Metallic CoN catalysts have been considered as one of the most promising non-noble materials for heterogeneous catalysis because of their high electrical conductivity, great magnetic property, and high intrinsic activity. However, the metastable properties seriously limit their applications for heterogeneous water phase catalysis. In this work, a novel Co-metal-organic framework (MOF)-derived hollow porous nanocages (PNCs) composed of metallic CoN and N-doped carbon (NC) were synthesized for the first time. This hollow three-dimensional (3D) PNC catalyst was synthesized by taking advantage of Co-MOF as a precursor for fabricating 3D hollow CoO@C PNCs, along with the NH treatment of Co-oxide frames to promote the in situ conversion of Co-MOF to CoN@NC PNCs, benefiting from the high intrinsic activity and electron conductivity of the metallic CoN phase and the good permeability of the hollow porous nanostructure as well as the efficient doping of N into the carbon layer. Besides, the covalent bridge between the active CoN surface and PNC shells also provides facile pathways for electron and mass transport. The obtained CoN@NC PNCs exhibit excellent catalytic activity and stability for 4-nitrophenol reduction in terms of low activation energy (E = 23.53 kJ mol), high turnover frequency (52.01 × 10 molecule g min), and high apparent rate constant (k = 2.106 min). Furthermore, its magnetic property and stable configuration account for the excellent recyclability of the catalyst. It is hoped that our finding could pave the way for the construction of other hollow transition metal-based nitride@NC PNC catalysts for wide applications.

A stable Z-scheme with well-defined architecture by in situ growth of COFs on CdS for photocatalytic water splitting is constructed. The T-COF shell can protect the catalytic center of CdS from deactivation and photocorrosion.

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Water-assisted proton hopping (WAPH) has been intensively investigated for promoting the performance of metal oxide-supported catalysts for hydrogenation. However, the effects of the structure of the metal oxide support on WAPH have received little attention. Herein, we construct oxygen vacancy-bearing, MoO3–x -supported Pd nanoparticle catalysts (Pd/MoO3–x -R), where the oxygen vacancies can promote WAPH, thereby facilitating catalytic hydrogenation. The experimental results and theoretical calculations show that the oxygen vacancies favor the adsorption of water, which assists the proton hopping across the surface of the metal oxide, enhancing the catalytic hydrogenation. Our finding will provide a potential approach to the design of metal oxide-supported catalysts for hydrogenation.

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