Reducing the Sampling Complexity of Energy Estimation in Quantum Many-Body Systems Using Empirical Variance Information.

IF 5.5 1区 化学 Q2 CHEMISTRY, PHYSICAL
Alexander Gresch, Uğur Tepe, Martin Kliesch
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引用次数: 0

Abstract

We consider the problem of estimating the energy of a quantum state preparation for a given Hamiltonian in Pauli decomposition. For various quantum algorithms, in particular, in the context of quantum chemistry, it is crucial to have energy estimates with error bounds, as captured by guarantees on the problem's sampling complexity. In particular, when limited to Pauli basis measurements, the smallest sampling complexity guarantee comes from a simple single-shot estimator via a straightforward argument based on Hoeffding's inequality. In this work, we construct an adaptive estimator using the state's actual variance. Technically, our estimation method is based on the empirical Bernstein stopping (EBS) algorithm and grouping schemes, and we provide a rigorous tail bound, which leverages the state's empirical variance. In a numerical benchmark of estimating ground-state energies of several Hamiltonians, we demonstrate that EBS consistently improves upon elementary readout guarantees up to 1 order of magnitude.

利用经验方差信息降低量子多体系统能量估计的采样复杂度。
我们考虑了泡利分解中给定哈密顿量的量子态制备能量估计问题。对于各种量子算法,特别是在量子化学的背景下,具有误差范围的能量估计是至关重要的,正如对问题采样复杂性的保证所捕获的那样。特别是,当限于泡利基测量时,通过基于Hoeffding不等式的直接论证,可以从简单的单次估计中获得最小的采样复杂度保证。在这项工作中,我们使用状态的实际方差构造了一个自适应估计器。从技术上讲,我们的估计方法是基于经验伯恩斯坦停止(EBS)算法和分组方案,我们提供了一个严格的尾界,它利用了状态的经验方差。在估计几个哈密顿量的基态能量的数值基准中,我们证明了EBS在基本读出保证上持续提高了1个数量级。
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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Theory and Computation invites new and original contributions with the understanding that, if accepted, they will not be published elsewhere.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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