2024 Journal Article A New Organic Laser Material Design Toward Ultra‐Low Amplified Spontaneous Red Emission and Ultra‐Bright ElectroluminescenceWallwork, Nicholle R., Shukla, Atul, Roseli, Ras Baizureen, Allison, Ilene, McGregor, Sarah K. M., Coles, Max, Gale, Innes, Rahane, Vijay P., Entoma, Volter, Moore, Evan G., Krenske, Elizabeth H., Namdas, Ebinazar B. and Lo, Shih‐Chun (2024). A New Organic Laser Material Design Toward Ultra‐Low Amplified Spontaneous Red Emission and Ultra‐Bright Electroluminescence. Small, 20 (52) 2406817, e2406817. doi: 10.1002/smll.202406817 |
2024 Journal Article End Cap Effect on Solution-Processable Deep Blue Lasing Materials with Low-Amplified Spontaneous Emission ThresholdsSugai, Yoshiki, Rahane, Vijay P., Gale, Innes, Verdi, Carla, Ireland, Alexander R., Canola, Sofia, McGregor, Sarah K. M., Moore, Evan G., Jain, Nidhi, Namdas, Ebinazar B. and Lo, Shih-Chun (2024). End Cap Effect on Solution-Processable Deep Blue Lasing Materials with Low-Amplified Spontaneous Emission Thresholds. ACS Applied Materials & Interfaces, 16 (35), 46506-46515. doi: 10.1021/acsami.4c07286 |
2024 Journal Article Highly Stable Red Emissive Organic Semiconductor Materials with Low Amplified Spontaneous Emission ThresholdsRahane, Vijay P., Roseli, Ras Baizureen, Ireland, Alexander R., Gale, Innes, Shukla, Atul, Moore, Evan G., Krenske, Elizabeth H., Namdas, Ebinazar B., Jain, Nidhi and Lo, Shih‐Chun (2024). Highly Stable Red Emissive Organic Semiconductor Materials with Low Amplified Spontaneous Emission Thresholds. Advanced Optical Materials, 12 (25) 2400892. doi: 10.1002/adom.202400892 |
2024 Journal Article Low amplified spontaneous emission threshold from solution processable excited‐state intramolecular proton transfer chromophoresRahane, Vijay P., Shukla, Atul, Roseli, Ras Baizureen, Ireland, Alexander R., Gale, Innes, Krenske, Elizabeth H., Moore, Evan G., Namdas, Ebinazar B., Jain, Nidhi and Lo, Shih‐Chun (2024). Low amplified spontaneous emission threshold from solution processable excited‐state intramolecular proton transfer chromophores. Advanced Optical Materials, 12 (24). doi: 10.1002/adom.202400840 |
2024 Journal Article Elucidating the Mechanism of Efficient Eu(III) and Yb(III) Sensitisation from a Re(I) Tetrazolato Triangular AssemblyWright, Phillip J., Pfrunder, Michael C., Etchells, Isaac M., Haghighatbin, Mohammad A., Raiteri, Paolo, Ogden, Mark I., Stagni, Stefano, Hogan, Conor F., Cameron, Lee J., Moore, Evan G. and Massi, Massimiliano (2024). Elucidating the Mechanism of Efficient Eu(III) and Yb(III) Sensitisation from a Re(I) Tetrazolato Triangular Assembly. Chemistry – A European Journal, 30 (49) e202401233, e202401233. doi: 10.1002/chem.202401233 |
2024 Journal Article Mechanistic and kinetic insights into intermolecular [2+2] photocycloadditionsQuach, Gina, Iranmanesh, Hasti, Luis, Ena T., Harper, Jason B., Beves, Jonathon E. and Moore, Evan G. (2024). Mechanistic and kinetic insights into intermolecular [2+2] photocycloadditions. ACS Catalysis, 14 (11), 8758-8766. doi: 10.1021/acscatal.4c01678 |
2024 Journal Article Accelerated redox reactions enable stable tin‐lead mixed perovskite solar cellsHe, Dongxu, Chen, Peng, Hao, Mengmeng, Lyu, Miaoqiang, Wang, Zhiliang, Ding, Shanshan, Lin, Tongen, Zhang, Chengxi, Wu, Xin, Moore, Evan, Steele, Julian A., Namdas, Ebinazar B., Bai, Yang and Wang, Lianzhou (2024). Accelerated redox reactions enable stable tin‐lead mixed perovskite solar cells. Angewandte Chemie, 136 (4) e202317446, 1-8. doi: 10.1002/ange.202317446 |
2024 Journal Article Accelerated redox reactions enable stable tin‐lead mixed perovskite solar cellsHe, Dongxu, Chen, Peng, Hao, Mengmeng, Lyu, Miaoqiang, Wang, Zhiliang, Ding, Shanshan, Lin, Tongen, Zhang, Chengxi, Wu, Xin, Moore, Evan, Steele, Julian A., Namdas, Ebinazar, Bai, Yang and Wang, Lianzhou (2024). Accelerated redox reactions enable stable tin‐lead mixed perovskite solar cells. Angewandte Chemie International Edition, 63 (4) e202317446, 1-8. doi: 10.1002/anie.202317446 |
2023 Journal Article Light blue rigid excited-state intramolecular proton transfer organic semiconductor laser chromophoresAllison, Ilene, Mamada, Mashashi, Shukla, Atul, McGregor, Sarah K. M., Roseli, Ras Baizureen, Gale, Innes, Rahane, Vijay P., Moore, Evan G., Krenske, Elizabeth H., Jain, Nidhi, Adachi, Chihaya, Namdas, Ebinazar B. and Lo, Shih-Chun (2023). Light blue rigid excited-state intramolecular proton transfer organic semiconductor laser chromophores. Journal of Materials Chemistry C, 11 (45), 15861-15872. doi: 10.1039/d3tc02707d |
2022 Journal Article Reduced singlet–triplet annihilation for low threshold amplified spontaneous emission from a blue polyfluorene electroluminescent organic semiconductorSardar, Gopa, Shukla, Atul, Moore, Evan G., Banappanavar, Gangadhar, Lo, Shih-Chun, Namdas, Ebinazar B. and Kabra, Dinesh (2022). Reduced singlet–triplet annihilation for low threshold amplified spontaneous emission from a blue polyfluorene electroluminescent organic semiconductor. The Journal of Physical Chemistry C, 126 (21), 9069-9075. doi: 10.1021/acs.jpcc.2c00648 |
2022 Journal Article Controlling triplet–triplet upconversion and singlet-triplet annihilation in organic light-emitting diodes for injection lasingShukla, Atul, Hasan, Monirul, Banappanavar, Gangadhar, Ahmad, Viqar, Sobus, Jan, Moore, Evan G., Kabra, Dinesh, Lo, Shih-Chun and Namdas, Ebinazar B. (2022). Controlling triplet–triplet upconversion and singlet-triplet annihilation in organic light-emitting diodes for injection lasing. Communications Materials, 3 (1) 27. doi: 10.1038/s43246-022-00248-0 |
2022 Journal Article Low light amplification threshold and reduced efficiency roll‐off in thick emissive layer OLEDs from a diketopyrrolopyrrole derivativeShukla, Atul, Entoma, Volter, McGregor, Sarah K. M., Hasan, Monirul, Mamada, Masashi, Moore, Evan G., Adachi, Chihaya, Lo, Shih‐Chun and Namdas, Ebinazar B. (2022). Low light amplification threshold and reduced efficiency roll‐off in thick emissive layer OLEDs from a diketopyrrolopyrrole derivative. Macromolecular Rapid Communications, 43 (16) 2200115, e2200115. doi: 10.1002/marc.202200115 |
2021 Journal Article Sensitised lanthanide luminescence using a RuII polypyridyl functionalised dipicolinic acid chelateRajah, Divya, Pfrunder, Michael C., Chong, Bowie S. K., Ireland, Alexander R., Etchells, Isaac M. and Moore, Evan G. (2021). Sensitised lanthanide luminescence using a RuII polypyridyl functionalised dipicolinic acid chelate. Dalton Transactions, 50 (21), 7400-7408. doi: 10.1039/d1dt00982f |
2021 Journal Article Light amplification and efficient electroluminescence from a solution‐processable diketopyrrolopyrrole derivative via triplet‐to‐singlet upconversionShukla, Atul, McGregor, Sarah K. M., Wawrzinek, Robert, Saggar, Siddhartha, Moore, Evan G., Lo, Shih‐Chun and Namdas, Ebinazar B. (2021). Light amplification and efficient electroluminescence from a solution‐processable diketopyrrolopyrrole derivative via triplet‐to‐singlet upconversion. Advanced Functional Materials, 31 (15) 2009817. doi: 10.1002/adfm.202009817 |
2021 Journal Article Dinuclear triple stranded phenyl-spaced 1,3-bis-β-diketonato lanthanide(iii) complexes: synthesis, structures and spectroscopyBrock, A. J., Etchells, I. M., Moore, E. G. and Clegg, J. K. (2021). Dinuclear triple stranded phenyl-spaced 1,3-bis-β-diketonato lanthanide(iii) complexes: synthesis, structures and spectroscopy. Dalton Transactions, 50 (14), 4874-4879. doi: 10.1039/d1dt00393c |
2020 Journal Article Solid cyclooctatetraene-based triplet quencher demonstrating excellent suppression of singlet–triplet annihilation in optical and electrical excitationMai, Van T. N., Ahmad, Viqar, Mamada, Masashi, Fukunaga, Toshiya, Shukla, Atul, Sobus, Jan, Krishnan, Gowri, Moore, Evan G., Andersson, Gunther G., Adachi, Chihaya, Namdas, Ebinazar B. and Lo, Shih-Chun (2020). Solid cyclooctatetraene-based triplet quencher demonstrating excellent suppression of singlet–triplet annihilation in optical and electrical excitation. Nature Communications, 11 (1) 5623, 1-9. doi: 10.1038/s41467-020-19443-z |
2020 Journal Article Enhanced near-infrared emission from eight-coordinate vs nine-coordinate YbIII complexes using 2-(5-methylpyridin-2-yl)-8-hydroxyquinolineChong, Bowie S. K., Rajah, Divya, Allen, Matthew F., Galán, Laura Abad, Massi, Massimiliano, Ogden, Mark and Moore, Evan G. (2020). Enhanced near-infrared emission from eight-coordinate vs nine-coordinate YbIII complexes using 2-(5-methylpyridin-2-yl)-8-hydroxyquinoline. Inorganic Chemistry, 59 (22) acs.inorgchem.0c01802, 16194-16204. doi: 10.1021/acs.inorgchem.0c01802 |
2020 Journal Article Lasing operation under long-pulse excitation in solution-processed organic gain medium: toward CW lasing in organic semiconductorsMai, Van T. N., Shukla, Atul, Senevirathne, A. M. Chathuranganie, Allison, Ilene, Lim, Hyunsoo, Lepage, Romain J., McGregor, Sarah K. M., Wood, Michael, Matsushima, Toshinori, Moore, Evan G., Krenske, Elizabeth H., Sandanayaka, Atula S. D., Adachi, Chihaya, Namdas, Ebinazar B. and Lo, Shih-Chun (2020). Lasing operation under long-pulse excitation in solution-processed organic gain medium: toward CW lasing in organic semiconductors. Advanced Optical Materials, 8 (21) 2001234, 2001234. doi: 10.1002/adom.202001234 |
2020 Journal Article Low amplified spontaneous emission and lasing thresholds from hybrids of fluorenes and vinylphenylcarbazoleShukla, Atul, Mai, Van T. N., Senevirathne, A. M. Chathuranganie, Allison, Ilene, McGregor, Sarah K. M., Lepage, Romain J., Wood, Michael, Matsushima, Toshinori, Moore, Evan G., Krenske, Elizabeth H., Sandanayaka, Atula S. D., Adachi, Chihaya, Namdas, Ebinazar B. and Lo, Shih‐Chun (2020). Low amplified spontaneous emission and lasing thresholds from hybrids of fluorenes and vinylphenylcarbazole. Advanced Optical Materials, 8 (20) 2000784, 1-9. doi: 10.1002/adom.202000784 |
2020 Journal Article A photophysical study of sensitization‐initiated electron transfer: insights into the mechanism of photoredox activityColes, Max S., Quach, Gina, Beves, Jonathon E. and Moore, Evan G. (2020). A photophysical study of sensitization‐initiated electron transfer: insights into the mechanism of photoredox activity. Angewandte Chemie, 132 (24), 9609-9613. doi: 10.1002/ange.201916359 |