Integrated xTB and simplified Tamm–Dancoff analysis of composition-dependent electronic structure in GaInZnP/ZnSeyS1-y core/shell quantum dots with DFT and TDDFPT benchmarking

IF 2.5 4区 化学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Oluwasesan Adegoke, Ojodomo J. Achadu
{"title":"Integrated xTB and simplified Tamm–Dancoff analysis of composition-dependent electronic structure in GaInZnP/ZnSeyS1-y core/shell quantum dots with DFT and TDDFPT benchmarking","authors":"Oluwasesan Adegoke,&nbsp;Ojodomo J. Achadu","doi":"10.1007/s00894-026-06728-1","DOIUrl":null,"url":null,"abstract":"<div><h3>Context</h3><p>Alloyed core/shell quantum dots (QDs) provide a platform for composition-controlled modulation of electronic structure and optical response. Using an integrated extended tight binding (xTB) and simplified Tamm Dancoff approximation (sTDA) framework, a composition-defined GaInZnP/ZnSe<sub>y</sub>S<sub>1-y</sub> core/shell QD series (<i>y</i> = 0.00, 0.25, 0.50, 0.75, 1.00) revealed a distinctly nonlinear dependence of electronic and excited-state behaviour on shell composition. Relative stability favoured S-rich shells, while mixed-shell compositions showed non-ideal energetic behaviour with a pronounced deviation at <i>y</i> = 0.75. The frontier electronic structure did not vary monotonically with Se content, while the optical response showed composition-dependent redistribution of low-energy transitions. Benchmark comparison with density functional theory (DFT) and time-dependent density functional perturbation theory (TDDFPT) confirmed that the nonlinear evolution of frontier-level separation and absorption behaviour was an intrinsic feature of the alloy series, although the exact magnitude and position of the extrema remain method dependent. A distinct anomaly at <i>y</i> = 0.75 indicated enhanced frontier state reorganisation within the mixed-shell environment.</p><h3>Method</h3><p>Atomistic GaInZnP/ZnSe<sub>y</sub>S<sub>1-y</sub> QDs spanning <i>y</i> = 0.00 to 1.00 were analysed under identical structural constraints to isolate shell anion substitution effects. Ground-state electronic structure and excited-state properties were evaluated using xTB and sTDA, with DFT and TDDFPT used as independent benchmarks for frontier electronic structure and optical absorption trends. Composition-dependent changes in energetic stability, frontier-orbital separation, density-of-states like distributions, absorption onset, and frontier-orbital localisation were then compared across the full alloy series using a consistent analysis framework.</p></div>","PeriodicalId":651,"journal":{"name":"Journal of Molecular Modeling","volume":"32 6","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2026-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00894-026-06728-1.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Modeling","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s00894-026-06728-1","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Context

Alloyed core/shell quantum dots (QDs) provide a platform for composition-controlled modulation of electronic structure and optical response. Using an integrated extended tight binding (xTB) and simplified Tamm Dancoff approximation (sTDA) framework, a composition-defined GaInZnP/ZnSeyS1-y core/shell QD series (y = 0.00, 0.25, 0.50, 0.75, 1.00) revealed a distinctly nonlinear dependence of electronic and excited-state behaviour on shell composition. Relative stability favoured S-rich shells, while mixed-shell compositions showed non-ideal energetic behaviour with a pronounced deviation at y = 0.75. The frontier electronic structure did not vary monotonically with Se content, while the optical response showed composition-dependent redistribution of low-energy transitions. Benchmark comparison with density functional theory (DFT) and time-dependent density functional perturbation theory (TDDFPT) confirmed that the nonlinear evolution of frontier-level separation and absorption behaviour was an intrinsic feature of the alloy series, although the exact magnitude and position of the extrema remain method dependent. A distinct anomaly at y = 0.75 indicated enhanced frontier state reorganisation within the mixed-shell environment.

Method

Atomistic GaInZnP/ZnSeyS1-y QDs spanning y = 0.00 to 1.00 were analysed under identical structural constraints to isolate shell anion substitution effects. Ground-state electronic structure and excited-state properties were evaluated using xTB and sTDA, with DFT and TDDFPT used as independent benchmarks for frontier electronic structure and optical absorption trends. Composition-dependent changes in energetic stability, frontier-orbital separation, density-of-states like distributions, absorption onset, and frontier-orbital localisation were then compared across the full alloy series using a consistent analysis framework.

集成xTB和简化tam - dancoff分析GaInZnP/ZnSeyS1-y核/壳量子点的成分相关电子结构与DFT和TDDFPT基准
上下文核/壳量子点(QDs)为电子结构和光响应的组合控制调制提供了一个平台。利用集成的扩展紧密结合(xTB)和简化的Tamm Dancoff近似(sTDA)框架,组成定义的GaInZnP/ZnSeyS1-y核/壳QD系列(y = 0.00, 0.25, 0.50, 0.75, 1.00)揭示了电子和激发态行为对壳组成的明显非线性依赖。相对稳定有利于富s壳层,而混合壳层组分表现出非理想的能量行为,在y = 0.75处有明显的偏差。前沿电子结构不随硒含量单调变化,而光学响应表现出组分依赖的低能跃迁重分布。与密度泛函理论(DFT)和时变密度泛函摄动理论(TDDFPT)的基准比较证实,边界层分离和吸收行为的非线性演化是合金系列的内在特征,尽管极值的确切大小和位置仍然依赖于方法。y = 0.75处的明显异常表明混合壳层环境中边界态重组增强。方法在相同的结构约束下,对y = 0.00 ~ 1.00的GaInZnP/ZnSeyS1-y量子点进行分析,分离出壳层阴离子取代效应。利用xTB和sTDA对基态电子结构和激发态性质进行了评估,DFT和TDDFPT作为前沿电子结构和光吸收趋势的独立基准。然后,使用一致的分析框架,在整个合金系列中比较了能量稳定性、边界轨道分离、态密度分布、吸收开始和边界轨道定位等成分依赖的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Molecular Modeling
Journal of Molecular Modeling 化学-化学综合
CiteScore
3.50
自引率
4.50%
发文量
362
审稿时长
2.9 months
期刊介绍: The Journal of Molecular Modeling focuses on "hardcore" modeling, publishing high-quality research and reports. Founded in 1995 as a purely electronic journal, it has adapted its format to include a full-color print edition, and adjusted its aims and scope fit the fast-changing field of molecular modeling, with a particular focus on three-dimensional modeling. Today, the journal covers all aspects of molecular modeling including life science modeling; materials modeling; new methods; and computational chemistry. Topics include computer-aided molecular design; rational drug design, de novo ligand design, receptor modeling and docking; cheminformatics, data analysis, visualization and mining; computational medicinal chemistry; homology modeling; simulation of peptides, DNA and other biopolymers; quantitative structure-activity relationships (QSAR) and ADME-modeling; modeling of biological reaction mechanisms; and combined experimental and computational studies in which calculations play a major role.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书