A facile microwave-hydrothermal method to fabricate B doped ZnWO4 nanorods with high crystalline and highly efficient photocatalytic activity

被引:54
作者
Liu, Zhen [1 ]
Tian, Jian [1 ]
Zeng, Debing [1 ]
Yu, Changlin [1 ,2 ,4 ]
Zhu, Lihua [1 ]
Huang, Weiya [1 ]
Yang, Kai [3 ]
Li, Dehao [4 ]
机构
[1] Jiangxi Univ Sci & Technol, Sch Met & Chem Engn, Ganzhou 341000, Jiangxi, Peoples R China
[2] Wuyi Univ, Sch Chem & Environm Engn, Jiangmen 529020, Guangdong, Peoples R China
[3] Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Fujian, Peoples R China
[4] Guangdong Univ Petrochem Technol, Fac Environm & Biol Engn, Maoming 525000, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Microwave-hydrothermal; ZnWO4; nanorods; Photocatalysis; B doping; High crystalline; OPTICAL-PROPERTIES; SONOCHEMICAL FABRICATION; COMPOSITE PHOTOCATALYST; DEGRADATION; PERFORMANCE; TIO2; CO; SEMICONDUCTORS; MICROSPHERE; TRANSPORT;
D O I
10.1016/j.materresbull.2017.06.021
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A series length of 50 similar to 200 nm B doped ZnWO4 nanorods with high crystallinity were fabricated via a fast microwave-hydrothermal method. The effects of B doping on the physical properties of ZnWO4 nanorods were intensively characterized by N-2 physical adsorption, XRD, TEM, FT-IR, XPS, ultraviolet-visible diffuse reflection spectrum (UV-vis DRS), photolunminescence spectrum (PL), transient photocurrent response (TPR). The results indicated that the doped B could replace the lattice tungsten kin in ZnWO4 crystals, which caused the lattice spacing contraction, particle size decrease, specific surface area increase. More importantly, the separation of the photogenerated electrons and holes in ZnWO4 was significantly enhanced by B doping. With doped optimum B concentration (2.42 wt%), B/ZnWO4 displayed super photocatalytic performance in dyes decomposition. The degradation rate constant (0.065 h(-1)) of Rhodamine B over B (2.42 wt%)/ZnWO4 is 4 times of that over ZnWO4 (0.016h(-1)). (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:298 / 306
页数:9
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