Femtosecond luminescence spectroscopy of core states in silicon nanocrystals

被引:31
作者
Zidek, K. [1 ,2 ]
Trojanek, F. [1 ]
Maly, P. [1 ]
Ondic, L. [1 ,2 ]
Pelant, I. [2 ]
Dohnalova, K. [2 ,3 ]
Siller, L. [4 ]
Little, R. [4 ]
Horrocks, B. R. [5 ]
机构
[1] Charles Univ Prague, Fac Math & Phys, CR-12116 Prague, Czech Republic
[2] Acad Sci Czech Republic, Inst Phys, Vvi, Prague 16253, Czech Republic
[3] Univ Amsterdam, Van der Waals Zeeman Inst, NL-1018 XE Amsterdam, Netherlands
[4] Newcastle Univ, Sch Chem Engn & Adv Mat, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[5] Newcastle Univ, Sch Chem, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
来源
OPTICS EXPRESS | 2010年 / 18卷 / 24期
基金
英国工程与自然科学研究理事会;
关键词
CARRIER RELAXATION; SI NANOCRYSTALS; CDSE NANOCRYSTALS; LIGHT-EMISSION; DYNAMICS; PHOTOLUMINESCENCE; ABSORPTION;
D O I
10.1364/OE.18.025241
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We present a study of ultrafast carrier transfer from highly luminescent states inside the core of silicon nanocrystal (due to quasidirect transitions) to states on the nanocrystal-matrix interface. This transfer leads to a sub-picosecond luminescence decay, which is followed by a slower decay component induced by carrier relaxation to lower interface states. We investigate the luminescence dynamics for two different surface passivation types and we propose a general model describing spectral dependence of ultrafast carrier dynamics. Our results stress the crucial role of the energy distribution of the interface states on surface-related quenching of quasidirect luminescence in silicon nanocrystals. We discuss how to avoid this quenching in order to bring the attractive properties of the quasidirect recombination closer to exploitation. (C) 2010 Optical Society of America
引用
收藏
页码:25241 / 25249
页数:9
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