Cited by 314Organic Light-Emitting Diodes ResearchLuminescence and Fluorescent MaterialsLuminescence Properties of Advanced Materials

The DOI matches its Crossref record; 62 of the 62 references it cites were found in a registry or an index.

Recent Progress of Highly Efficient Red and Near‐Infrared Thermally Activated Delayed Fluorescent Emitters

Kim, Ji Han, Yun, Ju Hui, Lee, Jun Yeob·2018·Advanced Optical Materials

DOI 10.1002/adom.201800255

Open this paper in CoChat — free account

Abstract

Organic emitters have been widely developed since the demonstration of high efficiency in pure organic emitters represented by thermally activated delayed fluorescent (TADF) emitters. Pure organic‐based TADF emitters are found to harvest all singlet and triplet excitons for radiative transition processes, like phosphorescent emitters that utilize all generated excitons for light emission by strong spin–orbit coupling. Red, green, and blue organic emitters are investigated, but major interest is focused on green and blue organic emitters. However, recent studies are being directed to red and even near‐infrared emitters because of their wide applications in bioimaging, sensors, telecommunications, and night vision. Although the external quantum efficiency of the red and near‐infrared TADF organic light‐emitting diodes (OLEDs) is low, the external quantum efficiency of red OLEDs has been advanced to close to 30% and that of near‐infrared OLEDs to the 10% level. Therefore, more attention is being paid to red and near‐infrared TADF emitters. In this work, recent progress of the red and near‐infrared TADF emitters is reviewed to understand the molecular design principle and the molecular structure–photophysical characteristics and molecular structure–device performance relationships. In addition, future prospect of the red and near‐infrared TADF emitters is proposed.

Integrity signals

Registry

Crossref · 10.1002/adom.201800255

Cites

62 of 62 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Highly efficient organic light-emitting diodes from delayed fluorescence
Uoyama, H., Goushi, K., Shizu, K., Nomura, H., & Adachi, C. (2012) · Nature · doi:10.1038/nature11687 · Cited by 8,219
Very high-efficiency green organic light-emitting devices based on electrophosphorescence
Baldo, M. A., Lamansky, S., Burrows, P. E., Thompson, M. E., & Forrest, S. R. (1999) · Applied Physics Letters · doi:10.1063/1.124258 · Cited by 2,868
Efficient blue organic light-emitting diodes employing thermally activated delayed fluorescence
Zhang, Q., Li, B., Huang, S., Nomura, H., Tanaka, H., & Adachi, C. (2014) · Nature Photonics · doi:10.1038/nphoton.2014.12 · Cited by 2,443
Recent advances in organic thermally activated delayed fluorescence materials
Yang, Z., Mao, Z., Xie, Z., Zhang, Y., Liu, S., Zhao, J., Xu, J., Chi, Z., & Aldred, M. P. (2017) · Chemical Society Reviews · doi:10.1039/c6cs00368k · Cited by 2,395
Thermally Activated Delayed Fluorescence Materials Towards the Breakthrough of Organoelectronics
Tao, Y., Yuan, K., Chen, T., Xu, P., Li, H., Chen, R., Zheng, C., Zhang, L., & Huang, W. (2014) · Advanced Materials · doi:10.1002/adma.201402532 · Cited by 2,011
Spin—Orbit Coupling and the Radiationless Processes in Nitrogen Heterocyclics
El‐Sayed, M. A. (1963) · The Journal of Chemical Physics · doi:10.1063/1.1733610 · Cited by 1,544
Highly efficient blue electroluminescence based on thermally activated delayed fluorescence
Hirata, S., Sakai, Y., Masui, K., Tanaka, H., Lee, S. Y., Nomura, H., Nakamura, N., Yasumatsu, M., Nakanotani, H., Zhang, Q., et al. (2014) · Nature Materials · doi:10.1038/nmat4154 · Cited by 1,328
Efficient up-conversion of triplet excitons into a singlet state and its application for organic light emitting diodes
Endo, A., Sato, K., Yoshimura, K., Kai, T., Kawada, A., Miyazaki, H., & Adachi, C. (2011) · Applied Physics Letters · doi:10.1063/1.3558906 · Cited by 1,213
Molecular Design Strategy of Organic Thermally Activated Delayed Fluorescence Emitters
Im, Y., Kim, M., Cho, Y. J., Seo, J., Yook, K. S., & Lee, J. Y. (2017) · Chemistry of Materials · doi:10.1021/acs.chemmater.6b05324 · Cited by 1,061
Self-citation
Anthraquinone-Based Intramolecular Charge-Transfer Compounds: Computational Molecular Design, Thermally Activated Delayed Fluorescence, and Highly Efficient Red Electroluminescence
Zhang, Q., Kuwabara, H., Potscavage, W. J., Huang, S., Hatae, Y., Shibata, T., & Adachi, C. (2014) · Journal of the American Chemical Society · doi:10.1021/ja510144h · Cited by 993

Flagged first, then by citations

Show all 62 references

Sorted by citations

Items 201–300 of 314

Near‐Infrared Electroluminescence beyond 800 nm with High Efficiency and Radiance from Anthracene Cored Emitters
Yu, Y., Hu, Y., Yang, S., Luo, W. D., Yuan, Y., Peng, C., Liu, J., Khan, A., Jiang, Z., & Liao, L. (2020) · Angewandte Chemie · doi:10.1002/ange.202006197 · Cited by 12
Computational descriptor analysis on excited state behaviours of a series of TADF and non-TADF compounds
Ulukan, P., Bas, E. E., Ozek, R. B., Kaynak, C. D., Monari, A., Avi̇yente, V., & Çatak, Ş. (2022) · Physical Chemistry Chemical Physics · doi:10.1039/d2cp01323a · Cited by 13
Computational design of efficient near-infrared TADF emitters with hot-exciton characteristics
Jacob, J. M., Samanta, P. K., & Ravva, M. K. (2023) · New Journal of Chemistry · doi:10.1039/d3nj01955a · Cited by 12
A theoretical perspective of the relationship between the structures and luminescence properties of red thermally activated delayed fluorescence molecules
Liu, H., Zhang, K., Zou, H., Mu, Q., Wang, X., Song, Y., Lin, L., Wang, C., & Fan, J. (2022) · Physical Chemistry Chemical Physics · doi:10.1039/d2cp01574a · Cited by 12
Oxygen sensing and OLED applications of di- tert -butyl-dimethylacridinyl disubstituted oxygafluorene exhibiting long-lived deep-blue delayed fluorescence
Gudeika, D., Bezvikonnyi, O., Volyniuk, D. Y., Skuodis, E., Lee, P.-H., Chen, C., Ding, W., Lee, J., Chiu, T., & Gražulevičius, J. V. (2020) · Journal of Materials Chemistry C · doi:10.1039/d0tc01648a · Cited by 12
Self-citation
Near-Infrared Conjugated Polymers Containing Thermally Activated Delayed Fluorescence Units Enable Enhanced Photothermal Therapy
Xu, Y., Chen, B., Su, D., Li, J., Qi, Q., Hu, Y., Wang, Q., Xia, F., Lou, X., Zhao, Z., et al. (2023) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.3c13821 · Cited by 11
Efficient red thermally activated delayed fluorescence emitters achieved through precise control of excited state energy levels
Zhang, B., Liu, S., Pei, J., Luo, M., Chen, Y., Jia, Q., Wu, Z., & Wang, D. (2024) · Chemical Science · doi:10.1039/d4sc00535j · Cited by 11
Constructing host-σ-guest structures to optimize the efficiency of non-doped solution-processed OLEDs
Liu, D., Zhang, M., Chen, H., Ma, D., Tian, W., Sun, K., Jiang, W., & Sun, Y. (2020) · Journal of Materials Chemistry C · doi:10.1039/d0tc04959j · Cited by 11
Efficient orange-red thermally activated delayed fluorescence material containing a cyano group
Huang, F.-X., Li, H., Xie, F., Zeng, X., Li, Y., Hu, Y., Tang, J., & Zhao, X. (2021) · Dyes and Pigments · doi:10.1016/j.dyepig.2021.109731 · Cited by 11
Efficient yellow and red thermally activated delayed fluorescence materials based on a quinoxaline-derived electron-acceptor
Ji, S.-C., Jiang, S., Zhao, T., Meng, L., Chen, X., & Lu, C. (2022) · New Journal of Chemistry · doi:10.1039/d2nj01072k · Cited by 11
Rational designs of structurally similar TADF and HLCT emitters with benzo- or naphtho-carbazole units as electron donors
Li, J., Li, T., Zhang, M., Guo, D., & Zhang, H. (2022) · Physical Chemistry Chemical Physics · doi:10.1039/d2cp03500f · Cited by 11
Equilibrating the key parameters of thermally activated delayed fluorescence emitters towards efficient red/near-infrared OLEDs
Fan, J., Xu, Y., Li, N., Miao, J., Zhou, C., Liu, T., Zhu, M., & Yin, X. (2022) · Journal of Materials Chemistry C · doi:10.1039/d2tc03933h · Cited by 11
Efficient solution processed hybrid white organic light-emitting diodes based on a blue thermally activated delayed fluorescence emitter
Joo, C. W., Huseynova, G., Kim, J. H., Yoo, J.-M., Kim, Y. H., Cho, N. S., Lee, J., Kim, Y.-H., & Lee, J. (2019) · Thin Solid Films · doi:10.1016/j.tsf.2019.137753 · Cited by 11
Self-citation
Room‐Temperature Multiple Phosphorescence from Functionalized Corannulenes: Temperature Sensing and Afterglow Organic Light‐Emitting Diode**
Si, C., Wang, T., Gupta, A. K., Cordes, D. B., Slawin, A. M. Z., Siegel, J. S., & Zysman‐Colman, E. (2023) · Angewandte Chemie · doi:10.1002/ange.202309718 · Cited by 11
Versatile Spiral Donor‐Based Thermally Activated Delayed Fluorescence Materials for Highly Efficient TADF‐OLED and TSF‐OLED Applications
Mu, X., Li, D., Liu, D., Wang, J., Li, J., Liu, C., Zhang, J., Feng, T., Fang, K., Li, W., et al. (2024) · Advanced Optical Materials · doi:10.1002/adom.202401735 · Cited by 10
Controlling emitting dipole orientations by N^O-ancillary electronic effects of [Ir(C^N) 2 (N^O)]-heteroleptic Ir( iii )-complexes towards efficient near-infrared (NIR) polymer light-emitting diodes (PLEDs)
Hou, S., Liu, J., Wang, B., Miao, T., Lü, X., Li, W., Fu, G., Feng, W., & Wong, W. (2021) · Journal of Materials Chemistry C · doi:10.1039/d1tc03485e · Cited by 10
C 1 -Symmetrical [Ir(C^N 1 )(C^N 2 )(N^O)]-tris-heteroleptic Ir( iii )-complexes with one strong N^O-ancillary π-donor for efficient all-solution-processed near-infrared (NIR) polymer light-emitting diodes (PLEDs)
Zhang, Y., Wang, B., Liu, J., Lü, X., Fu, G., Li, W., & Wong, W. (2022) · Journal of Materials Chemistry C · doi:10.1039/d1tc05662j · Cited by 10
Red/NIR Thermally Activated Delayed Fluorescence from Aza‐BODIPYs
Avellanal‐Zaballa, E., Prieto‐Castañeda, A., García‐Garrido, F., Agarrabeitia, A. R., Rebollar, E., Bañuelos, J., García‐Moreno, I., & Ortiz, M. J. (2020) · Chemistry - A European Journal · doi:10.1002/chem.202002916 · Cited by 9
Development of polymeric active layer for RGB light-emitting devices: a review
de Brito, E. B., Valaski, R., & Marques, M. D. F. V. (2020) · Journal of Materials Science Materials in Electronics · doi:10.1007/s10854-020-04809-2 · Cited by 10
Malononitrile based ternary AIE-ML materials: Experimental proof for emission switch from non-TADF to TADF
Luo, T., Lin, Z., Li, Z., Wang, Y., Xu, W., Zhao, C., Wang, H., & Luan, X. (2020) · Organic Electronics · doi:10.1016/j.orgel.2020.106003 · Cited by 10
A binaphthalimide motif as a chiral scaffold for thermally activated delayed fluorescence with circularly polarized luminescence activity
Tsuji, Y., Kanno, N., Goto, C., Katao, S., Okajima, Y., Reiné, P., Imbrasas, P., Reineke, S., Shizu, K., Nakashima, T., et al. (2023) · Journal of Materials Chemistry C · doi:10.1039/d3tc00316g · Cited by 9
Piezochromism of cyanostilbene derivatives: a small structural alteration makes a big photophysical difference
Zhu, C., Li, C., Li, W., Song, Q., Wang, K., Lv, C., & Zhang, Y. (2021) · New Journal of Chemistry · doi:10.1039/d1nj01945g · Cited by 9
Efficient Nondoped Pure Red/Near-Infrared TADF OLEDs by Designing and Adjusting Double Quantum Wells Structure
Sun, Y., Sun, W., Liu, W., Li, X., Yin, J., & Zhou, L. Y. (2022) · ACS Applied Electronic Materials · doi:10.1021/acsaelm.2c00531 · Cited by 9
AZABODIPY aggregates as a promising electroluminescent material for sustainable NIR OLED applications
Mróz, W., Squeo, B. M., Vercelli, B., Botta, C., & Pasini, M. (2023) · Materials Advances · doi:10.1039/d3ma00006k · Cited by 9
Green‐, Red‐, and Infrared‐Emitting Polymorphs of Sterically Hindered Push–Pull Substituted Stilbenes
Pauk, K., Luňák, S., Růžička, A., Marková, A., Mausová, A., Kratochvíl, M., Melánová, K., Weiter, M., Imramovský, A., & Vala, M. (2020) · Chemistry - A European Journal · doi:10.1002/chem.202004419 · Cited by 9
Synthesis and optical properties of the isomeric phenanthroimidazole Imidazo[1,2-a]pyridine conjugates: Effects of donor and their linking topology
Anupriya, Thomas, K. R. J., Nagar, M. R., & Jou, J. (2022) · Optical Materials · doi:10.1016/j.optmat.2022.112017 · Cited by 9
Efficient Red Thermally Activated Delayed Fluorescence Emitters Based on a Dibenzonitrile-Substituted Dipyrido[3,2-a:2′,3′-c]phenazine Acceptor
He, L., Zeng, X., Ning, W., Ying, A., Luo, Y., & Gong, S. (2021) · Molecules · doi:10.3390/molecules26092427 · Cited by 8
An electroluminescence efficiency of 30.3% for a yellow thermally activated delayed fluorescence emitter with a high horizontal emitting dipole ratio
Tang, Y., Zhou, J., Li, Y., Yang, D., Zeng, X., Zhang, K., He, Y., Ren, H., Ma, D., & Tang, J. (2023) · Journal of Materials Chemistry C · doi:10.1039/d2tc04968f · Cited by 8
Novel D-σ-A type thermally activated delayed fluorescence emitters with C–S σ bond for the orange-red OLEDs
Huang, F.-X., Wu, P., Li, H.-Z., Xie, F., Li, Y., Wei, H., Hu, Y., Tang, J., & Zhao, X. (2021) · Organic Electronics · doi:10.1016/j.orgel.2021.106245 · Cited by 8
Effect of Red Emissive Ligand Number on Dendronized Solution‐Processable Iridium(III) Complexes for Organic Light‐Emitting Diodes
Koodalingam, M., Jang, J., Ranasinghe, C. S. K., Gao, M., Burn, P. L., Kistemaker, J. C. M., Puttock, E. V., & Shaw, P. E. (2024) · Advanced Optical Materials · doi:10.1002/adom.202400640 · Cited by 7
Efficient Red TADF Emitter and Diode in High Doping Concentration via Steric Hindrance Engineering with Phosphine Oxide
Chang, P., Wang, H., Zhao, B., Man, Y., Qi, Q., Han, C., & Xu, H. (2024) · The Journal of Physical Chemistry C · doi:10.1021/acs.jpcc.4c02441 · Cited by 7
Designing solution-processed thermally activated delayed fluorescence emitters via introducing bulky steric hindrance groups for pure red OLEDs
Li, S., Chen, L., Li, M., Zhang, T., Yan, S., & Ren, Z. (2024) · Journal of Materials Chemistry C · doi:10.1039/d4tc01326c · Cited by 7
Precise Modulation of Donor–Acceptor Spatial Configuration and Excited-State Energy Alignment for Efficient Red-Shifted TADF Emitters
Zhang, B., Liu, S., Pei, J., Hao, C., Chen, Y., Li, Y., Dong, H., Jiao, B., Wu, Z., & Wang, D. (2025) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.5c17843 · Cited by 7
The photophysical properties of sulfone-based TADF emitters in relation to their structural properties
Hepguler, A., Ulukan, P., & Çatak, Ş. (2023) · Physical Chemistry Chemical Physics · doi:10.1039/d3cp03557c · Cited by 7
High‐Efficiency Deep Red Electroluminescence via a Spiro‐Based Pure Hydrogen Carbon Host
Yu, Y., Qu, Z., Ding, L., Wang, X., Meng, X., Li, M.-T., Zhou, D., Jiang, Z., & Liao, L. (2024) · Advanced Functional Materials · doi:10.1002/adfm.202405491 · Cited by 7
Achieving Highly Efficient Luminescence and Multiphoton Absorption Character in Thermally Activated Delayed Fluorescence Emitters Based on a Tetrabenzo[ a , c ]Phenazine Core
Mageswari, G. V., Chitose, Y., Li, Y., Fan, Z., Kao, Y., Balijapalli, U., Lin, J., Lin, T., & Adachi, C. (2025) · Angewandte Chemie International Edition · doi:10.1002/anie.202509348 · Cited by 7
Quantum simulations of thermally activated delayed fluorescence in an all-organic emitter
Francese, T., Kundu, A., Gygi, F., & Galli, G. (2022) · Physical Chemistry Chemical Physics · doi:10.1039/d2cp01147f · Cited by 7
Asymmetric donor–acceptor–host red thermally activated delayed fluorescent emitter for high-efficiency organic light emitting diodes
Li, H., Xie, F., Wu, P., Zhang, K., Zhao, X., Li, Y., & Tang, J. (2023) · Journal of Materials Chemistry C · doi:10.1039/d3tc01632c · Cited by 7
Deciphering the doublet luminescence mechanism in neutral organic radicals: spin-exchange coupling, reversed-quartet mechanism, excited-state dynamics
Lv, L., Zhang, Y., & Ning, Z. (2024) · RSC Advances · doi:10.1039/d4ra03566f · Cited by 6
Suppression and utilization of Kasha's rule: realizing the transformation from blue to near-infrared emission
Xie, M., Cai, J.-H., Zhang, G., Jung, S., Dong, D., Zhang, Z., Zhou, D., Liao, L., & Li, T. (2023) · Materials Chemistry Frontiers · doi:10.1039/d3qm00394a · Cited by 6
Tuning of the Singlet–Triplet Energy Gap of Donor-Linker-Acceptor Based Thermally Activated Delayed Fluorescent Emitters
Paras, & Ramachandran, C. N. (2023) · Journal of Fluorescence · doi:10.1007/s10895-023-03365-2 · Cited by 6
Intermolecular C–H⋯O hydrogen bond–induced H-aggregates for rapid, real-time detection of cyanide
Padghan, S. D., Hu, J., Wang, L., Hsu, Y.-H., & Chen, K. (2024) · Dyes and Pigments · doi:10.1016/j.dyepig.2024.112567 · Cited by 6
Effect of TADF Assistance on Performance Enhancement in Solution Processed Green Phosphorescent OLEDs
Witkowska, E., Wiosna-Sałyga, G., Głowacki, I., Ke, T., Malinowski, P. E., & Heremans, P. L. (2021) · Polymers · doi:10.3390/polym13071148 · Cited by 6
Deep-blue thermally activated delayed fluorescence emitter with a very high fluorescence rate
Wang, H., Cheng, C., Wang, D., Lou, W., Zhu, Y., Deng, C., Li, G., & Zhang, Q. (2021) · Organic Electronics · doi:10.1016/j.orgel.2021.106254 · Cited by 6
High-efficiency orange thermally activated delayed fluorescence by secondary acceptor modification
Zhou, J., Zeng, X., Xie, F., He, Y.-H., Tang, Y.-Q., Li, Y.-Q., & Tang, J. (2021) · Materials Today Energy · doi:10.1016/j.mtener.2021.100819 · Cited by 6
Efficient Intramolecular Charge‐Transfer Fluorophores Based on Substituted Triphenylphosphine Donors
Liu, Z., Deng, C., Su, L., Wang, D., Jiang, Y., Tsuboi, T., & Zhang, Q. (2021) · Angewandte Chemie · doi:10.1002/ange.202103075 · Cited by 6
Rational design of dibenzo[a,c]phenazine-derived isomeric thermally activated delayed fluorescence luminophores for efficient orange-red organic light-emitting diodes
Ye, H., Yang, J., Stavrou, K., Li, M., Liu, F., Li, F., Su, S., & Monkman, A. P. (2023) · Dyes and Pigments · doi:10.1016/j.dyepig.2023.111568 · Cited by 6
Solution-processable thermally activated delayed fluorescence red emitters poly(carbazole-fluorene) containing naphthalene imide units
Zhao, J., Liu, D., Lu, Y., Wu, Y., Liu, Y., Xu, S., Su, S., & Cao, S. (2023) · Polymer · doi:10.1016/j.polymer.2023.126316 · Cited by 6
Efficient and exclusively NIR-emitting (λem = 780 nm) [Ir(C^N)2(O^O)]-heteroleptic complexes with β-diketonate- or pyrazolonate-typed O^O-chelate ancillary
He, Y., Li, W., Fu, G., Wang, B., Miao, T., Tan, M., Feng, W., Lü, X., & He, H. (2019) · Journal of Luminescence · doi:10.1016/j.jlumin.2019.116983 · Cited by 6
Insights into Charge Transport in High-Efficiency Green Solution-Processed Thermally Activated Delayed Fluorescence Organic Light-Emitting Diodes with a Single Emitting Layer
Kumar, M., Chapran, M., Wiosna-Sałyga, G., Ślęczkowski, P., Łuszczyńska, B., & Pereira, L. (2020) · The Journal of Physical Chemistry C · doi:10.1021/acs.jpcc.0c04938 · Cited by 6
Highly Efficient Orange‐Red Thermally Activated Delayed Fluorescence Compounds Comprising Dual Dicyano‐Substituted Pyrazine/Quinoxaline Acceptors
Li, H., Yang, T., Wang, J., Xie, N., Wang, Q., Xu, Y., Zhao, Y., & Liang, B. (2020) · ChemPlusChem · doi:10.1002/cplu.202000703 · Cited by 6
Achieving near-infrared emission platinum (II) complex by introducing dimerized benzothiadiazole unit
Yang, X., Zhang, Y., Cao, L., Shao, M., Cao, J., Yu, J., Tan, H., & Zhu, W. (2021) · Optical Materials · doi:10.1016/j.optmat.2021.111896 · Cited by 6
Red and Near‐Infrared Emissive Organic Crystals: Molecular Design and Optoelectronic Applications
Lan, L., & Zhang, H. (2025) · Angewandte Chemie · doi:10.1002/ange.202509140 · Cited by 5
Precision design for high-performance TADF emitters with novel interlock D–A frameworks
Khan, A. H., Kong, F., Kazmi, J., Kumar, S., Leydecker, T., & Wang, Z. (2025) · Journal of Materials Chemistry C · doi:10.1039/d4tc05314a · Cited by 5
Theoretical insights into the central “acceptor” bridge function on the whole visible light and near-infrared emission in tetraphenylpyrazine-based luminogens
Gong, G., Dong, X., Ran, X., Mu, J., Zhang, T., & Wang, Z. (2022) · New Journal of Chemistry · doi:10.1039/d2nj03596k · Cited by 5
Phenoxazine-Dibenzothiophene Sulfoximine Emitters Featuring Both Thermally Activated Delayed Fluorescence and Aggregation Induced Emission
Yang, Y., Xiao, R., Cao, X., Chen, Z., Lv, X., Zhang, Y., Gong, S., Zou, Y., & Yang, C. (2021) · Molecules · doi:10.3390/molecules26175243 · Cited by 5
A theoretical study on the effects of intramolecular and intermolecular interactions on excited state properties of two NIR-TADF combined with AIE molecules
Liang, T., Jiang, X., Wang, J., Pan, Y., & Yang, B. (2022) · Computational and Theoretical Chemistry · doi:10.1016/j.comptc.2022.114000 · Cited by 5
Locally Excited States Guided Enhancement in Reverse Intersystem Crossing Rate in Unconventional Acceptor-free Thermally Activated Delayed Emitters
Mondal, M., & Vijayaraghavan, R. K. (2023) · The Journal of Physical Chemistry C · doi:10.1021/acs.jpcc.2c07848 · Cited by 5
Efficient Red Electroluminescent Copper Complexes with Fluorination-Balanced Dual Emission
Lou, X., Chen, G., Liu, C. X., Zhang, J., He, J., Niu, J., Duan, C., Han, C., Karasik, A. A., & Xu, H. (2025) · Research · doi:10.34133/research.1088 · Cited by 4
Secondary Donor Engineering for High‐Efficiency Orange‐Red Thermally Activated Delayed Fluorescence Emitters
Hua, L., Wu, H., Yan, S., Zhu, W., Ren, Z., & Wang, Y. (2025) · Chemistry - A European Journal · doi:10.1002/chem.202501391 · Cited by 4
Regulating through-space charge transfer interactions in donor–acceptor MOFs for thermally activated delayed fluorescence and X-ray scintillators
Yan, X., Song, S.-Y., Liang, S., Liu, K.-K., Liu, X., & Lu, C. (2025) · Chemical Science · doi:10.1039/d5sc02235e · Cited by 4
Improved performance of thermally activated delayed fluorescence white organic light-emitting diodes achieved by bulk-interfacial exciplex integrated system
Hu, X., Gu, Q., Xie, Y., Zhang, M., Sun, J., Wang, J., Sheng, R., & Chen, P. (2025) · Dyes and Pigments · doi:10.1016/j.dyepig.2025.113355 · Cited by 4
Selective decoration of dibenzofuran with multi-donors and a triazine acceptor for triplet to singlet up-conversion
Yun, J. H., Lee, K. H., Jeong, H., & Lee, J. Y. (2022) · Journal of Materials Chemistry C · doi:10.1039/d2tc01620f · Cited by 4
Self-citation
Towards red thermally activated delayed fluorescence emitter: Molecular design and property prediction of phenothiazine-triphenyltriazine derivative
An, L., Su, R., Sun, Y., Song, C., & Wang, Q. (2023) · Computational and Theoretical Chemistry · doi:10.1016/j.comptc.2023.114277 · Cited by 4
EXPLORING QUANTUM WELLS IN OLED TECHNOLOGIES: A COMPREHENSIVE REVIEW OF APPLICATIONS AND ADVANCEMENTS
Deva, L., Стахіра, П. Й., Fitio, V., Guminilovych, R. R., Bulavinets, T. O., Stanitska, M., & Volyniuk, D. Y. (2025) · Ukrainian Journal of Physical Optics · doi:10.3116/16091833/ukr.j.phys.opt.2025.02001 · Cited by 4
Combinatorial donor engineering for highly efficient blue thermally activated delayed fluorescence emitters with low efficiency roll-off
Shin, D. J., Lim, J., & Lee, J. Y. (2021) · Journal of Materials Chemistry C · doi:10.1039/d1tc03307g · Cited by 4
Self-citation
Computational Search to Find Efficient Red/Near‐Infrared Emitting Organic Molecules Based on Thermally Activated Delayed Fluorescence for Organic Light‐Emitting Diodes
Eskandarian, P., Fallah, H., Hajimahmoodzadeh, M., & Zabolian, H. (2021) · Advanced Theory and Simulations · doi:10.1002/adts.202100416 · Cited by 4
Highly efficient thermally activated delayed fluorescence emitter based on the 5 H -benzo[ d ]benzo[4,5]imidazo[1,2- a ]imidazole donor
Raikwar, M. M., Kim, S. C., & Lee, J. Y. (2022) · Materials Chemistry Frontiers · doi:10.1039/d2qm00806h · Cited by 4
Self-citation
Four‐Coordinate Organoboron Platforms for Efficient Red Phosphorescent Organic Light‐Emitting Diodes
Liu, X., Zhang, Y., Fei, X., Fung, M., & Fan, J. (2019) · ChemPlusChem · doi:10.1002/cplu.201900406 · Cited by 4
High-performance red and white organic light-emitting diodes based on a novel red thermally activated delayed fluorescence emitter in an exciplex matrix
Chen, J., Wang, H., Wang, K., Zhang, X., Zhou, L., Shi, Y., Yu, J., & Zhang, X. (2021) · Materials Today Energy · doi:10.1016/j.mtener.2021.100818 · Cited by 4
Deep‐red carbazole–furanonitrile emitters with linker‐dependent planarity and aggregation‐induced emission
Liu, S., Hsieh, C., Thomas, K. R. J., & Chen, C. (2025) · Journal of the Chinese Chemical Society · doi:10.1002/jccs.70111 · Cited by 3
Asymmetric TADF Emitters with 93% Horizontal Dipole Orientation Enable 20.1% EQE in Deep‐Red OLEDs and Spectral Tunability to NIR
Liu, Y., Lu, Z., Yang, J., Mao, Z., Yang, G., Zhao, J., Feng, H., Su, S., & Chi, Z. (2026) · Advanced Functional Materials · doi:10.1002/adfm.202529822 · Cited by 3
New sandwich-structured blue thermally activated delayed fluorescence molecules with through-space charge transfer effect
Lan, Z., Dong, X., Sun, R., Yang, Z., Tang, B. Z., & Zhao, Z. (2025) · Dyes and Pigments · doi:10.1016/j.dyepig.2025.112804 · Cited by 3
Eu3+-to-Cr3+ energy transfer for the improved Cr3+- characteristic near-infrared (NIR) phosphorescence in the Cr(III)-Eu(III)-Salen complex
Hou, S., Guo, Y., Zhang, Y., Wang, B., Li, W., Liu, J., Miao, T., & Lü, X. (2021) · Inorganic Chemistry Communications · doi:10.1016/j.inoche.2021.108811 · Cited by 3
Thermally activated delayed fluorescence and high-contrast mechanochromism of anthrone-based donor–acceptor systems
Sudhakar, P., Slawin, A. M. Z., & Zysman‐Colman, E. (2023) · Frontiers in Chemistry · doi:10.3389/fchem.2023.1248267 · Cited by 3
Highly Efficient Red, Green, and Blue Inverted Top‐Emitting Organic Light‐Emitting Diodes with Microstructured TiN Substrate
Shi, W. Y., Zheng, H., Zhao, Y., Pu, X., Shui, X., Lin, Y., Chen, G., Yang, X., Zhang, G., & Wei, B. (2024) · physica status solidi (RRL) - Rapid Research Letters · doi:10.1002/pssr.202400032 · Cited by 3
Intersystem crossing in a dibenzofuran-based room temperature phosphorescent luminophore investigated by non-adiabatic dynamics
Ulukan, P., Lognon, E., Çatak, Ş., & Monari, A. (2024) · Physical Chemistry Chemical Physics · doi:10.1039/d4cp02474e · Cited by 3
Efficient dual-phase visual detection of pesticides in real samples with electron-rich emitters carrying multiple twists
Tripathi, S., & Chakravarty, M. (2025) · Materials Advances · doi:10.1039/d5ma00630a · Cited by 2
Recent advances in triplet-state materials: A perspective towards bioimaging and biosensing
Rabiee, N., Daneshgar, H., Arghavani, P., Edrisi, M., Rabiee, M., Akrami‐Hasan‐Kohal, M., & Bencherif, S. A. (2025) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2025.217160 · Cited by 2
Strategic modification of the quinoxaline acceptor to induce broad-range orange to red thermally activated delayed fluorescence
Nanaware, S., Ren, Z., Ganesan, G., Zhou, D., Wang, Y., Liao, L., Kothavale, S., & Chaskar, A. C. (2025) · Journal of Materials Chemistry C · doi:10.1039/d5tc02803e · Cited by 2
Pillar[5]arene-cored hyper-structured molecular thermally activated delayed fluorescence orange-red emitters for OLEDs
Ma, C., Liu, D., Li, W., Liu, M., Wang, K., Liu, Y., Cao, S., Su, S., & Xu, S. (2026) · Journal of Photochemistry and Photobiology A Chemistry · doi:10.1016/j.jphotochem.2026.117155 · Cited by 2
Effects of Donor Rigidity on Coumarin Delayed Emission: New Tricks from Old Materials
Paredis, S., Cardeynaels, T., Kuila, S., Deckers, J., Lathouwers, A., Landeghem, M. V., Vandewal, K., Danos, A., Monkman, A. P., Champagne, B. R., et al. (2026) · The Journal of Physical Chemistry Letters · doi:10.1021/acs.jpclett.6c00210 · Cited by 2
Red hyperbranched conjugated polymers with thermally activated delayed fluorescence for solution-processed organic light-emitting diodes
Sun, J., Du, J., Yang, X., Fan, Z., Miao, Y., Dong, H., Liao, X., Wang, H., & Xu, B. (2024) · European Polymer Journal · doi:10.1016/j.eurpolymj.2024.113119 · Cited by 2
Effect of the Imidazole π‐Extension on TADF Emitters in Electrochemiluminescence
Pelorosso, E., Pavan, G., Scattolin, T., Orian, L., Antonello, S., Demitri, N., & Aliprandi, A. (2024) · Chemistry - An Asian Journal · doi:10.1002/asia.202400340 · Cited by 2
Highly Efficient, Low-Roll-Off, Red, “Hot Exciton” Organic Light-Emitting Diodes Promoted by the Heavy-Atom Effect of Selenium
Dong, X., Xie, X., Shen, S., Qin, Y., Pang, Z., Lv, X., & Wang, Y. (2024) · The Journal of Physical Chemistry Letters · doi:10.1021/acs.jpclett.4c02166 · Cited by 2
[Ir(C1^N1)(C2^N2)(O^O)]-tris-heteroleptic and [Ir(C1^N1)2(O^O)]-bis-heteroleptic Ir(III)-complexes with one or two color-responsible HC1^N1 ligands towards efficient color-purity near-infrared (NIR) phosphorescence
Chen, Y., Dong, X., Guo, W., Zhang, Y., Zhang, Z., Zhuang, Y., Lü, X., & Fu, G. (2025) · Journal of Luminescence · doi:10.1016/j.jlumin.2025.121149 · Cited by 2
Achieving Highly Efficient Luminescence and Multiphoton Absorption Character in Thermally Activated Delayed Fluorescence Emitters Based on a Tetrabenzo[ a , c ]Phenazine Core
Mageswari, G. V., Chitose, Y., Li, Y., Fan, Z., Kao, Y., Balijapalli, U., Lin, J., Lin, T., & Adachi, C. (2025) · Angewandte Chemie · doi:10.1002/ange.202509348 · Cited by 2
Pursuing red thermally activated delayed fluorescence upon increasing the degree of branching in phenothiazine-trithienyltriazine push–pull compounds
Mancini, P., Montanari, C., Yadav, K., Luzi, E., Misra, R., & Carlotti, B. (2025) · Journal of Materials Chemistry C · doi:10.1039/d5tc03179f · Cited by 2
Benzoylphenyltriazine as a new acceptor of donor–acceptor type thermally-activated delayed-fluorescent emitters
Yun, J. H., Lee, K. H., & Lee, J. Y. (2021) · Journal of Industrial and Engineering Chemistry · doi:10.1016/j.jiec.2021.07.011 · Cited by 2
Self-citation
Luminescence properties and mechanism studies of thermally activated delayed fluorescence molecules
Zhi-min, W., Wang, X., Li, R., Zhou, J., Cao, Y., Song, Y., Fan, J., Wang, C., Lin, L., & Wang, Z. (2025) · Organic Electronics · doi:10.1016/j.orgel.2025.107205 · Cited by 1
Developing Red and Near-Infrared Delayed Fluorescence Emission in Nitrogen-Substituted Donor–Acceptor Polycyclic Hydrocarbon OLED Emitters: A Theoretical Study
Sahoo, S. R., Baryshnikov, G., & Ågren, H. (2025) · The Journal of Physical Chemistry A · doi:10.1021/acs.jpca.4c07345 · Cited by 1
Meniscus‐Guided Molecular Alignment for High‐Efficiency Solution‐Processed DR/NIR‐OLEDs
Song, N., Xue, J., Chen, Y.-M., Xin, X., Wu, J., Liang, N., Ye, L., Zhai, T., & Wang, Z. (2025) · Advanced Optical Materials · doi:10.1002/adom.202501346 · Cited by 1
Dense ordered stacking co-planar self-assembled molecules for high-performance perovskite solar cells
Zhao, T., Guo, Y., Li, W., Huang, C., Wan, Q., ZHANG, J., Yang, X., Xiong, Z., Xiong, Q., & Zhang, D. (2026) · Chemical Engineering Journal · doi:10.1016/j.cej.2026.174722 · Cited by 1
Near-infrared-red-orange thermally activated delayed fluorescence emitters using a strong tetracoordinated difluoroboronated acceptor
Ren, Y., Nakagawa, H., Suzuki, K., Hu, W., & Kaji, H. (2022) · Japanese Journal of Applied Physics · doi:10.35848/1347-4065/ac7a7c · Cited by 1
Rational design of star-shaped triarylborane-based thermally activated delayed fluorescent emitters for organic light-emitting diodesPreprint
Jin, R., Xin, J., & Xiao, W. (2023) · Research Square · doi:10.21203/rs.3.rs-3230300/v1 · Cited by 1
Orange, red, and near-infrared thermally activated delayed fluorescent emitters
Zeng, W., & Yang, C. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-819810-0.00007-7
Pure Near-Infrared Thermally Activated Delay Fluorescence Materials Approaching 800 Nm Via Simple Malononitrile Condensation StrategyPreprint
Qiao, J., Li, Q., Dai, Y., Xu, J., Tan, S., & Xue, J. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4165520
Structure–Property Relationship of Triscarbazole-diphenyltriazine-type Blue Thermally Activated Delayed Fluorescent Emitters
Byeon, S. Y., Kim, S. C., & Lee, J. Y. (2022) · ACS Applied Electronic Materials · doi:10.1021/acsaelm.2c01245
Self-citation
High‐Efficiency Deep Red Fluorescent Material with Aggregation Induced Emission and the Application in Organic Light‐Emitting Diodes
Liu, H., Zhang, H., Pu, Y., Li, Z., Wan, L., Ge, S., Ma, X., Liu, F., & Lü, P. (2024) · ChemPhotoChem · doi:10.1002/cptc.202400098
Complexes of Rare Earth Metals with Bromine-Substituted (Benzoxazolyl)Naphtholate Ligands as Emissive Materials
Kuzyaev, D. M., Balashova, T. V., Polyakova, S. K., Ilichev, V. A., Yablonskiy, A. N., Baranov, E. V., Fukin, G. K., & Bochkarev, M. N. (2024) · Journal of Structural Chemistry · doi:10.1134/s0022476624110064

Authors: Kim, J. H., Yun, J. H., & Lee, J. Y.
Affiliations: Sungkyunkwan University (KR)
Corresponding author: Lee, Jun Yeob
ORCID: Lee, Jun Yeob
Venue: Advanced Optical Materials
Publisher: Wiley
Published: 2018-06-27
Volume: 6
Issue: 18
ISSN: 2195-1071 (ISSN-L)
DOI: 10.1002/adom.201800255
OpenAlex: W2811452226
Cited by: 314
References: 62
Citations by year: 2026: 11 · 2025: 30 · 2024: 32 · 2023: 44 · 2022: 52 · 2021: 61 · 2020: 47 · 2019: 34 · 2018: 3
FWCI: 13.87
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor)
Locations: Advanced Optical Materials (publishedVersion)
Funders: National Research Foundation of Korea
Ministry of Science, ICT and Future Planning (2016R1A2B3008845)
Ministry of Trade, Industry and Energy
Topics: Physical Sciences › Engineering › Electrical and Electronic Engineering › Organic Light-Emitting Diodes Research
Physical Sciences › Materials Science › Materials Chemistry › Luminescence and Fluorescent Materials
Physical Sciences › Materials Science › Materials Chemistry › Luminescence Properties of Advanced Materials
Keywords: thermally activated delayed fluorescence, red emitters, near-infrared emitters, organic light-emitting diodes, external quantum efficiency, molecular design, bioimaging

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Recent Progress of Highly Efficient Red and Near‐Infrared Thermally Activated Delayed Fluorescent Emitters

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Citations

Cites

Cited by

Related

Metadata

Record

About these checks