Band edge dynamics in CdSe nanocrystals observed by ultrafast fluorescence upconversion

被引:33
作者
Garrett, Maria Danielle [1 ]
Bowers, Michael J., II [1 ]
McBride, James R. [1 ]
Orndorff, Rebecca L. [1 ]
Pennycook, Stephen J. [2 ]
Rosenthal, Sandra J. [1 ,3 ]
机构
[1] Vanderbilt Univ, Dept Chem, Stevenson Ctr 7330, Stn B 351822, Nashville, TN 37235 USA
[2] Oak Ridge Natl Lab, Condensed Matter Sci Div, Oak Ridge, TN 37831 USA
[3] Vanderbilt Univ, Dept Phys & Astron, Nashville, TN 37235 USA
关键词
D O I
10.1021/jp7099306
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Fluorescence upconversion spectroscopy has been performed on high-quality, low size dispersion CdSe nanocrystals synthesized using the CdO precursor with tri-n-octylphosphine oxide and hexadecylamine cosurfactants. These measurements reveal that an increase in nanocrystal diameter, from 25 to 60 angstrom, is accompanied by an increase in both the short-lived (tau(1)) and long-lived (tau(2)) components of the fluorescence lifetime at the band edge. The increase in tau(1) is explained by the decrease in accessible trap sites through a reduction in surface-to-volume ratio. The addition of hexadecylamine as a cosolvent, through interaction with dangling selenium bonds on the nanocrystal surface, is shown to increase tau(1), as compared to nanocrystals synthesized only in tri-n-octylphosphine oxide. These results indicate that carrier dynamics are preparation dependent.
引用
收藏
页码:436 / 442
页数:7
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