Dye degradation of spherical and rod-shaped CuO semiconductor nanoparticles
Source abstract
Abstract
The chemical and physical properties of nanoparticles (NPs) are highly dependent on size, shape and structure. The smaller size of copper oxide (CuO) NPs paves the way for applications in sensor technology, solar cells, biology and photocatalysis. Here the authors report a wet chemical method for synthesis of stable CuO NPs by using copper acetate as the precursor and the cationic surfactant cetyltrimethylammonium bromide or hexadecyltrimethylammonium bromide (Ctab) ([(C16H33)N(CH3)3]Br). Ultraviolet (UV) spectroscopy shows that the CuO NPs have an absorbance peak at 289 nm, which gives a band gap of 2·5 eV, and Fourier transform infrared spectra confirm the capping of Ctab. Scanning electron microscopy images show that the NPs are spherical and rod-shaped and have diameters varying between 9 nm and 1 μm. The X-ray diffraction pattern shows that the synthesised NPs were high-purity CuO with average size = 10 nm, which is also confirmed by transmission electron microscopy results. The as-synthesised CuO NPs were subjected to a dye degradation study in time-specific mode on methyl orange (MO) and Congo red (CR) dyes by using a UV-irradiated source. The calculated degradation efficiencies of approximately 92% (MO) and 91% (CR) show promising application of CuO NPs in photocatalytic activity.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Copper-based nanomaterials and applications · ZnO doping and properties · Gold and Silver Nanoparticles Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Electronics and Communication Engineering, Desh Bhagat University, Mandi Gobindgarh, India
Department of Nanotechnology, Sri Guru Granth Sahib World University, Fatehgarh Sahib, India
Department of Chemistry and Biochemistry, Thapar University, Patiala, India
References (23)
Show source-provided references
1. Suleiman M · Journal of Materials and Environmental Science · 2013 · 4 · 792
2. 10.1007/s13204-013-0233-x10.1007/s13204-013-0233-x ↗
3. 10.1016/j.jssc.2011.12.01310.1016/j.jssc.2011.12.013 ↗
4. 10.1016/j.mseb.2009.10.00810.1016/j.mseb.2009.10.008 ↗
5. 10.1016/j.materresbull.2006.05.02010.1016/j.materresbull.2006.05.020 ↗
6. Amrut Lanje S · Advances in Applied Science Research · 2010 · 2 · 36
7. 10.5897/AJB2013.1305810.5897/AJB2013.13058 ↗
8. 10.1016/j.jallcom.2007.05.02310.1016/j.jallcom.2007.05.023 ↗
9. Ghane M · International Journal of Nano Dimensions · 2010 · 1 · 33
10. 10.1186/1556-276X-7-7010.1186/1556-276X-7-70 ↗
11. 10.1186/1556-276X-6-18110.1186/1556-276X-6-181 ↗
12. 10.1016/j.synthmet.2010.03.01210.1016/j.synthmet.2010.03.012 ↗
13. 10.1016/j.ijheatmasstransfer.2012.04.03510.1016/j.ijheatmasstransfer.2012.04.035 ↗
14. 10.2147/IJN.S2902010.2147/IJN.S29020 ↗
15. 10.1557/JMR.1997.005710.1557/JMR.1997.0057 ↗
16. 10.2298/JMMB1101073D10.2298/JMMB1101073D ↗
17. 10.1021/jp909742d10.1021/jp909742d ↗
18. Alabi AB · Ife Journal of Science · 2013 · 15 · 409
19. 10.1016/j.mssp.2014.05.04510.1016/j.mssp.2014.05.045 ↗
20. 10.1021/la703625a10.1021/la703625a ↗
21. Devi HS · Advances in Electronic and Electric Engineering · 2014 · 4 · 83
22. 10.24842/1611/001110.24842/1611/0011 ↗
23. 10.1016/j.ceramint.2014.03.13210.1016/j.ceramint.2014.03.132 ↗