Chinese Journal of Catalysis ›› 2016, Vol. 37 ›› Issue (3): 349-358.DOI: 10.1016/S1872-2067(15)61023-3

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Fabrication of a monoclinic/hexagonal junction in WO3 and its enhanced photocatalytic degradation of rhodamine B

Yuanyuan Lua, Guo Liua, Jing Zhanga, Zhaochi Fengb, Can Lib, Zhi Lic   

  1. a College of Chemistry, Chemical Engineering and Environmental Engineering, Liaoning Shihua University, Fushun 113001, Liaoning, China;
    b State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China;
    c Key Laboratory of Photochemical Conversion and Optoelectronic Materials, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190, China
  • Received:2015-11-25 Revised:2015-11-27 Online:2016-02-29 Published:2016-02-29
  • Contact: Jing Zhang
  • Supported by:

    This work was supported by the National Natural Science Foundation of China (21573101), the Liaoning Provincial Natural Science Foundation (2014020107), the Program for Liaoning Excellent Talents in University (LJQ2014041), the Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry ([2013]1792), the Opening Project of Key Laboratory of Photochemical Conversion and Optoelectronic Materials, TIPC, CAS, and the Opening Project of State Key Laboratory of Catalysis, DICP, CAS (N-09-06)

Abstract:

A series of WO3 samples with different crystalline phases were prepared by the thermal decomposition method from ammonium tungstate hydrate. X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy, and N2 adsorption-desorption were used to characterize the crystalline phase, morphology, particle size, chemical composition, and surface area of the WO3 samples. The formation of hexagonal (h-WO3) and monoclinic (m-WO3) crystal structures of WO3 at different temperatures or different times was confirmed by XRD. m-WO3 is formed at 600 ℃, while m-WO3 starts to transform into h-WO3 at 800 ℃. However, h-WO3, which forms at 800 ℃, may transform into m-WO3 by increasing the calcination temperature to 1000 ℃. SEM results indicate that m-WO3 particles exhibit a bulky shape with heavy aggregates, while h-WO3 particles exhibit a rod-like shape. Moreover, m-WO3 crystals are sporadically patched on the surface of the h-WO3 rod-like particles, resulting in the exposure of both m-WO3 and h-WO3 on the surface. It is observed that the monoclinic phase (m-WO3)/hexagonal phase (h-WO3) junction was fabricated by tuning the calcination temperature and calcination time. The relative ratios between m-WO3 and h-WO3 in the phase junction can readily be tailored by control of the calcination time. The photocatalytic activities of WO3 with different crystalline phases were evaluated by the photocatalytic degradation of rhodamine B as a model pollutant. A higher photocatalytic activity was observed in the WO3 sample with the m-WO3/h-WO3 junction as compared with the sample with only m-WO3. The improvement of photocatalytic activity can be attributed to the reduction of the electron-hole recombination rate owing to the formation of the phase junction, whose presence has been confirmed by HRTEM and photoluminescence spectra.

Key words: Tungsten oxide, Phase junction, Thermal decomposition method, Photocatalysis, Rhodamine B