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超越壳层填充:通过非侵入性定向外部电场强烈增强金属团簇的电子亲和能

Beyond Shell-Filling: Strong Enhancement of Electron Affinity of Metal Clusters through a Noninvasive Oriented External Electric Field.

作者信息

Liu Li-Ye, Li Jun, Liu Si-Qi, Du Shi-Hu, Siddique Muhammad Bilal Ahmed, Zhang Lei, Bu Yuxiang, Cheng Shi-Bo

机构信息

School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.

出版信息

J Phys Chem Lett. 2024 Jul 11;15(27):7028-7035. doi: 10.1021/acs.jpclett.4c01065. Epub 2024 Jul 1.

Abstract

Traditional electron counting rules, like the Jellium model, have long been successfully utilized in designing superhalogens by modifying clusters to have one electron less than a filled electronic shell. However, this shell-filling approach, which involves altering the intrinsic properties of the clusters, can be complex and challenging to control, especially in experiments. In this letter, we theoretically establish that the oriented external electric field (OEEF) can substantially enhance the electron affinity (EA) of diverse aluminum-based metal clusters with varying valence electron configurations, leading to the creation of superhalogen species without altering their shell arrangements. This OEEF approach offers a noninvasive alternative to traditional superatom design strategies, as it does not disrupt the clusters' geometrical structures and superatomic states. These findings contribute a vital piece to the puzzle of constructing superalkalis and superhalogens, extending beyond conventional shell-filling strategies and potentially expanding the range of applications for functional clusters.

摘要

传统的电子计数规则,如电子气模型,长期以来一直成功地用于通过修饰团簇使其电子数比充满的电子壳层少一个来设计超卤素。然而,这种涉及改变团簇固有性质的壳层填充方法可能很复杂且难以控制,尤其是在实验中。在本信函中,我们从理论上证明,定向外部电场(OEEF)可以显著提高具有不同价电子构型的各种铝基金属团簇的电子亲和能(EA),从而在不改变其壳层排列的情况下产生超卤素物种。这种OEEF方法为传统的超原子设计策略提供了一种非侵入性替代方案,因为它不会破坏团簇的几何结构和超原子态。这些发现为构建超碱和超卤素的难题提供了关键的一环,超越了传统的壳层填充策略,并有可能扩大功能团簇的应用范围。

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