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首页> 外文期刊>The Journal of Chemical Physics >Exchange potential from the common energy denominator approximation for the Kohn-Sham Green's function: Application to (hyper)polarizabilities of molecular chains
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Exchange potential from the common energy denominator approximation for the Kohn-Sham Green's function: Application to (hyper)polarizabilities of molecular chains

机译:Kohn-Sham Green函数的公共能分母近似的交换势:应用于分子链的(超)极化率

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An approximate Kohn-Sham (KS) exchange potential v(xsigma)(CEDA) is developed, based on the common energy denominator approximation (CEDA) for the static orbital Green's function, which preserves the essential structure of the density response function. v(xsigma)(CEDA) is an explicit functional of the occupied KS orbitals, which has the Slater v(Ssigma) and response v(respsigma)(CEDA) potentials as its components. The latter exhibits the characteristic step structure with "diagonal" contributions from the orbital densities psi(isigma)(2), as well as "off-diagonal" ones from the occupied-occupied orbital products psi(isigma)psi(j(not equal1)sigma). Comparison of the results of atomic and molecular ground-state CEDA calculations with those of the Krieger-Li-Iafrate (KLI), exact exchange (EXX), and Hartree-Fock (HF) methods show, that both KLI and CEDA potentials can be considered as very good analytical "closure approximations" to the exact KS exchange potential. The total CEDA and KLI energies nearly coincide with the EXX ones and the corresponding orbital energies epsilon(isigma) are rather close to each other for the light atoms and small molecules considered. The CEDA, KLI, EXX-epsilon(isigma) values provide the qualitatively correct order of ionizations and they give an estimate of VIPs comparable to that of the HF Koopmans' theorem. However, the additional off-diagonal orbital structure of v(xsigma)(CEDA) appears to be essential for the calculated response properties of molecular chains. KLI already considerably improves the calculated (hyper)polarizabilities of the prototype hydrogen chains H-n over local density approximation (LDA) and standard generalized gradient approximations (GGAs), while the CEDA results are definitely an improvement over the KLI ones. The reasons of this success are the specific orbital structures of the CEDA and KLI response potentials, which produce in an external field an ultranonlocal field-counteracting exchange potential. (C) 2002 American Institute of Physics. [References: 55]
机译:基于静态轨道格林函数的公共能量分母近似(CEDA),开发了近似的Kohn-Sham(KS)交换势v(xsigma)(CEDA)。 v(xsigma)(CEDA)是被占领的KS轨道的显式功能,它具有Slater v(Ssigma)和响应v(respsigma)(CEDA)电位。后者表现出具有特征性的阶跃结构,其中轨道密度 psi(isigma)(2)具有“对角线”贡献,而占据的轨道乘积psi(isigma)psi(j(不等于1)sigma)。原子和分子基态CEDA计算结果与Krieger-Li-Iafrate(KLI),精确交换(EXX)和Hartree-Fock(HF)方法的比较表明,KLI和CEDA势均可以被认为是对确切的KS交换势的很好的分析“闭合近似”。 CEDA和KLI的总能量几乎与EXX一致,并且对于所考虑的轻原子和小分子,相应的轨道能量epsilon(isigma)彼此非常接近。 CEDA,KLI,EXX-ε(isigma)值提供了定性的电离顺序,并且它们给出的VIP估计值与HF Koopmans定理相当。但是,v(xsigma)(CEDA)的其他非对角轨道结构似乎对于分子链的计算响应特性至关重要。与局部密度近似(LDA)和标准广义梯度近似(GGA)相比,KLI已经大大改善了原型氢链H-n的计算(超)极化率,而CEDA结果绝对是对KLI的改进。成功的原因是CEDA和KLI响应势的特定轨道结构,这些结构在外部场中产生了超非局部场抵消性交换势。 (C)2002美国物理研究所。 [参考:55]

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