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Electronic interaction of highly-dispersed Pd with defect-rich nickel disulfide nanoarrays for selective ethylene glycol-to-glycolate electroconversion
Nano Research 2026, 19(3): 94908315
Published: 09 March 2026
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Palladium (Pd) is regarded as one of the most active catalysts for electrochemical ethylene glycol oxidation reaction (EGOR) to value-added glycolate, but its large-scale application is still restricted by limited catalytic effectiveness and exorbitant cost. Herein, we designed and synthesized the defect-rich nickel sulfide nanosheet arrays on nickel foam (Ni3−xCoxS2@NF) as the self-supported substrate to anchor well-dispersive Pd nanoparticles (Pd-Ni3−xCoxS2@NF) with its loading as low as approximately 3.03 wt.%, which is conducive to the exposure and utilization of the active Pd sites. The optimal Pd-Ni3−xCoxS2@NF electrocatalyst (1 cm2 working area) could achieve an efficient EGOR performance, showing a current density of 100 mA·cm−2 at 0.77 V vs. reversible hydrogen electrode (RHE), and 98.1% Faradaic efficiency of glycolate. Furthermore, the in-situ Raman spectra reveal that the interaction between Pd and Ni3−xCoxS2@NF significantly increases the adsorption of EG, and Ni3−xCoxS2@NF enhances the *OH adsorption capacity, thus further improving the EGOR activity and stability. This study provides an effective paradigm for enhancing the utilization and electrocatalytic performance of noble metallic catalysts, and also offers a deep insight into the interaction between the active sites and substrate.

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