New Insights into the Complexities of Shell Growth and the Strong Influence of Particle Volume in Nonblinking "Giant" Core/Shell Nanocrystal Quantum Dots

被引:203
作者
Ghosh, Yagnaseni [1 ]
Mangum, Benjamin D. [1 ]
Casson, Joanna L. [2 ]
Williams, Darrick J. [1 ]
Htoon, Han [1 ]
Hollingsworth, Jennifer A. [1 ]
机构
[1] Los Alamos Natl Lab, Mat Phys & Applicat Div, Ctr Integrated Nanotechnol, Los Alamos, NM 87545 USA
[2] Los Alamos Natl Lab, Div Chem, Los Alamos, NM 87545 USA
关键词
ORIENTED ATTACHMENT; CDSE NANOCRYSTALS; MONODISPERSE; ROUTES;
D O I
10.1021/ja212032q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The growth of ultra-thick inorganic CdS shells over CdSe nanocrystal quantum clot (NQD) cores gives rise to a distinct class of NQD called the "giant" NQP (g-NQD). g-NQDs are characterized by unique photophysical properties compared to their conventional core/shell NQD counterparts, including suppressed fluorescence intermittency (blinking), photobleaching, and nonradiative Auger recombination. Here, we report new insights into the numerous synthetic conditions that influence the complex process of thick-shell growth. We show the individual and collective effects of multiple reaction parameters (noncoordinating solvent and coordinating-ligand identities and concentrations, precursor/NQD ratios, precursor reaction times, etc.) on determining g-NQD shape and crystalline phase, and the relationship between these structural features and optical properties. We find that hexagonally faceted wurzite g-NQDs afford the highest ensemble quantum yields in emission and the most complete suppression of blinking. Significantly, we also reveal a clear correlation between g-NQD particle volume and blinking suppression, such that larger cores afford blinking-suppressed behavior at relatively thinner shells compared to smaller starting core sizes, which require application of thicker shells to realize the same level of blinking suppression. We show that there is a common, threshold g-NQD volume (similar to 750 nm(3)) that is required to observe blinking suppression and that this particle volume corresponds to an NQD radiative lifetime of similar to 65 ns regardless of starting core size. Combining new understanding of key synthetic parameters with optimized core/shell particle volumes, we demonstrate effectively complete suppression of blinking even for long observation times of similar to 1 h.
引用
收藏
页码:9634 / 9643
页数:10
相关论文
共 24 条
[1]   Nano-engineered electron-hole exchange interaction controls exciton dynamics in core-shell semiconductor nanocrystals [J].
Brovelli, S. ;
Schaller, R. D. ;
Crooker, S. A. ;
Garcia-Santamaria, F. ;
Chen, Y. ;
Viswanatha, R. ;
Hollingsworth, J. A. ;
Htoon, H. ;
Klimov, V. I. .
NATURE COMMUNICATIONS, 2011, 2
[2]   Giant multishell CdSe nanocrystal quantum dots with suppressed blinking [J].
Chen, Yongfen ;
Vela, Javier ;
Htoon, Han ;
Casson, Joanna L. ;
Werder, Donald J. ;
Bussian, David A. ;
Klimov, Victor I. ;
Hollingsworth, Jennifer A. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (15) :5026-5027
[3]   Designing PbSe nanowires and nanorings through oriented attachment of nanoparticles [J].
Cho, KS ;
Talapin, DV ;
Gaschler, W ;
Murray, CB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (19) :7140-7147
[4]   Thermal Charging of Colloidal Quantum Dots in Apolar Solvents: A Current Transient Analysis [J].
Cirillo, Marco ;
Strubbe, Filip ;
Neyts, Kristiaan ;
Hens, Zeger .
ACS NANO, 2011, 5 (02) :1345-1352
[5]   Suppressed Auger Recombination in "Giant" Nanocrystals Boosts Optical Gain Performance [J].
Garcia-Santamaria, Florencio ;
Chen, Yongfen ;
Vela, Javier ;
Schaller, Richard D. ;
Hollingsworth, Jennifer A. ;
Klimov, Victor I. .
NANO LETTERS, 2009, 9 (10) :3482-3488
[6]   Highly Emissive Multiexcitons in Steady-State Photoluminescence of Individual "Giant" CdSe/CdS Core/Shell Nanocrystals [J].
Htoon, H. ;
Malko, A. V. ;
Bussian, D. ;
Vela, J. ;
Chen, Y. ;
Hollingsworth, J. A. ;
Klimov, V. I. .
NANO LETTERS, 2010, 10 (07) :2401-2407
[7]   On the use of time-resolved photoluminescence as a probe of nanocrystal photoexcitation dynamics [J].
Jones, Marcus ;
Scholes, Gregory D. .
JOURNAL OF MATERIALS CHEMISTRY, 2010, 20 (18) :3533-3538
[8]   Synthesis routes for the growth of complex nanostructures [J].
Kudera, Stefan ;
Carbone, Luigi ;
Carlino, Elvio ;
Cingolani, R. ;
Cozzoli, Pantaleo Davide ;
manna, Liberato .
PHYSICA E-LOW-DIMENSIONAL SYSTEMS & NANOSTRUCTURES, 2007, 37 (1-2) :128-133
[9]  
Kundu J., 2012, NANO LETT, DOI [10.1021/n13008659, DOI 10.1021/N13008659]
[10]   Large-scale synthesis of nearly monodisperse CdSe/CdS core/shell nanocrystals using air-stable reagents via successive ion layer adsorption and reaction [J].
Li, JJ ;
Wang, YA ;
Guo, WZ ;
Keay, JC ;
Mishima, TD ;
Johnson, MB ;
Peng, XG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (41) :12567-12575