Appearance of SERS activity in single silver nanoparticles by laser- induced reshaping

被引:23
作者
Chaudhari, Kamalesh [1 ,2 ]
Ahuja, Tripti [1 ,2 ]
Murugesan, Vasanthanarayan [1 ,2 ]
Subramanian, Vidhya [1 ,2 ]
Ganayee, Mohd Azhardin [1 ,2 ]
Thundat, Thomas [3 ]
Pradeep, Thalappil [1 ,2 ]
机构
[1] Indian Inst Technol Madras, Dept Chem, DST Unit NanoSci DST UNS, Madras 600036, Tamil Nadu, India
[2] Indian Inst Technol Madras, Dept Chem, Themat Unit Excellence, Madras 600036, Tamil Nadu, India
[3] Univ Alberta, Dept Chem & Mat Engn, Edmonton, AB T6G 2V4, Canada
关键词
ENHANCED RAMAN-SPECTROSCOPY; DARK-FIELD; MICROSCOPY; MOLECULE; NANOWIRE; BLINKING; SIZE;
D O I
10.1039/c8nr06497k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report simultaneous plasmonic scattering and Raman spectroscopic observations of single citrate capped silver nanoparticles (AgNPs) which exhibit surface enhanced Raman scattering (SERS) upon meeting specific conditions induced by laser (532 nm) exposure. We show that nanoparticles which are not initially SERS active become SERS active by laser-induced reshaping/reorientation. A set-up developed for these observations enabled in situ high speed time-lapse characterization using plasmonic and Raman spectroscopies in conjunction with dark-field microscopy (DFM). Changes in the AgNPs were confirmed by monitoring plasmonic scattering spectra and DFM images. Time-lapse observations have shown that laser-induced changes in the plasmonic properties of AgNPs resulted in the appearance of SERS. Spectral matching between plasmon resonance and downward molecular vibronic transitions for molecules adsorbed on the surface of plasmonic nanomaterials is attributed to the nanoparticle SERS. We have further shown that the release of silver ions by silver nanoparticles can be the probable reason for their plasmonic changes. Gold nanoparticles inert to such mild (850 W, 532 nm) laser-induced changes do not exhibit the appearance of SERS.
引用
收藏
页码:321 / 330
页数:10
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