Shows improved electrolysis activity and durability in water for platinum single atom catalysts, suggesting a new method for water splitting.
Enhancing the stability of Pt single atoms (SAs) remains a critical bottleneck for practical applications. Herein, we overcome this limitation by developing a ZrCl 3 –CH 4 system that enables an explosive nucleation to directly construct defect-rich ZrC nanoislands (NIs) on carbon cloth as ultrastable anchoring platforms for Pt single atoms (Pt 1 @ZrC NIs). This strategy dramatically enhances the surface number density of ZrC particles by 2 orders of magnitude over conventional methods and eliminates the long-standing issue of free carbon contamination. The Pt 1 @ZrC NI electrode exhibits a strong synergy, where ZrC promotes water adsorption/dissociation and Pt facilitates hydrogen migration/desorption, yielding a mass activity 116- and 132-fold greater than that of the commercial Pt@C catalyst in alkaline and acidic media, respectively. Moreover, owing to the excellent acid- and base-resistance of ZrC and its strong binding to Pt SAs and the substrate, the Pt 1 @ZrC NIs catalyst maintains exceptional stability in both acidic and alkaline media.
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Xiang et al. (2026) studied this question.
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