电容去离子
材料科学
堆积
电容感应
介孔材料
异质结
离子
超级电容器
插层(化学)
石墨烯
光电子学
化学工程
纳米技术
电极
化学
电化学
无机化学
计算机科学
催化作用
有机化学
工程类
物理化学
操作系统
生物化学
作者
Qian Li,Xingtao Xu,Jingru Guo,Jonathan P. Hill,Haishan Xu,Luoxing Xiang,Chen Li,Yusuke Yamauchi,Yiyong Mai
标识
DOI:10.1002/ange.202111823
摘要
Abstract The application of traditional electrode materials for high‐performance capacitive deionization (CDI) has been persistently limited by their low charge‐storage capacities, excessive co‐ion expulsion and slow salt removal rates. Here we report a bottom‐up approach to the preparation of a two‐dimensional (2D) Ti 3 C 2 T x MXene‐polydopamine heterostructure having ordered in‐plane mesochannels (denoted as mPDA/MXene). Interfacial self‐assembly of mesoporous polydopamine (mPDA) monolayers on MXene nanosheets leads to the mPDA/MXene heterostructure, which exhibits several unique features: (1) MXene undergoes reversible ion intercalation/deintercalation and possesses high conductivity; (2) mPDA layers establish redox capacitive characteristics and Na + selectivity, and also help to prevent self‐stacking and oxidation of MXene; (3) in‐plane mesochannels enable the smooth transport of ions at the internal spaces of this stacked 2D material. When applied as an electrode material for CDI, mPDA/MXene nanosheets exhibit top‐level CDI performance and cycling stability compared to those of the so far reported 2D materials. Our study opens an avenue for the rational construction of MXene‐organic hybrid heterostructures, and further motivates the development of high‐performance CDI electrode materials.
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