纳米片
材料科学
纳米技术
范德瓦尔斯力
可扩展性
超级电容器
领域(数学)
合理设计
工作(物理)
热的
磁场
能量收集
能量(信号处理)
纳米结构
领域(数学分析)
电极
瞬态(计算机编程)
能量转换
计算机科学
运动(物理)
动能
自组装
设计策略
力场(虚构)
能源景观
作者
Yubing Li,S. F. Xu,Dan Huang,ZhiQun Tian,Tangming Mo,Y M Wang,Ya Yang
标识
DOI:10.1002/aenm.202506366
摘要
ABSTRACT Controlling the macroscopic assembly of two‐dimensional (2D) nanosheets into functional, ordered architectures is a central challenge in materials science. Their intrinsic tendency to restack into dense, disordered films severely limits their potential in applications requiring directional transport, from catalysis to energy storage. Aligning atomically‐thin nanosheets has remained a major hurdle, a failure previously ascribed to thermal motion but which we identify as stemming from dominant, many‐body van der Waals interactions creating deep kinetic traps. Here, we overcome this barrier with a magnetic strategy enabling predictive architectural control at low field strengths (<50 mT). We establish a parameter‐matching model that deciphers the complex energy landscape, transforming assembly into a rational design framework. This approach allows us to sculpt architectures like vertically aligned, biaxially ordered MXene structures, creating ion superhighways with minimized tortuosity. As a demonstration, engineered MXene electrodes deliver exceptional rate capabilities in supercapacitors and sodium‐ion batteries. This work provides a universal, scalable platform for architecting 2D materials, unlocking their potential where directional transport is paramount.
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