Deciphering the emission dynamics of colloidal PbS quantum dots: a spectroscopic exploration under diverse environmental and experimental conditions.

This study employs a combination of spectroscopic techniques, including absorption, photoluminescence (PL), time-resolved PL kinetics, and transient absorption measurements, to elucidate the dynamics of excited states of oleic acid (OA)-capped colloidal PbS quantum dots (QDs) in toluene with a mean size of approximately 3 nm. PL decay profiles were properly treated employing either fitting or fitting-free models to extract average decay lifetimes and lifetime distributions. Our findings highlight the profound impact of factors such as particle concentration, size, surface treatment, and the surrounding environment on the optical properties of PbS QDs.

Correction: Inverse heavy-atom effect in near infrared photoluminescent gold nanoclusters.

Correction for 'Inverse heavy-atom effect in near infrared photoluminescent gold nanoclusters' by Goutam Pramanik et al., Nanoscale, 2021, DOI: 10.1039/d1nr02440j.

Inverse heavy-atom effect in near infrared photoluminescent gold nanoclusters.

Fluorophores functionalized with heavy elements show enhanced intersystem crossing due to increased spin-orbit coupling, which in turn shortens the fluorescence decay lifetime (τPL). This phenomenon is known as the heavy-atom effect (HAE). Here, we report the observation of increased τPL upon functionalisation of near-infrared photoluminescent gold nanoclusters with iodine.

Reversible photo- and thermal-effects on the luminescence of gold nanoclusters: implications for nanothermometry.

The optical properties of colloidal near-infrared (NIR) emitting gold nanoclusters (AuNCs) are thoroughly investigated at variable temperatures and excitation powers. Both absorption and photoluminescence (PL) excitation spectra reveal optical transitions expected from literature models of thiolated AuNCs - with the exception of the lowest energy transition which has the form of a featureless absorption tail partially overlapping with the PL band. The absorption cross section is determined via the PL saturation and PL modulation techniques to be in the range of 2-3 × 10 cm for excitation at 405 nm (relatively large value for such small clusters) and decreases ∼20 times toward 633 nm.