Legendre-spectral Dyson equation solver with super-exponential convergence

被引:21
|
作者
Dong, Xinyang [1 ]
Zgid, Dominika [1 ,2 ]
Gull, Emanuel [1 ]
Strand, Hugo U. R. [3 ,4 ]
机构
[1] Univ Michigan, Dept Phys, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
[3] Chalmers Univ Technol, Dept Phys, SE-41296 Gothenburg, Sweden
[4] Flatiron Inst, Ctr Computat Quantum Phys, New York, NY 10010 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2020年 / 152卷 / 13期
关键词
MOLECULAR WAVE-FUNCTIONS; CONFIGURATION-INTERACTION CALCULATIONS; GAUSSIAN-BASIS SETS; BENCHMARK CALCULATIONS; INTERMOLECULAR FORCES; ELECTRON-AFFINITIES; GREENS-FUNCTION; MOLLER-PLESSET; ENERGY; SYSTEMS;
D O I
10.1063/5.0003145
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
Quantum many-body systems in thermal equilibrium can be described by the imaginary time Green's function formalism. However, the treatment of large molecular or solid ab initio problems with a fully realistic Hamiltonian in large basis sets is hampered by the storage of the Green's function and the precision of the solution of the Dyson equation. We present a Legendre-spectral algorithm for solving the Dyson equation that addresses both of these issues. By formulating the algorithm in Legendre coefficient space, our method inherits the known faster-than-exponential convergence of the Green's function's Legendre series expansion. In this basis, the fast recursive method for Legendre polynomial convolution enables us to develop a Dyson equation solver with quadratic scaling. We present benchmarks of the algorithm by computing the dissociation energy of the helium dimer He-2 within dressed second-order perturbation theory. For this system, the application of the Legendre spectral algorithm allows us to achieve an energy accuracy of 10(-9)E(h) with only a few hundred expansion coefficients.
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页数:11
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