Open AccessWavelet-based decomposition of high resolution surface plasmon microscopy V (Z) curves at visible and near infrared wavelengths
Author(s) -
Elise Boyer-Provera,
Andrea Mario Rossi,
Luis Oriol,
Charles Dumontet,
A. Plesa,
Lotfi Berguiga,
Juan Elezgaray,
A. Arnéodo,
Françoise Argoul
Publication year - 2013
Publication title -
optics express
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.394
H-Index - 271
ISSN - 1094-4087
DOI - 10.1364/oe.21.007456
Subject(s) - optics , surface plasmon resonance , materials science , plasmon , surface plasmon , infrared , visible spectrum , microscopy , wavelength , microscope , resolution (logic) , spatial frequency , localized surface plasmon , physics , nanotechnology , nanoparticle , computer science , artificial intelligence
Surface plasmon resonance is conventionally conducted in the visible range and, during the past decades, it has proved its efficiency in probing molecular scale interactions. Here we elaborate on the first implementation of a high resolution surface plasmon microscope that operates at near infrared (IR) wavelength for the specific purpose of living matter imaging. We analyze the characteristic angular and spatial frequencies of plasmon resonance in visible and near IR lights and how these combined quantities contribute to the V(Z) response of a scanning surface plasmon microscope (SSPM). Using a space-frequency wavelet decomposition, we show that the V(Z) response of the SSPM for red (632.8 nm) and near IR (1550 nm) lights includes the frequential response of plasmon resonance together with additional parasitic frequencies induced by the objective pupil. Because the objective lens pupil profile is often unknown, this space-frequency decomposition turns out to be very useful to decipher the characteristic frequencies of the experimental V(Z) curves. Comparing the visible and near IR light responses of the SSPM, we show that our objective lens, primarily designed for visible light microscopy, is still operating very efficiently in near IR light. Actually, despite their loss in resolution, the SSPM images obtained with near IR light remain contrasted for a wider range of defocus values from negative to positive Z values. We illustrate our theoretical modeling with a preliminary experimental application to blood cell imaging.