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Register a new userComment on A tight distance-dependent estimator for screening three-center Coulomb integrals over Gaussian basis functions [J. Chem. Phys. 142, 154106 (2015)]
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We extend the tight distance-dependent estimator proposed by Hollman et al. [J. Chem. Phys. 142, 154106 (2015)] for the three-center Coulomb integrals over Gaussian atomic orbitals to handle the two-center case. We also propose minor modifications of the original three-center estimator for the case of contracted ket Gaussians and concentric bra Gaussians.
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We derive distance-dependent estimators for two-center and three-center electron repulsion integrals over a short-range Coulomb potential, $textrm{erfc}(omega r_{12})/r_{12}$. These estimators are much tighter than one based on the Schwarz inequality and can be viewed as a complement to the distance-dependent estimators for four-center short-range Coulomb integrals and for two-center and three-center full Coulomb integrals previously reported. Because the short-range Coulomb potential is commonly used in solid-state calculations, including those with the HSE functional and with our recently introduced range-separated periodic Gaussian density fitting, we test our estimators on a diverse set of periodic systems using a wide range of the range-separation parameter $omega$. These tests demonstrate the robust tightness of our estimators, which are then used with integral screening to calculate periodic three-center short-range Coulomb integrals with linear scaling in system size.
By using very general arguments, we show that the entropy loss conjecture at the glass transition violates the second law of thermodynamics and must be rejected.
The new combined formulas have been established for the complex and real rotation-angular functions arising in the evaluation of two-center overlap integrals over arbitrary atomic orbitals in molecular coordinate system. These formulas can be useful in the study of different quantum mechanical problems in both the theory and practice of calculations dealing with atoms, molecules, nuclei and solids when the integer and noninteger n complex and real atomic orbitals basis sets are emploed. This work presented the development of our previous paper (I.I. Guseinov, Phys. Rev. A, 32 (1985) 1864).
We discuss the relationship between modern time-dependent density functional theory and earlier time-period
In a series of publications, Kocherginsky and Gruebele presented a systematic framework for chemical transport and thermodiffusion to predict the Soret coefficients from thermodynamics. A macroscopic derivation of the Onsager reciprocal relations without recourse to microscopic fluctuations or equations of motion was also discussed. Their important contributions and some confusions are discussed.
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