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Composite Fe3O4-MXene-Carbon Nanotube Electrodes for Supercapacitors Prepared Using the New Colloidal Method.


ABSTRACT: MXenes, such as Ti3C2Tx, are promising materials for electrodes of supercapacitors (SCs). Colloidal techniques have potential for the fabrication of advanced Ti3C2Tx composites with high areal capacitance (CS). This paper reports the fabrication of Ti3C2TX-Fe3O4-multiwalled carbon nanotube (CNT) electrodes, which show CS of 5.52 F cm-2 in the negative potential range in 0.5 M Na2SO4 electrolyte. Good capacitive performance is achieved at a mass loading of 35 mg cm-2 due to the use of Celestine blue (CB) as a co-dispersant for individual materials. The mechanisms of CB adsorption on Ti3C2TX, Fe3O4, and CNTs and their electrostatic co-dispersion are discussed. The comparison of the capacitive behavior of Ti3C2TX-Fe3O4-CNT electrodes with Ti3C2TX-CNT and Fe3O4-CNT electrodes for the same active mass, electrode thickness and CNT content reveals a synergistic effect of the individual capacitive materials, which is observed due to the use of CB. The high CS of Ti3C2TX-Fe3O4-CNT composites makes them promising materials for application in negative electrodes of asymmetric SC devices.

SUBMITTER: Liang W 

PROVIDER: S-EPMC8199491 | biostudies-literature | 2021 May

REPOSITORIES: biostudies-literature

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Composite Fe<sub>3</sub>O<sub>4</sub>-MXene-Carbon Nanotube Electrodes for Supercapacitors Prepared Using the New Colloidal Method.

Liang Wenyu W   Zhitomirsky Igor I  

Materials (Basel, Switzerland) 20210529 11


MXenes, such as Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub>, are promising materials for electrodes of supercapacitors (SCs). Colloidal techniques have potential for the fabrication of advanced Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> composites with high areal capacitance (C<sub>S</sub>). This paper reports the fabrication of Ti<sub>3</sub>C<sub>2</sub>T<sub>X</sub>-Fe<sub>3</sub>O<sub>4</sub>-multiwalled carbon nanotube (CNT) electrodes, which show C<sub>S</sub> of 5.52 F cm<sup>-2</sup> in the n  ...[more]

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