Hostname: page-component-cd9895bd7-dzt6s Total loading time: 0 Render date: 2024-12-24T12:27:56.541Z Has data issue: false hasContentIssue false
  • English
  • Français

Electronic Energy Transfer from Excitons Confined in Silicon Nanocrystals to Molecular Oxygen

Published online by Cambridge University Press:  10 February 2011

E. Gross ,
D. Kovalev ,
N. Künzner ,
J. Diener ,
F. Koch ,
V.Yu. Timoshenko  and
Minoru Fujii
E. Gross
Affiliation:
Technische Universität München, Physik Department E16, 85747 Garching, Germany
D. Kovalev
Affiliation:
Technische Universität München, Physik Department E16, 85747 Garching, Germany
N. Künzner
Affiliation:
Technische Universität München, Physik Department E16, 85747 Garching, Germany
J. Diener
Affiliation:
Technische Universität München, Physik Department E16, 85747 Garching, Germany
F. Koch
Affiliation:
Technische Universität München, Physik Department E16, 85747 Garching, Germany
V.Yu. Timoshenko
Affiliation:
Faculty of Physics, Moscow State M.V. Lomonosov University, 119992 Moscow, Russia
Minoru Fujii
Affiliation:
Department of Electrical and Electronics Engineering, Faculty of Engineering, Kobe University, Rokkodai, Nada, Kobe 657-8501, Japan
Get access

Abstract

We report on efficient electronic energy transfer from excitons confined in silicon (Si) nanocrystals to molecular oxygen (MO). The remarkable photosensitizing properties of Si nanocrystal assemblies result from a broad energy spectrum of photoexcited excitons, a long triplet exciton lifetime and a highly developed surface area. Quenching of photoluminescence (PL) of Si nanocrystals by MO physisorbed on their surface is found to be most efficient when the energy of excitons coincides with the triplet-singlet splitting energy of oxygen molecules. Spectroscopic analysis of the quenched PL spectrum evidences that energy transfer is accompanied by multi-phonon emission. From time-resolved measurements the characteristic time of energy transfer is found to be in the range of microseconds. The dependence of PL quenching efficiency on the surface termination of nanocrystals is consistent with short-range resonant electron exchange mechanism of energy transfer. The energy transfer to oxygen molecules in the gaseous phase at elevated temperatures is demonstrated.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 770: Symposium I – Optoelectronics of Group-IV-Based Materials , 2003 , I1.4
Copyright
Copyright © Materials Research Society 2003

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Krupenie, P. H., J. Phys. Chem. Ref. Data 423, 423 (1972).Google Scholar
2. Turro, N. J., Modern Molecular Photochemistry (Benjamin/Cummings, Menlo Park, CA, 1978).Google Scholar
3. Cullis, A. G., Canham, L. T., and Calcott, P. D. J., J. Appl. Phys. 909, 909 (1997).Google Scholar
4. Bisi, O., Ossicini, S., and Pavesi, L., Surface Science Reports 1, 1 (2000).Google Scholar
5. Weber, W., Phys. Rev. B. 4789, 4789 (1977).Google Scholar
6. Förster, T., Ann. Phys. (N.Y.) 55, 55 (1948).Google Scholar
7. Dexter, D. L., J. Chem. Phys. 836, 836 (1953).Google Scholar
8. CRC Handbook of Chemistry and Physics, edited by Linde, D. R. (CRCPress, New York, 1997-1998), 78th ed.Google Scholar
9. Langmuir, I., J. Am. Chem. Soc. 2221, 2221 (1916).Google Scholar