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A covalent organic framework-based route to the in situ encapsulation of metal nanoparticles in N-rich hollow carbon spheres

机译:在富氮空心碳球中将金属纳米粒子原位封装的基于共价有机框架的途径

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摘要

Metal nanoparticles (NPs) encapsulated in hollow nanostructures hold great promise for a variety of applications. Herein, we demonstrate a new concept where covalent organic frameworks (COFs) doped with metal cations can be readily used as novel precursors for the in situ encapsulation of metal NPs into N doped hollow carbon spheres (NHCS) through a controlled carbonization process. The obtained Pd@NHCS composites show a significantly enhanced catalytic activity and selectivity in the hydrogenation of nitrobenzene in ethanol and oxidation of cinnamyl alcohol compared with that of the conventional Pd/N–C and commercial Pd/C catalysts. The excellent catalytic performance should be related to the synergism of the porous hollow spheric structure, highly dispersed Pd NPs, and uniform distribution of N dopants on the materials. We believe that this newly developed methodology could be extended to the synthesis of other metal NPs@NHCS composites for a variety of advanced applications.
机译:封装在空心纳米结构中的金属纳米颗粒(NPs)在各种应用中都具有广阔的前景。在这里,我们展示了一个新概念,其中掺杂有金属阳离子的共价有机骨架(COF)可以很容易地用作通过控制碳化过程将金属NP原位封装到N掺杂空心碳球(NHCS)中的新型前体。与传统的Pd / N–C和商业Pd / C催化剂相比,所获得的Pd @ NHCS复合材料在乙醇中硝基苯加氢和肉桂醇氧化方面显示出显着增强的催化活性和选择性。优异的催化性能应与多孔空心球形结构的协同作用,高度分散的Pd NP和材料中N掺杂剂的均匀分布有关。我们认为,这种新开发的方法可以扩展到其他金属NPs @ NHCS复合材料的合成,以用于各种高级应用。

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