Preparation of several Z-scheme CuBi2O4/Bi2O3 photocatalyst films loaded on different metal foils for efficient methylene blue degradation with synchronous hydrogen evolution

被引:1
作者
Chi, Shengwei [1 ]
Tu, Yuning [1 ]
Li, Xican [1 ]
Dang, Jiaqi [1 ]
Jin, Taiyu [2 ]
Fang, Dawei [1 ,2 ]
Wang, Jun [1 ]
机构
[1] Liaoning Univ, Coll Chem, Shenyang 110036, Peoples R China
[2] Liaoning Univ, Inst Dispersed Element Chem, Shenyang 110036, Peoples R China
关键词
Different metal foil; Z-scheme; Photocatalytic degradation; H2; evolution; PERFORMANCE;
D O I
10.1016/j.ijhydene.2024.10.222
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
The Z-scheme CuBi2O4/Bi2O3 photocatalyst films were prepared on copper foil, titanium foil and 430-stainless steel foil, respectively, by using incomplete solid-state reaction method. The photocatalytic organic pollutants degradation and simultaneous hydrogen production were achieved on both sides of the metal foils, respectively. The microstructure, composition and performance of photocatalyst films were studied through XRD, SEM, TEM, XPS, EDX, TPR, PL and EIS. In photocatalytic MB degradation and hydrogen evolution experiments, the influences of the Bi(OH)3 precipitation spin-coating number, calcination temperature and calcination time on the photocatalytic activity of Z-scheme CuBi2O4/Bi2O3 photocatalyst films were investigated. The effects of the three different metal foils were comprehensively compared when the experimental conditions of 2 coating layer Bi (OH)3 precipitation, 500 degrees C calcination temperature, 2.0 h calcination time and 10 mg/L and 50 mg/L MB concentrations were adopted. Experimental results show that Cu|CuBi2O4/Bi2O3 photocatalyst film has the best photocatalytic performance in three photocatalyst films. MB degradation ratio and H2 evolution amount are 92.90% and 491.07 mu mol/dm2, respectively, for Cu|CuBi2O4/Bi2O3 photocatalyst film under visible light irradiation for 180 min, and that for Ti|CuBi2O4/Bi2O3 photocatalyst film and SSF|CuBi2O4/Bi2O3 photocatalyst film they are 89.70% and 415.18 mu mol/dm2, 83.90% and 401.79 mu mol/dm2, respectively. The MB degradation and H2 evolution mechanisms of the Z-scheme CuBi2O4/Bi2O3 photocatalytic system were proposed. In theory, this method may have broad application prospects in repairing organic wastewater and large-scale hydrogen evolution.
引用
收藏
页码:1009 / 1024
页数:16
相关论文
共 56 条
  • [51] Preparation, characterization and visible photocatalytic activity of CuBi2O4 photocatalyst by a novel sol-gel method
    Zhang, Jiwen
    Jiang, Yanyan
    [J]. JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS, 2015, 26 (06) : 4308 - 4312
  • [52] Electrospinning directly synthesis of 0D/1D CuBi2O4@WO3 nanofiber photocatalyst with S-scheme heterojunction
    Zhang, Liruhua
    Shen, Qianhong
    Huang, Feilong
    Jiang, Libei
    Liu, Jie
    Sheng, Jiansong
    Li, Yue
    Yang, Hui
    [J]. APPLIED SURFACE SCIENCE, 2023, 608
  • [53] Fixed Z-scheme TiO2|Ti|WO3 composite film as recyclable and reusable photocatalyst for highly effective hydrogen production
    Zhang, Meng
    Piao, Congcong
    Wang, Di
    Liu, Zhiyu
    Liu, Jize
    Zhang, Zhaohong
    Wang, Jun
    Song, Youtao
    [J]. OPTICAL MATERIALS, 2020, 99 (99)
  • [54] Construction of Ag/ CuBi2O4/ Ag2MoO4 composites for enhanced degradation of methylene blue and the proposed possible photocatalytic mechanism
    Zhang, Xiaofang
    Wang, Shoufeng
    Pan, Chuanjiang
    Zeng, Ying
    [J]. MATERIALS LETTERS, 2021, 288
  • [55] Ternary TiO2@Bi2O3@TiO2 hollow photocatalyst drives robust visible-light photocatalytic performance and excellent recyclability
    Zhang, Xuan-xuan
    Xiao, Ying-guan
    Cao, Shun-sheng
    Yin, Zheng-liang
    Liu, Zhao-Qing
    [J]. JOURNAL OF CLEANER PRODUCTION, 2022, 352
  • [56] TiO2 NTAs decorated with thin CuBi2O4 nanosheets for efficient photocatalytic dye degradation and hydrogen generation
    Zhu, Shuxu
    Cui, Yuming
    Wang, Xiaoyu
    Liu, Yao
    Chen, Wenyi
    Zhang, Yihan
    Wang, Qingyao
    [J]. CERAMICS INTERNATIONAL, 2022, 48 (05) : 6627 - 6637