Insight into the mechanism and outcoupling enhancement of excimer-associated white light generation. Issue 6 (22nd February 2016)
- Record Type:
- Journal Article
- Title:
- Insight into the mechanism and outcoupling enhancement of excimer-associated white light generation. Issue 6 (22nd February 2016)
- Main Title:
- Insight into the mechanism and outcoupling enhancement of excimer-associated white light generation
- Authors:
- Chen, Ying-Hsiao
Tang, Kuo-Chun
Chen, Yi-Ting
Shen, Jiun-Yi
Wu, Yu-Sin
Liu, Shih-Hung
Lee, Chun-Shu
Chen, Chang-Hsuan
Lai, Tzu-Yu
Tung, Shih-Huang
Jeng, Ru-Jong
Hung, Wen-Yi
Jiao, Min
Wu, Chung-Chih
Chou, Pi-Tai - Abstract:
- Abstract : Fundamental insight into excimer formation ofCz 9 PhAn, achieving a single-component, high-performance WOLED. Abstract : Fundamental insight into excimer formation has been gained by using 9, 10-bis[4-(9-carbazolyl)phenyl]anthracene] (Cz 9 PhAn ) as a probe.Cz 9 PhAn exhibits a highly emissive blue fluorescence in solution and is found to emit a panchromatic white light spectrum (400–750 nm) in film, powder and single crystal, in which an additional excimer band appears at ∼550 nm. Detailed structural analyses, emission relaxation dynamics and a theoretical approach conclude the formation of an anthracene*/phenyl ring excimer through an overlap between π* (anthracene) and π (phenyl ring) orbitals in a face-to-edge stacking orientation. The rate of excimer formation is determined to be 2.2 × 10 9 s −1 at room temperature, which requires coupling with lattice motion with an activation energy of 0.44 kcal mol −1 . ExploitingCz 9 PhAn as a single emitter, a fluorescent white organic light emitting diode (WOLED) is fabricated with a maximum external quantum efficiency ( η ext ) of 3.6% at 1000 cd m −2 (4.2 V) and Commission Internationale de L'Eclairage (CIE) coordinates of (0.30, 0.33). The white-lightCz 9 PhAn reveals a preferred orientation of the transition dipole moment in the emitting layer to enhance light outcoupling. This non-doped, single component (Cz 9 PhAn ) WOLED greatly reduces the complexity of the fabrication process, rendering a green andAbstract : Fundamental insight into excimer formation ofCz 9 PhAn, achieving a single-component, high-performance WOLED. Abstract : Fundamental insight into excimer formation has been gained by using 9, 10-bis[4-(9-carbazolyl)phenyl]anthracene] (Cz 9 PhAn ) as a probe.Cz 9 PhAn exhibits a highly emissive blue fluorescence in solution and is found to emit a panchromatic white light spectrum (400–750 nm) in film, powder and single crystal, in which an additional excimer band appears at ∼550 nm. Detailed structural analyses, emission relaxation dynamics and a theoretical approach conclude the formation of an anthracene*/phenyl ring excimer through an overlap between π* (anthracene) and π (phenyl ring) orbitals in a face-to-edge stacking orientation. The rate of excimer formation is determined to be 2.2 × 10 9 s −1 at room temperature, which requires coupling with lattice motion with an activation energy of 0.44 kcal mol −1 . ExploitingCz 9 PhAn as a single emitter, a fluorescent white organic light emitting diode (WOLED) is fabricated with a maximum external quantum efficiency ( η ext ) of 3.6% at 1000 cd m −2 (4.2 V) and Commission Internationale de L'Eclairage (CIE) coordinates of (0.30, 0.33). The white-lightCz 9 PhAn reveals a preferred orientation of the transition dipole moment in the emitting layer to enhance light outcoupling. This non-doped, single component (Cz 9 PhAn ) WOLED greatly reduces the complexity of the fabrication process, rendering a green and cost-effective alternative among the contemporary display/lighting technologies. … (more)
- Is Part Of:
- Chemical science. Volume 7:Issue 6(2016:Jun.)
- Journal:
- Chemical science
- Issue:
- Volume 7:Issue 6(2016:Jun.)
- Issue Display:
- Volume 7, Issue 6 (2016)
- Year:
- 2016
- Volume:
- 7
- Issue:
- 6
- Issue Sort Value:
- 2016-0007-0006-0000
- Page Start:
- 3556
- Page End:
- 3563
- Publication Date:
- 2016-02-22
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/SC ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5sc04902d ↗
- Languages:
- English
- ISSNs:
- 2041-6520
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3151.490000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 7584.xml