Fauser Steffen, Förster Arno, Redeker Leon, Neiss Christian, Erhard Jannis, Trushin Egor, Görling Andreas
Lehrstuhl für Theoretische Chemie, Universität Erlangen-Nürnberg, Egerlandstr. 3, D-91058 Erlangen, Germany.
Theoretical Chemistry, Vrije Universiteit, De Boelelaan 1083, NL-1081 HV Amsterdam, The Netherlands.
J Chem Theory Comput. 2024 Mar 26;20(6):2404-2422. doi: 10.1021/acs.jctc.3c01132. Epub 2024 Mar 11.
σ-Functionals belong to the class of Kohn-Sham (KS) correlation functionals based on the adiabatic-connection fluctuation-dissipation theorem and are technically closely related to the random phase approximation (RPA). They have the same computational demand as the latter, with the computational effort of an energy evaluation for both methods being lower than that of a preceding hybrid DFT calculation for typical systems but yield much higher accuracy, reaching chemical accuracy of 1 kcal/mol for quantities such as reactions and transition energies in main group chemistry. In previous work on σ-functionals, rather large Gaussian basis sets have been used. Here, we investigate the actual basis set requirements of σ-functionals and present three setups that employ smaller Gaussian basis sets ranging from quadruple-ζ (QZ) to triple-ζ (TZ) quality and represent a good compromise between accuracy and computational efficiency. Furthermore, we introduce an implementation of σ-functionals based on Slater-type basis sets and present two setups of QZ and TZ quality for this implementation. We test the accuracy of these setups on a large database of various physical properties and types of reactions, as well as equilibrium geometries and vibrational frequencies. As expected, the accuracy of σ-functional calculations becomes somewhat lower with a decreasing basis set size. However, for all setups considered here, calculations with σ-functionals are clearly more accurate than those within the RPA and even more so than those of the conventional KS methods. For the smallest setup using Gaussian-type basis functions and Slater-type basis functions, we introduce a reparametrization that reduces the loss in accuracy due to the basis set error to some extent. A comparison with the range-separated hybrid ωB97X-V and the double hybrid DSD-BLYP-D3 shows that σ functionals outperform in accuracy both of these accurate and, for their class, representative functionals.
σ泛函属于基于绝热连接涨落耗散定理的科恩-沈(KS)相关泛函类别,在技术上与随机相位近似(RPA)密切相关。它们与RPA具有相同的计算需求,对于这两种方法,能量评估的计算量低于典型系统先前混合密度泛函理论(DFT)计算的计算量,但能产生更高的精度,对于主族化学中的反应和跃迁能量等量,能达到1千卡/摩尔的化学精度。在先前关于σ泛函的工作中,使用了相当大的高斯基组。在此,我们研究了σ泛函实际的基组要求,并给出了三种设置,这些设置采用了从四重ζ(QZ)到三重ζ(TZ)质量的较小高斯基组,在精度和计算效率之间实现了良好的折衷。此外,我们介绍了基于斯莱特型基组的σ泛函实现,并给出了此实现的两种QZ和TZ质量的设置。我们在一个包含各种物理性质、反应类型、平衡几何结构和振动频率的大型数据库上测试了这些设置的精度。正如预期的那样,随着基组大小的减小,σ泛函计算的精度会有所降低。然而,对于这里考虑的所有设置,使用σ泛函的计算明显比RPA中的计算更准确,甚至比传统KS方法的计算更准确。对于使用高斯型基函数和斯莱特型基函数的最小设置,我们引入了一种重新参数化方法,在一定程度上减少了由于基组误差导致的精度损失。与范围分离的杂化ωB97X-V和双杂化DSD-BLYP-D3的比较表明,σ泛函在精度上优于这两种准确且在其类别中具有代表性的泛函。