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Enabling Heteroatom Doping of Flexible MXene Film in Seconds: A Microwave‐Induced Targeted Thermal‐Shock Method.

Authors :
Zhong, Geng
Yang, Haiyan
Zeng, Minling
Liu, Sisi
Chen, Shengnan
Fan, Zhimin
Zhu, Caizhen
Xu, Jian
Yu, Jiali
Source :
Advanced Functional Materials. May2024, Vol. 34 Issue 22, p1-10. 10p.
Publication Year :
2024

Abstract

Heteroatom doping can efficiently tailor the physicochemical properties of 2D MXene materials for enhancing the energy storage performance. However, in mostly applied doping strategies, the wet chemistry method typically suffers tedious separation and abstersion process while the solid‐phase thermal strategy (traditional furnace heating) employed long‐time (several hours) high‐temperature treatment may cause degradation of MXene. In this work, a universal, energy efficient and environmental‐friendly strategy is reported to realize the heteroatom doping of MXene within seconds by microwave‐induced targeted thermal shock. The MXene film can self‐heat to >800 °C within seconds followed by generating dazzling plasma under microwave field. The high temperature combined with plasma create a localized ultrahigh‐energy environment in MXenes, which promotes the rapid decomposition of preloaded dopant precursors and lattice/surface functional group substitutions between dopant atoms and MXene. The resulted nitrogen (N) and sulfur (S) co‐doped MXene showed significantly improved capacity and performance stability under deformations. Compared with the traditional furnace heating, the targeted heating strategy have significantly higher energy and time efficiencies and reduced carbon footprint. In addition, this method can be readily extended to various element doping of MXene. The microwave‐induced targeted thermal‐shock represents a general and efficient strategy for the fast heteroatom doping of MXene. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1616301X
Volume :
34
Issue :
22
Database :
Academic Search Index
Journal :
Advanced Functional Materials
Publication Type :
Academic Journal
Accession number :
177563189
Full Text :
https://doi.org/10.1002/adfm.202313845