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arXiv 2406.03545nucl-th
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核结合能上的相关性影响

Impact of correlations on nuclear binding energies

KU Leuven(荷语鲁汶大学);ExtreMe Matter Institute EMMI, GSI Helmholtzzentrum für Schwerionenforschung GmbH(极端物质研究所EMMI,GSI重离子研究中心有限公司);Max-Planck-Institut für Kernphysik(马克斯·普朗克核物理研究所);IRFU, CEA, Université Paris-Saclay(IRFU,法国原子能和替代能源委员会,巴黎萨克雷大学);CEA, DES, IRESNE, DER, SPRC, LEPh(法国原子能和替代能源委员会,DES,IRESNE,DER,SPRC,LEPh);Technische Universität Darmstadt(达姆施塔特工业大学)

Alberto Scalesi, Thomas Duguet, Pepijn Demol, Mikael Frosini, Vittorio Somà, Alexander Tichai

AI总结:

本文通过分析多体相关性对钙和铬同位素结合能的影响,展示了多项式扩展方法在扩展初态计算到重核中的优势。

摘要:

在未来几年,将致力于扩展从初态核结构计算到重双开壳核的范围。为此,必须确定最有效的策略,以纳入此类核中占主导地位的多体相关性。基于此动机,本文教科书式地分析了多体相关性的纳入及其对钙和铬同位素结合能的影响。利用一个从旋轮有效场理论构建的实证最优哈密顿量,通过基于多项式扩展多体方法的层次近似,研究了两个同位素链上的结合能。相应的结果与实验数据以及在正常有序二级近似下通过值空间中等介质相似重整化群计算的结果进行比较,后者在本研究中作为参考。球形平均场近似在钙同位素中显示出特定的不足,这些不足可以被解析地理解,并且通过在其上一致地添加低阶动力学相关性得以有效纠正。虽然相同的设置无法正确再现双开壳铬同位素的结合能,但允许未受扰动的平均场态打破旋转对称性,可以有效地捕捉导致两种同位素链之间现象差异的静态相关性。最终,本文以教科书的方式证明了基于可能打破(并恢复)对称性的未受扰动态的多项式扩展方法,是扩展到重闭壳和开壳核的初态计算的最优途径。

英文摘要:

A strong effort will be dedicated in the coming years to extend the reach of ab initio nuclear-structure calculations to heavy doubly open-shell nuclei. In order to do so, the most efficient strategies to incorporate dominant many-body correlations at play in such nuclei must be identified. With this motivation in mind, the present work pedagogically analyses the inclusion of many-body correlations and their impact on binding energies of Calcium and Chromium isotopes. Employing an empirically-optimal Hamiltonian built from chiral effective field theory, binding energies along both isotopic chains are studied via a hierarchy of approximations based on polynomially-scaling expansion many-body methods. The corresponding results are compared to experimental data and to those obtained via valence-space in-medium similarity renormalization group calculations at the normal-ordered two-body level that act as a reference in the present study. The spherical mean-field approximation is shown to display specific shortcomings in Ca isotopes that can be understood analytically and that are efficiently corrected via the consistent addition of low-order dynamical correlations on top of it. While the same setting cannot appropriately reproduce binding energies in doubly open-shell Cr isotopes, allowing the unperturbed mean-field state to break rotational symmetry permits to efficiently capture the static correlations responsible for the phenomenological differences observed between the two isotopic chains. Eventually, the present work demonstrates in a pedagogical way that polynomially-scaling expansion methods based on unperturbed states that possibly break (and restore) symmetries constitute an optimal route to extend ab initio calculations to heavy closed- and open-shell nuclei.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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