Harvesting triplet excitons in lead-halide perovskites for room-temperature phosphorescence

Room-temperature phosphorescence (RTP) has a much longer lifetime than fluorescence as it involves triplet excitons. This extended lifetime enables the design of advanced optoelectronics and biological sensing technologies. Despite the omnipresence of triplet states, harnessing these triplet exciton...

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Main Authors: Hu, Hongwei, Zhao, Daming, Gao, Yang, Qiao, Xianfeng, Salim, Teddy, Chen, Bingbing, Chia, Elbert Ee Min, Grimsdale, Andrew C., Lam, Yeng Ming
Other Authors: School of Materials Science and Engineering
Format: Article
Language:English
Published: 2021
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Online Access:https://hdl.handle.net/10356/151310
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1513102021-07-06T02:46:29Z Harvesting triplet excitons in lead-halide perovskites for room-temperature phosphorescence Hu, Hongwei Zhao, Daming Gao, Yang Qiao, Xianfeng Salim, Teddy Chen, Bingbing Chia, Elbert Ee Min Grimsdale, Andrew C. Lam, Yeng Ming School of Materials Science and Engineering School of Physical and Mathematical Sciences Engineering::Materials Excitons Layers Room-temperature phosphorescence (RTP) has a much longer lifetime than fluorescence as it involves triplet excitons. This extended lifetime enables the design of advanced optoelectronics and biological sensing technologies. Despite the omnipresence of triplet states, harnessing these triplet excitons remains challenging for most organic materials because of forbidden transitions between singlet and triplet states. Here, we report novel organic–inorganic hybrid perovskites based on conjugated organic cations with low-lying triplet energy levels to extract triplet excitons from the inorganic component, thereby generating RTP with a long lifetime in the millisecond range. Dexter-type energy transfer was confirmed to occur in this type of hybrid perovskites with transfer efficiency of up to 80%. More impressively, multiple-colored phosphorescence was achieved by a facile design of the system using organic cations with different triplet exciton energies. These results are expected to greatly expand the prospects of hybrid perovskites with functional organic cations for versatile display applications. Ministry of Education (MOE) Nanyang Technological University H.H., and Y.M.L. acknowledge financial support from Institute for Sports Research, Nanyang Technological University. E.E.M.C. acknowledges support from the Singapore Ministry of Education AcRF Tier 2 (MOE2015-T2-2-065 and MOE2016-T2-1-054). We would like to acknowledge the Facility for Analysis, Characterization, Testing and Simulation (FACTS), Nanyang Technological University, Singapore, for use of their electron microscopy and XRD facilities. 2021-07-06T02:46:28Z 2021-07-06T02:46:28Z 2019 Journal Article Hu, H., Zhao, D., Gao, Y., Qiao, X., Salim, T., Chen, B., Chia, E. E. M., Grimsdale, A. C. & Lam, Y. M. (2019). Harvesting triplet excitons in lead-halide perovskites for room-temperature phosphorescence. Chemistry of Materials, 31(7), 2597-2602. https://dx.doi.org/10.1021/acs.chemmater.9b00315 0897-4756 0000-0001-8633-8771 0000-0003-2498-3024 0000-0001-9390-8074 https://hdl.handle.net/10356/151310 10.1021/acs.chemmater.9b00315 2-s2.0-85064264447 7 31 2597 2602 en MOE2015-T2-2-065 MOE2016-T2-1-054 Chemistry of Materials © 2019 American Chemical Society. All rights reserved.
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Materials
Excitons
Layers
spellingShingle Engineering::Materials
Excitons
Layers
Hu, Hongwei
Zhao, Daming
Gao, Yang
Qiao, Xianfeng
Salim, Teddy
Chen, Bingbing
Chia, Elbert Ee Min
Grimsdale, Andrew C.
Lam, Yeng Ming
Harvesting triplet excitons in lead-halide perovskites for room-temperature phosphorescence
description Room-temperature phosphorescence (RTP) has a much longer lifetime than fluorescence as it involves triplet excitons. This extended lifetime enables the design of advanced optoelectronics and biological sensing technologies. Despite the omnipresence of triplet states, harnessing these triplet excitons remains challenging for most organic materials because of forbidden transitions between singlet and triplet states. Here, we report novel organic–inorganic hybrid perovskites based on conjugated organic cations with low-lying triplet energy levels to extract triplet excitons from the inorganic component, thereby generating RTP with a long lifetime in the millisecond range. Dexter-type energy transfer was confirmed to occur in this type of hybrid perovskites with transfer efficiency of up to 80%. More impressively, multiple-colored phosphorescence was achieved by a facile design of the system using organic cations with different triplet exciton energies. These results are expected to greatly expand the prospects of hybrid perovskites with functional organic cations for versatile display applications.
author2 School of Materials Science and Engineering
author_facet School of Materials Science and Engineering
Hu, Hongwei
Zhao, Daming
Gao, Yang
Qiao, Xianfeng
Salim, Teddy
Chen, Bingbing
Chia, Elbert Ee Min
Grimsdale, Andrew C.
Lam, Yeng Ming
format Article
author Hu, Hongwei
Zhao, Daming
Gao, Yang
Qiao, Xianfeng
Salim, Teddy
Chen, Bingbing
Chia, Elbert Ee Min
Grimsdale, Andrew C.
Lam, Yeng Ming
author_sort Hu, Hongwei
title Harvesting triplet excitons in lead-halide perovskites for room-temperature phosphorescence
title_short Harvesting triplet excitons in lead-halide perovskites for room-temperature phosphorescence
title_full Harvesting triplet excitons in lead-halide perovskites for room-temperature phosphorescence
title_fullStr Harvesting triplet excitons in lead-halide perovskites for room-temperature phosphorescence
title_full_unstemmed Harvesting triplet excitons in lead-halide perovskites for room-temperature phosphorescence
title_sort harvesting triplet excitons in lead-halide perovskites for room-temperature phosphorescence
publishDate 2021
url https://hdl.handle.net/10356/151310
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