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成分复杂合金中析氧反应的晶面-活性相关性

Crystal Facets-Activity Correlation for Oxygen Evolution Reaction in Compositional Complex Alloys.

作者信息

Zhao Hui-Feng, Yao Jun-Qing, Wang Ya-Song, Gao Niu, Zhang Tao, Li Li, Liu Yuyao, Chen Zheng-Jie, Peng Jing, Liu Xin-Wang, Yu Hai-Bin

机构信息

Wuhan National High Magnetic Field Center & School of Physic, Huazhong University of Science and Technology, Wuhan, 430074, China.

State Key Laboratory of Materials Processing and Die and Mould Technology, School of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan, 430074, China.

出版信息

Adv Sci (Weinh). 2024 Sep;11(36):e2404095. doi: 10.1002/advs.202404095. Epub 2024 Jul 23.

Abstract

Compositional complex alloys, including high and medium-entropy alloys (HEAs/MEAs) have displayed significant potential as efficient electrocatalysts for the oxygen evolution reaction (OER), but their structure-activity relationship remains unclear. In particular, the basic question of which crystal facets are more active, especially considering the surface reconstructions, has yet to be answered. This study demonstrates that the lowest index {100} facets of FeCoNiCr MEAs exhibit the highest activity. The underlying mechanism associated with the {100} facet's low in-plane density, making it easier to surface reconstruction and form amorphous structures containing the true active species is uncovered. These results are validated by experiments on single crystals and polycrystal MEAs, as well as DFT calculations. The discoveries contribute to a fundamental comprehension of MEAs in electrocatalysis and offer physics-based strategies for developing electrocatalysts.

摘要

包括高熵合金和中熵合金在内的成分复杂合金,已显示出作为析氧反应(OER)高效电催化剂的巨大潜力,但其结构-活性关系仍不清楚。特别是,关于哪些晶面更具活性这一基本问题,尤其是考虑到表面重构时,仍未得到解答。本研究表明,FeCoNiCr中熵合金的最低指数{100}晶面表现出最高活性。揭示了与{100}晶面低面内密度相关的潜在机制,这使得其更容易进行表面重构并形成包含真正活性物种的非晶结构。这些结果通过单晶和多晶中熵合金实验以及密度泛函理论(DFT)计算得到验证。这些发现有助于从根本上理解中熵合金在电催化中的作用,并为开发电催化剂提供基于物理的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e94f/11423224/0df9dd2dfd58/ADVS-11-2404095-g006.jpg

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