Tunable NIR-II emitting silver chalcogenide quantum dots using thio/selenourea precursors: preparation of an MRI/NIR-II multimodal imaging agent

Aqueous-stable, Cd- and Pb-free colloidal quantum dots with fluorescence properties in the second near-infrared region (NIR-II, 1000-1400) are highly desirable for non-invasive deep-tissue optical imaging and biosensing. The low band-gap semiconductor, silver chalcogenide, offers a non-toxic and sta...

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Veröffentlicht in:Dalton transactions : an international journal of inorganic chemistry 2020-11, Vol.49 (43), p.15425-15432
Hauptverfasser: Bhardwaj, Karishma, Pradhan, Sajan, Basel, Siddhant, Clarke, Mitchell, Brito, Beatriz, Thapa, Surakcha, Roy, Pankaj, Borthakur, Sukanya, Saikia, Lakshi, Shankar, Amit, Stasiuk, Graeme J, Pariyar, Anand, Tamang, Sudarsan
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Sprache:eng
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Zusammenfassung:Aqueous-stable, Cd- and Pb-free colloidal quantum dots with fluorescence properties in the second near-infrared region (NIR-II, 1000-1400) are highly desirable for non-invasive deep-tissue optical imaging and biosensing. The low band-gap semiconductor, silver chalcogenide, offers a non-toxic and stable alternative to existing Pd, As, Hg and Cd-based NIR-II colloidal quantum dots (QDs). We report facile access to NIR-II emission windows with Ag 2 X (X = S, Se) QDs using easy-to-prepare thio/selenourea precursors and their analogues. The aqueous phase transfer of these QDs with a high conservation of fluorescence quantum yield (retention up to ∼90%) and colloidal stability is demonstrated. A bimodal NIR-II/MRI contrast agent with a tunable fluorescence and high T 1 relaxivity of 408 mM −1 s −1 per QD (size ∼ 2.2 nm) and 990 mM −1 s −1 per QD (size ∼ 4.2 nm) has been prepared by grafting 50 and 120 monoaqua Gd( iii ) complexes respectively to two differently sized Ag 2 S QDs. The size of the nanocrystals is crucial for tuning the Gd payload and the relaxivity. Precursor-controlled synthesis of silver chalcogenide quantum dots with tunable fluorescence in the second near-infrared window.
ISSN:1477-9226
1477-9234
DOI:10.1039/d0dt02974b