{"title":"Temperature-dependent photoluminescence and exciton recombination processes in naphthalene/TCNB charge-transfer cocrystal","authors":"Wei-Long Xu, Xiangrun Chen, Qiuyu Gu, Fei Zhao, Yannan Zhang, Yuebin Lian","doi":"10.1016/j.jlumin.2025.121371","DOIUrl":null,"url":null,"abstract":"<div><div>Cocrystal engineering offers a promising strategy to synthesize materials with novel physicochemical properties by integrating electron-rich donors and electron-deficient acceptors through non-covalent interactions. This work focuses on the preparation and characterization of naphthalene/1,2,4,5-tetracyanobenzene (TCNB) charge-transfer cocrystal using a controlled slow solvent evaporation method. Millimeter-scale cocrystals with preferential growth along the (110) plane were synthesized by mixing equimolar acetonitrile solutions of naphthalene and TCNB. Temperature-dependent photoluminescence (PL) studies demonstrated a significant redshift in emission peaks and a broadening of the full width at half maximum (FWHM) from 122 nm to 173 nm, attributed to enhanced electron-phonon coupling and thermal quenching. An exciton binding energy of 142 meV was derived, supporting efficient radiative recombination. Power-dependent PL spectra revealed exciton annihilation effects under high excitation intensity, suppressing short-wavelength emission. The relatively uniform fluorescence lifetime across the sample was observed in time-resolved fluorescence lifetime imaging (FLIM) image. Two decay components were assigned to localized exciton (14.4 ns) and charge transfer exciton (40.3 ns) recombination. These results highlight the tunable optoelectronic properties of naphthalene/TCNB cocrystals and their potential for applications in light-emitting devices and photonic systems.</div></div>","PeriodicalId":16159,"journal":{"name":"Journal of Luminescence","volume":"286 ","pages":"Article 121371"},"PeriodicalIF":3.3000,"publicationDate":"2025-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Luminescence","FirstCategoryId":"101","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022231325003114","RegionNum":3,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OPTICS","Score":null,"Total":0}
引用次数: 0
Abstract
Cocrystal engineering offers a promising strategy to synthesize materials with novel physicochemical properties by integrating electron-rich donors and electron-deficient acceptors through non-covalent interactions. This work focuses on the preparation and characterization of naphthalene/1,2,4,5-tetracyanobenzene (TCNB) charge-transfer cocrystal using a controlled slow solvent evaporation method. Millimeter-scale cocrystals with preferential growth along the (110) plane were synthesized by mixing equimolar acetonitrile solutions of naphthalene and TCNB. Temperature-dependent photoluminescence (PL) studies demonstrated a significant redshift in emission peaks and a broadening of the full width at half maximum (FWHM) from 122 nm to 173 nm, attributed to enhanced electron-phonon coupling and thermal quenching. An exciton binding energy of 142 meV was derived, supporting efficient radiative recombination. Power-dependent PL spectra revealed exciton annihilation effects under high excitation intensity, suppressing short-wavelength emission. The relatively uniform fluorescence lifetime across the sample was observed in time-resolved fluorescence lifetime imaging (FLIM) image. Two decay components were assigned to localized exciton (14.4 ns) and charge transfer exciton (40.3 ns) recombination. These results highlight the tunable optoelectronic properties of naphthalene/TCNB cocrystals and their potential for applications in light-emitting devices and photonic systems.
期刊介绍:
The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid.
We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.