Klopper Wim
Lehrstuhl fur Theoretische Chemie, Institut fur Physikalische Chemie, Universitat Karlsruhe, D-76128 Karlsruhe, Germany.
J Chem Phys. 2004 Jun 15;120(23):10890-5. doi: 10.1063/1.1742904.
In the framework of second-order Møller-Plesset linear-r(12) (MP2-R12) perturbation theory, a method is developed and implemented that uses an auxiliary basis set for the resolution-of-the-identity (RI) approximation for the three- and four-electron integrals. In contrast to previous work, the two-electron integrals that must be evaluated never involve more than one auxiliary basis function. The new method therefore scales linearly with the number of auxiliary basis functions and is much more efficient than the previous one, which scaled quadratically. A general formulation of MP2-R12 theory is presented for various ansatze, approximations, and orbitals (canonical or localized). The new method is assessed by computations of the valence-shell second-order Møller-Plesset correlation energy of a few small closed-shell systems. The preliminary calculations indicate that the difference between the new and previous methods is about one order of magnitude smaller than the errors that occur due to basis-set truncations and RI approximations and under the assumptions of generalized and extended Brillouin conditions.
在二阶莫勒-普列斯特定理线性-r(12)(MP2-R12)微扰理论框架下,开发并实现了一种方法,该方法使用辅助基组对三电子和四电子积分进行恒等式解析(RI)近似。与先前的工作不同,必须计算的双电子积分从不涉及超过一个辅助基函数。因此,新方法与辅助基函数的数量呈线性比例关系,并且比之前呈二次方比例关系的方法效率高得多。针对各种假设、近似和轨道(正则或定域),给出了MP2-R12理论的一般表述。通过对几个小的闭壳层体系的价层二阶莫勒-普列斯特相关能进行计算,对新方法进行了评估。初步计算表明,在广义和扩展布里渊条件的假设下,新方法与先前方法之间的差异比由于基组截断和RI近似所产生的误差小约一个数量级。