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Highly Efficient Oxygen Reduction Reaction Electrocatalysts Synthesized under Nanospace Confinement of Metal-Oganic Framework

机译:基于金属 - Oganic框架的纳米空间限制合成的高效氧还原反应电催化剂

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摘要

The output energy capacity of green electrochemical devices, e.g., fuel cells, depends strongly on the sluggish oxygen reduction reaction (ORR), which requires catalysts. One of the desired features for highly efficient ORR electrocatalytic materials is the richness of welldefined activate sites. Herein, we developed a facile approach to prepare highly efficient nonprecious metal and nitrogen-doped carbon-based ORR catalysts based on covalent organic polymers (COPs) synthesized in situ, in the nanoconfined space of highly ordered metal organic frameworks (MOFs). The MOF templet ensured the developed electrocatalysts possess a high surface area with homogeneously distributed small metal/nitrogen active sites, as confirmed by X-ray absorption fine structure measurements and first-principles calculations, leading to highly efficient ORR electrocatalytic activity. Notably, the developed COP-TPP(Fe)@MOF-900 exhibits a 16 mV positive half wave potential compared with the benchmarked Pt/C.
机译:绿色电化学器件的输出能量,例如燃料电池,在需要催化剂的缓慢氧还原反应(ORR)上的强烈依赖。 高效ORR电催化材料的所需特征之一是井义的活性位点的丰富性。 在此,我们开发了一种基于原位合成的共价有机聚合物(COP)的高效的非佛得多金属和氮掺杂碳基ORR催化剂的容易方法,在高度有序的金属有机骨架(MOF)的纳米核空间中。 MOF模板确保开发的电催化剂具有具有均匀分布的小金属/氮活性位点的高表面积,如X射线吸收细结构测量和第一原理计算所证实,导致高效的ORR电催化活性。 值得注意的是,与基准PT / C相比,发达的COP-TPP(FE)@ MOF-900表现出16mV正半波电位。

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