Quantum dot surface engineering: Toward inert fluorophores with compact size and bright, stable emission

被引:80
作者
Lim, Sung Jun [1 ,2 ]
Ma, Liang [1 ,3 ]
Schleife, Andre [3 ]
Smith, Andrew M. [1 ,2 ,3 ]
机构
[1] Univ Illinois, Micro & Nanotechnol Lab, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Bioengn, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Mat Sci & Engn, Urbana, IL 61801 USA
基金
美国国家科学基金会;
关键词
Semiconductor; Nanoparticle; Photoluminescence; CdSe; Bioimaging; Probe; SELF-ASSEMBLED MONOLAYERS; EXCITATION-WAVELENGTH DEPENDENCE; CRYSTAL-STRUCTURE CONTROL; FREE CLICK CHEMISTRY; CDSE NANOCRYSTALS; HIGHLY LUMINESCENT; LIGAND-EXCHANGE; COLLOIDAL NANOCRYSTALS; GOLD NANOPARTICLES; SEMICONDUCTOR NANOCRYSTALS;
D O I
10.1016/j.ccr.2016.03.012
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The surfaces of colloidal nanocrystals are complex interfaces between solid crystals, coordinating ligands, and liquid solutions. For fluorescent quantum dots, the properties of the surface vastly influence the efficiency of light emission, stability, and physical interactions, and thus determine their sensitivity and specificity when they are used to detect and image biological molecules. But after more than 30 years of study, the surfaces of quantum dots remain poorly understood and continue to be an important subject of both experimental and theoretical research. In this article, we review the physics and chemistry of quantum dot surfaces and describe approaches to engineer optimal fluorescent probes for applications in biomolecular imaging and sensing. We describe the structure and electronic properties of crystalline facets, the chemistry of ligand coordination, and the impact of ligands on optical properties. We further describe recent advances in compact coatings that have significantly improved their properties by providing small hydrodynamic size, high stability and fluorescence efficiency, and minimal nonspecific interactions with cells and biological molecules. While major progress has been made in both basic and applied research, many questions remain in the chemistry and physics of quantum dot surfaces that have hindered key breakthroughs to fully optimize their properties. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:216 / 237
页数:22
相关论文
共 275 条
[1]   Nanocrystal targeting in vivo [J].
Åkerman, ME ;
Chan, WCW ;
Laakkonen, P ;
Bhatia, SN ;
Ruoslahti, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) :12617-12621
[2]   Short Ligands Affect Modes of QD Uptake and Elimination in Human Cells [J].
Al-Hajaj, Noura A. ;
Moquin, Alexandre ;
Neibert, Kevin D. ;
Soliman, Ghareb M. ;
Winnik, Francoise M. ;
Maysinger, Dusica .
ACS NANO, 2011, 5 (06) :4909-4918
[3]   Size-dependent dissociation pH of thiolate ligands from cadmium chalcogenide nanocrystals [J].
Aldana, J ;
Lavelle, N ;
Wang, YJ ;
Peng, XG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (08) :2496-2504
[4]   Photochemical instability of CdSe nanocrystals coated by hydrophilic thiols [J].
Aldana, J ;
Wang, YA ;
Peng, XG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (36) :8844-8850
[5]   Perspectives on the physical chemistry of semiconductor nanocrystals [J].
Alivisatos, AP .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (31) :13226-13239
[6]   Ligand Exchange and the Stoichiometry of Metal Chalcogenide Nanocrystals: Spectroscopic Observation of Facile Metal-Carboxylate Displacement and Binding [J].
Anderson, Nicholas C. ;
Hendricks, Mark P. ;
Choi, Joshua J. ;
Owen, Jonathan S. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (49) :18536-18548
[7]   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
[8]  
[Anonymous], 2013, Physical Foundations of Materials Science, DOI DOI 10.1007/978-3-662-09291-0
[9]   Ligand Induced Spectral Changes in CdSe Quantum Dots [J].
Azpiroz, Jon M. ;
De Angelis, Filippo .
ACS APPLIED MATERIALS & INTERFACES, 2015, 7 (35) :19736-19745
[10]   Ionization, atomization, and bond energies as functions of distances in inorganic molecules and crystals [J].
Batsanov, S. S. .
RUSSIAN JOURNAL OF INORGANIC CHEMISTRY, 2007, 52 (08) :1223-1229