J Colloid Interface Sci
August 2025
Whether stress at the micro-structural level exhibited self-limiting characteristics similar to macroscopic conditions, thus affecting the performance of catalysts in relation to the scope of stress influence, remained a topic requiring further investigation. In this study, we designed a CuAg@NiAg core-shell structure to induce lattice expansion and generate stress at the core-shell interface through the simultaneous action of displacement and co-reduction reactions. By adjusting the shell thickness, we investigated the impact of atomic-scale stress influence range (self-limiting behavior) on catalytic performance.
View Article and Find Full Text PDFThe enhanced selectivity for C products in the electrochemical CO reduction reaction (ECORR) is critically dependent on the regulation of the elemental existence state on the surface of the electrocatalyst. In this study, CuO nanowires featuring multiple grain boundaries were successfully synthesized. Two distinct model catalysts were prepared: one through surface adsorption of Br (denoted as CuO_Br) and the other via surface bromination (denoted as CuO@CuBr).
View Article and Find Full Text PDFJ Colloid Interface Sci
October 2023
Cobalt-nitride-carbide (Co-N-C) catalysts are promising cost-efficient transition metal catalysts for electrocatalytic hydrogen evolution, but few works investigate the metal-support interaction (MSI) effect on hydrogen evolution reaction (HER) performance. Herein, efficient Co-N-C catalysts with controllable MSI between encapsulated Co nanoparticles and nitrogen-doped graphitic carbon nanosheets were synthesized via a facile organic-inorganic hybridization method. Results demonstrate that the Co-N-C catalyst with the coexistence of single-atom Co sites and Co nanoparticles prepared by 0.
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