Temperature Dependence of the CdS Bandgap in the Extreme Confinement Regime

A non-empirical equation describing the effect of size on the temperature dependence of the optical bandgap of CdS (dE(g)/dT) is obtained on the basis of the Brus equation. Intriguingly, we find that dE(g)/dT diverges strongly from bulk values only within the extreme confinement (EC) regime. We conducted both experimental and theoretical investigations of the absorption spectra of CdS clusters and quantum dots as a function of temperature above room temperature. Our results show that the value of dE(g)/dT obtained from absorption spectra in the EC regime is 2.5 times higher than in the strong confinement regime. Notable ligand sensitivities are also observed for dE(g)/dT in the case of CdS clusters. Ab initio molecular dynamics simulations and density functional theory calculations reveal that thermal fluctuations are the crucial factor influencing the bandgap temperature coefficient. Our results help resolve some long-standing debates regarding the dE(g)/dT behavior of semiconductor quantum dots.

Automated summary

A non-empirical equation for describing the temperature dependence of the optical bandgap of CdS, based on the Brus equation, reveals that the value of dE(g)/dT differs significantly from bulk values only within the extreme confinement (EC) regime. Both experimental and theoretical investigations of absorption spectra of CdS clusters and quantum dots show that dE(g)/dT in the EC regime is 2.5 times higher than in the strong confinement regime. Ligand sensitivities are also observed for dE(g)/dT in the case of CdS clusters. Ab initio molecular dynamics simulations and density functional theory calculations highlight thermal fluctuations as the crucial factor influencing the bandgap temperature coefficient.