Pulsed laser-patterned high-entropy single-atomic sites and alloy coordinated graphene oxide for pH-universal water electrolysis

Abstract

Synthesizing catalysts with multiple single-metal atoms remains challenging. Here, we introduce high-entropy single-atom catalysts (HESACs) co-coordinated with six elements from a FeRuPtNiCoPd high-entropy alloy (HEA) on graphene oxide supports (HESAC-HEA/GO) via single-pot pulsed laser irradiation in liquids (PLIL). This method leverages tailored surface composition and diverse active sites for electrochemical overall water splitting (OWS) across a wide pH range. The synergistic interactions in high-entropy systems and rapid photoreduction of Fe2+via PLIL enhance nuclei generation and active sites compared to Fe3+, achieving high hydrogen evolution reaction in 0.5 M H2SO4 with eta of 49 mV at 10 mA cm-2, and record-high oxygen evolution reaction in 1.0 M KOH with eta of 398 mV. Optimized HESAC-HEA/GO-Fe2+ shows exceptional OWS performance with lower cell voltage compared to HESACC-HEA/GO-Fe3+ and Pt/C. This study offers a robust pathway for fabricating versatile catalysts and facilitates mechanistic insights through in situ Raman and density functional theory analyses.