Fan Zhang, Ke Wang, Hui Zhang, Shiliu Yang, Mai Xu, Yi He, Lecheng Lei, Pengfei Xie, Xingwang Zhang
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引用次数: 0
摘要
析氧反应(OER)动力学迟缓严重限制了阴离子交换膜电解(AEMWE)的效率。本文设计了一种掺铈双金属Fe2P/NiCoP杂化预催化剂,通过动态重构激活高效OER通路。优化后的Ce0.1-Fe2P/NiCoP在0.5 A cm−2下的过电位为280 mV,在1.0 M KOH下的Tafel斜率很小,为55.3 mV dec−1。值得注意的是,当作为阳极集成在AEMWE电解槽中时,它在1.0 a cm - 2时提供1.812 V的低电池电压,并在60°C下保持500小时以上的稳定性能。原位表征和密度泛函理论(DFT)计算表明,ce掺杂增强了表面重建并调节了电子结构,从而降低了中间体(ΔG*OH和ΔG*OOH)形成的能垒,加速了OER动力学。本文介绍了一种利用催化剂改造的新策略,促进了其在AEMWE系统中的应用。
Dynamic Reconstruction of Ce-Doped Fe2P/NiCoP Hybrid for Ampere-Level Oxygen Evolution in Anion Exchange Membrane Water Electrolysis
The sluggish kinetics of the oxygen evolution reaction (OER) critically limit the efficiency of anion exchange membrane water electrolysis (AEMWE). Herein, a Ce-doped bimetallic Fe2P/NiCoP hybrid pre-catalyst that undergoes dynamic reconstruction to activate a highly efficient OER pathway is designed. The optimized Ce0.1-Fe2P/NiCoP exhibits an impressively low overpotential of 280 mV at 0.5 A cm−2 and a small Tafel slope of 55.3 mV dec−1 in a 1.0 M KOH. Remarkably, when integrated as the anode in an AEMWE electrolyzer, it delivers a low cell voltage of 1.812 V at 1.0 A cm−2 and maintains stable performance for over 500 h at 60 °C. In situ characterizations and density functional theory (DFT) calculations reveal that Ce-doping enhances surface reconstruction and modulates the electronic structure, thereby reducing energy barriers for intermediates (ΔG*OH and ΔG*OOH) formation and accelerating OER kinetics. This work introduces a novel strategy to utilize catalyst reconstruction, advancing their applications in AEMWE systems.
期刊介绍:
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