The core ionization energies calculated by delta SCF and Slater's transition state theory

被引:11
作者
Hirao, Kimihiko [1 ]
Nakajima, Takahito [2 ]
Chan, Bun [3 ]
Lee, Ho-Jin [4 ]
机构
[1] Kyoto Univ, Fukui Inst Fundamental Chem, Nishihiraki cho 34 4, Sakyo ku, Kyoto 6068103, Japan
[2] RIKEN Ctr Computat Sci, 7 1 26, Minatojima minami machi, Chuo ku, Kobe 6500047, Japan
[3] Nagasaki Univ, Grad Sch Engn, Bunkyo 1 14, Nagasaki 8528521, Japan
[4] Southwest Tennessee Community Coll, Dept Nat Sci, Memphis, TN 38015 USA
关键词
ELECTRON BINDING-ENERGIES; DENSITY-FUNCTIONAL THEORY; 2P PHOTOELECTRON SHIFTS; K-ABSORPTION SPECTRA; X-RAY-SPECTRA; EXCITED-STATES; PHOTOABSORPTION SPECTRA; EXCHANGE-ENERGY; BETA-EMISSION; HARTREE-FOCK;
D O I
10.1063/5.0140032
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The core ionization energies of the second-period and third-period elements are studied by Lambda SCF and Slater's transition state (STS) theory by using Hartree-Fock (HF) and Kohn-Sham (KS) approximations. Electron correlation increases the estimated core ionization energies, while the self-interaction error (SIE) decreases them, especially for the third-period elements and is a more significant factor. As a result, while HF lacks electron correlation, it is free of SIE and reasonably predicts the core ionization energies. The core ionization energies calculated by HF STS are very close to those calculated by HF Delta SCF, showing that STS reasonably describes the relaxation of the core hole. The core ionization energies calculated by KS are particularly sensitive to the SIE of the functional used, with functionals having less SIE yielding more accurate.SCF core ionization energies. Consequently, BH&HLYP gives better results than B3LYP and LC-BOP since BH&HLYP is the hybrid functional with high proportion of the exact HF exchange. Although the core ionization energies are underestimated by Delta SCF due to SIE, STS gives larger core ionization energies than Delta SCF due to a concave behavior of the error curves of STS, which is also related to SIE. The mean absolute deviations of STS relative to Delta SCF, and relative to the experiment, are almost constant regardless of the nuclei among the element in the second period, and likewise among those in the third period. The systematic nature suggests that shifting the STS core ionization energies may be useful. We propose the shifted STS (1) for reproducing Delta SCF values, and the shifted STS (2) to reproduce the observed ones for KS calculations. Both schemes work quite well. The calculated results of KS Delta SCF and STS vary depending on the functional. However, the variation of each species' shifted STS (2) is very small, and all shifted STS (2) values are close to the observed ones. As the shifted STS require only one SCF calculation, they are simple and practical for predicting the core ionization energies.
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页数:17
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共 73 条
[1]  
Abramowitz M., 1972, HDB MATH FUNCTIONS F, P916
[2]   DIRECT NEAR-HARTREE-FOCK CALCULATIONS ON 1S HOLE STATES OF NO+ [J].
BAGUS, PS ;
SCHAEFER, HF .
JOURNAL OF CHEMICAL PHYSICS, 1971, 55 (03) :1474-&
[3]   A NEW MIXING OF HARTREE-FOCK AND LOCAL DENSITY-FUNCTIONAL THEORIES [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (02) :1372-1377
[4]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[5]   DENSITY-FUNCTIONAL EXCHANGE-ENERGY APPROXIMATION WITH CORRECT ASYMPTOTIC-BEHAVIOR [J].
BECKE, AD .
PHYSICAL REVIEW A, 1988, 38 (06) :3098-3100
[6]   Self-consistent-field calculations of core excited states [J].
Besley, Nicholas A. ;
Gilbert, Andrew T. B. ;
Gill, Peter M. W. .
JOURNAL OF CHEMICAL PHYSICS, 2009, 130 (12)
[7]   SINGLE-ELECTRON AND MULTIPLE-ELECTRON EFFECTS IN THE SI 1S PHOTOABSORPTION SPECTRA OF SIX4 (X=H,D,F,CL,BR,CH3,C2H5,OCH3,OC2H5) MOLECULES - EXPERIMENT AND THEORY [J].
BODEUR, S ;
MILLIE, P ;
NENNER, I .
PHYSICAL REVIEW A, 1990, 41 (01) :252-263
[8]   CHLORINE-K SHELL PHOTOABSORPTION SPECTRA OF GAS-PHASE HCL AND CL2 MOLECULES [J].
BODEUR, S ;
MARECHAL, JL ;
REYNAUD, C ;
BAZIN, D ;
NENNER, I .
ZEITSCHRIFT FUR PHYSIK D-ATOMS MOLECULES AND CLUSTERS, 1990, 17 (04) :291-298
[9]   RELATIVISTIC CORRECTIONS TO REPORTED SULFUR 1S IONIZATION ENERGIES [J].
CARROLL, TX ;
DE, J ;
MACLAREN, DC ;
THOMAS, TD ;
SAETHRE, LJ .
JOURNAL OF ELECTRON SPECTROSCOPY AND RELATED PHENOMENA, 1987, 42 (03) :281-284
[10]   Accurate density-functional calculation of core-electron binding energies by a total-energy difference approach [J].
Cavigliasso, G ;
Chong, DP .
JOURNAL OF CHEMICAL PHYSICS, 1999, 111 (21) :9485-9492