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首页> 外文期刊>Advanced Materials >Unveiling the Activity Origin of Electrocatalytic Oxygen Evolution over Isolated Ni Atoms Supported on a N-Doped Carbon Matrix
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Unveiling the Activity Origin of Electrocatalytic Oxygen Evolution over Isolated Ni Atoms Supported on a N-Doped Carbon Matrix

机译:在N掺杂碳基质上支撑的孤立Ni原子上揭示电催化氧放出的活性起源

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摘要

Exploring highly efficient electrocatalysts for the oxygen evolution reaction (OER) and unveiling their activity origin are pivotal for energy conversion technologies. Herein, atomically distributed Ni sites over a N-doped hollow carbon matrix are reported as a promising electrocatalyst for OER in alkaline conditions. Significantly boosted activity is observed after the decoration of the active Ni sites with well-controlled coordination geometry. Results of X-ray absorption spectroscopy investigation and density functional theory (DFT) calculation reveal that the effective electronic coupling via the Ni-N coordination can move down the Fermi level and lower the adsorption energy of intermediates, thus resulting in the facilitated OER kinetics.
机译:探索用于氧释放反应(OER)的高效电催化剂并揭示其活性来源对于能量转换技术至关重要。在此,据报道在N掺杂的空心碳基质上原子分布的Ni位点是在碱性条件下用于OER的有希望的电催化剂。在以良好控制的配位几何结构修饰活性镍位点后,观察到活性显着增强。 X射线吸收光谱研究和密度泛函理论(DFT)计算的结果表明,通过Ni-N配位进行有效的电子偶联可以降低费米能级并降低中间体的吸附能,从而促进了OER动力学。

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