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On the accuracy of the potential harmonic functions

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【作者】 王沂轩; 李林尉; 边文生; 刘成卜; 邓从豪;

【Author】 WANG, Yi-Xuan LI, Lin-Wei BIAN, Wen-ShengLIU, Cheng-Bu Deng, Cong-Hao Institute of Theoretical Chemistry, Shandong University, Jinan, Shandong 250100, China Department of Chemistry, Liaocheng Teachers University, Liaocheng, Shandong 252059, China

【机构】 Institute of Theoretical Chemistry; Shandong University; Jinan; Shandong 250100; China; Department of Chemistry; Liaocheng Teachers University; Liaocheng; Shandong 252059; China;

【摘要】 <正> The matrix elements of the correlation function between symmetric potential harmonics are simplified into the analytical summations of the grand angular momenta by smartly using the recurrence and coupling relations of the potential harmonics. The correlation-function potential-harmonic and generalized-Laguerre-function method (CFPHGLF) , recently developed by us, is applied to the S states of the helium-like systems for Z = 2 to 9. The results exhibit good convergence with the bases in terms of both the angular and radial directions. The final eigen-energies agree excellently with the best s-limits of the variational configuration interaction (CI) method for the involved low-lying S states. The accuracy of the potential harmonic (PH) expansion scheme is discussed relative to the exact Hylleraas CI results (HCI), and Hartree-Fock results. Moreover, suggestion is given for the future improvement of the PH scheme.

【Abstract】 The matrix elements of the correlation function between symmetric potential harmonics are simplified into the analytical summations of the grand angular momenta by smartly using the recurrence and coupling relations of the potential harmonics. The correlation-function potential-harmonic and generalized-Laguerre-function method (CFPHGLF) , recently developed by us, is applied to the S states of the helium-like systems for Z = 2 to 9. The results exhibit good convergence with the bases in terms of both the angular and radial directions. The final eigen-energies agree excellently with the best s-limits of the variational configuration interaction (CI) method for the involved low-lying S states. The accuracy of the potential harmonic (PH) expansion scheme is discussed relative to the exact Hylleraas CI results (HCI), and Hartree-Fock results. Moreover, suggestion is given for the future improvement of the PH scheme.

【基金】 Project (No. 29703003) supported by the National Natural Science Foundation of China.
  • 【文献出处】 Chinese Journal of Chemistry ,中国化学(英文版) , 编辑部邮箱 ,1999年06期
  • 【分类号】O174
  • 【下载频次】3
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