We present an automated setup to measure the surface plasmon resonance (SPR)-enhanced optical absorption spectra of molecular adsorbates. The setup detects the reflectivity at the SPR resonance angle as a function of the incident light wavelength. Because the resonance angle is wavelength dependent, a feedback mechanism adjusts the photodetector position to follow the resonance angle when the wavelength varies. Both theoretical calculations and experimental measurements show a signal enhancement of up to ∼40 times over the conventional absorption spectroscopy. The SPR-based absorption spectroscopy is surface specific because the optical field is localized near the surface at resonance. In addition, the SPR angular shift is simultaneously measured, which provides adsorbate coverage and adsorption kinetic information. We anticipate that with our automated system, the method could be used in the study of adsorbed molecules and in chemical and biosensor applications.
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July 2001
Research Article|
July 01 2001
Surface plasmon resonance enhanced optical absorption spectroscopy for studying molecular adsorbates Available to Purchase
S. Wang;
S. Wang
Department of Physics, Florida International University, Miami, Florida 33199
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S. Boussaad;
S. Boussaad
Department of Physics, Florida International University, Miami, Florida 33199
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N. J. Tao
N. J. Tao
Department of Physics, Florida International University, Miami, Florida 33199
Search for other works by this author on:
S. Wang
Department of Physics, Florida International University, Miami, Florida 33199
S. Boussaad
Department of Physics, Florida International University, Miami, Florida 33199
N. J. Tao
Department of Physics, Florida International University, Miami, Florida 33199
Rev. Sci. Instrum. 72, 3055–3060 (2001)
Article history
Received:
February 20 2001
Accepted:
April 23 2001
Citation
S. Wang, S. Boussaad, N. J. Tao; Surface plasmon resonance enhanced optical absorption spectroscopy for studying molecular adsorbates. Rev. Sci. Instrum. 1 July 2001; 72 (7): 3055–3060. https://doi.org/10.1063/1.1379604
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