Reversible Constrained Dissociation and Reassembly of MXene Films

Author:

Zhang Xuefeng1,Liu Xudong2,Liu Qingqiang1,Feng Yufa1,Qiu Si1,Wang Ting1,Xu Huayu1,Li Hao1,Yin Liang3,Kang Hui4,Fan Zhimin23ORCID

Affiliation:

1. School of chemistry and Materials Engineering Guangdong Provincial Key Laboratory for Electronic Functional Materials and Devices Huizhou University Huizhou 516007 China

2. School of Materials Science and Engineering Harbin Institute of Technology Harbin 150001 China

3. MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage School of Chemistry and Chemical Engineering Harbin Institute of Technology Harbin 150001 China

4. Advanced Materials Thrust The Hong Kong University of Science and Technology (Guangzhou) Guangzhou 510000 China

Abstract

AbstractEnabling materials to undergo reversible dynamic transformations akin to the behaviors of living organisms represents a critical challenge in the field of material assembly. The pursuit of such capabilities using conventional materials has largely been met with limited success. Herein, the discovery of reversible constrained dissociation and reconfiguration in MXene films, offering an effective solution to overcome this obstacle is reported. Specifically, MXene films permit rapid intercalation of water molecules between their distinctive layers, resulting in a significant expansion and exhibiting confined dissociation within constrained spaces. Meanwhile, the process of capillary compression driven by water evaporation reinstates the dissociated MXene film to its original compact state. Further, the adhesive properties emerging from the confined disassociation of MXene films can spontaneously induce fusion between separate films. Utilizing this attribute, complex structures of MXene films can be effortlessly foamed and interlayer porosity precisely controlled, using only water as the inducer. Additionally, a parallel phenomenon has been identified in graphene oxide films. This work not only provides fresh insights into the microscopic mechanisms of 2D materials such as MXene but also paves a transformative path for their macroscopic assembly applications in the future.

Funder

National Natural Science Foundation of China

Key Research and Development Program of Heilongjiang

Publisher

Wiley

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