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Enhanced capacitive performance of cathodically reduced titania nanotubes pulsed deposited with Mn(2)O(3) as supercapacitor electrode

A facile and simple pulse electrodeposition method was employed to deposit Mn(2)O(3) nanoparticles on cathodically reduced titania nanotubes (R-TNTs) at different deposition time in the range of 3–15 min to investigate the influence of mass loading of Mn(2)O(3) on the electrochemical performance of...

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Autores principales: Muzakir, Muhammad Muhammad, Zainal, Zulkarnain, Lim, Hong Ngee, Abdullah, Abdul Halim, Bahrudin, Noor Nazihah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037482/
https://www.ncbi.nlm.nih.gov/pubmed/35479972
http://dx.doi.org/10.1039/d1ra00564b
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author Muzakir, Muhammad Muhammad
Zainal, Zulkarnain
Lim, Hong Ngee
Abdullah, Abdul Halim
Bahrudin, Noor Nazihah
author_facet Muzakir, Muhammad Muhammad
Zainal, Zulkarnain
Lim, Hong Ngee
Abdullah, Abdul Halim
Bahrudin, Noor Nazihah
author_sort Muzakir, Muhammad Muhammad
collection PubMed
description A facile and simple pulse electrodeposition method was employed to deposit Mn(2)O(3) nanoparticles on cathodically reduced titania nanotubes (R-TNTs) at different deposition time in the range of 3–15 min to investigate the influence of mass loading of Mn(2)O(3) on the electrochemical performance of Mn(2)O(3)/R-TNTs nanocomposite for supercapacitor application. Mn(2)O(3) nanoparticles were deposited on circumference of R-TNTs as well as in the nanotubes as revealed by FESEM images for all the deposited time. XPS result confirmed the presence of MnO(2) (Mn(4+)) and MnO (Mn(2+)) on the Mn(2)O(3)/R-TNTs composite which provide pseudocapacitive behaviour for the electrode. Mass loading of Mn(2)O(3) increased linearly with deposition time as confirmed by EDX analysis. The sample deposited for 12 min exhibits the highest areal capacitance of 51 mF cm(−2) (which is 22 times enhancement over R-TNTs) at a current density of 0.1 mA cm(−2) and specific capacitance of 325 F g(−1) at 6 A g(−1). The sample also show a high-rate capability by retaining 80% of its capacitance even at higher current density of 30 A g(−1). Interestingly, it retained 98% of the capacitance over 5000 charge discharge cycles at 10 A g(−1) after initial drop to 95% at 200th cycles suggesting an excellent long-term chemical stability. A considerably low equivalent series resistance (ESR) and charge transfer resistance (R(ct)) of 9.6 Ω and 0.4 Ω respectively was deduced from electrochemical impedance spectroscopy (EIS) analysis indicating good conductivity and improved charge transfer efficiency of Mn(2)O(3)/R-TNTs nanocomposite.
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spelling pubmed-90374822022-04-26 Enhanced capacitive performance of cathodically reduced titania nanotubes pulsed deposited with Mn(2)O(3) as supercapacitor electrode Muzakir, Muhammad Muhammad Zainal, Zulkarnain Lim, Hong Ngee Abdullah, Abdul Halim Bahrudin, Noor Nazihah RSC Adv Chemistry A facile and simple pulse electrodeposition method was employed to deposit Mn(2)O(3) nanoparticles on cathodically reduced titania nanotubes (R-TNTs) at different deposition time in the range of 3–15 min to investigate the influence of mass loading of Mn(2)O(3) on the electrochemical performance of Mn(2)O(3)/R-TNTs nanocomposite for supercapacitor application. Mn(2)O(3) nanoparticles were deposited on circumference of R-TNTs as well as in the nanotubes as revealed by FESEM images for all the deposited time. XPS result confirmed the presence of MnO(2) (Mn(4+)) and MnO (Mn(2+)) on the Mn(2)O(3)/R-TNTs composite which provide pseudocapacitive behaviour for the electrode. Mass loading of Mn(2)O(3) increased linearly with deposition time as confirmed by EDX analysis. The sample deposited for 12 min exhibits the highest areal capacitance of 51 mF cm(−2) (which is 22 times enhancement over R-TNTs) at a current density of 0.1 mA cm(−2) and specific capacitance of 325 F g(−1) at 6 A g(−1). The sample also show a high-rate capability by retaining 80% of its capacitance even at higher current density of 30 A g(−1). Interestingly, it retained 98% of the capacitance over 5000 charge discharge cycles at 10 A g(−1) after initial drop to 95% at 200th cycles suggesting an excellent long-term chemical stability. A considerably low equivalent series resistance (ESR) and charge transfer resistance (R(ct)) of 9.6 Ω and 0.4 Ω respectively was deduced from electrochemical impedance spectroscopy (EIS) analysis indicating good conductivity and improved charge transfer efficiency of Mn(2)O(3)/R-TNTs nanocomposite. The Royal Society of Chemistry 2021-08-05 /pmc/articles/PMC9037482/ /pubmed/35479972 http://dx.doi.org/10.1039/d1ra00564b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Muzakir, Muhammad Muhammad
Zainal, Zulkarnain
Lim, Hong Ngee
Abdullah, Abdul Halim
Bahrudin, Noor Nazihah
Enhanced capacitive performance of cathodically reduced titania nanotubes pulsed deposited with Mn(2)O(3) as supercapacitor electrode
title Enhanced capacitive performance of cathodically reduced titania nanotubes pulsed deposited with Mn(2)O(3) as supercapacitor electrode
title_full Enhanced capacitive performance of cathodically reduced titania nanotubes pulsed deposited with Mn(2)O(3) as supercapacitor electrode
title_fullStr Enhanced capacitive performance of cathodically reduced titania nanotubes pulsed deposited with Mn(2)O(3) as supercapacitor electrode
title_full_unstemmed Enhanced capacitive performance of cathodically reduced titania nanotubes pulsed deposited with Mn(2)O(3) as supercapacitor electrode
title_short Enhanced capacitive performance of cathodically reduced titania nanotubes pulsed deposited with Mn(2)O(3) as supercapacitor electrode
title_sort enhanced capacitive performance of cathodically reduced titania nanotubes pulsed deposited with mn(2)o(3) as supercapacitor electrode
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037482/
https://www.ncbi.nlm.nih.gov/pubmed/35479972
http://dx.doi.org/10.1039/d1ra00564b
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