Quantitative modeling of the role of surface traps in CdSe/CdS/ZnS nanocrystal photoluminescence decay dynamics

被引:315
作者
Jones, Marcus
Lo, Shun S.
Scholes, Gregory D. [1 ]
机构
[1] Univ Toronto, Dept Chem, Inst Opt Sci, Toronto, ON M5S 3H6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
quantum dot; states; electron transfer; time-correlated single-photon counting; fluorescence intermittency; CDSE QUANTUM DOTS; DETECTED MAGNETIC-RESONANCE; FLUORESCENCE INTERMITTENCY; COLLOIDAL NANOCRYSTALS; OPTICAL-PROPERTIES; RADIATIVE DECAY; EMISSION; LUMINESCENCE; TEMPERATURE; RECOMBINATION;
D O I
10.1073/pnas.0809316106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Charge carrier trapping is an important phenomenon in nanocrystal (NC) decay dynamics because it reduces photoluminescence (PL) quantum efficiencies and obscures efforts to understand the interaction of NC excitons with their surroundings. Particularly crucial to our understanding of excitation dynamics in, e.g., multiNC assemblies, would be a way of differentiating between processes involving trap states and those that do not. Direct optical measurement of NC trap state processes is not usually possible because they have negligible transition dipole moments; however, they are known to indirectly affect exciton photoluminescence. Here, we develop a framework, based on Marcus electron transfer theory, to determine NC trap state dynamics from time-resolved NC exciton PL measurements. Our results demonstrate the sensitivity of PL to interfacial dynamics, indicating that the technique can be used as an indirect but effective probe of trap distribution changes. We anticipate that this study represents a step toward understanding how excitons in nanocrystals interact with their surroundings: a quality that must be optimized for their efficient application in photovoltaics, photodetectors, or chemical sensors.
引用
收藏
页码:3011 / 3016
页数:6
相关论文
共 53 条
[11]   Surface effects on quantum dot-based energy transfer [J].
Dayal, Smita ;
Burda, Clemens .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (25) :7977-7981
[12]   Size- and temperature-dependence of exciton lifetimes in CdSe quantum dots [J].
Donega, C. de Mello ;
Bode, M. ;
Meijerink, A. .
PHYSICAL REVIEW B, 2006, 74 (08)
[13]   Study of colloidal quantum-dot surfaces using an innovative thin-film positron 2D-ACAR method [J].
Eijt, SWH ;
Van Veen, A ;
Schut, H ;
Mijnarends, PE ;
Denison, AB ;
Barbiellini, B ;
Bansil, A .
NATURE MATERIALS, 2006, 5 (01) :23-26
[14]   Small is different: Shape-, size-, and composition-dependent properties of some colloidal semiconductor nanocrystals [J].
El-Sayed, MA .
ACCOUNTS OF CHEMICAL RESEARCH, 2004, 37 (05) :326-333
[15]   Emission intensity dependence and single-exponential behavior in single colloidal quantum dot fluorescence lifetimes [J].
Fisher, BR ;
Eisler, HJ ;
Stott, NE ;
Bawendi, MG .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (01) :143-148
[16]   Universal emission intermittency in quantum dots, nanorods and nanowires [J].
Frantsuzov, Pavel ;
Kuno, Masaru ;
Janko, Boldizsar ;
Marcus, Rudolph A. .
NATURE PHYSICS, 2008, 4 (07) :519-522
[17]   Air-stable all-inorganic nanocrystal solar cells processed from solution [J].
Gur, I ;
Fromer, NA ;
Geier, ML ;
Alivisatos, AP .
SCIENCE, 2005, 310 (5747) :462-465
[18]   Comparative study of the quenching of core and core-shell CdSe quantum dots by binding and non-binding nitroxides [J].
Heafey, Eve ;
Laferriere, Marie ;
Scaiano, J. C. .
PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES, 2007, 6 (05) :580-584
[19]   Hybrid nanorod-polymer solar cells [J].
Huynh, WU ;
Dittmer, JJ ;
Alivisatos, AP .
SCIENCE, 2002, 295 (5564) :2425-2427
[20]   Ligand bonding and dynamics on colloidal nanocrystals at room temperature: The case of alkylamines on CdSe nanocrystals [J].
Ji, Xiaohui ;
Copenhaver, Danis ;
Sichmeller, Christopher ;
Peng, Xiaogang .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (17) :5726-5735