Exciton recombination dynamics in CdSe nanowires: Bimolecular to three-carrier Auger kinetics

被引:129
|
作者
Robel, Istvan
Bunker, Bruce A.
Kamat, Prashant V. [1 ]
Kuno, Masaru
机构
[1] Univ Notre Dame, Radiat Lab, Dept Chem & Biochem, Dept Chem & Biomol Engn, Notre Dame, IN 46556 USA
[2] Univ Notre Dame, Dept Phys, Notre Dame, IN 46556 USA
关键词
D O I
10.1021/nl060199z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ultrafast relaxation dynamics of charge carriers in CdSe quantum wires with diameters between 6 and 8 nm are studied as a function of carrier density. At high electron-hole pair densities above 10(19) cm(-3) the dominant process for carrier cooling is the "bimolecular" Auger recombination of one-dimensional (1D) excitons. However, below this excitation level an unexpected transition from a bimolecular (exciton-exciton) to a three-carrier Auger relaxation mechanism occurs. Thus, depending on excitation intensity, electron-hole pair relaxation dynamics in the nanowires exhibit either 1D or 0D ( quantum dot) character. This dual nature of the recovery kinetics defines an optimal intensity for achieving optical gain in solution-grown nanowires given the different carrier-density-dependent scaling of relaxation rates in either regime.
引用
收藏
页码:1344 / 1349
页数:6
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