磷化铟
量子点
光致发光
材料科学
光电子学
异质结
铟
近红外光谱
纳米颗粒
磷化镓
红外线的
光激发
纳米技术
光学
砷化镓
激发
工程类
物理
电气工程
作者
Alexander M. Saeboe,A. Yu. Nikiforov,Reyhaneh Toufanian,Joshua Kays,Margaret Chern,J. Paolo Casas,Keyi Han,Andrei Piryatinski,Dennis Jones,Allison M. Dennis
出处
期刊:Nano Letters
[American Chemical Society]
日期:2021-03-23
卷期号:21 (7): 3271-3279
被引量:63
标识
DOI:10.1021/acs.nanolett.1c00600
摘要
This report of the reddest emitting indium phosphide quantum dots (InP QDs) to date demonstrates tunable, near-infrared (NIR) photoluminescence (PL) as well as PL multiplexing in the first optical tissue window while avoiding toxic constituents. This synthesis overcomes the InP "growth bottleneck" and extends the emission peak of InP QDs deeper into the first optical tissue window using an inverted QD heterostructure, specifically ZnSe/InP/ZnS core/shell/shell nanoparticles. The QDs exhibit InP shell thickness-dependent tunable emission with peaks ranging from 515-845 nm. The high absorptivity of InP yields effective photoexcitation of the QDs with UV, visible, and NIR wavelengths. These nanoparticles extend the range of tunable direct-bandgap emission from InP-based nanostructures, effectively overcoming a synthetic barrier that has prevented InP-based QDs from reaching their full potential as NIR imaging agents. Multiplexed lymph node imaging in a mouse model demonstrates the potential of the NIR-emitting InP particles for in vivo imaging.
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