Abstract

AbstractFormamidinium iodide (FAI) based perovskite absorbers have been shown to be ideal candidates for highly efficient and operationally stable perovskite solar cells (PSC). A major challenge for formamidinium lead iodide (FAPbI3) is to suppress the phase transition from the photoactive black phase into yellow nonperovskite δ‐phase. Several approaches to stabilize the black phase have been developed for solution‐based perovskites, whereas so far, vacuum‐deposited FAPbI3 has rarely been reported. This study demonstrates the preparation of FAPbI3 by co‐evaporation and discusses the influence of the subjacent hole transporting layer (HTL) on its phase stability. By using FAI excess in the evaporation process in combination with phosphonic acids groups from the HTL, the black perovskite phase is stabilized at room temperature. Further addition of 32–59% methylammonium iodide (MAI) during the co‐evaporation process leads to good absorption properties and high PSC efficiencies of 20.4%. In addition, excellent stability is achieved for optimized MAI to FAI ratios, maintaining 100% of the initial PSC performance after 1000 h under constant operation. This highly stable perovskite composition enables the first monolithic fully textured perovskite/silicon tandem solar cells with co‐evaporated perovskite absorbers. Due to the conformally covered pyramid texture, these tandem cells show minimal reflection losses and reach an efficiency of 24.6%.

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.