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Amine-Capped Co Nanoparticles for Highly Efficient Dehydrogenation of Ammonia Borane

机译:胺基包覆的钴纳米粒子对氨硼烷的高效脱氢

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Highly efficient heterogeneous catalysts are desired for the development of new energy storage materials, The rational choice and use of capping ligands are of significant importance for performance optimization of metal nanoparticle (NP) catalysts. By exploiting amine-rich polyethylenimine (PEI) and graphene oxide (GO) as a NP support, we demonstrate that as a capping ligand, PEI deposited on GO provides a novel pathway able to simultaneously control the morphology, spatial distribution, surface active sites of cobalt (Co) NPs, and remarkably enhances their catalytic properties for the hydrolytic dehydrogenation of ammonia borane (AB). Such a synergistic effect enables the synthesized PEI-GO/Co catalysts to reveal extremely high dehydrogenation activities under atmosphere condition. A total turnover frequency of 39.9 mol_(H2) min~(-1) mol_(Co)~(-1) and an apparent activation energy of 28.2 kJ mol~(-1) make the catalytic performance of these PEI-GO/Co catalysts comparable to those of noble metal-based catalysts, including bimetallic and multimetallic catalysts.
机译:高效多相催化剂是开发新型储能材料所需要的。封端配体的合理选择和使用对于优化金属纳米颗粒(NP)催化剂的性能至关重要。通过利用富胺的聚乙烯亚胺(PEI)和氧化石墨烯(GO)作为NP载体,我们证明了作为封端配体,PEI沉积在GO上提供了一种新颖的途径,能够同时控制其形态,空间分布,表面活性位点钴(Co)NPs,并显着增强了它们对氨硼烷(AB)水解脱氢的催化性能。这种协同作用使得合成的PEI-GO / Co催化剂在大气条件下具有极高的脱氢活性。这些PEI-GO / Co的总转换频率为39.9 mol_(H2)min〜(-1)mol_(Co)〜(-1),表观活化能为28.2 kJ mol〜(-1)。与贵金属基催化剂可比的催化剂,包括双金属和多金属催化剂。

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