External electric field induced emission behavior for ESIPT-based 2-(benzo[d]thiazol-2-yl)-4-(pyren-1-yl)phenol towards near-infrared region.
Spectrochim Acta A Mol Biomol Spectrosc
; 325: 125045, 2024 Aug 29.
Article
en En
| MEDLINE
| ID: mdl-39216142
ABSTRACT
Organic light-emitting diodes (OLEDs) for low energy transfer and double emission, but the current methods for regulating ESIPT processes are mostly solvent and substituent effects. Here, utilizing the density theory functional (DFT) and time-dependent density functional theory (TD-DFT) methods, the ESIPT process controlled by an external electric field (EEF) is proposed, and the changes in photophysical properties of 2-(benzo[d]thiazol-2-yl)-4-(pyren-1-yl)phenol (PyHBT) are investigated. Structural parameter variations and IR vibrational spectra measure the prerequisite for the ESIPT process, namely, intramolecular hydrogen bond (IHB) strength, and the scanned potential energy curves (PECs) demonstrate that the ESIPT process of PyHBT is harder to execute as the positive EEF increases, and the opposite is true for the negative EEF. The absorption and fluorescence spectra show shifts under the distinct EEFs, and even the emission wavelength reaches the short-wave near-infrared (SW-NIR) region (780-1100 nm), such as 815.2 nm for a positive EEF of + 30 × 10-4 a.u. in the keto form. Additionally, the fluorescence intensity of PyHBT is strongly influenced by the positive EEF, especially in the enol form, and the investigation of the mechanism by hole-electron analysis demonstrates that under the positive EEF, the twisted intramolecular charge transfer (TICT) process is induced, which triggers the weakening of the fluorescence intensity. In summary, our work not only complements the theoretical approach to modulate the ESIPT process, but also reveals that the photophysical properties of materials affected by the external electric field are even expected to reach the NIR region.
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Colección:
01-internacional
Base de datos:
MEDLINE
Idioma:
En
Revista:
Spectrochim Acta A Mol Biomol Spectrosc
Asunto de la revista:
BIOLOGIA MOLECULAR
Año:
2024
Tipo del documento:
Article
País de afiliación:
China
Pais de publicación:
Reino Unido