Synthesis, surface and optical properties of Ag2Cu(VO3)4 and Cu(VO3)2 vanadates

被引:5
作者
Qiao, Xuebin [1 ]
Wan, Yingpeng [2 ]
Li, Yuze [2 ]
Qin, Lin [3 ,4 ]
Seo, Hyo Jin [3 ,4 ]
机构
[1] Jiangsu Normal Univ, Sch Phys & Elect Engn, Jiangsu Key Lab Adv Laser Mat & Devices, Xuzhou 221116, Peoples R China
[2] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
[3] Pukyong Natl Univ, Dept Phys, Busan 608737, South Korea
[4] Pukyong Natl Univ, Interdisciplinary Program Biomed Mech & Elect Eng, Busan 608737, South Korea
基金
中国国家自然科学基金; 新加坡国家研究基金会;
关键词
Inorganic compounds; Semiconductors; Catalytic properties; Optical properties; Electronic band structure; Photocatalysis; PHOTOCATALYTIC ACTIVITY; DEGRADATION; SEMICONDUCTOR; MICROSPHERES; IRRADIATION; OXIDES; BIVO4;
D O I
10.1016/j.apsusc.2016.01.221
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
Ag2Cu(VO3)(4) and Cu(VO3)(2) were prepared via the sol-gel chemical synthesis. The phase formation was confirmed by X-ray powder polycrystalline diffraction (XRD) measurements. The surface properties were measured with the scanning electron microscope (SEM), energy dispersive spectra (EDS), transmission electron microscopy (TEM), and nitrogen adsorption-desorption isotherms. The optical properties and the band-gap structures were investigated. The vanadates have efficient optical absorption in the UV to visible wavelength region with an indirect allowed transition. Ag2Cu(VO3)(4) has smaller band gap (1.85 eV) than that of Cu(VO3)(2) (2.03 eV). The narrowed band gap is due to the hybridization between the Ag-4d and O-2p in the valence band. The photocatalysis was investigated by photodegradation of methylene blue (MB) solutions excited by the light with wavelength longer than 420 nm. Correspondingly Ag2Cu(VO3)(4) has more efficient photocatalytic activity on MB photodegradation than that of Cu(VO3)(2). The photocatalytic mechanisms were suggested according to the band positions and the trapping experiments. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:63 / 68
页数:6
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