Tuning platinum for cleaner hydrogen
Peer-Reviewed Publication
Updates every hour. Last Updated: 27-Oct-2026 13:17 ET (27-Oct-2026 17:17 GMT/UTC)
Clean hydrogen production depends on catalysts that can split water efficiently while using precious metals more wisely. A new catalyst design addresses one of the long-standing barriers in alkaline water electrolysis: the slow breakdown of water molecules on platinum (Pt) surfaces. By placing Pt clusters on a symbiotic oxide support made from titanium dioxide quantum dots and cobalt oxide (TiO₂ QDs/Co₃O₄), the study reshapes the electronic state of Pt and creates paired active sites. These sites separately accelerate water dissociation and hydrogen adsorption, enabling faster hydrogen evolution reaction (HER) activity, stronger stability, and a clearer path toward more efficient alkaline electrolyzers.
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Recently, Professor Hanjun Sun and his team from Nanjing Normal University proposed a novel Csp–π–d conjugation design strategy. By incorporating carbon–carbon triple bonds (C≡C) into a metalloporphyrin framework, they constructed a Csp–π–d conjugated structure with unique electronic modulation capability, enabling precise regulation of the adsorption behavior of the key oxygen reduction intermediate *OH and thereby significantly enhancing the performance of non-precious-metal catalysts. The resulting p-Co-TEPP/rGO catalyst not only exhibited outstanding oxygen reduction activity in alkaline media, but also delivered superior overall performance to the Pt/C–RuO2 cathode in zinc–air batteries, offering a new strategy for the design of low-cost, high-performance energy catalysts.
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Researchers demonstrate a giant insulator-to-metal transition and room-temperature superparamagnetism by controlling defect reconstruction and nickel nanoparticle formation in perovskite oxide thin films.