Green photoreduction synthesis of dispersible gold nanoparticles and their direct in situ assembling in multidimensional substrates for SERS detection

被引:15
|
作者
Chen, Zhengyi [1 ]
Lu, Shengyong [2 ]
Zhang, Zhi [2 ]
Huang, Xuemei [1 ]
Zhao, Hao [1 ]
Wei, Jiaxin [1 ]
Li, Fengling [1 ]
Yuan, Kunting [3 ]
Su, Linjing [2 ]
Xiong, Yuhao [2 ]
机构
[1] Guilin Med Univ, Pharm Sch, Guilin 541004, Peoples R China
[2] Hezhou Univ, Coll Food & Bioengn, Hezhou 542899, Peoples R China
[3] Guilin Med Univ, Capital Construct Dept, Guilin 541004, Peoples R China
基金
中国国家自然科学基金;
关键词
Gold nanoparticles; Photoreduction synthesis; Green synthesis; Surface-enhanced Raman scattering; Multidimensional materials; ENHANCED RAMAN-SCATTERING; GROWTH; ACID;
D O I
10.1007/s00604-022-05379-2
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Gold nanoparticles (AuNPs) and their composites have been applied in surface-enhanced Raman scattering (SERS) detection methods, owing to their stable and excellent surface plasmon resonance. Unfortunately, methods for synthesizing AuNPs often require harsh conditions and complicated external steps. Additionally, removing residual surfactants or unreacted reductants is critical for improving the sensitivity of SERS detection, especially when employing AuNPs-assembled multidimensional substrates. In this study, we propose a simple and green method for AuNPs synthesis via photoreduction, which does not require external surfactant additives or stabilizers. All the processes were completed within 20 min. Along this way, only methanol was employed as the electron acceptor. Based on this photoreduction synthesis strategy, AuNPs can be directly and circularly assembled in situ in multidimensional substrates for SERS detection. The removal of residual methanol was easy because of its low boiling point. This strategy was employed for the preparation of three different dimensional SERS substrates: filter paper@AuNPs, g-C3N4@AuNPs, and MIL-101(Cr)@AuNPs. The limit of detection of filter paper@AuNPs for thiabendazole SERS detection was 1.0 x 10(-7) mol/L, while the limits of detection of g-C3N4@AuNPs and MIL-101(Cr)@AuNPs for malachite green SERS detection were both 5.0 x 10(-11) mol/L. This strategy presents potential in AuNP doping materials and SERS detection.
引用
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页数:10
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