单层
分子
表面等离子共振
材料科学
吸光度
等离子体子
吸收(声学)
化学物理
金属
表面等离子体子
吸收光谱法
共振(粒子物理)
胶体
纳米技术
纳米颗粒
纳米结构
化学
光学
光电子学
物理化学
原子物理学
物理
有机化学
复合材料
冶金
作者
Brendan L. Darby,Baptiste Auguié,Matthias Meyer,Andres E. Pantoja,Eric C. Le Ru
出处
期刊:Nature Photonics
[Nature Portfolio]
日期:2015-11-02
卷期号:10 (1): 40-45
被引量:150
标识
DOI:10.1038/nphoton.2015.205
摘要
Enhanced optical absorption of molecules in the vicinity of metallic nanostructures is key to a number of surface-enhanced spectroscopies and of great general interest to the fields of plasmonics and nano-optics. However, experimental access to this absorbance has long proven elusive. Here, we present direct measurements of the surface absorbance of dye molecules adsorbed onto silver nanospheres and, crucially, at sub-monolayer concentrations where dye–dye interactions become negligible. With a large detuning from the plasmon resonance, distinct shifts and broadening of the molecular resonances reveal the intrinsic properties of the dye in contact with the metal colloid, in contrast to the often studied strong-coupling regime where the optical properties of the dye molecules cannot be isolated. The observation of these shifts together with the ability to routinely measure them has broad implications in the interpretation of experiments involving resonant molecules on metallic surfaces, such as surface-enhanced spectroscopies and many aspects of molecular plasmonics. Direct measurements of silver spheres with sub-monolayer concentrations of dye-molecules reveal shifts and broadening of molecular resonances.
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