纳米囊
光催化
共价键
化学
纳米技术
光化学
材料科学
化学工程
有机化学
纳米颗粒
催化作用
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/ange.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.
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