材料科学
纳米技术
离解(化学)
合并(版本控制)
介孔材料
氧化物
多孔性
石墨烯
融合
薄膜
计算机科学
化学
复合材料
物理化学
生物化学
语言学
哲学
冶金
情报检索
催化作用
作者
Xuefeng Zhang,Xudong Li,Q. Liu,Yufa Feng,Si Qin,Ting Wang,Honggang Xu,Hao Li,Liang Yin,Hyeok-Gu Kang,Zhimin Fan
标识
DOI:10.1002/advs.202309171
摘要
Abstract Enabling 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.
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