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Understanding Bonding Nature of α-Keggin Polyoxometalates [XW12O40]n- (X = Al, Si, P, S): A Generalized Superatomic Perspective

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energy & ENVIRONMENTAL MATERIALS 2024年第6期7卷 176-183页

作者： Li, Rui Shi, Yulei Yu, Famin Wang, Rui Yan, Haitao Teo, Boon K. Wang, Zhigang Capital Normal Univ Dept Phys Beijing 100048 Peoples R China Jilin Univ Coll Phys Key Lab Mat Simulat Methods & Software Minist Educ Changchun 130012 Peoples R China Jilin Univ Inst Atom & Mol Phys Changchun 130012 Peoples R China Jilin Univ Inst Theoret Chem Coll Chem Changchun 130012 Peoples R China Xiamen Univ Coll Chem & Chem Engn State Key Lab Phys Chem Solid Surfaces Xiamen 361005 Peoples R China

alpha-Keggin polyoxometalates (POMs) [XW12O40](n-) (X = Al, Si, P, S) are widely used in batteries owing to their remarkable redox activity. However, the mechanism underlying the applications appears inconsistent with the widely accepted covalent bonding nature. Here, first-principles calculations show that XW12 are core-shell structures composed of a shell and an XO4n- core, both are stabilized by covalent interactions. Interestingly, owing to the presence of a substantial number of electrons in W12O36 shell, the frontier molecular orbitals of XW12 are not only strongly delocalized but also exhibit superatomic properties with high-angular momentum electrons that do not conform to the Jellium model. Detailed analysis indicates that energetically high lying filled molecular orbitals (MOs) have reached unusually high-angular momentum characterized by quantum number K or higher, allowing for the accommodation of numerous electrons. This attribute confers strong electron acceptor ability and redox activity to XW12. Moreover, electrons added to XW12 still occupy the K orbitals and will not cause rearrangement of the MOs, thereby maintaining the stability of these structures. Our findings highlight the structure-activity relationship and provide a direction for tailor-made POMs with specific properties at atomic level.

关键词： first principles molecular orbital polyoxometalate redox activity superatom ELECTRONIC SHELL STRUCTURE correlation-energy BASIS-SET DENSITY STABILITY CHEMISTRY HETEROPOLYANIONS ORBITALS MODEL DFT

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Geometric and Electronic Properties of Highly Fluorinated Fullerene C74F38

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Chinese Physics Letters 2006年第9期23卷 2563-2565页

作者：吴海平卢功利袁勇波邓开明刘玉真杨金龙 Department of Applied Physics Naniing University of Science and Technology Nanjing 210014 Laboratory of Bond Selective Chemistry University of Science and Technology of China Hefei 230026

Geometric and electronic properties of highly fluorinated fullerene C74F38 have been studied using the density functional theory at BLYP level with the double numerical atomic orbital basis sets with polarization functions （DNP）. The optimized geometry of C74F38, quite different from that of C74, turns into a pronounced hexahedron shape because the six stabilizing isolated benzenoid rings tend to be as far apart as possible. The HOMO-LUMO energy gap and the binding energy of C74F38 indicate that C74F38 is not only kinetically but also dynamically stable. The shorter F-C bond lengths together with the analysis of the density of states and the Mulliken populations indicate that the F-C bonds in C74F38 have both covalent and ionic characters. The Mulliken populations show that the fluorine atoms obtain about 10 electrons from the C74 cage.

关键词： correlation-energy KINETIC STABILITY DENSITY C-60 GAS DERIVATIVES EXCHANGE ANIONS C60F36 CARBON

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