| Literature DB >> 29870579 |
Yu Tong1,2, En-Ping Yao1,2, Aurora Manzi1,2, Eva Bladt3, Kun Wang2,4, Markus Döblinger5, Sara Bals3, Peter Müller-Buschbaum2,4, Alexander S Urban1,2, Lakshminarayana Polavarapu1,2, Jochen Feldmann1,2.
Abstract
Self-assembly of nanoscale building blocks into ordered nanoarchitectures has emerged as a simple and powerful approach for tailoring the nanoscale properties and the opportunities of using these properties for the development of novel optoelectronic nanodevices. Here, the one-pot synthesis of CsPbBr3 perovskite supercrystals (SCs) in a colloidal dispersion by ultrasonication is reported. The growth of the SCs occurs through the spontaneous self-assembly of individual nanocrystals (NCs), which form in highly concentrated solutions of precursor powders. The SCs retain the high photoluminescence (PL) efficiency of their NC subunits, however also exhibit a redshifted emission wavelength compared to that of the individual nanocubes due to interparticle electronic coupling. This redshift makes the SCs pure green emitters with PL maxima at ≈530-535 nm, while the individual nanocubes emit a cyan-green color (≈512 nm). The SCs can be used as an emissive layer in the fabrication of pure green light-emitting devices on rigid or flexible substrates. Moreover, the PL emission color is tunable across the visible range by employing a well-established halide ion exchange reaction on the obtained CsPbBr3 SCs. These results highlight the promise of perovskite SCs for light emitting applications, while providing insight into their collective optical properties.Entities:
Keywords: CsPbX3 perovskite; electronic coupling; green LEDs; supercrystals; superlattices
Year: 2018 PMID: 29870579 DOI: 10.1002/adma.201801117
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849