Using surface enhanced Raman spectroscopy (SERS), we observed Raman enhancements (104-105) for pyridine molecules adsorbed on II-VI semiconductor quantum dots on (uncapped CdSe/ZnBeSe) produced by molecular beam epitaxy. When a monolayer of pyridine is adsorbed on these structures, excitation at 488 nm produces intense Raman spectra, a very large enhancement of the a1, b1, and b2 modes. This indicates the presence of charge transfer as a contributor to the enhancement. Furthermore, the excitation wavelength is in the vicinity of several interband transitions located both in the quantum dots and the wetting layer, and it is likely that these resonances also contribute to the enhancement factor.

Surface Enhanced Raman Spectroscopy of Pyridine on CdSe/ZnBeSe Quantum Dots Grown by Molecular Beam Epitaxy

2010

Abstract

Using surface enhanced Raman spectroscopy (SERS), we observed Raman enhancements (104-105) for pyridine molecules adsorbed on II-VI semiconductor quantum dots on (uncapped CdSe/ZnBeSe) produced by molecular beam epitaxy. When a monolayer of pyridine is adsorbed on these structures, excitation at 488 nm produces intense Raman spectra, a very large enhancement of the a1, b1, and b2 modes. This indicates the presence of charge transfer as a contributor to the enhancement. Furthermore, the excitation wavelength is in the vicinity of several interband transitions located both in the quantum dots and the wetting layer, and it is likely that these resonances also contribute to the enhancement factor.
2010
Istituto di fotonica e nanotecnologie - IFN
Surface Enhanced Raman Scattering (SERS)
semiconductor quantum-dots
Raman enhancement
charge-transfer enhancement
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/14914
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? 58
social impact