The development of a resilient economy requires advanced electrochemical technologies for efficient power generation and storage, together with materials that reduce reliance on noble and critical raw materials. High-entropy materials offer a promising strategy to meet these demands. Here, we report a high-entropy perovskite electrolyte, BaCe0.2Zr0.2Gd0.2La0.2Y0.2O3−δ (BCZGLY), designed to enhance chemical robustness and sinterability while retaining proton conductivity at intermediate temperatures. BCZGLY forms a single-phase perovskite and achieves improved densification at 1400 °C. Under humid atmospheres, conductivities of 54 mS cm−1 at 500 °C and 0.71 S cm−1 at 700 °C are obtained, comparable to state-of-the-art BaZr0.8Y0.2O3−δ under similar conditions. Thermogravimetric and structural analyses reveal enhanced resistance to carbonation and controlled hydration, consistent with a stabilized defect landscape. First-principles calculations support a proton-friendly defect chemistry. Overall, these results identify BCZGLY as a promising electrolyte for intermediate-temperature protonic devices, while device-level validation is reserved for future studies and practical electrochemical applications.

High-entropy BCZGLY as a proton-conducting electrolyte: Material-level validation and implications for electrochemical cells

Dell'Agli, G.;Spiridigliozzi, L.;
2026-01-01

Abstract

The development of a resilient economy requires advanced electrochemical technologies for efficient power generation and storage, together with materials that reduce reliance on noble and critical raw materials. High-entropy materials offer a promising strategy to meet these demands. Here, we report a high-entropy perovskite electrolyte, BaCe0.2Zr0.2Gd0.2La0.2Y0.2O3−δ (BCZGLY), designed to enhance chemical robustness and sinterability while retaining proton conductivity at intermediate temperatures. BCZGLY forms a single-phase perovskite and achieves improved densification at 1400 °C. Under humid atmospheres, conductivities of 54 mS cm−1 at 500 °C and 0.71 S cm−1 at 700 °C are obtained, comparable to state-of-the-art BaZr0.8Y0.2O3−δ under similar conditions. Thermogravimetric and structural analyses reveal enhanced resistance to carbonation and controlled hydration, consistent with a stabilized defect landscape. First-principles calculations support a proton-friendly defect chemistry. Overall, these results identify BCZGLY as a promising electrolyte for intermediate-temperature protonic devices, while device-level validation is reserved for future studies and practical electrochemical applications.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11580/123663
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