• Alessi, Bruno
• Švrček, Vladimir
• Macias-Montero, Manuel
• Mariotti, Davide
• Bürkle, Marius
• Lozach, Mickaël

Abstract

<jats:title>Abstract</jats:title><jats:p>Nanocrystals in the regime between molecules and bulk give rise to unique electronic properties. Here, a thorough study focusing on quantum‐confined nanocrystals (NCs) is provided. At the level of density functional theory an approximate (quasi) band structure which addresses both the molecular and bulk aspects of finite‐sized NCs is calculated. In particular, how band‐like features emerge with increasing particle diameter is shown. The quasiband structure is used to discuss technological‐relevant direct bandgap NCs. It is found that ultrasmall <jats:styled-content>Sn</jats:styled-content> NCs have a direct bandgap in their at‐nanoscale‐stable α‐phase and for high enough <jats:styled-content>Sn</jats:styled-content> concentration (≈41%) alloyed <jats:styled-content>Si–Sn</jats:styled-content> NCs transition from indirect to direct bandgap semiconductors. The calculations strongly support recent experiments suggesting a direct bandgap for these systems. For a quantitative comparison many‐body <jats:italic>GW</jats:italic> + Bethe–Salpeter equation (BSE) calculations are performed. The predicted optical gaps are close to the experimental data and the calculated absorbance spectra compare well with the corresponding measurements.</jats:p>

Topics

• density
• impedance spectroscopy
• phase
• theory
• experiment
• semiconductor
• density functional theory
• band structure