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Abstract Photoluminescence of ultrasmall, atomically precise gold nanoclusters constitutes an area of significant interest in recent years for both fundamental research and biological applications. However, the exploration of near-infrared photoluminescence of gold nanoclusters is still in its infancy due to the limitations of synthetic methods and characterization techniques. Herein, the photoluminescence properties of an Au 38 (PET) 26 (PET = 2-phenylethanethiolate) nanocluster are investigated in detail. The Au 38 (PET) 26 exhibits an emission peak at 865 nm, which is revealed to be a mix of fluorescence, thermally activated delayed fluorescence, and phosphorescence via the combined analyses of time-resolved and temperature-dependent photoluminescence measurements. The quantum yield of Au 38 (PET) 26 is determined to be 1.8% at room temperature under ambient conditions, which increases to above 90% by suppressing the non-radiative relaxation pathway at a cryogenic temperature (80 K). Overall, the results of this work discover the coexistence of three radiative processes in thiolate-protected Au nanoclusters and will pave the way for understanding the intriguing photoluminescence properties of gold nanoclusters in future studies. 

Fluorescent organic nanoparticles (FoNPs) encapsulating aggregation-induced emission (AIE) luminogens were synthesizedviamicroemulsion ATRP, revealing that the increased intraparticle rigidity significantly enhanced photoluminescence.