Adiabatic Connection without Coupling Constant Integration

• Published in: Journal of chemical theory and computation Vol. 14; no. 6; pp. 2979 - 2990
• Main Authors: Bates, Jefferson E, Sengupta, Niladri, Sensenig, Jonathon, Ruzsinszky, Adrienn
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 12.06.2018
• Subjects: Approximation; Correlation; Coupling (molecular); Density; Exchanging; Kernels; Mathematical analysis; Perturbation theory; Response functions
• ISSN: 1549-9618; 1549-9626
• DOI: 10.1021/acs.jctc.8b00067

Using a second-order approximation to Random Phase Approximation renormalized (RPAr) many-body perturbation theory for the interacting density–density response function, we have developed a so-called higher-order terms (HOT) approximation for the correlation energy. In combination with the first-order RPAr correction, our new method faithfully captures the infinite-order correlation for a given exchange-correlation kernel, yielding errors of the total correlation energy on the order of 1% or less for most systems. For exchange-like kernels, our new method has the further benefit that the coupling-strength integration can be completely eliminated resulting in a modest reduction in computational cost compared to the traditional approach. When the correlation energy is accurately reproduced by the HOT approximation, structural properties and energy differences are also accurately reproduced, as we demonstrate for several periodic solids and some molecular systems. Energy differences involving fragmentation are challenging for the HOT method, however, due to errors that may not cancel between a composite system and its constituent pieces.