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Fabrication of highly luminescent and thermally stable composites of sulfur nanodots through surface modification and assembly

Sulfur nanodots (S-dots) have emerged as a promising luminescent material to excel over traditional heavy metal-based quantum dots. However, their relatively low emission efficiency and poor thermal stability in the solid state have limited their wide applications in photoelectric devices. In this w...

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Bibliographic Details
Published in:Nanoscale 2024-02, Vol.16 (7), p.3492-3497
Main Authors: Sun, Bingye, Shi, Yu-e, Guo, Jiaqi, Wang, Zhenguang
Format: Article
Language:English
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Summary:Sulfur nanodots (S-dots) have emerged as a promising luminescent material to excel over traditional heavy metal-based quantum dots. However, their relatively low emission efficiency and poor thermal stability in the solid state have limited their wide applications in photoelectric devices. In this work, highly luminescent, with a photoluminescence quantum yield higher than 50%, and thermally stable composites of S-dots were produced through modulating their surface states and aggregation behaviors by introducing pyromellitic dianhydride (PMDA) and benzoyleneurea (BEU), respectively. PMDA eliminated the relatively short-lived surface states and defects on the surface of S-dots and BEU regulated the aggregation states and facilitated the energy transfer from BEU to S-dots. The as-obtained composites also showed significantly improved thermal stability compared to S-dots, aided by the hydrophobic chemical groups and dense matrix of PMDA and BEU, which extended their applications in fabricating light-emitting diodes. Our presented results provide a new approach to produce highly luminescent S-dots, which widen their applications in the fields of bioimaging, sensing, photoelectric devices, and environmental science. Highly luminescent and thermally stable composites of S-dots were produced through modulating their surface states and aggregation behaviours by introducing pyromellitic dianhydride and benzoyleneurea.
ISSN:2040-3364
2040-3372
DOI:10.1039/d3nr06292a