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三阶莫勒-普莱塞特微扰理论变得实用了?轨道的选择和标度极大地提高了热化学、动力学和分子间相互作用的精度。

Third-Order Møller-Plesset Perturbation Theory Made Useful? Choice of Orbitals and Scaling Greatly Improves Accuracy for Thermochemistry, Kinetics, and Intermolecular Interactions.

作者信息

Bertels Luke W, Lee Joonho, Head-Gordon Martin

机构信息

Department of Chemistry , University of California , Berkeley , California 94720 , United States.

Chemical Sciences Division , Lawrence Berkeley National Laboratory , Berkeley , California 94720 , United States.

出版信息

J Phys Chem Lett. 2019 Aug 1;10(15):4170-4176. doi: 10.1021/acs.jpclett.9b01641. Epub 2019 Jul 12.

Abstract

We develop and test methods that include second- and third-order perturbation theory (MP3) using orbitals obtained from regularized orbital-optimized second-order perturbation theory, κ-OOMP2, denoted as MP3:κ-OOMP2. Testing MP3:κ-OOMP2 shows RMS errors that are 1.7-5 times smaller than those of MP3 across 7 data sets. To do still better, empirical training of the scaling factors for the second- and third-order correlation energies and the regularization parameter on one of those data sets led to an unregularized scaled ( = 1.0; = 0.8) denoted as MP2.8:κ-OOMP2. MP2.8:κ-OOMP2 yields significant additional improvement over MP3:κ-OOMP2 in 4 of 6 test data sets on thermochemistry, kinetics, and noncovalent interactions. Remarkably, these two methods outperform coupled cluster with singles and doubles in 5 of the 7 data sets considered, at greatly reduced cost (no iterations).

摘要

我们开发并测试了一些方法,这些方法包括使用从正则化轨道优化二阶微扰理论(κ-OOMP2)获得的轨道进行二阶和三阶微扰理论(MP3)计算,记为MP3:κ-OOMP2。对MP3:κ-OOMP2的测试表明,在7个数据集上,其均方根误差比MP3小1.7至5倍。为了进一步提高性能,在其中一个数据集上对二阶和三阶相关能的缩放因子以及正则化参数进行经验训练,得到了一个非正则化缩放( = 1.0; = 0.8)的方法,记为MP2.8:κ-OOMP2。在热化学、动力学和非共价相互作用的6个测试数据集中,有4个数据集上MP2.8:κ-OOMP2相对于MP3:κ-OOMP2有显著的额外改进。值得注意的是,在考虑的7个数据集中的5个数据集中,这两种方法的性能优于单双激发耦合簇方法,且成本大幅降低(无需迭代)。

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