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Synthesis of Au NP@MoS(2) Quantum Dots Core@Shell Nanocomposites for SERS Bio-Analysis and Label-Free Bio-Imaging

In this work, we report a facile method using MoS(2) quantum dots (QDs) as reducers to directly react with HAuCl(4) for the synthesis of Au nanoparticle@MoS(2) quantum dots (Au NP@MoS(2) QDs) core@shell nanocomposites with an ultrathin shell of ca. 1 nm. The prepared Au NP@MoS(2) QDs reveal high sur...

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Detalles Bibliográficos
Autores principales: Fei, Xixi, Liu, Zhiming, Hou, Yuqing, Li, Yi, Yang, Guangcun, Su, Chengkang, Wang, Zhen, Zhong, Huiqing, Zhuang, Zhengfei, Guo, Zhouyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5554031/
https://www.ncbi.nlm.nih.gov/pubmed/28773010
http://dx.doi.org/10.3390/ma10060650
Descripción
Sumario:In this work, we report a facile method using MoS(2) quantum dots (QDs) as reducers to directly react with HAuCl(4) for the synthesis of Au nanoparticle@MoS(2) quantum dots (Au NP@MoS(2) QDs) core@shell nanocomposites with an ultrathin shell of ca. 1 nm. The prepared Au NP@MoS(2) QDs reveal high surface enhanced Raman scattering (SERS) performance regarding sensitivity as well as the satisfactory SERS reproducibility and stability. The limit of detection of the hybrids for crystal violet can reach 0.5 nM with a reasonable linear response range from 0.5 μM to 0.5 nM (R(2) ≈ 0.974). Furthermore, the near-infrared SERS detection based on Au NP@MoS(2) QDs in living cells is achieved with distinct Raman signals which are clearly assigned to the various cellular components. Meanwhile, the distinguishable SERS images are acquired from the 4T1 cells with the incubation of Au NP@MoS(2) QDs. Consequently, the straightforward strategy of using Au NP@MoS(2) QDs exhibits great potential as a superior SERS substrate for chemical and biological detection as well as bio-imaging.