Comparing between steady-state excitonic transitions and ultrafast polaronic photoexcitations in layered perovskites: the role of electron–phonon interaction
We have studied four 2D layered perovskites, including OA2PbI4 (RP phase), ODAPbI4 and BDAPbI4 (DJ phase), (GA)MAPbI4 (ACI phase), where OA is [(CmH2m+1)NH3](m = 8), ODA is [NH3(CH2)mNH3](m = 8), BDA is [NH3(CH2)mNH3](m = 4), and GA is [C(NH2)3]; RP, DJ, and ACI means Ruddlesden–Popper, Dion–Jacobso...
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De Gruyter
2023-04-01
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Online Access: | https://doi.org/10.1515/nanoph-2023-0015 |
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author | Yan Pingyuan Li Tao Zhou Haoxiang Hu Shu Xiang Chenhong Zhang Yang Wang Chengqiang Wu Zihan Li Heng Zhao Haibin Sheng ChuanXiang |
author_facet | Yan Pingyuan Li Tao Zhou Haoxiang Hu Shu Xiang Chenhong Zhang Yang Wang Chengqiang Wu Zihan Li Heng Zhao Haibin Sheng ChuanXiang |
author_sort | Yan Pingyuan |
collection | DOAJ |
description | We have studied four 2D layered perovskites, including OA2PbI4 (RP phase), ODAPbI4 and BDAPbI4 (DJ phase), (GA)MAPbI4 (ACI phase), where OA is [(CmH2m+1)NH3](m = 8), ODA is [NH3(CH2)mNH3](m = 8), BDA is [NH3(CH2)mNH3](m = 4), and GA is [C(NH2)3]; RP, DJ, and ACI means Ruddlesden–Popper, Dion–Jacobson and alternating cations in the interlayer, respectively. The temperature dependence of absorption and photoluminescence (PL) spectra have been measured. From which the average phonon energy (electron-phonon interaction strength) is analyzed as around 34 (80), 47 (184), 50 (402), and 63 (758) with the unit of meV for OA2PbI4, ODAPbI4, BDAPbI4, and (GA)MAPbI4, respectively. Larger phonon energy indicates the involvement of more phonons in organic spacer layer, with the corresponding stronger electron-phonon interaction. Furthermore, ultrafast transient absorption spectroscopy proves that, when the excitation photon energy is serval hundred meV higher than bandgap, the excitons still are the major photoexcitations in OA2PbI4, but polarons are major one in ODAPbI4, BDAPbI4, and (GA)MAPbI4 films, no matter the excitonic transitions dominate the absorption at their band edges. This work proves the organic spacers can regulate electron–phonon interaction then optoelectronic properties in 2D perovskites profoundly, which have implications toward future rational design for relevant devices. |
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spelling | doaj.art-5eddc519310a464eb70dbe039a3813422023-05-31T06:55:50ZengDe GruyterNanophotonics2192-86062192-86142023-04-0112111965197710.1515/nanoph-2023-0015Comparing between steady-state excitonic transitions and ultrafast polaronic photoexcitations in layered perovskites: the role of electron–phonon interactionYan Pingyuan0Li Tao1Zhou Haoxiang2Hu Shu3Xiang Chenhong4Zhang Yang5Wang Chengqiang6Wu Zihan7Li Heng8Zhao Haibin9Sheng ChuanXiang10Department of Optical Science and Engineering, School of Information Science and Technology, Fudan University, Shanghai, 200433, ChinaDepartment of Optical Science and Engineering, School of Information Science and Technology, Fudan University, Shanghai, 200433, ChinaDepartment of Optical Science and Engineering, School of Information Science and Technology, Fudan University, Shanghai, 200433, ChinaSchool of Electronic and Optical Engineering, Nanjing University of Science and Technology, Nanjing, 210094, ChinaSchool of Electronic and Optical Engineering, Nanjing University of Science and Technology, Nanjing, 210094, ChinaSchool of Electronic and Optical Engineering, Nanjing University of Science and Technology, Nanjing, 210094, ChinaSchool of Electronic and Optical Engineering, Nanjing University of Science and Technology, Nanjing, 210094, ChinaSchool of Electronic and Optical Engineering, Nanjing University of Science and Technology, Nanjing, 210094, ChinaSchool of Electronic and Optical Engineering, Nanjing University of Science and Technology, Nanjing, 210094, ChinaDepartment of Optical Science and Engineering, School of Information Science and Technology, Fudan University, Shanghai, 200433, ChinaDepartment of Optical Science and Engineering, School of Information Science and Technology, Fudan University, Shanghai, 200433, ChinaWe have studied four 2D layered perovskites, including OA2PbI4 (RP phase), ODAPbI4 and BDAPbI4 (DJ phase), (GA)MAPbI4 (ACI phase), where OA is [(CmH2m+1)NH3](m = 8), ODA is [NH3(CH2)mNH3](m = 8), BDA is [NH3(CH2)mNH3](m = 4), and GA is [C(NH2)3]; RP, DJ, and ACI means Ruddlesden–Popper, Dion–Jacobson and alternating cations in the interlayer, respectively. The temperature dependence of absorption and photoluminescence (PL) spectra have been measured. From which the average phonon energy (electron-phonon interaction strength) is analyzed as around 34 (80), 47 (184), 50 (402), and 63 (758) with the unit of meV for OA2PbI4, ODAPbI4, BDAPbI4, and (GA)MAPbI4, respectively. Larger phonon energy indicates the involvement of more phonons in organic spacer layer, with the corresponding stronger electron-phonon interaction. Furthermore, ultrafast transient absorption spectroscopy proves that, when the excitation photon energy is serval hundred meV higher than bandgap, the excitons still are the major photoexcitations in OA2PbI4, but polarons are major one in ODAPbI4, BDAPbI4, and (GA)MAPbI4 films, no matter the excitonic transitions dominate the absorption at their band edges. This work proves the organic spacers can regulate electron–phonon interaction then optoelectronic properties in 2D perovskites profoundly, which have implications toward future rational design for relevant devices.https://doi.org/10.1515/nanoph-2023-00152d perovskiteelectron-phonon interactionexcitonic transitionsoptical propertiespolarons |
spellingShingle | Yan Pingyuan Li Tao Zhou Haoxiang Hu Shu Xiang Chenhong Zhang Yang Wang Chengqiang Wu Zihan Li Heng Zhao Haibin Sheng ChuanXiang Comparing between steady-state excitonic transitions and ultrafast polaronic photoexcitations in layered perovskites: the role of electron–phonon interaction Nanophotonics 2d perovskite electron-phonon interaction excitonic transitions optical properties polarons |
title | Comparing between steady-state excitonic transitions and ultrafast polaronic photoexcitations in layered perovskites: the role of electron–phonon interaction |
title_full | Comparing between steady-state excitonic transitions and ultrafast polaronic photoexcitations in layered perovskites: the role of electron–phonon interaction |
title_fullStr | Comparing between steady-state excitonic transitions and ultrafast polaronic photoexcitations in layered perovskites: the role of electron–phonon interaction |
title_full_unstemmed | Comparing between steady-state excitonic transitions and ultrafast polaronic photoexcitations in layered perovskites: the role of electron–phonon interaction |
title_short | Comparing between steady-state excitonic transitions and ultrafast polaronic photoexcitations in layered perovskites: the role of electron–phonon interaction |
title_sort | comparing between steady state excitonic transitions and ultrafast polaronic photoexcitations in layered perovskites the role of electron phonon interaction |
topic | 2d perovskite electron-phonon interaction excitonic transitions optical properties polarons |
url | https://doi.org/10.1515/nanoph-2023-0015 |
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