In-situ Hf/Zr co-doped Fe2O3 nanorod decorated with CuOx/CoOx: Enhanced photocatalytic performance for antibacterial and organic pollutants

被引:1
|
作者
Hwang I.-S. [1 ]
Mahadik M.A. [1 ,2 ]
Anushkkaran P. [3 ]
Song M.S. [1 ]
Jo Y.J. [1 ]
Chae W.-S. [4 ]
Park J.-H. [1 ]
Choi S.H. [5 ]
Jang J.S. [1 ,3 ]
机构
[1] Division of Biotechnology, Safety, Environment and Life Science Institute, College of Environmental and Bioresource Sciences, Jeonbuk National University, Iksan
[2] School of Civil and Environmental Engineering, Cornell University, Ithaca, 14853, NY
[3] Department of Integrative Environmental Biotechnology, College of Environmental and Bioresource Sciences, Jeonbuk National University, Iksan
[4] Daegu Center, Korea Basic Science Institute, Daegu
[5] Pohang Accelerator Laboratory, Pohang University of Science and Technology (POSTECH), Pohang
基金
新加坡国家研究基金会;
关键词
Bacteria inactivation; CuO[!sub]x[!/sub] and CoO[!sub]x[!/sub] co-catalysts; Fe[!sub]2[!/sub]O[!sub]3[!/sub] NRs; Hydrothermal synthesis; Orange II dye degradation; Zr/Hf co-doping;
D O I
10.1016/j.chemosphere.2024.142450
中图分类号
学科分类号
摘要
Herein, we successfully synthesized Hf/Zr co-doping on Fe2O3 nanorod photocatalyst by a hydrothermal process and quenching methods. The synergistic roles of Hf and Zr double-doping on the bacteria inactivation test and decomposition of organic pollutants were investigated in detail for the 1 wt% CoOx loaded Hf/Zr–Fe2O3 NRs and CuOx/CoOx loaded Hf/Zr–Fe2O3 NRs photocatalyst. Initially, the rod-like porous morphology of the Hf/Zr-doped Fe2O3 NRs was produced via a hydrothermal method at various Hf co-doping (0, 2, 4, 7 and 10)%. Further, CoOx and CuOx loaded by a wet impregnation approach on the Hf/Zr–Fe2O3 NRs and a highly photoactive Hf(4)/Zr–Fe2O3 [CoOx/CuOx] NRs photocatalyst were developed. After the Hf(4)/Zr–Fe2O3 [CoOx/CuOx] NRs photocatalyst treatment, the Bio–TEM imagery of bacterial cells showed extensive morphological deviations in cell membranes. Hf(4)/Zr–Fe2O3 NR achieved 84.1% orange II degradation upon 3 h illumination, which is higher than that of Hf–Fe2O3 and Zr–Fe2O3 (68.7 and 73.5%, respectively). Additionally, the optimum sample, Hf(4)/Zr–Fe2O3 [CoOx/CuOx] photocatalyst, exhibited 95.5% orange II dye degradation after light radiation for 3 h. Optimized Hf(4)/Zr–Fe2O3 [CoOx/CuOx] catalysts exhibited 99.9% and 99.7% inactivation of E. coli and S. aureus with 120 min, respectively. Further, scavenger experiments revealed that the electrons are the primary responsible species for photocatalytic kinetics. This work will provide a rapid method for the development of high photocatalytic performance materials for bacterial disinfection and organic degradation. © 2024 Elsevier Ltd
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