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通过界面调制制备的含/不含空位填充的钴-锰双金属纳米线作为用于水分解的活性和耐用电催化剂

Co─Mn Bimetallic Nanowires by Interfacial Modulation with/without Vacancy Filling as Active and Durable Electrocatalysts for Water Splitting.

作者信息

Jiang Yimin, Song Zekuan, Qu Meijiao, Jiang Yong, Luo Wei, He Rongxing

机构信息

School of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, China.

School of Materials Science and Engineering, Nankai University, Tianjin, 300350, China.

出版信息

Small. 2024 Aug;20(33):e2400859. doi: 10.1002/smll.202400859. Epub 2024 Mar 22.

Abstract

Active and stable nonnoble electrocatalysts for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) are required for water splitting by sustainable electricity. Here, Mn bonded with O and P is incorporated to modulate CoS and CoP respectively to enhance the catalytic activity and extend the catalyst lifetime. MnO adjusts the electronic structure of CoS and Co atom fills the oxygen vacancy in MnO. The interfacial interaction endows CoS/MnO to a lower reaction barrier due to ideal binding energies for OER intermediates. Structure stability of active sites and enhanced Co─S bonds by Operando Raman spectroscopy and theoretical calculations reduce the dissolution of CoS/MnO, resulting in a lifetime of 500 h at 50 mA cm for OER. The modulation of CoP by MnP weakens the interaction between Co sites and adsorbed H, achieving a high activity under a large current for HER. The assembled electrolyzer affords 50 mA cm at 1.58 V and exhibits a lifetime of 350 h at 50 mA cm. The calculations disclose the electron interaction for the activity and stability, as well as the enhanced conductivity. The findings develop new avenues toward promoting catalytic activity and stability, making Co─Mn bimetallic nanowires efficient electrocatalysts for nonnoble water electrolyzers.

摘要

通过可持续电力进行水分解需要用于析氧反应(OER)和析氢反应(HER)的活性且稳定的非贵金属电催化剂。在此,将与O和P键合的Mn分别引入以调节CoS和CoP,从而提高催化活性并延长催化剂寿命。MnO调节CoS的电子结构,且Co原子填充MnO中的氧空位。由于OER中间体具有理想的结合能,界面相互作用使CoS/MnO具有较低的反应势垒。通过原位拉曼光谱和理论计算表明,活性位点的结构稳定性以及增强的Co─S键减少了CoS/MnO的溶解,从而在50 mA cm²的电流密度下实现了500小时的OER寿命。MnP对CoP的调节减弱了Co位点与吸附H之间的相互作用,从而在大电流下实现了HER的高活性。组装的电解槽在1.58 V电压下可提供50 mA cm²的电流密度,并且在50 mA cm²的电流密度下表现出350小时的寿命。计算结果揭示了活性和稳定性的电子相互作用以及增强的导电性。这些发现为提高催化活性和稳定性开辟了新途径,使Co─Mn双金属纳米线成为非贵金属水电解槽的高效电催化剂。

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