Expressivity of Determinantal Ansatzes for Neural Network Wave Functions

IF 5.5 1区 化学 Q2 CHEMISTRY, PHYSICAL
Ni Zhan, , , William A. Wheeler, , , Gil Goldshlager, , , Elif Ertekin, , , Ryan P. Adams, , and , Lucas K. Wagner*, 
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Abstract

Neural network wave functions have shown promise as a way to achieve high accuracy in solving the many-body quantum problem. These wave functions most commonly use a determinant or a sum of determinants to antisymmetrize many-body orbitals, which are described by a neural network. In many cases, the wave function is projected onto a fixed-spin state. Such a treatment is allowed for spin-independent operators; however, it cannot be applied to spin-dependent problems, such as Hamiltonians containing spin–orbit interactions. We show that for spin-independent Hamiltonians, a strict upper bound property is obeyed between a traditional Hartree–Fock-like determinant, full spinor wave function, the full determinant wave function, and a generalized spinor wave function. The relationship between a spinor wave function and the full determinant arises because the full determinant wave function is the spinor wave function projected onto a fixed-spin, after which antisymmetry is implicitly restored in the spin-independent case. For spin-dependent Hamiltonians, the full determinant wave function is not applicable, because it is not antisymmetric. Numerical experiments on the H3 molecule and two-dimensional homogeneous electron gas confirm these bounds.

Abstract Image

神经网络波函数的行列式分析的表达性。
神经网络波函数在求解多体量子问题中具有很高的精度。这些波函数通常使用行列式或行列式的和来反对称多体轨道,这是由神经网络描述的。在许多情况下,波函数被投射到一个固定的自旋状态。这种处理对于自旋独立算子是允许的;然而,它不能应用于自旋相关的问题,例如包含自旋轨道相互作用的哈密顿量。我们证明了对于自旋无关的哈密顿量,在传统的hartree - fock类行列式、完全旋量波函数、完全行列式波函数和广义旋量波函数之间有严格的上界性质。旋量波函数和完全行列式之间的关系出现是因为完全行列式波函数是投射到固定自旋上的旋量波函数,之后在自旋无关的情况下隐式地恢复了反对称。对于自旋相关的哈密顿量,完全行列式波函数是不适用的,因为它不是反对称的。对H3分子和二维均相电子气体的数值实验证实了这些边界。
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来源期刊
Journal of Chemical Theory and Computation
Journal of Chemical Theory and Computation 化学-物理:原子、分子和化学物理
CiteScore
9.90
自引率
16.40%
发文量
568
审稿时长
1 months
期刊介绍: The Journal of Chemical Theory and Computation invites new and original contributions with the understanding that, if accepted, they will not be published elsewhere. Papers reporting new theories, methodology, and/or important applications in quantum electronic structure, molecular dynamics, and statistical mechanics are appropriate for submission to this Journal. Specific topics include advances in or applications of ab initio quantum mechanics, density functional theory, design and properties of new materials, surface science, Monte Carlo simulations, solvation models, QM/MM calculations, biomolecular structure prediction, and molecular dynamics in the broadest sense including gas-phase dynamics, ab initio dynamics, biomolecular dynamics, and protein folding. The Journal does not consider papers that are straightforward applications of known methods including DFT and molecular dynamics. The Journal favors submissions that include advances in theory or methodology with applications to compelling problems.
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