Journal
SCIENTIFIC REPORTS
Volume 5, Issue -, Pages -Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/srep10923
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Funding
- National Natural Science Foundation of China [21274065, 21304049, 21001065, 61136003, 51173081]
- Ministry of Education of China [IRT1148]
- priority academic program development of Jiangsu higher education institutions (PAPD) [YX03001]
- Qing Lan project of Jiangsu province
- National Basic Research Program of China (973 Program) [2012CB933301, 2012CB723402, 2014CB648300]
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Developing organic optoelectronic materials with desired photophysical properties has always been at the forefront of organic electronics. The variation of singlet-triplet splitting (Delta E-ST) can provide useful means in modulating organic excitons for diversified photophysical phenomena, but controlling Delta E-ST in a desired manner within a large tuning scope remains a daunting challenge. Here, we demonstrate a convenient and quantitative approach to relate Delta E-ST to the frontier orbital overlap and separation distance via a set of newly developed parameters using natural transition orbital analysis to consider whole pictures of electron transitions for both the lowest singlet (S-1) and triplet (T-1) excited states. These critical parameters revealed that both separated S-1 and T-1 states leads to ultralow Delta E-ST; separated S-1 and overlapped T-1 states results in small Delta E-ST; and both overlapped S-1 and T-1 states induces large Delta E-ST. Importantly, we realized a widely-tuned Delta E-ST in a range from ultralow (0.0003 eV) to extra-large (1.47 eV) via a subtle symmetric control of triazine molecules, based on time-dependent density functional theory calculations combined with experimental explorations. These findings provide keen insights into Delta E-ST control for feasible excited state tuning, offering valuable guidelines for the construction of molecules with desired optoelectronic properties.
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