Please use this identifier to cite or link to this item: https://doi.org/10.1021/acsmaterialslett.1c00138
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dc.titleRevisiting Carbazole: Origin, Impurity, and Properties
dc.contributor.authorChen, Chengjian
dc.contributor.authorChong, Kok Chan
dc.contributor.authorPan, Yutong
dc.contributor.authorQi, Guobin
dc.contributor.authorXu, Shidang
dc.contributor.authorLiu, Bin
dc.date.accessioned2022-02-17T05:26:10Z
dc.date.available2022-02-17T05:26:10Z
dc.date.issued2021-06-21
dc.identifier.citationChen, Chengjian, Chong, Kok Chan, Pan, Yutong, Qi, Guobin, Xu, Shidang, Liu, Bin (2021-06-21). Revisiting Carbazole: Origin, Impurity, and Properties. ACS MATERIALS LETTERS 3 (7) : 1081-1087. ScholarBank@NUS Repository. https://doi.org/10.1021/acsmaterialslett.1c00138
dc.identifier.issn2639-4979,
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/215477
dc.description.abstractPhotoluminescence quantum yield (PLQY) is one of the most important characteristics for organic luminescent materials. However, when carbazole prepared from the lab was compared to that from a commercial source, a remarkable change of PLQY was observed to vary from 37.1% to 69.8%. Taking 9-(4-bromobenzyl)-9H-carbazole (CzBBr) as an example of carbazole derivatives, the PLQYs of CzBBr synthesized from different origins of carbazole were varied from 16.0% to 91.1%. Our studies demonstrated that efficient radiative transition pathways were activated for commercial carbazole based luminescence, leading to a large enhancement in PLQY with fluorescence (from 16.0% to 54.4%) and phosphorescence (from <1% to 36.7%) for CzBBr. These results suggest that the origin of carbazole plays a very important role in determining the optical properties of carbazole derivatives, alerting us to carefully revisit carbazole and its derivatives, especially those with record-high efficiency.
dc.description.urihttps://scholarbank.nus.edu.sg/handle/10635/215477
dc.language.isoen
dc.publisherAMER CHEMICAL SOC
dc.sourceElements
dc.subjectScience & Technology
dc.subjectTechnology
dc.subjectMaterials Science, Multidisciplinary
dc.subjectMaterials Science
dc.subjectTEMPERATURE PHOSPHORESCENCE
dc.subjectDELAYED FLUORESCENCE
dc.subjectCYCLIZATION
dc.subjectLUMINOGENS
dc.subjectARYLATION
dc.typeArticle
dc.date.updated2022-02-17T05:19:53Z
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1021/acsmaterialslett.1c00138
dc.description.sourcetitleACS MATERIALS LETTERS
dc.description.volume3
dc.description.issue7
dc.description.page1081-1087
dc.published.statePublished
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