Metal–Organic Framework-Derived Ni–S/C Catalysts for Selective Alkyne Hydrogenation
Source abstract
Abstract
A carbon matrix-supported Ni catalyst with surface/subsurface S species is prepared using a sacrificial metal–organic framework synthesis strategy. The resulting highly dispersed Ni–S/C catalyst contains surface discontinuous and electron-deficient Ni δ+ sites modified by p-block S elements. This catalyst proved to be extremely active and selective for alkyne hydrogenation. Specifically, high intrinsic activity (TOF = 0.0351 s –1 ) and superior selectivity (>90%) at complete conversion were achieved, whereas an analogous S-free sample prepared by the same synthetic route performed poorly. That is, the incorporation of S in Ni particles and the carbon matrix exerts a remarkable positive effect on catalytic behavior for alkyne hydrogenation, breaking the activity–selectivity trade-off. Through comprehensive experimental studies, enhanced performance of Ni–S/C was ascribed to the presence of discontinuous Ni ensembles, which promote desorption of weakly π-bonded ethylene and an optimized electronic structure modified via obvious p–d orbital hybridization.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Catalysis and Hydrodesulfurization Studies · Nanomaterials for catalytic reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Chemical Resource Engineering, Beijing Engineering Center for Hierarchical Catalysts, Beijing University of Chemical Technology, Beijing 100029, China
Quzhou Institute for Innovation in Resource Chemical Engineering, Quzhou 324000, China
Department of Chemistry, University of Aberdeen, Aberdeen AB24 3UE, U.K.
Funding
Beijing Association for Science and Technology · Fundamental Research Funds for the Central Universities · National Natural Science Foundation of China
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