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Demonstrates optimized electrocatalytic efficiency in MXene-supported single-atom sites, suggesting a new strategy for selective reactions.
with a 200 h stability. In situ/operando spectroscopy and DFT calculations unveil that Pt/Co DSAs synergistically induce charge redistribution on the MXene surface, thus optimizing the active-site electronic states and intermediate adsorption to lower the reaction energy barrier. Our strategy serves as a pathway for atomically precise control of MXene-supported single-atom sites toward selective electrocatalysis.
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Zhang et al. (2026) studied this question.
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