纳米囊
介孔材料
材料科学
化学工程
阳离子聚合
光催化
催化作用
纳米材料基催化剂
乳状液
亚胺
共价键
肺表面活性物质
单体
纳米技术
共价有机骨架
纳米颗粒
化学
高分子化学
有机化学
聚合物
复合材料
工程类
作者
Yuting Ma,Shenhui Yu,Wei Li,Di Chen,Zhenqian Zheng,Linjie Mao,Xuan Yang,Wenjun Wang,Pingwei Liu
标识
DOI:10.1002/anie.202416980
摘要
Synthesis and assembly of two‐dimensional (2D) polymeric materials present a tricky trade‐off between the high reaction rate and precise morphology control. Here we report a nanoconfined synthesis of imine‐based 2D covalent organic frameworks (COFs) at the interface of oil‐in‐water (O/W) emulsion droplets stabilized by cationic surfactants. Highly uniform nanocapsules (NCs) could be prepared without adding extra catalysts at room temperature in just 4.5 h at a yield of 86%. The NCs have tunable average diameters and shell thicknesses, depending on the monomer and surfactant types/concentrations. Their BET‐specific surface areas are up to 139.0 m2/g, mainly contributed by narrowly‐distributed mesopores at ~5.0 nm and micropores at 1.4 nm. The surfactant plays the role of a catalyst during the reaction and interestingly, it also regulates the formation of mesopores and their sizes. Both theoretical and experimental studies confirm that the reaction has been accelerated by two orders of magnitude at the microdroplet interface, compared to that without emulsification. The resulting NCs could be well dispersed in water, and they have been demonstrated to be highly efficient nanocatalysts in application of water‐based hydrogen evolution. Such microdroplet interface‐confined synthesis may facilitate the future development of 2D polymeric materials for more advanced applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI