journal article·2023-02Open access

Electrochemical detection of dopamine using green and chemical synthesized CuO/PANI nanocomposite modified electrode

Seleke J. Mokole, Ahmed Aliyu, Omolola E. Fayemi

Applied Physics A· Volume 129· Issue 2

Abstract

Abstract Copper oxide (CuO) nanoparticles were synthesized using the chemical and green method routes and doped with polyaniline (PANI) to form PANI/CuOchand PANI/CuOgrnanocomposite. The microstructural properties of the nanocomposites were characterized by UV–Vis spectroscopy (UV), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy equipped with energy-dispersive X-ray spectroscopy (EDS) detector. The electrochemical behavior of the CuOch, CuOgr, PANI/CuOch, and PANI/CuOgrelectrodes was investigated using cyclic voltammetry (CV), and square wave voltammetry (SWV), and the results showed an enhanced electrochemical catalytic activity toward dopamine (DA) on PANI/CuOgrelectrodes. SWV was conducted for the determination of DA with a linear range from 26 to 95 μM and a low limit of detection (LOD) of 8.22 μM. A comparison between the PANI/CuOchand PANI/CuOgrelectrodes and other modified electrodes toward detection of DA are comparable with the reported literature results.
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Research context

OpenAlex topics: Electrochemical sensors and biosensors · Conducting polymers and applications · Electrochemical Analysis and Applications

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References (38)

Show source-provided references
1. H. Li, K. Zhou, J. Cao, Q. Wei, C.T. Lin, S.E. Pei, L. Ma, N. Hu, Y. Guo, Z. Deng, Z. Yu, S. Zeng, W. Yang, L. Meng, Carbon 171, 16–28 (2021)10.1016/j.carbon.2020.08.019 ↗
2. J.G. Nutt, G.F. Wooten, N. Engl, J. Med. 353, 1021–1027 (2005)
3. K. Chaiendoo, S. Ittisanronnachai, V. Promarak, W. Ngeontae, Carbon 146, 728–735 (2019)10.1016/j.carbon.2019.02.030 ↗
4. R.M. Wightman, L.J. May, A.C. Michael, Anal. Chem. 60, 769A-779A (1988)10.1021/ac00164a001 ↗
5. R.D. Badgaiyan, Front. Neurosci. 7, 125 (2013)10.3389/fnins.2013.00125 ↗
6. B.B. Anderson, A.G. Ewing, J. Pharmaceut. Biomed. Anal. 19, 15–32 (1999)10.1016/S0731-7085(98)00088-0 ↗
7. J.F. van Staden, R.I.S. van Staden, Talanta 102, 34–43 (2012)10.1016/j.talanta.2012.05.017 ↗
8. A. Suzuki, T.A. Ivandini, K. Yoshimi, A. Fujishima, G. Oyama, T. Nakazato, N. Hattori, S. Kitazawa, Y. Einaga, Anal. Chem. 79, 8608–8615 (2007)10.1021/ac071519h ↗
9. W. Cai, J. Lai, T. Lai, H. Xie, J. Ye, Sens. Actuators B-Chem. 224, 225–232 (2016)10.1016/j.snb.2015.09.079 ↗
10. V.K. Jha, Nep. J. Integr. Sci. 2, 42–46 (2012)
11. O.E. Fayemi, O.G. Pooe, F.A. Adesanya, I.P. Ejidike, Nanomater. 12, 1825 (2022)10.3390/nano12111825 ↗
12. B. Uma, K.S. Anantharaju, L. Renuka, S. Malini, S.S. More, Y.S. Vidya, S. Meena, Ceram. Int. 47, 10355–10369 (2021)10.1016/j.ceramint.2020.10.223 ↗
13. X. Huang, H. Wu, S. Pu, W. Zhang, X. Liao, B. Shi, Green Chem. 13, 950 (2011)10.1039/c0gc00724b ↗
14. Z. Wang, C. Fang, M. Megharaj, A.C.S. Sustain, Chem. Eng. 2, 1022 (2014)
15. E.C. Okpara, O.E. Fayemi, E.M. Sherif, P.S. Ganesh, B.E.K. Swamy, E.E. Ebenso, Sens. Bio-Sens. Res. 35, 100476 (2022)10.1016/j.sbsr.2022.100476 ↗
16. K.R. Shubhashree, R. Reddy, A.K. Gangula, G.S. Nagananda, P.K. Badiya, S.S. Ramamurthy, P. Aramwit, N. Reddy, Mater. Chem. Phys. 280, 125795 (2022)10.1016/j.matchemphys.2022.125795 ↗
17. A.B. Samui, A.S. Patanakar, R.S. Satpute, P.C. Deb, Synth. Met. 125, 423–427 (2002)10.1016/S0379-6779(01)00487-8 ↗
18. D.C. Sindhimeshram, M.C. Gupta, Indian J. Chem. 34A, 260–277 (1995)
19. Q. Qin, Y. Guo, J. Nanomater. 1, 6 (2012)
20. Q. Jia, S. Shan, L. Jiang, Y. Wang, D. Li, J. Appl. Poly. Sci. 125, 3560–3566 (2012)10.1002/app.36257 ↗
21. R.A. Nyquist, R.O. Kagel, Infrared Spectra of Inorganic Compounds, 1st edn. (Academic Press, New York, 1971) p. 220
22. M. Abdelaziz, E.M. Abdelrazek, M. Phys. B 390, 1–7 (2007)10.1016/j.physb.2006.07.067 ↗
23. S.S. Shankar, A. Ahmad, M. Sastry, Biotechnol. Prog. 19, 1627–1631 (2003)10.1021/bp034070w ↗
24. V.K. Patel, S. Bhattacharya, A.C.S. Appl, Mater. Interfaces 5, 13364–13374 (2013)10.1021/am404308s ↗
25. F. Kanwal, S.A. Siddiqi, S. Tasleem, J. Chem. Soc. Pak. 31, 882–887 (2009)
26. S.M. Reda, S.M. Al-Ghannam, Adv. mater. Phys. Chem. 2, 75 (2012)10.4236/ampc.2012.22013 ↗
27. J. Vivekanandan, V. Ponnusamy, A. Mahudeswaran, P.S. Vijayanand, Arch. Appl. Sci. Res. 3, 147–153 (2011)
28. H.R. Humud, T.K. Aubais, Phys. Sci. Res. Int. 5, 110–122 (2013)
29. L. Zhang, Electrochim. Acta 52, 6969–6975 (2007)10.1016/j.electacta.2007.05.012 ↗
30. S.E. Elugoke, O.E. Fayemi, A.S. Adekunle, B.B. Mamba, T.T.I. Nkambule, E.E. Ebenso, FlatChem 33, 100372 (2022)10.1016/j.flatc.2022.100372 ↗
31. J. Ping, J. Wu, Y. Wang, Y. Ying, Biosens. Bioelectron. 34, 70–76 (2012)10.1016/j.bios.2012.01.016 ↗
32. Y.J. Yang, Sens. Actuators B Chem. 221, 750–759 (2015)10.1016/j.snb.2015.06.150 ↗
33. E. Laviron, J. Electroanal. Chem. 52, 355–393 (1974)10.1016/S0022-0728(74)80448-1 ↗
34. E. Laviron, J. Electroanal. Chem. 101, 19–28 (1979)10.1016/S0022-0728(79)80075-3 ↗
35. H. Yu, Y. Pang, J. Tang, Int. J. Electrochem. Sci. 10, 8353–8360 (2015)10.1016/S1452-3981(23)11101-1 ↗
36. S. Liu, J. Yan, G.W. He, D.D. Zhong, J.X. Chen, L.Y. Shi, X.M. Zhou, H.J. Jiang, J. Electroanal. Chem. 672, 40–44 (2012)10.1016/j.jelechem.2012.03.007 ↗
37. M. Ouellette, J. Mathault, S.D. Niyonambaza, A. Miled, E. Boisselier, Coatings 9, 496 (2019)10.3390/coatings9080496 ↗
38. J.B. Raoof, A. Kiani, R. Ojani, R. Valiollahi, S. Rashid-Nadimi, J. Solid State Electrochem. 14, 1171–1176 (2010)10.1007/s10008-009-0917-z ↗