Photoluminescence dynamics in solid formulations of colloidal PbSe quantum dots: Three-dimensional versus two-dimensional films

被引:10
|
作者
Quintero-Torres, Rafael [1 ,2 ]
Foell, Charles A. [2 ]
Pichaandi, Jothirmayanantham [3 ]
van Veggel, Frank C. J. M. [3 ]
Young, Jeff F. [2 ]
机构
[1] Ctr Fis Aplicada & Tecnol Avanzada, Juriquilla Queretaro 76230, Mexico
[2] Univ British Columbia, Dept Phys & Astron, Vancouver, BC V6T 1Z1, Canada
[3] Univ Victoria, Dept Chem, Victoria, BC V8W 3V6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
ENERGY-TRANSFER; NANOCRYSTALS; CORE/SHELL; LASER; CHIP;
D O I
10.1063/1.4752737
中图分类号
O59 [应用物理学];
学科分类号
摘要
Time-resolved photoluminescence spectroscopy is used to compare decay dynamics of colloidal PbSe quantum dots as (i) dilute dispersions in hexanes, (ii) thick, dense, emulsive films, and (iii) sub-monolayer films on silicon surfaces. Accounting for the effect of each dielectric environment on exciton radiative decay rates, we deduce the non-radiative decay rate of excitons increases going from solution to thick films by approximate to 6 fold and to sub-monolayer films by approximate to 7-16 fold. This is attributed to surface passivation degradation due to a lack of mobile ligands when the particles are taken out of solution. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.4752737]
引用
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页数:4
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