Hellmann Lars, Neugebauer Johannes
Theoretische Organische Chemie, Organisch-Chemisches Institut and Center for Multiscale Theory and Computation, Universität Münster, Corrensstraße 36, 48149 Münster, Germany.
J Phys Chem A. 2023 Oct 19;127(41):8698-8711. doi: 10.1021/acs.jpca.3c04282. Epub 2023 Oct 6.
Density fitting techniques that use automatically generated auxiliary basis sets generally rely on the formation of basis function products. Recently, Lehtola [ 2021, 17, 6886-6900] presented a procedure making use of a purely spherical representation by adding auxiliary basis functions coupled to the required angular momentum quantum numbers for the product of spherical harmonics and then removing linear dependencies by means of a Cholesky decomposition. In this work, we extend this idea by making use of the explicit equations for the product of two spherical harmonics in the angular part of the basis function product. Some of the resulting terms are not directly accessible when popular standard integral libraries are used, which could prevent the widespread use of the exact product form. For these terms, we introduce four approximations of increasing sophistication that require integrals involving only standard Gaussian-type orbitals and thus can be computed with standard libraries. We assess the accuracy of the different schemes in the context of the aCD for the reconstruction of the electron repulsion integral matrix and absolute and relative single point energies and in the framework of optimally tuned range-separated hybrid functionals.
使用自动生成的辅助基组的密度拟合技术通常依赖于基函数乘积的形成。最近,莱托拉[2021, 17, 6886 - 6900]提出了一种程序,通过添加与球谐函数乘积所需的角动量量子数耦合的辅助基函数,利用纯球形表示,然后通过Cholesky分解消除线性相关性。在这项工作中,我们通过在基函数乘积的角部分使用两个球谐函数乘积的显式方程来扩展这一思想。当使用流行的标准积分库时,一些结果项无法直接获得,这可能会阻碍精确乘积形式的广泛使用。对于这些项,我们引入了四种复杂度逐渐增加的近似方法,这些方法只需要涉及标准高斯型轨道的积分,因此可以用标准库进行计算。我们在用于重建电子排斥积分矩阵和绝对及相对单点能量的aCD背景下,以及在最优调整的范围分离混合泛函框架内,评估了不同方案的准确性。