Electron Propagator Methods for Vertical Electron Detachment Energies of Anions: Benchmarks and Case Studies

被引:19
作者
Diaz-Tinoco, Manuel [1 ]
Corzo, H. H. [1 ]
Ortiz, J. V. [1 ]
机构
[1] Auburn Univ, Dept Chem & Biochem, Auburn, AL 36849 USA
基金
美国国家科学基金会;
关键词
GAUSSIAN-BASIS SETS; CORRELATED MOLECULAR CALCULATIONS; QUASI-PARTICLE THEORY; IONIZATION ENERGIES; BINDING ENERGIES; ATOMS ALUMINUM; SELF-ENERGY; AFFINITIES; EFFICIENT; SPECTRA;
D O I
10.1021/acs.jctc.8b00736
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
Ab initio electron propagator methods are efficient and accurate means of calculating vertical electron detachment energies of closed-shell, molecular anions with nuclei from the first three periods. Basis set extrapolations enable definitive comparisons between electron propagator results and benchmarks defined by total energy differences obtained with coupled-cluster, single, double, plus perturbative triple substitution theory. The best compromises of accuracy and efficiency are provided by the renormalized, partial third-order, diagonal (P3+) self-energy and by the nondiagonal, renormalized, second-order (NR2) approximation. The outer-valence Green function, the two-particle-one-hole Tamm Dancoff approximation, the third-order algebraic diagrammatic construction, and the renormalized third-order methods also are examined. A detailed analysis of errors for small anions is performed. Case studies include F-(H2O) and C1-(H2O) complexes, C5H5-, two P2N3- pentagonal rings, and a superhalide, Al(BO2)(4)(-), whose electron detachment energy is more than double those of the halide anions. These applications illustrate the versatility of electron propagator methods, their utility for interpreting negative-ion photoelectron spectra, and their promise in the discovery of unusual properties and patterns of chemical bonding. Composite methods, which combine basis set effects calculated at the relatively efficient diagonal, second-order level and higher correlation effects calculated with small basis sets, provide excellent estimates of basis set extrapolated P3+ or NR2 results and facilitate applications to large molecules. In the P3+ and NR2 methods, a judicious choice of low-order couplings between hole operators that correspond to the assumptions of Koopmans's theorem and operators that describe final-state relaxation and polarization and initial-state correlation leads to predictive accuracy, computational efficiency, and interpretive lucidity.
引用
收藏
页码:5881 / 5895
页数:15
相关论文
共 71 条
[1]  
[Anonymous], 1981, Second Quantization-Based Methods in Quantum Chemistry
[2]  
[Anonymous], 2007, ADV CHEM PHYS
[3]   Beyond classical stoichiometry: Experiment and theory [J].
Boldyrev, AI ;
Wang, LS .
JOURNAL OF PHYSICAL CHEMISTRY A, 2001, 105 (48) :10759-10775
[4]   Beyond organic chemistry: aromaticity in atomic clusters [J].
Boldyrev, Alexander I. ;
Wang, Lai-Sheng .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2016, 18 (17) :11589-11605
[5]   Delocalized water and fluoride contributions to Dyson orbitals for electron detachment from the hydrated fluoride anion [J].
Canuto, Sylvio ;
Coutinho, Kaline ;
Cabral, Benedito J. C. ;
Zakrzewski, V. G. ;
Ortiz, J. V. .
JOURNAL OF CHEMICAL PHYSICS, 2010, 132 (21)
[6]  
Cederbaum L. S., 1977, ADV CHEM PHYS, V36, P205, DOI DOI 10.1002/9780470142554.ch4
[7]   CORRELATION-EFFECTS IN THE IONIZATION OF MOLECULES - BREAKDOWN OF THE MOLECULAR-ORBITAL PICTURE [J].
CEDERBAUM, LS ;
DOMCKE, W ;
SCHIRMER, J ;
VONNIESSEN, W .
ADVANCES IN CHEMICAL PHYSICS, 1986, 65 :115-159
[8]   DIRECT CALCULATION OF IONIZATION POTENTIALS OF CLOSED-SHELL ATOMS AND MOLECULES [J].
CEDERBAUM, LS .
THEORETICA CHIMICA ACTA, 1973, 31 (03) :239-260
[9]   EFFICIENT DIFFUSE FUNCTION-AUGMENTED BASIS SETS FOR ANION CALCULATIONS. III. THE 3-21+G BASIS SET FOR FIRST-ROW ELEMENTS, LI-F [J].
CLARK, T ;
CHANDRASEKHAR, J ;
SPITZNAGEL, GW ;
SCHLEYER, PV .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 1983, 4 (03) :294-301
[10]   NR2 and P3+: Accurate, Efficient Electron-Propagator Methods for Calculating Valence, Vertical Ionization Energies of Closed-Shell Molecules [J].
Corzo, H. H. ;
Galano, Annia ;
Dolgounitcheva, O. ;
Zakrzewski, V. G. ;
Ortiz, J. V. .
JOURNAL OF PHYSICAL CHEMISTRY A, 2015, 119 (33) :8813-8821