Thermally activated delayed fluorescence (TADF) and room temperature phosphorescence (RTP) are most promising processes for harvesting triplet excitons in organic light-emitting diodes. In this work, the effect of the linkage between the carbazole (Cz) donor (D) and the naphthalenediimide (NDI) acceptor (A) on the TADF and RTP propensities is elucidated using density functional theory computations employing D-A, D-A-D, D-π-A, and D-π-A-π-D structural designs. The effects of the dihedral angle between the donor and acceptor units on the energy difference between the singlet and triplet excited states (Δ), the spin-orbit coupling (SOC) constants, and radiative (), intersystem crossing () and reverse intersystem crossing () rates are unravelled. The molecules possessing a direct linkage between Cz and NDI exhibit large Δ values due to substantial overlap between the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO). However, the insertion of a phenyl spacer between the Cz and NDI units led to disjoint HOMO and LUMO and consequently resulted in a small Δ. Furthermore, the presence of two donors with and without a phenyl spacer on NDI resulted in a high-lying triplet state (T) that is energetically lower than the lowest singlet excited state (S), hence providing additional channels to the TADF and RTP processes. Also, the orientation of Cz and NDI in the -positions of the phenyl unit resulted in a T state with dominant LE character which led to moderate spin-orbit coupling constants and highest rates compared to the analogous - and -linked derivatives. Thus, the -derivatives possessed small Δ, charge transfer dominated S, joint holes and electrons for the T state, characteristic of local excitation, high SOC, and promising rISC and rates. Overall, the phenyl linked derivatives possess TADF characteristics, while the directly linked analogues show RTP propensity.
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http://dx.doi.org/10.1039/d4cp02636e | DOI Listing |
Angew Chem Int Ed Engl
December 2024
Guangdong Basic Research Center of Excellence for Energy and Information Polymer Materials, State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Wushan Road 381, Tianhe District, Guangzhou, 510640, Guangdong Province, P. R. China.
The exploration of circularly polarized luminescence is important for advancing display and lighting technologies. Herein, by utilizing isomeric molecular engineering, a novel series of chiral molecules are designed to exploit both thermally activated delayed fluorescence (TADF) and room-temperature phosphorescence (RTP) mechanisms for efficient luminescence. The cooperation of a small singlet-triplet energy gap, moderate spin-orbital coupling (SOC), and large oscillator strength enables efficient TADF emission, with photoluminescence quantum yields exceeding 90 %.
View Article and Find Full Text PDFACS Mater Au
November 2024
Kaunas University of Technology, Baršausko 59, Kaunas 51423, Lithuania.
To enhance the usually low-charge carrier mobilities of highly twisted donor-acceptor-type compounds that exhibit thermally activated delayed fluorescence, we designed a rodlike acceptor benzodioxinoquinoxaline. This acceptor and two donor-acceptor-donor derivatives were synthesized via microwave Buchwald-Hartwig cross-coupling reactions with yields of up to 91%. The compounds exhibit three different types of photoluminescence, which is well-explained by quantum chemical calculations.
View Article and Find Full Text PDFPhys Chem Chem Phys
January 2025
Organic Materials Laboratory, Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee - 247667, India.
RSC Adv
October 2024
Guangzhou Institute of Chemistry, Chinese Academy of Sciences Guangzhou 510650 China
This study reports the synthesis and photophysical analysis of three isomeric compounds, namely 3Fmo, 3Fmm, and 3Fmp, which were engineered using carbazole as the electron donor, phthalimide as the electron acceptor, and a benzene ring as the bridging moiety. Among these, 3Fmm was distinguished by its ability to exhibit immediate room-temperature white phosphorescence following the cessation of UV illumination, whereas 3Fmo and 3Fmp demonstrated TADF properties. Crystallographic analysis revealed unique intermolecular π-π stacking interactions within 3Fmm, absent in the other two isomers.
View Article and Find Full Text PDFACS Appl Mater Interfaces
October 2024
Key Laboratory for Advanced Materials and Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry Institute of Fine Chemicals, School of Chemistry and Molecular Engineering, East China University of Science & Technology, Meilong Road 130, Shanghai 200237, China.
Organic emitters with both thermally activated delayed fluorescence (TADF) and room-temperature phosphorescence (RTP) have attracted widespread interest for their intriguing luminescent properties. Herein, a series of triphenylamine-substituted isoquinoline derivatives possessing monomeric TADF and aggregated RTP properties are reported. As the molecules exhibited various forms of π-π and charge transfer (CT) stacking with different intensities, inter/intramolecular CT can be meticulously modulated to achieve tunable TADF-RTP.
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