Volume 8, Issue 3 pp. 979-984
EMRS-J – Contributed Article

Ultrafast photoluminescence dynamics of blue-emitting silicon nanostructures

K. Židek

Corresponding Author

K. Židek

Faculty of Mathematics and Physics, Charles University in Prague, Ke Karlovu 3, 121 16 Prague 2, Czech Republic

Institute of Physics, Academy of Sciences of the Czech Republic, v.v.i., Cukrovarnická 10, 162 53 Prague 6, Czech Republic

Phone: +420 221 911 629, Fax: +420 221 911 249Search for more papers by this author
F. Trojánek

F. Trojánek

Faculty of Mathematics and Physics, Charles University in Prague, Ke Karlovu 3, 121 16 Prague 2, Czech Republic

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P. Malý

P. Malý

Faculty of Mathematics and Physics, Charles University in Prague, Ke Karlovu 3, 121 16 Prague 2, Czech Republic

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I. Pelant

I. Pelant

Institute of Physics, Academy of Sciences of the Czech Republic, v.v.i., Cukrovarnická 10, 162 53 Prague 6, Czech Republic

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P. Gilliot

P. Gilliot

IPCMS – DON Unité mixte CNRS – ULP (UMR 7504), 23 rue du Loess, Boîte Postale 43, 67034 Strasbourg Cedex 2, France

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B. Hönerlage

B. Hönerlage

IPCMS – DON Unité mixte CNRS – ULP (UMR 7504), 23 rue du Loess, Boîte Postale 43, 67034 Strasbourg Cedex 2, France

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First published: 25 January 2011
Citations: 6

Abstract

We report on ultrafast photoluminescence (PL) spectroscopy of blue and red-emitting silicon nanostructures. We prepared samples of porous Si with different dominating PL bands in time-integrated PL spectrum. These samples show also striking differences in ultrafast PL dynamics. For the red-emitting samples we observe rapid PL onset followed by a two-exponential decay, which is spectrally dependent. For the blue-emitting porous Si the PL builds up several picoseconds and decays mono-exponentially with spectrally independent PL rise and decay times.

Our results indicate that a dominant part of the blue and red emission comes from two distinct species with different energy states structures. This is furthermore supported by two-photon absorption induced PL mea-surements. The two-photon and one-photon absorption induced PL spectra, which are identical for the red-emitting samples, differ substantially for the blue-emitting ones. However, polarization properties of PL suggest that the blue PL band originates from several overlapping PL bands with sample-dependent importance. (© 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)

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