Equivalence of the Wei potential model and Tietz potential model for diatomic molecules

被引:166
|
作者
Jia, Chun-Sheng [1 ]
Diao, Yong-Feng [2 ]
Liu, Xiang-Jun [1 ]
Wang, Ping-Quan [1 ]
Liu, Jian-Yi [1 ]
Zhang, Guang-Dong [1 ]
机构
[1] SW Petr Univ, State Key Lab Oil & Gas Reservoir Geol & Exploita, Chengdu 610500, Peoples R China
[2] China W Normal Univ, Sch Educ, Nanchong 637002, Peoples R China
来源
JOURNAL OF CHEMICAL PHYSICS | 2012年 / 137卷 / 01期
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
LINE-POSITION DATA; GROUND-STATE; ENERGY CURVE; FORCE-FIELD; FIT ANALYSIS; VIBRATIONAL LEVELS; HYDROGEN-FLUORIDE; X-1-SIGMA(+)(G); LI-2; SIMULATIONS;
D O I
10.1063/1.4731340
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
By employing the dissociation energy and the equilibrium bond length for a diatomic molecule as explicit parameters, we generate improved expressions for the well-known Rosen-Morse, Manning-Rosen, Tietz, and Frost-Musulin potential energy functions. It is found that the well-known Tietz potential function that is conventionally defined in terms of five parameters [T. Tietz, J. Chem. Phys. 38, 3036 (1963)] actually only has four independent parameters. It is shown exactly that the Wei [Phys. Rev. A 42, 2524 (1990)] and the well-known Tietz potential functions are the same solvable empirical function. When the parameter h in the Tietz potential function has the values 0, + 1, and -1, the Tietz potential becomes the standard Morse, Rosen-Morse, and Manning-Rosen potentials, respectively. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.4731340]
引用
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页数:4
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