A. de J. Ríos-Roldán, J. A. Munguía-Valadez, E. J. Sambriski, J. A. Moreno-Razo
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The stability of the nematic region is enhanced as s→1, corresponding to the conventional Lennard-Jones interaction. The stability of the nematic phase for nearly-spherical mesogens with increasing s leads to a gradual loss in spherical symmetry despite no imposed shape anisotropy. Thus, the energy anisotropy becomes more pronounced and is capable of prompting the emergence of the nematic phase in this model.Keywords: Phase diagramsnematicmesogenanisotropyliquid crystals AcknowledgmentsJAMR gratefully acknowledges the support provided through grants UNAM-DGAPA-PAPIIT IN114721, LANCAD-UNAM-DGTIC-276, and LANCAD-UNAM-DGTIC-247, in addition to the generous computing time provided by the Laboratorio de Supercómputo y Visualización en Paralelo at UAMI (LSVP-UAMI).Disclosure statementNo potential conflict of interest was reported by the author(s).Additional informationFundingJMV and AJRR are thankful for the financial support received through a CONACYT graduate fellowship (No. 947695 and 1234731).","PeriodicalId":18817,"journal":{"name":"Molecular Physics","volume":"1 11","pages":"0"},"PeriodicalIF":1.6000,"publicationDate":"2023-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nematic phases from nearly spherical mesogens: applying the approximate non-conformal (ANC) theory\",\"authors\":\"A. de J. 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引用次数: 0
摘要
摘要利用近似非共形(ANC)理论中的相互作用势,建立了一个较为粗糙的Gay-Berne介圈模型。非国大的潜力既有令人反感的贡献,也有吸引人的贡献。我们修改分子间的吸引力,通过调节他们与Hess-Su取向相关的项。这使得系统的能量具有各向异性。探讨了ANC电位的柔软参数s,以定性地确定能够维持向列相的阈值。我们从分子动力学模拟中为每个s值构建相图,并对大块样品进行表征以勾勒相区域。我们发现柔软度参数s ~ 0.6或更高支持向列相的出现。向列区域的稳定性随着s→1而增强,与传统的Lennard-Jones相互作用相对应。随着s的增加,向列相的稳定性导致球面对称性的逐渐丧失,尽管没有施加形状各向异性。因此,能量各向异性变得更加明显,并且能够促使该模型中向列相的出现。jamr感谢通过赠款UNAM-DGAPA-PAPIIT IN114721, LANCAD-UNAM-DGTIC-276和LANCAD-UNAM-DGTIC-247提供的支持,以及UAMI (LSVP-UAMI)平行实验室Supercómputo y Visualización提供的慷慨计算时间。披露声明作者未报告潜在的利益冲突。jmv和AJRR感谢通过CONACYT研究生奖学金(No. 947695和1234731)获得的财政支持。
Nematic phases from nearly spherical mesogens: applying the approximate non-conformal (ANC) theory
AbstractA coarser model for the Gay-Berne mesogen is developed using the interaction potential from the Approximate Non-Conformal (ANC) theory. The ANC potential contains both repulsive and attractive contributions. We modify intermolecular attractions by conditioning them with a Hess-Su orientation-dependent term. This imparts an anisotropic contribution to the energy of the system. The softness parameter s of the ANC potential is probed to qualitatively identify a threshold capable of sustaining a nematic phase. We construct phase diagrams for each value of s from molecular dynamics simulations and characterise bulk samples to outline phase regions. We find that a softness parameter s∼0.6 or higher supports the emergence of a nematic phase. The stability of the nematic region is enhanced as s→1, corresponding to the conventional Lennard-Jones interaction. The stability of the nematic phase for nearly-spherical mesogens with increasing s leads to a gradual loss in spherical symmetry despite no imposed shape anisotropy. Thus, the energy anisotropy becomes more pronounced and is capable of prompting the emergence of the nematic phase in this model.Keywords: Phase diagramsnematicmesogenanisotropyliquid crystals AcknowledgmentsJAMR gratefully acknowledges the support provided through grants UNAM-DGAPA-PAPIIT IN114721, LANCAD-UNAM-DGTIC-276, and LANCAD-UNAM-DGTIC-247, in addition to the generous computing time provided by the Laboratorio de Supercómputo y Visualización en Paralelo at UAMI (LSVP-UAMI).Disclosure statementNo potential conflict of interest was reported by the author(s).Additional informationFundingJMV and AJRR are thankful for the financial support received through a CONACYT graduate fellowship (No. 947695 and 1234731).
期刊介绍:
Molecular Physics is a well-established international journal publishing original high quality papers in chemical physics and physical chemistry. The journal covers all experimental and theoretical aspects of molecular science, from electronic structure, molecular dynamics, spectroscopy and reaction kinetics to condensed matter, surface science, and statistical mechanics of simple and complex fluids. Contributions include full papers, preliminary communications, research notes and invited topical review articles.