Porous Au-Ag Nanoparticles from Galvanic Replacement Applied as Single-Particle SERS Probe for Quantitative Monitoring

被引:37
|
作者
Wang, Lu [1 ]
Patskovsky, Sergiy [1 ]
Gauthier-Soumis, Bastien [1 ]
Meunier, Michel [1 ]
机构
[1] Polytech Montreal, Dept Engn Phys, Laser Proc & Plasmon Lab, CP 6079, Montreal, PQ H3C 3A7, Canada
关键词
galvanic replacement; nanoprobe; plasmonic nanostructure; porous nanoparticles; single particle; surface-enhanced Raman spectroscopy; METAL NANOSTRUCTURES; HOLLOW NANOSTRUCTURES; GOLD; EVOLUTION; RELEASE; SPECTROSCOPY; NANOSPHERES; DOXORUBICIN; NANOSHELLS; NANOBOXES;
D O I
10.1002/smll.202105209
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Plasmonic nanostructures have raised the interest of biomedical applications of surface-enhanced Raman scattering (SERS). To improve the enhancement and produce sensitive SERS probes, porous Au-Ag alloy nanoparticles (NPs) are synthesized by dealloying Au-Ag alloy NP-precursors with Au or Ag core in aqueous colloidal environment through galvanic replacement reaction. The novel designed core-shell Au-Ag alloy NP-precursors facilitate controllable synthesis of porous nanostructure, and dealloying degree during the reaction has significant effect on structural and spectral properties of dealloyed porous NPs. Narrow-dispersed dealloyed NPs are obtained using NPs of Au/Ag ratio from 10/90 to 40/60 with Au and Ag core to produce solid core@porous shell and porous nanoshells, having rough surface, hollowness, and porosity around 30-60%. The clean nanostructure from colloidal synthesis exhibits a redshifted plasmon peak up to near-infrared region, and the large accessible surface induces highly localized surface plasmon resonance and generates robust SERS activity. Thus, the porous NPs produce intensely enhanced Raman signal up to 68-fold higher than 100 nm AuNP enhancement at single-particle level, and the estimated Raman enhancement around 7800, showing the potential for highly sensitive SERS probes. The single-particle SERS probes are effectively demonstrated in quantitative monitoring of anticancer drug Doxorubicin release.
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页数:13
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