Relativistic coupled-cluster method application

Energy levels of heavy and super-heavy (Z>100) elements are calculated by the relativistic coupled cluster method. The method starts from the four-component solutions of the Dirac-Fock or Dirac-Fock-Breit equations, and correlates them by the coupled-cluster approach. Simultaneous inclusion of relativistic terms in the Hamiltonian (to order o , where a is the fine-structure constant) and correlation effects (all products smd powers of single and double virtual excitations) is achieved. The Fock-space coupled-cluster method yields directly transition energies (ionization potentials, excitation energies, electron affinities). Results are in good agreement (usually better than 0.1 eV) with known experimental values. Properties of superheavy atoms which are not known experimentally can be predicted. Examples include the nature of the ground states of elements 104 md 111. Molecular applications are also presented. 

U. Kaldor, Relativistic coupled cluster method and applications, in R.J. Bartlett (Ed.), Recent advances in coupled-cluster methods, Recent advances in computational chemistry, Vol. 3, World Scientific Publishing, Singapore, 1997, pp. 125-153, and references 45-58 therein. 

L. K. Sorensen, J. Olsen, T. Fleig. Two- and four-component relativistic generalized-active-space coupled cluster method Implementation and application to BiH. /. Chem. Phys., 134 (2011) 214102. 

SS. Fleig, L. K. Sorensen, J. Olsen. A relativistic 4-component general-order multireference coupled cluster method initial implementation and application to HBr. Theor. Chem. Acc., 118 (2007) 347-356. 

E. Ehav and U. Kaldor, Relativistic four-component multireference coupled cluster methods Towards a covariant approach, in Recent Progress in Coupled Cluster Methods Theory and Applications, eds. J. Pittner, P. Charsky, and J. Paldus (Springer, 2010), p. 113. 

In spite of the impressive progress which has been achieved with conventional ab-initio methods as the Configuration-Interaction or Coupled-Cluster schemes in recent years density functional theory (DFT) still represents the method of choice for the study of complex many-electron systems (for an overview of DFT see [1]). Today DFT covers an enormous variety of fields, ranging from atomic [2,3], cluster [4,5] and surface physics [6,7] to the material sciences [8-10]. and theoretical biophysics [11-13]. Moreover, since the introduction of the generalized gradient approximation DFT has become an accepted method also for standard quantum chemical applications [14,15]. Given this tremendous success of nonrelativistic DFT the question for a relativistic extension (RDFT) arises quite naturally in view of the large number of problems in which relativistic effects play an important role (see e.g. Refs.[16,17]). 

Field (CASSCF) Second-order Perturbation Theory (CAS-PT2) Configuration Interaction Core-Valence Correlation Effects Coupled-cluster Theory Experimental Data Evaluation and Quality Control G2 Theory Heats of Formation Isoelectronic Isogyric Reactions M0ller-Plesset Perturbation Theory Numerical Hartree-Fock Methods for Molecules r 12-Dependent Wavefunctions Relativistic Theory and Applications Spectroscopy Computational Methods Spin Contamination Transition Metals Applications,... 

The coupled cluster (CC) approach is the most powerful and accurate of generally applicable electron correlation methods. This has been shown in many benchmark applications of 4-component relativistic CC methods to atoms [11-18] and molecules [19-31]. The CC method is an all-order, size-extensive, and systematic many-body approach. Multireference variants of relativistic 4-component CC methods capable of handling quasidegeneracies, which are important for open-shell heavy atomic and molecular systems, have been developed in recent years [15,17-19,21,31]. In particular, the multireference FSCC scheme [32,33] is applicable to systems with a variable number of particles, and is an ideal candidate for merging with QED theory to create an infinite-order size-extensive covariant many-body method applicable to systems with variable numbers of fermions and bosons [6,7]. 

Basis Sets Correlation Consistent Sets Benchmark Studies on Small Molecules Complete Active Space Self-consistent Field (CASSCF) Second-order Perturbation Theory (CASPT2) Configuration Interaction Configuration Interaction PCI-X and Applications Core-Valence Correlation Effects Coupled-cbister Theory Density Functional Applications Density Functional Theory (DFT), Har-tree-Fock (HF), and the Self-consistent Field Density Functional Theory Applications to Transition Metal Problems Electronic Structure of Meted and Mixed Nonstoi-chiometric Clusters G2 Theory Gradient Theory Heats of Formation Hybrid Methods Metal Complexes Relativistic Effective Core Potential Techniques for Molecules Containing Very Heavy Atoms Relativistic Theory and Applications Semiempiriced Methetds Transition Metals Surface Chemi-ced Bond Transition Meted Chemistry. 

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