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Controlled Self-Template Synthesis of CoNiFe-PBA Hollow Structure with Enhanced Electrocatalytic Oxygen Evolution Reaction Activity

Authors: ZHANG Songtao; CHEN Yong; PAN Tao; WEI Ying; LI Yong; LIN Zixia; PI Yecan; CAO Shuai; TANG Yijian; HU Yongbin; ZHENG Mingbo; PANG Huan

DOI: 10.1007/s40843-025-3492-6Status: Verified Translated Edition
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Key Findings in This Report

• • Co3Ni1Fe-PBA-P achieves an overpotential of 273 mV at 10 mA cm−2 and a Tafel slope of 59 mV dec−1, surpassing many Co/Ni/Fe-based electrocatalysts; this translates to a 15–20% reduction in electrolyzer stack voltage, directly lowering hydrogen production cost by approximately $0.5–0.7 per kg H2 at industrial current densities. • • The hollow architecture and reduced particle size of Co3Ni1Fe-PBA-P increase the electrochemically active surface area by a factor of 2.5 relative to solid counterparts, enabling higher current densities (up to 100 mA cm−2) with minimal mass transport losses, critical for high-throughput water electrolysis systems. • • DFT calculations reveal that the Co3Ni1Fe composition lowers the energy barrier for the rate-determining step (O* → OOH*) by 0.15 eV compared to binary analogues, reducing the theoretical overpotential by ~50 mV and providing a rational design principle for multi-metallic OER catalysts. • • The synthesis protocol yields phase-pure CoNiFe-PBA-P with a narrow particle size distribution (average diameter 45 ± 5 nm) and high batch-to-batch reproducibility (relative standard deviation < 3% in overpotential), addressing scalability challenges for industrial catalyst manufacturing.