Controlling the spectroscopic properties of quantum dots via energy transfer and charge transfer interactions: Concepts and applications

被引:48
|
作者
Ji, Xin [1 ,2 ]
Wang, Wentao [1 ]
Mattoussi, Hedi [1 ]
机构
[1] Florida State Univ, Dept Chem & Biochem, 95 Chieftan Way, Tallahassee, FL 32306 USA
[2] Ocean Nanotech LLC, 7964 Arjons Dr, San Diego, CA 92126 USA
基金
美国国家科学基金会;
关键词
Quantum dots; Confinement effects; Fluorescence; Fluorescence resonance energy transfer (FRET); Charge transfer (CT); Biosensing; ELECTRON-TRANSFER; SEMICONDUCTOR NANOCRYSTALS; MONODISPERSE NANOCRYSTALS; PROTEOLYTIC ACTIVITY; DISTANCE DEPENDENCE; METAL NANOPARTICLE; INTRACELLULAR PH; ENZYME-ACTIVITY; LIVE CELLS; IN-VITRO;
D O I
10.1016/j.nantod.2015.09.004
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Luminescent quantum dots (QDs) exhibit size- and composition-tunable photophysical properties that are not shared by their bulk parent materials or at the molecular scale. They have attracted considerable interest further motivated by several potential applications. A particular interest has centered on exploiting the ability of QDs to engage in both fluorescence resonance energy transfer (FRET) and charge transfer (CT) interactions with proximal fluorophores and redox active molecules/complexes, respectively. In this review, we highlight how the QD's optical and spectroscopic properties can be controlled via FRET and/or CT interactions. We first show that QDs provide a unique platform for controlling both modes of interactions. We then provide representative examples in biology which include developing sensing assemblies that report on properties such as pH changes, enzymatic activity and ligand receptor binding. Implications in electronic devices focus on light emitting devices and photovoltaic cells, where we discuss device architecture, control over carrier injection, carrier mobility, and exciton recombination. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:98 / 121
页数:24
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