Multishelled Hollow Covalent Organic Framework Nanospheres for Stable Potassium Storage

共价键 结晶 无定形固体 纳米复合材料 化学工程 蚀刻(微加工) 制作 化学 水溶液 材料科学 纳米技术 有机化学 工程类 医学 替代医学 图层(电子) 病理
作者
Yanfei Chen,Ying Fang,Ningning Zhu,Luo Xiao,Guo-Yu Zhu,Menghua Yang,Run-Hang Chen,Xian Zeng,Ji‐Miao Xiao,Lin Liu,Guo‐Hong Ning,De‐Shan Bin,Dan Li
出处
期刊:Angewandte Chemie [Wiley]
被引量:1
标识
DOI:10.1002/anie.202424641
摘要

Multishelled hollow covalent organic framework nanospheres (MH-COFs) with at least two shells integrate the merits of the porous crystalline covalent organic framework (COF) matrix with the complex hollow architecture, which can motivate new functions for exceptional performance. However, the fabrication of MH-COFs is still uncultivated and remains a formidable challenge. Herein, we reported a facile template-free protocol for the general synthesis of different MH-COFs by controlling the simultaneous processes of surface crystallization and core etching of the crystalline-inhomogeneity nanospheres of COFs precursor. The crystalline-inhomogeneity solid covalent organic polymer nanospheres (COPs) with robust crystalline surface but vulnerable amorphous core were designed. Subsequently, an acetic acid aqueous solution treatment of crystalline-inhomogeneity COPs not only induced selective etching of the vulnerable cores but also promote the further crystallization of the surface layers, thereby producing hollow COFs. A further step-by-step expansion of seeded growth for inhomogeneous COP layers and then similar acid solution treatment can output the intriguing MH-COFs. An extraordinarily stable K-ion battery anode with high capacity was demonstrated with a MH-COFs/S nanocomposite fabricated by covalently bonding chain sulfur into the MH-COFs matrix. This work opened a simple but powerful avenue in designing complex hollow COFs architectures to boost their potential for applications.
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