Metal nanoclusters (NCs) with aggregation-induced emission (AIE) characteristics have garnered substantial interest due to their intense photoluminescence and extensive potential applications. Elucidating the mechanisms underlying their high-efficiency luminescence is critical for advancing high-performance luminescent metal NCs materials. In recent years, Au(0)@Au(I)-thiolate nanoclusters featuring core-shell architectures have demonstrated exceptional luminescent properties, offering an attractive strategy for engineering highly emissive Au NCs. This study presents a facile method for synthesizing novel green-emitting homocysteine stabilized Au NCs (Hcy-Au NCs) with core-shell structure. The critical mechanistic feature involves precisely controlled HCl etching of Au(I)-thiolate complexes, driving their decomposition to generate the Au(0) cores essential for the core-shell structures, thereby enabling the formation of luminescent Hcy-Au NCs. This convenient one-pot methodology demonstrates remarkable versatility, having been successfully extended beyond the preparation of luminescent Hcy-Au NCs and glutathione stabilized Au NCs (GSH-Au NCs) to include the synthesis of luminescent cysteine stabilized Au NCs (Cys-Au NCs) and D-Penicillamine stabilized Au NCs (DPA-Au NCs). Our work provides valuable insights for developing novel highly luminescent metal NCs.
No takes yet. Share an insight, caveat, or question.
Wang et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: