Abstract
Removing long-chain ligands on the surface of perovskite nanocrystals (NCs) is a promising strategy to facilitate charge transport towards a high-performance perovskite light-emitting diode (PeLED). However, perovskite NCs, especially CsPbI 3 NCs, tend to decompose in the ligand removal procedure due to their poor stability of perovskite NCs and high polarity of solvents. Here, we report Sr 2+ -doped CsPbI 3 NCs that were synthesized by a modified hot injection method. These NCs show enhanced stability and near-unity photoluminescence quantum yield (PLQY, 99.8%). More importantly, the CsPbI 3 :Sr 2+ NCs still maintain a high PLQY (97.5%) after removing surface ligands by a polar solvent (ethyl acetate, EA). Furthermore, a mixture of EA and octane was used to prepare smooth and dense CsPbI 3 :Sr 2+ NC films with an exceedingly high PLQY of 73.2% and a high stability under ambient conditions. Finally, the red-emitting CsPbI 3 :1.8% Sr 2+ PeLEDs demonstrate a world-record peak external quantum efficiency (EQE) of 17.1%. Sr 2+ -doped CsPbI 3 NCs with near-unity photoluminescence quantum yield (PLQY, 99.8%) and enhanced stability were synthesized. By modifying the wetting behavior of NCs solution, uniform and smooth perovskite films were prepared, which shows the highest PLQY of 73.2%. Moreover, by employing the CsPbI 3 :1.8% Sr 2+ NC films as the emission layer, a red PeLED was fabricated with a new record peak EQE of 17.1%. • Sr 2+ -doped CsPbI 3 NCs with near-unity photoluminescence quantum yield and enhanced stability • The perovskite films were optimized by modifying the wetting behavior of NCs solution. • A CsPbI 3 : Sr 2+ NC films based PeLED was fabricated with a new record peak EQE of 17.1%.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.