纳米探针
纳米颗粒
荧光
材料科学
胶体金
纳米技术
光学
物理
作者
Jiazhou Ye,Zikang Chen,Weiwei Chen,Yu Zhao,Caiping Ding,Youju Huang
出处
期刊:ACS applied nano materials
[American Chemical Society]
日期:2024-02-16
卷期号:7 (5): 5543-5553
标识
DOI:10.1021/acsanm.4c00243
摘要
Traditional methods of decorating silica shells with gold nanoparticles (Au NPs) have problems with being time-consuming (usually over 10 h) and easy agglomeration. An ultrasonic–polymer collaborative-assisted synthesis method is presented in this article for the preparation of monodisperse gold nanoparticles decorated with controlled SiO2 shells (Au NPs@SiO2). Mercaptan-based poly(ethylene glycol) (SH-PEG) was used to modify Au NPs to improve dispersibility. Then, an ultrasound technique was introduced to accelerate the formation of Au NPs@SiO2 with superior monodispersity within 2 h. Controlling the SiO2 shell thickness (7.2–31.1 nm) can be accomplished by changing the injection of tetraethyl orthosilicate (TEOS) during the synthesis process. An ultrasonic–polymer collaborative-assisted synthesis approach is proposed for the rapid and precise synthesis of monodisperse Au NPs@SiO2 nanoparticles with controllable shell thicknesses. In addition, a fluorescence nanoprobe with an adjustable shell Au NPs@SiO2 was constructed, resulting in a strong enhancement factor of 17 717. Moreover, 29 mg of Au NPs@SiO2 can be synthesized at once (generally less than 10 mg). This method will improve the synthesis of core–shell-structured nanomaterials and promote their application in the biomedical field.
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