| Literature DB >> 28834091 |
Yu Tong1,2, Bernhard J Bohn1,2, Eva Bladt3, Kun Wang4, Peter Müller-Buschbaum4, Sara Bals3, Alexander S Urban1,2, Lakshminarayana Polavarapu1,2, Jochen Feldmann1,2.
Abstract
The colloidal synthesis and assembly of semiconductor nanowires continues to attract a great deal of interest. Herein, we describe the single-step ligand-mediated synthesis of single-crystalline CsPbBr3 perovskite nanowires (NWs) directly from the precursor powders. Studies of the reaction process and the morphological evolution revealed that the initially formed CsPbBr3 nanocubes are transformed into NWs through an oriented-attachment mechanism. The optical properties of the NWs can be tuned across the entire visible range by varying the halide (Cl, Br, and I) composition through subsequent halide ion exchange. Single-particle studies showed that these NWs exhibit strongly polarized emission with a polarization anisotropy of 0.36. More importantly, the NWs can self-assemble in a quasi-oriented fashion at an air/liquid interface. This process should also be easily applicable to perovskite nanocrystals of different morphologies for their integration into nanoscale optoelectronic devices.Entities:
Keywords: oriented attachment; perovskite nanowires; polarized emission; self-assembly; ultrasonication
Year: 2017 PMID: 28834091 DOI: 10.1002/anie.201707224
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336