Abstract Herein, the preparation of tunable NIR‐I emitting (700–900 nm) Au‐alloyed Ag 2 S QDs is outlined, controlled through Au:Ag reaction stoichiometry. Increasing Au:Ag results in blue‐shifted emission ( λ em = 1180–715 nm), accompanied with an increased measured bandgap (E g = 1.6–2.3 eV). Au‐alloyed Ag 2 S QDs exhibited enhanced PLQYs (φ = 26.7%) and prolonged lifetimes (τ = 4.57 µs) compared to their parent Ag 2 S QDs (φ = 5.9%, τ = 1.87 µs). Detailed structural characterization revealed that the series of NIR QDs possessed uniform size distributions with morphological changes due to the nucleation of Au on the QD surface. Cationic exchange of Ag + for Au + occurs, originating from these nucleation sites. Phase transformations in the crystal structure were evident, giving rise to the evolution of Ag 3 AuS 2 , AgAuS, and AgAu 3 species. AgAuS QDs were transferred to aqueous media through ligand exchange with dihydrolipoic acid (DHLA), to produce colloidally stable QDs with an emission maximum in the far NIR‐I region at 845 nm. NIR‐I imaging phantoms were additionally measured to confirm their compatibility with commercial instrumentation. To our knowledge, this is the first report elucidating the relationship between structural evolution and optoelectronic properties of tunable NIR‐I emitting Au‐alloyed Ag 2 S QDs.
Chelani et al. (2025) studied this question.