scholarly journals Ground-State Clusters for Short-Range Attractive and Long-Range Repulsive Potentials

Langmuir ◽  
2004 ◽  
Vol 20 (24) ◽  
pp. 10756-10763 ◽  
Author(s):  
S. Mossa ◽  
F. Sciortino ◽  
P. Tartaglia ◽  
E. Zaccarelli
2014 ◽  
Vol 89 (17) ◽  
Author(s):  
Oleg Rivin ◽  
Hagai Shaked ◽  
Arsen Gukasov ◽  
El'ad N. Caspi

2021 ◽  
Vol 14 (3) ◽  
pp. 239-247

Abstract: The second virial coefficient B for low-dense 7Lithium (7Li) gas is calculated over a wide temperature range 1 K40000 K. In the ‘high’-T limit (600 K45000 K), the classical coefficient, Bcl, and the contribution of the first quantum-mechanical correction, Bqc, are computed from standard expressions, using a suitable binary potential. The classical coefficient, Bcl, together with the Boyle temperature, TB, are determined and their values are in good agreement with previous results. In addition, the interface between the classical and quantum regimes is systematically investigated. Furthermore, the calculation of the quantum-mechanical second virial coefficient, Bq, is evaluated using the Beth-Uhlenbeck formula in the temperature range 1 K500 K. A positive value of Bq indicates that the net interaction energy is repulsive, implying that the short-range repulsive forces dominate the long-range attractive forces. However, quite the opposite occurs for negative values of Bq, which are indicative of net attractive interaction. The general behavior of Bq is similar to the potential energy itself, such that the long-range attractive and the short-range repulsive potentials can be deduced from the measurements of Bq. Keywords: Second virial coefficient, Low-density Lithium-7 Gas, Short-range repulsive forces, Long-range attractive forces. PACS: 51.30.+i.


Nature ◽  
2021 ◽  
Author(s):  
Siyu Chen ◽  
Linda Lee ◽  
Tasmin Naila ◽  
Susan Fishbain ◽  
Annie Wang ◽  
...  

2021 ◽  
Vol 5 (1) ◽  
Author(s):  
Roman Sherrod ◽  
Eric C. O’Quinn ◽  
Igor M. Gussev ◽  
Cale Overstreet ◽  
Joerg Neuefeind ◽  
...  

AbstractThe structural response of Dy2TiO5 oxide under swift heavy ion irradiation (2.2 GeV Au ions) was studied over a range of structural length scales utilizing neutron total scattering experiments. Refinement of diffraction data confirms that the long-range orthorhombic structure is susceptible to ion beam-induced amorphization with limited crystalline fraction remaining after irradiation to 8 × 1012 ions/cm2. In contrast, the local atomic arrangement, examined through pair distribution function analysis, shows only subtle changes after irradiation and is still described best by the original orthorhombic structural model. A comparison to Dy2Ti2O7 pyrochlore oxide under the same irradiation conditions reveals a different behavior: while the dysprosium titanate pyrochlore is more radiation resistant over the long-range with smaller degree of amorphization as compared to Dy2TiO5, the former involves more local atomic rearrangements, best described by a pyrochlore-to-weberite-type transformation. These results highlight the importance of short-range and medium-range order analysis for a comprehensive description of radiation behavior.


1977 ◽  
Vol 38 (C7) ◽  
pp. C7-202-C7-206 ◽  
Author(s):  
R. MORET ◽  
M. HUBER ◽  
R. COMÈS

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
R. S. Markiewicz ◽  
J. Lorenzana ◽  
G. Seibold ◽  
A. Bansil
Keyword(s):  

2002 ◽  
Vol 14 (03) ◽  
pp. 273-302 ◽  
Author(s):  
HERIBERT ZENK

We give a short summary on how to combine and extend results of Combes and Hislop [2] (short range Anderson model with additional displacements), Kirsch, Stollmann and Stolz [13] and [14] (long range Anderson model without displacements) to get localization in an energy interval above the infimum of the almost sure spectrum for a continuous multidimensional Anderson model including long range potentials and displacements.


2014 ◽  
Vol 45 (1) ◽  
pp. 33-47 ◽  
Author(s):  
Xue Lin ◽  
Chengguo Wang ◽  
Meijie Yu ◽  
Zhitao Lin ◽  
Yuzhen Liu

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