Bast Radovan, Saue Trond, Henriksson Johan, Norman Patrick
Institut de Chimie, Laboratoire de Chimie Quantique, CNRS et Université Louis Pasteur, 4 rue Blaise Pascal, BP 1032, F-67070 Strasbourg Cedex, France.
J Chem Phys. 2009 Jan 14;130(2):024109. doi: 10.1063/1.3054302.
The quadratic response function has been derived and implemented at the adiabatic four-component Kohn-Sham density functional theory level with inclusion of noncollinear spin magnetization and gradient corrections in the exchange-correlation functional-a work that is an extension of our previous report where magnetization dependencies in the exchange-correlation functional were ignored [J. Henriksson, T. Saue, and P. Norman, J. Chem. Phys. 128, 024105 (2008)]. The electric-field induced second-harmonic generation experiments on CF(3)Cl and CF(3)Br are addressed by a determination of beta(-2omega;omega, omega) for a wavelength of 694.3 nm, and the same property is also determined for CF(3)I. The relativistic effects on the static hyperpolarizability for the series of molecules amount to 1%, 5%, and 9%, respectively. At the experimental wavelength, the contributions to beta due to the magnetization dependence in the exchange-correlation functional are negligible for CF(3)Cl and CF(3)Br and small for CF(3)I. The noticeable effect of magnetization in the latter case is attributed to a near two-photon resonance with the excited state 1 (3)E (nonrelativistic notation). It is emphasized, however, that the effect of magnetization on beta for CF(3)I is negligible both in comparison to the total relativistic correction as well as to the effects of electron correlation. It is concluded that, in calculations of hyperpolarizabilities under nonresonant conditions, the magnetization dependence in the exchange-correlation functional may be ignored.
二次响应函数已在绝热四分量Kohn-Sham密度泛函理论水平上推导并实现,其中在交换关联泛函中包含了非共线自旋磁化和梯度校正——这项工作是我们之前报告的扩展,在之前的报告中忽略了交换关联泛函中的磁化依赖性[J. Henriksson, T. Saue, and P. Norman, J. Chem. Phys. 128, 024105 (2008)]。通过测定波长为694.3 nm时的β(-2ω;ω, ω),对CF(3)Cl和CF(3)Br的电场诱导二次谐波产生实验进行了研究,并且也测定了CF(3)I的相同性质。对于该系列分子,相对论对静态超极化率的影响分别为1%、5%和9%。在实验波长下,对于CF(3)Cl和CF(3)Br,交换关联泛函中由于磁化依赖性对β的贡献可忽略不计,而对于CF(3)I则较小。在后一种情况下,磁化的显著影响归因于与激发态1 (3)E(非相对论符号)的近双光子共振。然而需要强调的是,与总相对论校正以及电子关联效应相比,磁化对CF(3)I的β的影响都可忽略不计。得出的结论是,在非共振条件下超极化率的计算中,交换关联泛函中的磁化依赖性可以忽略。