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Title: SERS of semiconducting nanoparticles (TiO{sub 2} hybrid composites).

Journal Article · · J. Am. Chem. Soc.
DOI:https://doi.org/10.1021/ja808277u· OSTI ID:1010887

Raman scattering of molecules adsorbed on the surface of TiO{sub 2} nanoparticles was investigated. We find strong enhancement of Raman scattering in hybrid composites that exhibit charge transfer absorption with TiO{sub 2} nanoparticles. An enhancement factor up to {approx}10{sup 3} was observed in the solutions containing TiO{sub 2} nanoparticles and biomolecules, including the important class of neurotransmitters such as dopamine and dopac (3,4-dihydroxy-phenylacetic acid). Only selected vibrations are enhanced, indicating molecular specificity due to distinct binding and orientation of the biomolecules coupled to the TiO{sub 2} surface. All enhanced modes are associated with the asymmetric vibrations of attached molecules that lower the symmetry of the charge transfer complex. The intensity and the energy of selected vibrations are dependent on the size and shape of nanoparticle support. Moreover, we show that localization of the charge in quantized nanoparticles (2 nm), demonstrated as the blue shift of particle absorption, diminishes SERS enhancement. Importantly, the smallest concentration of adsorbed molecules shows the largest Raman enhancements suggesting the possibility for high sensitivity of this system in the detection of biomolecules that form a charge transfer complex with metal oxide nanoparticles. The wavelength-dependent properties of a hybrid composite suggest a Raman resonant state. Adsorbed molecules that do not show a charge transfer complex show weak enhancements probably due to the dielectric cavity effect.

Research Organization:
Argonne National Lab. (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE Office of Science (SC); Univ. of Queensland Graduate School Research Travel Grant; ARCNN Overseas Travel Fellowship
DOE Contract Number:
DE-AC02-06CH11357
OSTI ID:
1010887
Report Number(s):
ANL/CNM/JA-63872; TRN: US201109%%158
Journal Information:
J. Am. Chem. Soc., Vol. 131, Issue 17 ; Apr. 13. 2009
Country of Publication:
United States
Language:
ENGLISH

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