Akademik Veri Yönetim Sistemi
ACS Omega, cilt.11, sa.12, ss.19345-19355, 2026 (SCI-Expanded, Scopus)
Zinc-air batteries are limited by sluggish, reversible oxygen electrocatalysis at the air cathode. High-entropy sulfides (HESs) are introduced as bifunctional oxygen catalysts, leveraging multication disorder to create robust, tunable active sites. Three pyrite-type, single-phase compositions: HES-TM [(FeNiCoCrMn)S2], HES-CuTi [(FeNiCoCuTi)S2], and HES-Co0.4 [(FeNiCo0.4CrMn)S2], exhibit homogeneous elemental distributions and nanoscale particles. Among them, HES-TM delivers the strongest overall bifunctionality (0.94 V), combining lower OER overpotential with more favorable ORR polarization. Koutecký-Levich analysis indicates mixed pathways consistent with partially four-electron ORR. XPS reveals predominantly Co3+ with mixed Ni and Fe valence, while HES-TM shows a higher sulfide (S22–) fraction with a thin SOx surface layer, signatures of stronger metal–sulfur coordination, and optimized *OH/*OOH binding. Despite higher conductivity in HES-CuTi, activity trends confirm that active-site chemistry, not conductivity alone, governs performance. In full zinc-air cells, HES-TM reduces the charge–discharge voltage gap and enhances power and energy delivery, consistent with its low bifunctional index. These results position disorder-engineered pyrite HESs as cost-effective, scalable cathodes and provide design rules that link surface sulfur chemistry and mixed metal valence to reversible oxygen electrocatalysis.