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
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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.
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.