scholarly journals Slave-boson approach to the size-dependent transition from van der Waals to covalent bonding in Hgn clusters

1994 ◽  
Vol 2 (3-4) ◽  
pp. 481-487 ◽  
Author(s):  
M.E. Garcia ◽  
K.H. Bennemann
1992 ◽  
Vol 114 (1) ◽  
pp. 108-115 ◽  
Author(s):  
M. A. Dvorak ◽  
R. S. Ford ◽  
R. D. Suenram ◽  
F. J. Lovas ◽  
K. R. Leopold

2017 ◽  
Vol 19 (21) ◽  
pp. 13756-13766 ◽  
Author(s):  
Ersen Mete ◽  
Merve Yortanlı ◽  
Mehmet Fatih Danışman

Coverage and size dependent chain–chain electronic interactions counteract with the alkyl chain–gold surface interactions and the surface relaxation of the metal in the formation of standing up monolayer structures.


2021 ◽  
Vol 154 (7) ◽  
pp. 074304
Author(s):  
Manuel Brand ◽  
Karan Ahmadzadeh ◽  
Xin Li ◽  
Zilvinas Rinkevicius ◽  
Wissam A. Saidi ◽  
...  

2008 ◽  
Vol 06 (04) ◽  
pp. 693-707 ◽  
Author(s):  
ALEXEI V. FINKELSTEIN ◽  
MICHAEL Y. LOBANOV ◽  
NIKITA V. DOVIDCHENKO ◽  
NATALIA S. BOGATYREVA

Strict physical theory and numerical calculations show that a specific coupling of many-atom van der Waals interactions with covalent bonding can significantly (half as much) increase the strength of attractive dispersion interactions when the direction of interaction coincides with the direction of the covalent bond, and decrease this strength when the direction of interaction is perpendicular to the direction of the covalent bond. The energy effect is comparable to that caused by the replacement of atoms (e.g. N by C or O ) in conventional pairwise van der Waals interactions. Analysis of protein structures shows that they bear an imprint of this effect. This means that many-atom van der Waals interactions cannot be ignored in refinement of protein structures, in simulations of their folding, and in prediction of their binding affinities.


Author(s):  
Alok Ghanekar ◽  
Yi Zheng ◽  
Weixing Zhang ◽  
Zongqin Zhang

Near-field thermal radiation and van der Waal force between flat plates and curved surfaces have been probed in the past; however the peculiarities of radiative heat transfer and van der Waals stress due to fluctuations of electromagnetic fields for micro/nano-sized spherical objects have not been studied in great details. We demonstrate how fluctuational electrodynamics can be used to determine emissivity and van der Waals contribution to surface energy for various spherical shapes in a homogeneous and isotropic medium. The dyadic Green’s function formalism of radiative energy and fluctuation-induced van der Waals stress for different spherical configurations has been developed. We present the calculations for a single sphere, a bubble, a spherical shell and a coated sphere. We observe that emission spectrum ofmicro/nanoscale spheres displays several sharp peaks as the size of object reduces. Our calculations indicate that surface energy becomes size dependent (r-3) due to van der Waals phenomena for small radii.


1990 ◽  
Vol 94 (4) ◽  
pp. 1619-1624 ◽  
Author(s):  
M. Todd. Coolbaugh ◽  
William R. Peifer ◽  
James F. Garvey

Author(s):  
M. A. Listvan ◽  
R. P. Andres

Knowledge of the function and structure of small metal clusters is one goal of research in catalysis. One important experimental parameter is cluster size. Ideally, one would like to produce metal clusters of regulated size in order to characterize size-dependent cluster properties.A source has been developed which is capable of producing microscopic metal clusters of controllable size (in the range 5-500 atoms) This source, the Multiple Expansion Cluster Source, with a Free Jet Deceleration Filter (MECS/FJDF) operates as follows. The bulk metal is heated in an oven to give controlled concentrations of monomer and dimer which were expanded sonically. These metal species were quenched and condensed in He and filtered to produce areosol particles of a controlled size as verified by mass spectrometer measurements. The clusters were caught on pre-mounted, clean carbon films. The grids were then transferred in air for microscopic examination. MECS/FJDF was used to produce two different sizes of silver clusters for this study: nominally Ag6 and Ag50.


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