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Dynamic Emission Tuning of X‐ray Radioluminescent Crystalline Colloidal Arrays: Coupling the Optical Stop Band with Sequential Förster Resonance Energy Transfers
Author(s) -
Burdette Mary K.,
Bandera Yuriy P.,
Gray Gary M.,
Foulger Stephen H.
Publication year - 2019
Publication title -
advanced optical materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.89
H-Index - 91
ISSN - 2195-1071
DOI - 10.1002/adom.201801142
Subject(s) - radioluminescence , materials science , förster resonance energy transfer , nanoparticle , optoelectronics , phosphorescence , luminescence , acceptor , scattering , resonance (particle physics) , exciton , nanotechnology , optics , fluorescence , atomic physics , physics , detector , condensed matter physics , scintillation , quantum mechanics
Abstract X‐ray radiation exhibits diminished scattering and a greater penetration depth in tissue relative to the visible spectrum and has spawned new medical imaging techniques that exploit X‐ray luminescence of nanoparticles. The majority of the nanoparticles finding applications in this field incorporate metals with high atomic numbers and pose potential toxicity effects. Here, a general strategy for the preparation of a fully organic X‐ray radioluminescent colloidal platform that can be tailored to emit anywhere in the visible spectrum through a judicious choice in donor/acceptor pairing and multiple sequential Förster resonance energy transfers (FRETs) is presented. This is demonstrated with three different types of ≈100 nm particles that are doped with anthracene as the scintillating molecule to “pump” subsequent FRET dye pairs that result in emissions from ≈400 nm out past 700 nm. The particles can be self‐assembled in crystalline colloidal arrays, and the radioluminescence of the particles can be dynamically tuned by coupling the observed rejection wavelength with the dyes' emission.