SERS of Individual Nanoparticles on a Mirror: Size Does Matter, but so Does Shape

被引:185
作者
Benz, Felix [1 ]
Chikkaraddy, Rohit [1 ]
Salmon, Andrew [1 ]
Ohadi, Hamid [1 ]
de Nijs, Bart [1 ]
Mertens, Jan [1 ]
Carnegie, Cloudy [1 ]
Bowman, Richard W. [1 ]
Baumberg, Jeremy J. [1 ]
机构
[1] Univ Cambridge, Cavendish Lab, Dept Phys, NanoPhoton Ctr, JJ Thompson Ave, Cambridge CB3 0HE, England
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2016年 / 7卷 / 12期
基金
英国工程与自然科学研究理事会;
关键词
ENHANCED RAMAN-SCATTERING; MOLECULES;
D O I
10.1021/acs.jpclett.6b00986
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Coupling noble metal nanoparticles by a 1 nm gap to an underlying gold mirror confines light to extremely small volumes, useful for sensing on the nanoscale. Individually measuring 10 000 of such gold nanoparticles of increasing size dramatically shows the different scaling of their optical scattering (far-field) and surface-enhanced Raman emission (SERS, near-field). Linear red-shifts of the coupled plasmon modes are seen with increasing size, matching theory. The total SERS from the few hundred molecules under each nanoparticle dramatically increases with increasing size. This scaling shows that maximum SERS emission is always produced from the largest nanoparticles, irrespective of tuning to any plasmonic resonances. Changes of particle facet with nanoparticle size result in vastly weaker scaling of the near-field SERS, without much modifying the far-field, and allows simple approaches for optimizing practical sensing.
引用
收藏
页码:2264 / 2269
页数:6
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