Tripodal Pd metallenes mediated by Nb2C MXenes for boosting alkynes semihydrogenation

2D metallene nanomaterials have spurred considerable attention in heterogeneous catalysis by virtue of sufficient unsaturated metal atoms, high specific surface area and surface strain. Nevertheless, the strong metallic bonding in nanoparticles aggravates the difficulty in the controllable regulation of the geometry of metallenes. Here we propose an efficient galvanic replacement strategy to construct Pd metallenes loaded on Nb2C MXenes at room temperature, which is triggered by strongmetal-support interaction based on MD simulations. The Pdmetallenes feature a chair structure of six-membered ring with the coordination number of Pd as low as 3. Coverage-dependent kinetic analysis based on first-principles calculations reveals that the tripodal Pd metallenes promote the diffusion of alkene and inhibit its overhydrogenation. As a consequence, Pd/Nb2C delivers an outstanding turnover frequency of 10372 h(-1) and a high selectivity of 96% at 25 degrees C in the semihydrogenation of alkynes without compromising the stability. This strategy is general and scalable considering the plentiful members of the MXene family, which can set a foundation for the design of novel supported-metallene catalysts for demanding transformations.

Automated summary

This study presents an efficient galvanic replacement strategy to load Pd metallenes on Nb2C MXenes at room temperature. The Pd metallenes have a chair structure of six-membered ring with a coordination number of Pd as low as 3. The strategy exhibits outstanding catalytic activity and selectivity in the semihydrogenation of alkynes.