RESUMO
The metal salts of fatty acid (M-FA) are the most widely used metal precursors to colloidal semiconductor nanocrystals (NCs). They play a key role in controlling the composition, shape, and size of semiconductor NCs, and their purity is essential for attaining impeccable batch-to-batch reproducibility in the optical and electrical properties of the NCs. Herein, we report a novel, one-pot synthesis of a library of highly pure M-FAs at near-quantitative yields (up to 91%) using 1,8-diazabicyclo[5.4.0]undec-7-ene or the related nonionic/noncoordinating base as an inexpensive and ecofriendly catalyst in a green solvent medium. The method is highly general and scalable with vast academic and industrial potential. As a practical application, we also demonstrate the use of these high-quality M-FAs in the synthesis of the spectrum of colloidal semiconductor NCs (III-V, II-VI, IV-VI, I-VI, I-III-VI, and perovskite) having absorption/emission in visible to the near-infrared region.
RESUMO
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 Ag2X (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 â¼90%) and colloidal stability is demonstrated. A bimodal NIR-II/MRI contrast agent with a tunable fluorescence and high T1 relaxivity of 408 mM-1 s-1 per QD (size â¼ 2.2 nm) and 990 mM-1 s-1 per QD (size â¼ 4.2 nm) has been prepared by grafting 50 and 120 monoaqua Gd(iii) complexes respectively to two differently sized Ag2S QDs. The size of the nanocrystals is crucial for tuning the Gd payload and the relaxivity.
RESUMO
We report unprecedented phase stability of cubic CsPbBr3 quantum dots in ambient air obtained by using Br2 as halide precursor. Mechanistic investigation reveals the decisive role of temperature-controlled in situ generated, oleylammonium halide species from molecular halogen and amine for the long term stability and emission tunability of CsPbX3 (X = Br, I) nanocrystals.