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BULLETIN OF THE CHINESE CERAMIC SOCIETY ›› 2021, Vol. 40 ›› Issue (12): 4137-4143.

• New Functional Materials • Previous Articles     Next Articles

Preparation and Photoelectrocatalytic Perfermance of Bi2MoO6@CQDs/TiO2 Nanotube Arrays

ZHANG Dalong1,2, HE Shuo1, LIN Zuxiang1, DAI Gaopeng1,2, LIU Suqin1,2, XIAO Zuoan2, CAI Shuang2   

  1. 1. Hubei Key Laboratory of Power System Design and Test for Electrical Vehicle, Hubei University of Arts and Science, Xiangyang 441053, China;
    2. School of Food Science and Technology & School of Chemical Engineering, Hubei University of Arts and Science, Xiangyang 441053, China
  • Online:2021-12-15 Published:2022-01-07

Abstract: In this work, TiO2 nanotube arrays (TNA) were modified through the incorporation of Bi2MoO6 and carbon quantum dots (CQDs), to improve the visible light photocatalytic activity of TiO2. The CQDs, Bi(NO3)3·5H2O, and Na2MoO4 were used as the starting materials, a facile solvothermal method was employed to fabricate the novel Bi2MoO6@CQDs/TNA composite through the deposition of CQDs and Bi2MoO6 into the TNA. Based on the SEM and elemental mapping results, CQD and Bi2MoO6 are successfully coated on the tube wall of TNA. Moreover, the photocatalytic performance of Bi2MoO6@CQDs/TNA composite was investigated through the degradation of methyorange (MO) solution under the visible light irradiation. The corresponding photoelelctrocatalytic test results confirm that the as-prepared Bi2MoO6@CQDs/TNA exhibits an enhanced photoelectrocatalytic activity. Bi2MoO6@CQDs/TNA has a 32% higher removal rate of MO than Bi2MoO6/TNA. The enhanced activity can be attributed to the excellent up-conversion photoluminescence (UCPL) of CQDs, promoting TiO2 to generate photogenerated carriers under the visible light. Meanwhile, the heterojunction between Bi2MoO6 and TiO2 can also effectively inhibit the recombination of photogenerated carriers.

Key words: TiO2 nanotube arrays, carbon quantum dots, Bi2MoO6, visible light, photoelectrocatalytic, up-conversion photoluminescence

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