Surface Doping Quantum Dots with Chemically Active Native Ligands: Controlling Valence without Ligand Exchange

被引:34
作者
Tavasoli, Elham [1 ]
Guo, Yijun [1 ]
Kunal, Pranaw [1 ]
Grajeda, Javier [2 ]
Gerber, Allison [1 ]
Vela, Javier [1 ,2 ]
机构
[1] Iowa State Univ, Dept Chem, Ames, IA 50011 USA
[2] Ames Lab, Ames, IA 50011 USA
基金
美国国家科学基金会;
关键词
quantum dot; valence; loading; chemical surface modification; SEMICONDUCTOR NANOCRYSTALS; COLLOIDAL NANOCRYSTALS; OPTICAL-PROPERTIES; PARAMAGNETIC-SUSCEPTIBILITY; CDSE; NMR; NANOPARTICLES; SPECTROSCOPY; METATHESIS; PRECURSOR;
D O I
10.1021/cm3026957
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
One remaining challenge in the field of colloidal semiconductor nanocrystal quantum dots is learning to control the degree of functionalization or "Valence" per nanocrystal. Current quantum dot surface modification strategies rely heavily on ligand exchange, which consists of replacing the nanocrystal's native ligands with carboxylate- or amine-terminated thiols, usually added in excess. Removing the nanocrystal's native ligands can cause etching and introduce surface defects, thus affecting the nanocrystal's optical properties. More importantly, ligand exchange methods fail to control the extent of surface modification or number of functional groups introduced per nanocrystal Here, we report a fundamentally new surface ligand modification or "doping" approach aimed at controlling the degree of functionalization or valence per nanocrystal while retaining the nanocrystal's original colloidal and photostability. We show that surface-doped quantum dots capped with chemically active native ligands can be prepared. directly from a mixture of ligands with similar chain lengths. Specifically, vinyl and azide-terminated carboxylic acid ligands survive, the high temperatures needed for nanocrystal synthesis. The ratio between chemically active and inactive terminated ligands is maintained on the nanocrystal surface, allowing to control the extent of surface modification by straightforward organic reactions. Using a combination of optical and structural characterization tools, including IR and 2D NMR; We show that carboxylates bind in a bidentate chelate fashion, forming a single monolayer of ligands that are perpendicular to the nanocrystal surface. Moreover, we show that mixtures of ligands with similar chain lengths homogeneously distribute themselves on the nanocrystal surface. We expect this new surface doping approach will be widely applicable to other nanocrystal compositions and morphologies, as well as to many specific applications in biology and materials science.
引用
收藏
页码:4231 / 4241
页数:11
相关论文
共 82 条
[1]   Semiconductor Quantum Dots in Bioanalysis: Crossing the Valley of Death [J].
Algar, W. Russ ;
Susumu, Kimihiro ;
Delehanty, James B. ;
Medintz, Igor L. .
ANALYTICAL CHEMISTRY, 2011, 83 (23) :8826-8837
[2]   Covalent Inhibition of Bacterial Quorum Sensing [J].
Amara, Neri ;
Mashiach, Roi ;
Amar, Dotan ;
Krief, Pnina ;
Spieser, Stephane A. H. ;
Bottomley, Matthew J. ;
Aharoni, Amir ;
Meijler, Michael M. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (30) :10610-10619
[3]   Quantum Dot Light-Emitting Devices with Electroluminescence Tunable over the Entire Visible Spectrum [J].
Anikeeva, Polina O. ;
Halpert, Jonathan E. ;
Bawendi, Moungi G. ;
Bulovic, Vladimir .
NANO LETTERS, 2009, 9 (07) :2532-2536
[4]  
[Anonymous], MACROMOLECULES
[5]   Synthesis and characterization of zinc bis(O-isopropylxanthate) as a single-source chemical vapor deposition precursor for ZnS [J].
Barreca, D ;
Gasparotto, A ;
Maragno, C ;
Seraglia, R ;
Tondello, E ;
Venzo, A ;
Krishnan, V ;
Bertagnolli, H .
APPLIED ORGANOMETALLIC CHEMISTRY, 2005, 19 (09) :1002-1009
[6]   NMR analysis of surfaces and interfaces in 2-nm CdSe [J].
Berrettini, MG ;
Braun, G ;
Hu, JG ;
Strouse, GF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (22) :7063-7070
[7]   Rapid Covalent Ligation of Fluorescent Peptides to Water Solubilized Quantum Dots [J].
Blanco-Canosa, Juan B. ;
Medintz, Igor L. ;
Farrell, Dorothy ;
Mattoussi, Hedi ;
Dawson, Philip E. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (29) :10027-10033
[8]   Ruthenium-catalyzed azide-alkyne cycloaddition: Scope and mechanism [J].
Boren, Brant C. ;
Narayan, Sridhar ;
Rasmussen, Lars K. ;
Zhang, Li ;
Zhao, Haitao ;
Lin, Zhenyang ;
Jia, Guochen ;
Fokin, Valery V. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (28) :8923-8930
[9]   Size limitations for the formation of ordered striped nanoparticles [J].
Carney, Randy P. ;
DeVries, Gretchen A. ;
Dubois, Cedric ;
Kim, Hyewon ;
Kim, Jin Young ;
Singh, Chetana ;
Ghorai, Pradip K. ;
Tracy, Joseph B. ;
Stiles, Rebecca L. ;
Murray, Royce W. ;
Glotzer, Sharon C. ;
Stellacci, Francesco .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (03) :798-+
[10]  
Centrone A, 2007, SMALL, V3, P814, DOI 10.1002/smll.20060073