The incorporation of chloride (Cl) into methylammonium lead iodide (MAPbI) perovskites has attracted much attention because of the significantly improved performance of the MAPbI-based optoelectronic devices with a negligible small amount of Cl incorporation. It is expected that the Cl incorporation in 2D perovskites with layered nature would be much more efficient and thus can greatly alter the morphology, optical properties, phase transition, and charge transport; however, studies on those aspects in 2D perovskites remain elusive up to date. Here, a one-pot solution method to synthesize the Cl-doped lead-free 2D perovskite (BA)SnI with various Cl incorporation concentrations is reported and how the Cl incorporation affects the morphology change, photoluminescence, phase transition, and charge transport is investigated. The Cl element is successfully incorporated into the crystal lattice in the solution-processed perovskite materials, confirmed by X-ray photoelectron spectroscopy and energy dispersive X-ray spectroscopy measurements. The temperature-dependent photoluminescence studies indicate that the emission properties and phase transition behavior in (BA)SnI Cl can be tuned by varying the Cl incorporation concentration. Electrical measurement suggests that the charge transport behavior can also be greatly altered by the Cl doping concentration and the electrical conductivity can be significantly improved under a higher Cl incorporation concentration.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402407PMC
http://dx.doi.org/10.1002/advs.201802019DOI Listing

Publication Analysis

Top Keywords

phase transition
16
charge transport
16
transition charge
12
incorporation
8
lead-free perovskite
8
perovskite basni
8
photoluminescence phase
8
properties phase
8
incorporation concentration
8
concentration electrical
8

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!