Mass-independent Dunham analysis of the known electronic states of platinum sulfide, PtS, and analysis of the electronic field-shift effect

2019 ◽  
Vol 151 (9) ◽  
pp. 094303 ◽  
Author(s):  
Jack C. Harms ◽  
Leah C. O’Brien ◽  
James J. O’Brien

2011 ◽  
Vol 1 (1) ◽  
pp. 387-392 ◽  
Author(s):  
T. Fujii ◽  
F. Moynier ◽  
A. Agranier ◽  
E. Ponzevera ◽  
M. Abe

AbstractLead isotopes were fractionated by the liquid-liquid extraction technique between an aqueous phase and a crown ether. After purification by ion-exchange chemistry, the 207Pb/206Pb and 208Pb/206Pb isotopic ratios were measured by multiple-collector inductively coupled plasma mass spectrometry (MC-ICP-MS). Isotope fractionations > 0.05‰ have been found. The conventional equilibrium mass-dependent isotope effect estimated by an ab initio calculation was smaller than the Pb isotope fractionation experimentally obtained. Conventional mass-dependent isotope fractionation is not a valuable explanation for our results. The nuclear field shift effect, which results from the isotopic change in the nuclear size and shape, was also estimated by an ab initio method combined with a finite nucleus model. The nuclear field shift effect calculated was in agreement with our experimental results. Therefore, this study reports the first nuclear field shift effect of Pb in an equilibrium ligand exchange reaction.



2007 ◽  
Vol 21 (17) ◽  
pp. 1065-1075 ◽  
Author(s):  
HAIYU LI

We study the system of vertically coupled two quantum dots in confined single electron. Coulomb interaction between two electrons and Rashba type spin-orbit coupling are taken into account. It is a two-Fermion system, hence the antisymmetric requirement of electronic states must be considered. Four lower antisymmetric eigenfunctions are found out. Based on the rotation wave approximation, the coherent manipulation of quantum state in an external electric pulse with some resonance harmonic frequencies are investigated. The instantaneous degree of quantum entanglement of the state in time-dependent external electronic field is calculated.





2009 ◽  
Vol 267 (3-4) ◽  
pp. 139-156 ◽  
Author(s):  
Toshiyuki Fujii ◽  
Frédéric Moynier ◽  
Francis Albarède


2008 ◽  
Vol 10 (15) ◽  
pp. 2078 ◽  
Author(s):  
Barbara M. Giuliano ◽  
Luca Bizzocchi ◽  
Stephen Cooke ◽  
Deike Banser ◽  
Mareike Hess ◽  
...  


2012 ◽  
Vol 296 (1) ◽  
pp. 261-265 ◽  
Author(s):  
Toshiyuki Fujii ◽  
Frédéric Moynier ◽  
Arnaud Agranier ◽  
Emmanuel Ponzevera ◽  
Minori Abe ◽  
...  


2009 ◽  
Vol 267 (3-4) ◽  
pp. 157-163 ◽  
Author(s):  
Toshiyuki Fujii ◽  
Frédéric Moynier ◽  
Philippe Telouk ◽  
Francis Albarède


2002 ◽  
Vol 106 (30) ◽  
pp. 6911-6914 ◽  
Author(s):  
Toshiyuki Fujii ◽  
Daisuke Suzuki ◽  
Katsubumi Gunji ◽  
Kazuo Watanabe ◽  
Hirotake Moriyama ◽  
...  


2002 ◽  
Vol 57 (5) ◽  
pp. 247-254 ◽  
Author(s):  
Ibrahim M. Ismail ◽  
Masao Nomura ◽  
Yasuhiko Fujii ◽  
Masao Aida

The uranium isotope effect in the exchange system uranyl(VI)-malate ligand at 288-343 K has been studied by ion exchange displacement chromatography. At all temperatures 235U is enriched at the front of the uranium band. The single stage separation coefficient, (Ɛ = α - 1), increased from (0.9 ± 0.1) × 10-4 at 288 K to (2.9 ± 0.3) × 10-4 at 343 K. The equilibrium constant of the isotope exchange reaction equaled the separation factor at the current experimental conditions. The increase of the separation coefficient with temperature, which is in contrast to the uranium(IV)-ligand exchange systems, can be explained by the introduction of the field shift effect.



1993 ◽  
Vol 78 (1-4) ◽  
pp. 247-250 ◽  
Author(s):  
R. E. Silverans ◽  
L. Vermeeren ◽  
A. Klein ◽  
R. Neugart ◽  
C. Schulz ◽  
...  


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