{"title":"Phase-Engineered α/δ-FAPbI3 Heterojunctions for Valleytronics, Band Alignment, and Stability","authors":"Lingkun Kong, , , Yulong Tang, , , Mengjia Feng, , , Wei Wang, , , Chenyang Zha, , and , Linghai Zhang*, ","doi":"10.1021/acs.jpcc.5c02507","DOIUrl":null,"url":null,"abstract":"<p >Cubic FAPbI<sub>3</sub> perovskite exhibits exceptional optoelectronic properties, yet the α-to-δ phase transition mechanism remains incompletely understood. In this work, we construct α-FAPbI<sub>3</sub> (111)/δ-FAPbI<sub>3</sub> (0001) heterojunctions and employ density functional theory to investigate the impact of δ-phase formation on thermodynamic stability, along with electronic and optical properties. Our results demonstrate that a higher δ-phase content significantly enhances stability, with the α-to-δ phase transition occurring at a low energy barrier. Tuning the α/δ phase ratio induces a transition from type-I to type-II band alignment. Moreover, the hexagonal structures of α/δ-FAPbI<sub>3</sub> heterojunctions exhibit spin-valley coupling, indicating their potential as valleytronic materials─an effect rarely reported in halide perovskites. This allows for valley-selective excitation of spin-polarized carriers using left- or right-handed circularly polarized light. Additionally, the difference in work function between the two phases drives the spontaneous flow of electrons from α-FAPbI<sub>3</sub> to δ-FAPbI<sub>3</sub> and holes in the opposite direction. Careful design of the α/δ phase ratio allows for effective tuning of the optical properties of FAPbI<sub>3</sub>. These findings highlight the crucial role of α/δ phase engineering in tailoring the electronic and optical properties of FAPbI<sub>3</sub>, offering a theoretical foundation for the design of high-performance perovskite-based optoelectronic devices.</p>","PeriodicalId":61,"journal":{"name":"The Journal of Physical Chemistry C","volume":"129 38","pages":"17185–17194"},"PeriodicalIF":3.2000,"publicationDate":"2025-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry C","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jpcc.5c02507","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Cubic FAPbI3 perovskite exhibits exceptional optoelectronic properties, yet the α-to-δ phase transition mechanism remains incompletely understood. In this work, we construct α-FAPbI3 (111)/δ-FAPbI3 (0001) heterojunctions and employ density functional theory to investigate the impact of δ-phase formation on thermodynamic stability, along with electronic and optical properties. Our results demonstrate that a higher δ-phase content significantly enhances stability, with the α-to-δ phase transition occurring at a low energy barrier. Tuning the α/δ phase ratio induces a transition from type-I to type-II band alignment. Moreover, the hexagonal structures of α/δ-FAPbI3 heterojunctions exhibit spin-valley coupling, indicating their potential as valleytronic materials─an effect rarely reported in halide perovskites. This allows for valley-selective excitation of spin-polarized carriers using left- or right-handed circularly polarized light. Additionally, the difference in work function between the two phases drives the spontaneous flow of electrons from α-FAPbI3 to δ-FAPbI3 and holes in the opposite direction. Careful design of the α/δ phase ratio allows for effective tuning of the optical properties of FAPbI3. These findings highlight the crucial role of α/δ phase engineering in tailoring the electronic and optical properties of FAPbI3, offering a theoretical foundation for the design of high-performance perovskite-based optoelectronic devices.
期刊介绍:
The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.