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Encapsulation of C–N-decorated metal sub-nanoclusters/single atoms into a metal–organic framework for highly efficient catalysis

机译:将装饰有C–N的金属亚纳米簇/单原子封装到金属有机框架中以实现高效催化

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摘要

Fabrication and modification of few-atom metal clusters and even single atoms in the pores of porous materials for catalysis are highly desired from an atom-efficiency aspect but remain a great challenge. Herein, we propose a facile and efficient strategy for the encapsulation of C–N-decorated Pd sub-nanoclusters (MSNCs)/single atoms (SAs) into MOFs by the confined thermolysis of Pd-based metal–organic polyhedra (MOPs) in MOF pores. The obtained hybrids contained both Pd MSNCs (∼0.8 nm) and Pd SAs, which were stabilized by the in situ formed C–N fragments and the confinement effect of MOF pores. Benefiting from the highly exposed Pd atoms and synergistic effect between Pd and C–N fragments, these catalysts exhibited extremely high catalytic activity and stability in various important chemical processes, making them comparable to the most active Pd-based catalysts reported in the literature even under milder reaction conditions. Considering the high tunability of MOPs, this proposed strategy might provide a new toolbox for enriching the family of decorated MSNC/SA catalysts.
机译:从原子效率的角度出发,非常需要在多孔材料的孔中制造和修饰少量原子的金属簇,甚至是单原子以进行催化,但仍然是一个巨大的挑战。本文中,我们提出了一种通过在MOF中对Pd基金属有机多面体(MOP)进行有限的热解,将C–N装饰的Pd亚纳米簇(MSNC)/单原子(SAs)封装到MOF中的一种简便有效的策略。毛孔。获得的杂化物同时包含Pd MSNC(〜0.8 nm)和Pd SA,它们通过原位形成的C–N片段和MOF孔的封闭作用而得以稳定。得益于高度暴露的Pd原子以及Pd和C–N片段之间的协同作用,这些催化剂在各种重要的化学过程中均表现出极高的催化活性和稳定性,使其甚至可以与文献中报道的活性最高的Pd基催化剂媲美。反应条件温和。考虑到MOP的高度可调性,该提议的策略可能会提供一个新的工具箱,以丰富装饰MSNC / SA催化剂系列。

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