, Jalan Tungku Link, BE-1410 Gadong, Brunei
基金
新加坡国家研究基金会;
关键词
ZnO; ZnS; Cubic and hexagonal; CO oxidation; Photocatalytic dye degradation; 2-hydroxyterephthalic acid; ZINC-SULFIDE NANOPARTICLES; OPTICAL-PROPERTIES; METHYL-ORANGE; RHODAMINE-B; ASSISTED SYNTHESIS; NANOSTRUCTURES; WATER; CEO2; PHOTOACTIVITY; NANOCRYSTALS;
D O I
10.1016/j.jallcom.2016.03.070
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
This paper reports the synthesis of ZnS microspheres with cubic and hexagonal crystal phases using a solvothermal method. These materials were characterized by a range of techniques. The effects of Au and Ag-doping on ZnS were also examined. Hexagonal phase ZnO microspheres could be obtained by a CO oxidation process over the ZnS microspheres. The onset of CO oxidation occurred above 350 degrees C, which was increased by Au and Ag doping. The synthesized materials were used for the photocatalytic degradation of mixed dyes {methylene blue (MB) + methyl orange (MO) + rhodamine B (RhB)}. The observed photocatalytic degradation rate over the photocatalysts was in the order, RhB < MB << MO. The photocatalytic degradation activity of the synthesized materials was observed in the order, Au-ZnS approximate to Ag-ZnS << ZnS < ZnO. ZnO was similar to 6 times more efficient in the photocatalytic synthesis of 2-hydroxyterephthalic acid than the ZnS and metal-doped ZnS. These results further support the importance and wide applications of the synthesized ZnS, Ag-ZnS, Au-ZnS and ZnO microspheres. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:46 / 56
页数:11
相关论文
共 57 条
  • [51] Inhibition of photocorrosion and photoactivity enhancement for ZnO via specific hollow ZnO core/ZnS shell structure
    Yu, Linhui
    Chen, Wei
    Li, Danzhen
    Wang, Jubao
    Shao, Yu
    He, Miao
    Wang, Peng
    Zheng, Xiuzhen
    [J]. APPLIED CATALYSIS B-ENVIRONMENTAL, 2015, 164 : 453 - 461
  • [52] Plasmonic-enhanced self-cleaning activity on asymmetric Ag/ZnO surface-enhanced Raman scattering substrates under UV and visible light irradiation
    Zang, Yashu
    Yin, Jun
    He, Xu
    Yue, Chuang
    Wu, Zhiming
    Li, Jing
    Kang, Junyong
    [J]. JOURNAL OF MATERIALS CHEMISTRY A, 2014, 2 (21) : 7747 - 7753
  • [53] Low temperature synthesis of wurtzite zinc sulfide (ZnS) thin films by chemical spray pyrolysis
    Zeng, Xin
    Pramana, Stevin S.
    Batabyal, Sudip K.
    Mhaisalkar, Subodh G.
    Chen, Xiaodong
    Jinesh, K. B.
    [J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2013, 15 (18) : 6763 - 6768
  • [54] Photocatalytic activity of Ag/ZnO heterostructure nanocatalyst: Correlation between structure and property
    Zheng, Yuanhui
    Chen, Chongqi
    Zhan, Yingying
    Lin, Xingyi
    Zheng, Qi
    Wei, Kemei
    Zhu, Jiefang
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (29) : 10773 - 10777
  • [55] Development of polyacrylic acid-functionalized porous zinc sulfide nanospheres for a non-aqueous solid phase extraction procedure toward alkaloids
    Zhu, Dong
    Li, Wei
    Wen, Hong-Mei
    Hu, Yue
    Wang, Jun
    Zhu, Jun-Min
    Ni, Wen-Ting
    Gu, Chao-Qian
    [J]. RSC ADVANCES, 2015, 5 (38): : 29820 - 29827
  • [56] Sonochemistry-assisted synthesis and optical properties of mesoporous ZnS nanomaterials
    Zhu, Yun-Pei
    Li, Jie
    Ma, Tian-Yi
    Liu, Yu-Ping
    Du, Gaohui
    Yuan, Zhong-Yong
    [J]. JOURNAL OF MATERIALS CHEMISTRY A, 2014, 2 (04) : 1093 - 1101
  • [57] Double-sided ZnO nanorod arrays on single-crystal Ag holed microdisks with enhanced photocataltytic efficiency
    Zuo, Yuanhui
    Qin, Yao
    Jin, Chao
    Li, Ying
    Shi, Donglu
    Wu, Qingsheng
    Yang, Jinhu
    [J]. NANOSCALE, 2013, 5 (10) : 4388 - 4394