The size effect of Ti <sub>3</sub> C <sub>2</sub> T <sub>x</sub> nanosheet on the charge storage capability

This study explores the influence of lateral dimensions on the electrochemical performance of Ti 3 C 2 T x . Both Ti 3 C 2 T x with big lateral (Ti 3 C 2 T x -B) and Ti 3 C 2 T x with medium lateral (Ti 3 C 2 T x -M) exhibit a surface-controlled charge storage mechanism across all scan rates, with Ti 3 C 2 T x -M showing a significant contribution from surface capacitance. In contrast, only the small lateral Ti 3 C 2 T x (Ti 3 C 2 T x -S) displayed a diffusion-controlled process, and, within the same electrochemical potential range, it demonstrated significant hydrogen evolution performance. Ti 3 C 2 T x -M achieves the highest specific capacitance of 412 F g −1 at 0.5 A g −1 , surpassing Ti 3 C 2 T x -B, which reaches 350 F g −1 . These findings indicate that the lateral size restrict ion diffusion in the electrolyte, impacting the reaction rate, as smaller dimensions allow ions more time to traverse pores while their diffusion is influenced by the availability of active sites on the electrode surface.

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Publication Details

Journal
Journal of Chemical Research
Published
2025-03-01
DOI
https://doi.org/10.1177/17475198251330484
Primary Topic
MXene and MAX Phase Materials
Type
article
Field-Weighted Citation Impact
0.00

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article

The size effect of Ti 3 C 2 T x nanosheet on the charge storage capability

Baozhi Gong, Mingyue Chen, S. Wu, Kunyan Wang et al.
Journal of Chemical Research
MXene and MAX Phase Materials
article

The size effect of Ti 3 C 2 T x nanosheet on the charge storage capability

Baozhi Gong, Mingyue Chen, S. Wu, Kunyan Wang, Yangbin Ding, Jia-Yu Pan, Tang Pei-song
article en

Abstract

This study explores the influence of lateral dimensions on the electrochemical performance of Ti 3 C 2 T x . Both Ti 3 C 2 T x with big lateral (Ti 3 C 2 T x -B) and Ti 3 C 2 T x with medium lateral (Ti 3 C 2 T x -M) exhibit a surface-controlled charge storage mechanism across all scan rates, with Ti 3 C 2 T x -M showing a significant contribution from surface capacitance. In contrast, only the small lateral Ti 3 C 2 T x (Ti 3 C 2 T x -S) displayed a diffusion-controlled process, and, within the same electrochemical potential range, it demonstrated significant hydrogen evolution performance. Ti 3 C 2 T x -M achieves the highest specific capacitance of 412 F g −1 at 0.5 A g −1 , surpassing Ti 3 C 2 T x -B, which reaches 350 F g −1 . These findings indicate that the lateral size restrict ion diffusion in the electrolyte, impacting the reaction rate, as smaller dimensions allow ions more time to traverse pores while their diffusion is influenced by the availability of active sites on the electrode surface.

Journal of Chemical ResearchVol. 49(2)
Huzhou Normal University (CN), Northeast Petroleum University (CN)
National College Students Innovation and Entrepreneurship Training Program
Openalex Percentile: Top 94%
MXene and MAX Phase Materials
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