Nicholas P. Sloane, Christopher G. Bailey, Jared H. Cole, Timothy W. Schmidt, Dane R. McCamey, Mykhailo V. Klymenko
{"title":"Electronic Structure at the Perovskite/Rubrene Interface: The Effect of Surface Termination","authors":"Nicholas P. Sloane, Christopher G. Bailey, Jared H. Cole, Timothy W. Schmidt, Dane R. McCamey, Mykhailo V. Klymenko","doi":"10.1021/acs.jpcc.4c07074","DOIUrl":null,"url":null,"abstract":"Perovskite films have rapidly emerged as leading active materials in optoelectronic devices due to their strong optical absorption, high carrier mobility, and ease of fabrication. While proving to be promising materials for solar cells and light-emitting diodes, another application of perovskites, which makes effective use of their unique properties, is sensitization for photon upconversion. Consisting of a bulk perovskite sensitizer alongside an adjacent organic semiconductor film, the upconverting system can absorb multiple low-energy photons to emit high-energy photons. In this work, density functional theory, in conjunction with GW theory, is utilized to investigate the electronic structure at the MAPbI<sub>3</sub>/rubrene interface for different surface terminations of MAPbI<sub>3</sub>. From this investigation, we reveal that the surface termination of the perovskite layer greatly affects the charge density at the interface and within the rubrene layer, driven by the formation of interfacial dipole layers. The formation of a strong interfacial dipole for the lead-iodide-terminated perovskite alters the band alignment of the heterojunction and is expected to facilitate more efficient hole transfer, which should enhance triplet generation in rubrene through sequential charge transfer from the perovskite layer. The formation of this dipole layer is explained by the slight ionization of rubrene molecules due to the passivation of surface states and orbital hybridization. For the perovskite surface terminated with the methylammonium iodide layer, the highest occupied molecular orbital of the adjacent rubrene layer lies deep within the perovskite band gap. This termination type is further characterized by a lower density of states near the band edges and lower electron density, thereby acting as a spacer, which is anticipated to decrease the probability of charge transfer across the interface. Thus, based on our results, PbI<sub>2</sub>-terminated perovskite surfaces are predicted to be favorable for applications where hole transfer to a rubrene layer is ideal, highlighting the significance of surface termination not only for upconverting systems but for all systems where the electronic environment at the interface is crucial to performance.","PeriodicalId":61,"journal":{"name":"The Journal of Physical Chemistry C","volume":"201 1","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2024-12-16","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://doi.org/10.1021/acs.jpcc.4c07074","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
Perovskite films have rapidly emerged as leading active materials in optoelectronic devices due to their strong optical absorption, high carrier mobility, and ease of fabrication. While proving to be promising materials for solar cells and light-emitting diodes, another application of perovskites, which makes effective use of their unique properties, is sensitization for photon upconversion. Consisting of a bulk perovskite sensitizer alongside an adjacent organic semiconductor film, the upconverting system can absorb multiple low-energy photons to emit high-energy photons. In this work, density functional theory, in conjunction with GW theory, is utilized to investigate the electronic structure at the MAPbI3/rubrene interface for different surface terminations of MAPbI3. From this investigation, we reveal that the surface termination of the perovskite layer greatly affects the charge density at the interface and within the rubrene layer, driven by the formation of interfacial dipole layers. The formation of a strong interfacial dipole for the lead-iodide-terminated perovskite alters the band alignment of the heterojunction and is expected to facilitate more efficient hole transfer, which should enhance triplet generation in rubrene through sequential charge transfer from the perovskite layer. The formation of this dipole layer is explained by the slight ionization of rubrene molecules due to the passivation of surface states and orbital hybridization. For the perovskite surface terminated with the methylammonium iodide layer, the highest occupied molecular orbital of the adjacent rubrene layer lies deep within the perovskite band gap. This termination type is further characterized by a lower density of states near the band edges and lower electron density, thereby acting as a spacer, which is anticipated to decrease the probability of charge transfer across the interface. Thus, based on our results, PbI2-terminated perovskite surfaces are predicted to be favorable for applications where hole transfer to a rubrene layer is ideal, highlighting the significance of surface termination not only for upconverting systems but for all systems where the electronic environment at the interface is crucial to performance.
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.