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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 84 (1986), S. 3301-3310 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Silicon and germanium clusters containing three to seven atoms have been studied with the pseudopotential MO-LCAO method followed by configuration interaction procedure. Si and Ge clusters have very similar electronic structures and consequently analogous physico-chemical properties but differ substantially from small carbon clusters. Linear structures are clearly less favorable than more compact structures. On the other hand, some planar geometries possess considerable stability. The Si and Ge clusters which are sections of the diamond-type crystal lattice are less stable than clusters which can be considered as segments of closed-packed lattices or as steps in pentagonal crystal growth. The reason is that the majority of atoms in small clusters are surface atoms which cannot assume the tetrahedral coordination characteristic of Si and Ge bulk atoms. The appearance of typical bulk properties is expected only for very large Si and Ge clusters with small surface atoms/bulk atoms ratio.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 83 (1985), S. 1722-1735 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A general formulation of the alternancy symmetry adaptation for the semiempirical Pariser–Parr–Pople (PPP) type Hamiltonians is presented at both the spin-orbital and spin-adapted many-electron levels. The derivation of the general form of the alternancy symmetry conjugation operators is based solely on the tight-binding approximation for the short range one-particle part of the Hamiltonian considered. It starts by a simple formulation of the desired invariance properties of the PPP type Hamiltonian. Using algebraic properties of the unitary group generators and of their particle number nonconserving extensions, it leads to a completely explicit and general form for the alternancy symmetry conjugation operators. In this way the prior descriptions, which become special cases of this general formulation, are interrelated and unified. The spin and quasispin character of certain components of these operators are also pointed out and explicitly derived. The spin-adapted version is based on the unitary group formulation of the valence bond-type approach. A completely general formulation is given which applies to many-electron states of an arbitrary multiplicity of neutral systems, either of the normal kind with an identical number of starred and nonstarred sites, or of the radicaloid character with different numbers of starred and nonstarred sites. An explicit form of the dependence of the relative phase factor of the alternancy symmetry conjugation operator on the total spin, total electron number and on the number of starred and nonstarred sites is also given. General rules for the construction of spin and alternancy symmetry-adapted states are illustrated on a few simple examples. Finally, a brief discussion of the implications of the alternancy symmetry is presented.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 88 (1988), S. 5657-5662 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Geometric structure of Li−n (n=2–9) clusters is determined with the analytical gradient minimization procedure of the Hartree–Fock energy using a relatively small AO basis set. The energies of the Li−n clusters for the SCF optimized geometries are calculated with the multireference diexcited configuration interaction method. The geometries of Li−n (n〈5) differ appreciately from those of neutral as well as of cationic Li clusters. Linear geometries of Li− trimer and Li− tetramer can be ascribed to the electrostatic repulsion. The atomization energy of Li−n clusters as function of cluster nuclearity shows a generally increasing tendency. The calculated electron affinities of Lin clusters exhibit features which are in details analogous to the features of the adiabatic electron affinities determined experimentally for Cun clusters.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 5794-5802 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Electronic and geometric structure of mixed neutral BeLik and cationic BeLi+k clusters (k=1–9) has been investigated employing ab initio configuration interaction quantum chemical methods. The values of atomization energies per atom for BeLik with k〈7 and for BeLi+k with k〈8 increase strongly with the cluster size. The binding energy per atom remains nearly unchanged for neutral BeLik with k=7–9 and cationic BeLi+k clusters with k=8 and 9. The quantities which measure cluster stability towards fragmentation processes predict high stabilities for BeLi6 and BeLi+7. The geometries of cluster, their stabilities as well as other properties can be easily interpreted as simple consequences of the nodal properties of the cluster MOs. The connection between the results obtained from this work and from the superatom model has been pointed out. The specific nature of the chemical bonding in mixed clusters obtained from quantum chemical investigations has been analyzed.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 3802-3825 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The configuration-interaction (CI) study of excited states of alkali metal clusters accounts for spectroscopical patterns obtained from (i) the photoelectron detachment spectra of their anions and from (ii) the photodepletion spectra of the neutral species, reproduces observed excitation energies, intensities for allowed transitions, and permits an assignment of cluster structures. For Na−2–4 the linear anionic geometries are responsible for the photoelectron detachment spectra. In the case of Na−5, both planar and linear anionic isomers seem to contribute to the recorded spectrum. The calculation of optically allowed states for Na3(C2v) and Na4(D2h) structures and oscillator strengths yield rich spectra which have been fully assigned to the observed ones. In the case of Na8, the Td and the related D2d forms give rise to an intense transition located at ∼495 nm and the weak fine structure shifted to the red in full agreement with the measured spectrum. A molecular versus collective excitation interpretation of absorption spectra is discussed.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 4861-4866 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The favorable geometries of small sodium clusters Na+n (n=3–9) are determined with the analytical gradient method in the framework of the ab initio SCF approximation. The transition from the planar towards three-dimensional cluster geometries is understood in terms of some basic quantum theoretical concepts. The binding energies per atom for Na+n clusters calculated with the MRD CI procedure increase, in general, as a function of n. Nevertheless, the atomization energy per atom as well as the ionization potential as functions of the nuclearity n exhibit well developed oscillations for even–odd n. Consequently, the fragmentation energy for the channel Na+n→Na+n−1+Na shows strong oscillations as well. This explains large abundances of cationic clusters with odd nuclearity found in some detection devices. The possible consequences for the fragmentation process of Na+n is discussed. It is found that the process Na+n→Na+n−2+Na2 is favorable for Na+5, Na+7, and Na+9.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 91 (1987), S. 2658-2664 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 87 (1983), S. 1096-1097 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Chemical reviews 86 (1986), S. 539-587 
    ISSN: 1520-6890
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1520-6890
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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