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用于高效水氧化的FeCoNiCrMo高熵合金纳米颗粒的原子结构非晶化和电子结构重构

Atomic Structure Amorphization and Electronic Structure Reconstruction of FeCoNiCrMo High-Entropy Alloy Nanoparticles for Highly Efficient Water Oxidation.

作者信息

Zhou Xuechun, Zhu He, Fu Shu, Lan Si, Hahn Horst, Zeng Jianrong, Feng Tao

机构信息

Herbert Gleiter Institute of Nanoscience, School of Material Science and Engineering, Nanjing Nanjing University of Science and Technology, Nanjing, 210094, P. R. China.

Institute of Nanotechnology, Karlsruhe Institute of Technology, 76021, Karlsruhe, Germany.

出版信息

Small. 2024 Nov;20(47):e2405596. doi: 10.1002/smll.202405596. Epub 2024 Aug 15.

Abstract

The complexity of the multielement interaction in high-entropy alloys (HEAs) may provide more active sites to adapt different catalytic reaction steps in oxygen evolution reaction (OER). Investigating the correlation between structure and performance of HEAs electrocatalysts is both essential and challenging. In this work, FeCoNiCrMo HEA nanoparticles are successfully fabricated utilizing a unique nanofabrication method called inert gas condensation. With the increase of high-valence metal component Mo, the atomic structure amorphization and electronic structure reconstruction are unveiled. According to the X-ray photoelectron spectroscopy valence spectra, the d-band center of FeCoNiCrMo is ascending, and thus enhancing the adsorption energy. Synchrotron pair distribution function analysis reflects the degree of structural disorder and reveals a robust correlation with the intrinsic OER activities of the electrocatalysts. FeCoNiCrMo high-entropy metallic glass nanoparticles exhibit an outstanding OER performance with an ultralow overpotential of 294.5 mV at a high current density of 100 mA cm. This work brings fundamental and practical insights into the modulation mechanism of metal components of HEAs catalysts for developing OER.

摘要

高熵合金(HEAs)中多元素相互作用的复杂性可为析氧反应(OER)中不同的催化反应步骤提供更多活性位点。研究高熵合金电催化剂的结构与性能之间的相关性既至关重要又具有挑战性。在这项工作中,利用一种名为惰性气体凝聚的独特纳米制造方法成功制备了FeCoNiCrMo高熵合金纳米颗粒。随着高价金属组分Mo含量的增加,揭示了原子结构的非晶化和电子结构的重构。根据X射线光电子能谱价带谱,FeCoNiCrMo的d带中心上升,从而提高了吸附能。同步辐射对分布函数分析反映了结构无序程度,并揭示了与电催化剂本征OER活性的强相关性。FeCoNiCrMo高熵金属玻璃纳米颗粒在100 mA cm的高电流密度下表现出出色的OER性能,过电位低至294.5 mV。这项工作为开发用于OER的高熵合金催化剂的金属组分调控机制带来了基础和实际的见解。

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