Abstract

AbstractInorganic 2D layered CsPbI3 is awaiting to overcome the phase instability of traditional 3D components. However, the most reported Ruddlesden–Popper (RP) phase 2D CsPbI3 leads to larger interlayer distance and weaker interlayer coupling since the existence of the van der Waals gap, which deteriorates the performance of the device and makes the improvement of stability unsatisfactory. Herein, this work resorts ethylenediamine cations (EDA2+) to construct a series of Dion–Jacobson (DJ) phase 2D CsPbI3 as (EDA)Csn−1PbnI3n+1 with van der Waals gap eliminated. Combining simulation calculations and experiments, it is found that the (EDA)Csn−1PbnI3n+1 has enhanced intermolecular forces to overcome the problem of insufficient crystallization power caused by large steric hindrance in the film assembly process compared to phenethylammonium‐based RP phase analogues. In addition, profit from the reduced interlayer distance and stronger coupling, the rigidity of the structure is increased, and the annoying non‐radiative recombination caused by structural fluctuations is alleviated. As a result, the 2D layered DJ phase CsPbI3‐based solar cells deliver eminent performance than RP phase analogues, especially the 2D (EDA)(Cs)4Pb5I16 (n = 5) device exhibits a record PCE of 10.43% in this work, and significantly enhanced stability.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

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.