Leveraging the Heterostructure-Driven Synergy in Lychee-Like Ni–Mn Telluride Amalgamated with Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> MXene for Binder-Free All-Solid-State Hybrid Supercapacitors

The incorporation of a stratified structure for electrode fabrication proffers an advanced solution to stimulate the energy density of supercapacitors while maintaining the power density. The provision of interface engineering in heterostructure electrode constitutes a highly effective strategy for tuning their corresponding physical and chemical characteristics, which augments the storage capacity. Thus, this study reports the fabrication of a Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> MXene and nickel manganese telluride (NMTe)-based composite, synthesized through an acid etching followed by a straightforward one-step <i>in situ</i> hydrothermal process, encompassing lychee-like NMTe into a multilayered Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub>. Remarkably, the binder-free NMTe@Ti<sub>3</sub>C<sub>2</sub>Tx electrode surpasses the performance of its individual counterparts, i.e., NMTe and Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub>, benefiting from the synergistic interplay between the two constituents and a distinctive architectural framework that optimizes electrode-electrolyte interaction. The composite effectually remediated the self-restacking of multilayered MXene and the conglomeration of NMTe particles. The battery-type NMTe@Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> electrode exhibited an exceptional specific capacitance of 2139.1 F g<sup>-1</sup> at a current density of 1 A g<sup>-1</sup> with cyclic stability of 96.5% for over 10,000 cycles with trivial alteration in surface morphology. Mechanistically, an in-depth examination unveiled a more nuanced understanding of interfacial charge flux modulation and electronic state reconfiguration in the charge storage mechanism. Further, two separate devices were fabricated in symmetric and asymmetric configurations utilizing the binder-free NMTe@Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> electrodes. Prodigiously, the asymmetric device unveiled a larger potential window of 1.6 V and an outstanding energy density of 114.2 Wh kg<sup>-1</sup> at a power density of 756.8 W kg<sup>-1</sup>. Thus, the present research bestows a stepping stone for the broader integration of telluride and MXene-based composite into energy storage technologies.

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Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2025-06-06
DOI
https://doi.org/10.1021/acsami.5c05172
Citations
4
Primary Topic
MXene and MAX Phase Materials
Type
article
Field-Weighted Citation Impact
2.07

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article

Leveraging the Heterostructure-Driven Synergy in Lychee-Like Ni–Mn Telluride Amalgamated with Ti3C2Tx MXene for Binder-Free All-Solid-State Hybrid Supercapacitors

H. S. Chauhan, Antra Choubey, Ashish Yadav
4 citations
ACS Applied Materials & Interfaces
MXene and MAX Phase Materials
2.07
article

Leveraging the Heterostructure-Driven Synergy in Lychee-Like Ni–Mn Telluride Amalgamated with Ti3C2Tx MXene for Binder-Free All-Solid-State Hybrid Supercapacitors

H. S. Chauhan, Antra Choubey, Ashish Yadav
article en
4 citations

Abstract

The incorporation of a stratified structure for electrode fabrication proffers an advanced solution to stimulate the energy density of supercapacitors while maintaining the power density. The provision of interface engineering in heterostructure electrode constitutes a highly effective strategy for tuning their corresponding physical and chemical characteristics, which augments the storage capacity. Thus, this study reports the fabrication of a Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> MXene and nickel manganese telluride (NMTe)-based composite, synthesized through an acid etching followed by a straightforward one-step <i>in situ</i> hydrothermal process, encompassing lychee-like NMTe into a multilayered Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub>. Remarkably, the binder-free NMTe@Ti<sub>3</sub>C<sub>2</sub>Tx electrode surpasses the performance of its individual counterparts, i.e., NMTe and Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub>, benefiting from the synergistic interplay between the two constituents and a distinctive architectural framework that optimizes electrode-electrolyte interaction. The composite effectually remediated the self-restacking of multilayered MXene and the conglomeration of NMTe particles. The battery-type NMTe@Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> electrode exhibited an exceptional specific capacitance of 2139.1 F g<sup>-1</sup> at a current density of 1 A g<sup>-1</sup> with cyclic stability of 96.5% for over 10,000 cycles with trivial alteration in surface morphology. Mechanistically, an in-depth examination unveiled a more nuanced understanding of interfacial charge flux modulation and electronic state reconfiguration in the charge storage mechanism. Further, two separate devices were fabricated in symmetric and asymmetric configurations utilizing the binder-free NMTe@Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> electrodes. Prodigiously, the asymmetric device unveiled a larger potential window of 1.6 V and an outstanding energy density of 114.2 Wh kg<sup>-1</sup> at a power density of 756.8 W kg<sup>-1</sup>. Thus, the present research bestows a stepping stone for the broader integration of telluride and MXene-based composite into energy storage technologies.

ACS Applied Materials & InterfacesVol. 17(24)
Indian Institute of Technology Roorkee (IN)
Indian Institute of Technology Roorkee, Ministry of Education, India
Openalex Percentile: Top 13%
MXene and MAX Phase Materials
2.07
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