纳米团簇
发光
光致发光
量子产额
分子内力
水溶液
席夫碱
星团(航天器)
材料科学
光化学
纳米材料
金属
纳米技术
化学
荧光
物理化学
高分子化学
光电子学
立体化学
物理
光学
计算机科学
冶金
程序设计语言
作者
Hao‐Hua Deng,Kai‐Yuan Huang,Ling-Fang Xiu,Wei‐Ming Sun,Qiaofeng Yao,Xiangyu Fang,Xin Huang,Hamada A. A. Noreldeen,Hua‐Ping Peng,Jianping Xie,Wei Chen
标识
DOI:10.1038/s41467-022-30760-3
摘要
Abstract Metal nanoclusters (NCs) have been developed as a new class of luminescent nanomaterials with potential applications in various fields. However, for most of the metal NCs reported so far, the relatively low photoluminescence quantum yield (QY) in aqueous solution hinders their applications. Here, we describe the utilization of bis-Schiff base linkages to restrict intramolecular motion of surface motifs at the single-cluster level. Based on Au 22 (SG) 18 (SG: glutathione) NCs, an intracluster cross-linking system was constructed with 2,6-pyridinedicarboxaldehyde (PDA), and water-soluble gold NCs with luminescence QY up to 48% were obtained. The proposed approach for achieving high emission efficiency can be extended to other luminescent gold NCs with core-shell structure. Our results also show that the content of surface-bound Au(I)-SG complexes has a significant impact on the PDA-induced luminescence enhancement, and a high ratio of Au(I)-SG will be beneficial to increasing the photoluminescence intensity of gold NCs.
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