Facile synthesis and characterization of Te-doped CuO nanoparticles for increased antibacterial and photocatalytic activity

被引:5
作者
Saumya
Dasauni, Khushboo [2 ]
Nailwal, Tapan [2 ]
Nenavathu, Bhavani Prasad [1 ]
机构
[1] Indira Gandhi Delhi Tech Univ Women, Dept Appl Sci & Humanities, Delhi 110006, India
[2] Kumaun Univ, Dept Biotechnol, JC Bose Tech Campus, Bhimtal 263136, Uttaranchal, India
关键词
Tellurium doping; CuO Nanoparticles; Reactive oxygen species (ROS); Antibacterial activity; 2; 4-Dichlorophenol; Photocatalysis; ZNO NANOPARTICLES; OPTICAL-PROPERTIES; DEGRADATION;
D O I
10.1016/j.matpr.2022.05.387
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Te-doped CuO nanoparticles (NPs) are fabricated via the facile co-precipitation method for aquaculture wastewater remediation. The phase, crystallite size, and morphological studies of the fabricated Te-doped CuO NPs were studied by scanning electron microscopy and powder X-ray diffraction. XRD of pristine and Te-doped CuO NPs (4 wt%) exhibited crystallite size of 10-17 nm. FE-SEM shows that the nanostructured material exhibited a rice grain-like morphology. The antibacterial activity of prepared samples was investigated against an aquatic fish pathogenic gram-negative (Aeromonas Salmonicida strain MTCC 1522) bacteria using the disc diffusion method. This method displayed that 4 wt% Te-doped CuO NPs exhibited excellent antibacterial activity compared to Pristine CuO NPs. Further, 4 wt% Te-doped CuO exhibited higher photocatalytic activity (76.6 %) compared to pristine CuO (39.4%) towards the photodecomposition of 2,4-Dichlorophenol in a water medium by UV light. Taking into consideration the facile synthesis process and the efficient antibacterial activity of Te-doped CuO NPs, this study opens up a marvellous possibility for this material in wastewater treatment.Copyright (c) 2022 Elsevier Ltd. All rights reserved. Selection and peer-review under responsibility of the scientific committee of the 2nd International Con-ference on Advances in Smart Materials & Emerging Technologies.
引用
收藏
页码:456 / 461
页数:6
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