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Ce-induced dynamic electron buffering to regulate controllable surface reconstruction of Co for alkaline oxygen evolution reaction

Authors: ZHAN Yiqin; GONG Ruixue; YANG Tao; LIU Shuang; ZHOU Linlin; WANG Kang; CAO Sheng; WANG Hongyang; HOU Xinmei

DOI: 10.1007/s40843-026-4505-9Status: Verified Translated Edition
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Key Findings in This Report

• • Optimized Ce-Co(OH)2 achieves an overpotential of 236 mV at 10 mA cm-2, outperforming undoped Co(OH)2 and many Ni-based catalysts, directly reducing energy consumption in alkaline electrolyzers. • • The catalyst demonstrates 200 h of continuous operation at 10 mA cm-2 with negligible degradation, addressing the critical durability bottleneck that plagues transition metal hydroxide anodes. • • In an AEMWE system, the Ce-Co(OH)2 anode delivers 2.04 V at 1 A cm-2 and sustains 500 h at 500 mA cm-2, meeting industrial current density requirements and demonstrating scalability for green hydrogen production. • • Precise control of the Ce3+/Ce4+ ratio via electrodeposition temperature (optimized at 40°C) enables dynamic electron buffering, preventing Co over-oxidation and structural collapse, a mechanism that can be generalized to other lanthanide-doped catalysts.