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Dr. Rajendra S. Dhayal Jian‐Hong Liao Dr. Yu‐Chiao Liu Dr. Ming‐His Chiang Dr. Samia Kahlal Prof. Jean‐Yves Saillard Prof. C. W. Liu 《Angewandte Chemie (International ed. in English)》2015,54(12):3702-3706
A novel discrete [Ag21{S2P(OiPr)2}12](PF6) nanocluster has been synthesized and characterized by single‐crystal X‐ray diffraction and also NMR spectroscopy (1H, 31P), ESI mass spectrometry, and other analytic techniques (XPS, EDS, UV/Vis spectroscopy). The Ag21 skeleton has an unprecedented silver‐centered icosahedron that is capped by eight additional metal atoms. The whole framework is protected by twelve dithiophosphate ligands. According to the spherical Jellium model, the stability of monocationic nanocluster can be described by an 8‐electron superatom with 1S2 1P6 configuration, as confirmed by DFT calculations. 相似文献
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Jianyu Wei Dr. Rémi Marchal Prof. Didier Astruc Prof. Jean-Yves Saillard Prof. Jean-François Halet Dr. Samia Kahlal 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(24):5508-5514
The electronic structure of the spherical Mackay icosahedral nanosized cluster Pd55(PiPr3)12(μ3-CO)20 is analyzed by using DFT calculations. Results reveal that it can be considered as a regular superatom with a “magic” electron count of 20, characterized by a 1S2 1P6 1D10 2S2 jellium configuration. Its open shell nature is associated with partial occupation of non-jellium, 4d-type, levels located on the interior of the Pd55 kernel. This shows that the superatom model can be used to rationalize the bonding and stability of spherical ligated group 10 clusters, despite their apparent 0-electron count. 相似文献
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Franck Gam Ramiro Arratia-Perez Samia Kahlal Jean-Yves Saillard Alvaro Muñoz-Castro 《International journal of quantum chemistry》2019,119(6):e25827
Attempts to expand the versatility of well defined clusters are a relevant issue in the design of building blocks for functional nanostructures. Here, we investigate the plausible formation of related structures from the emblematic highly symmetrical 18-e [W@Au12] cluster. The calculated [W@Au12Ptn] series, with n = 0, 1, 2, 3, and 4, show cohesion energies, HOMO-LUMO gap, adiabatic electron affinities (AEAs) and adiabatic ionization potentials (AIPs), indicating a relative stability to the parent cluster [W@Au12] experimentally characterized, where clusters with n = 1 and n = 4 are suggested as the most stable with respect to oxidation. The resulting symmetry lowering away from the high icosahedral symmetry upon adding Pt atoms induces a sizable splitting of the frontiers shells, which in turn effectively modify the properties of the calculated clusters, as observed from calculated optical properties. The estimated absorption spectra show an interesting broadening effect of the absorption peaks, which appears as a useful approach for further design of broad black absorbers, which are able to absorb light in a wider range, with potential capabilities to enhance the efficiency of thin film solar cells and photocatalysis processes, among other applications. 相似文献