Yen Chi-Yang, Rana Shailesh, Awasthi Kamlesh, Ohta Nobuhiro, Oh-E Masahito
Institute of Photonics Technologies, Department of Electrical Engineering, National Tsing Hua University, 101 Sec. 2 Kuang-Fu Road, Hsinchu, 300044, Taiwan.
Department of Applied Chemistry, Institute of Molecular Science, Center for Emergent Functional Matter Science, National Yang Ming Chiao Tung University, 1001 Ta-Hsueh Road, Hsinchu, 300093, Taiwan.
Sci Rep. 2024 Oct 31;14(1):26223. doi: 10.1038/s41598-024-72773-6.
Although many dyes have been introduced into cellulose, whether bound to its backbone or within a cellulose matrix, few studies have determined whether the backbone statically or dynamically quenches the photoluminescence of the dye. To advance cellulosic fluorescent films, the influence of the cellulose backbone on photoluminescence must be understood. We determined the fluorescence properties of fluorescein isothiocyanate (FITC) and fluorescein-labeled cellulose (FLC) in water and alcohol, including their quantum yields [Formula: see text], lifetimes [Formula: see text], and rates of radiative [Formula: see text] and nonradiative [Formula: see text] decay. Dissolved FLC had a ~ 30× lower [Formula: see text] than FITC, suggesting that incorporating FITC into the cellulose backbone remarkably reduces the fluorescence efficiency. The FLC solutions had a six-fold lower [Formula: see text] than their FITC counterparts but a 10-20 times higher [Formula: see text]. Presumably, this was because the cellulose backbone interacted weakly with the fluorescein moieties, suggesting a quenching mechanism that can be termed quasi-static, corresponding to static quenching between the fluorescein moieties and cellulose backbone, in addition to the fluorescence quenching caused by the intramolecular nonradiative processes of fluorescein, as observed in conventional molecules. Using the Strickler‒Berg formula, we deduced the analytical radiative decay rate constants [Formula: see text] and eventually estimated the number of very short-lived fluorescein moieties per single fluorescent fluorescein moiety, corresponding well with static quenching.
尽管许多染料已被引入纤维素中,无论是与纤维素主链结合还是存在于纤维素基质内,但很少有研究确定主链是静态还是动态淬灭染料的光致发光。为了推进纤维素荧光薄膜的发展,必须了解纤维素主链对光致发光的影响。我们测定了异硫氰酸荧光素(FITC)和荧光素标记的纤维素(FLC)在水和醇中的荧光特性,包括它们的量子产率[公式:见正文]、寿命[公式:见正文]以及辐射[公式:见正文]和非辐射[公式:见正文]衰减速率。溶解的FLC的[公式:见正文]比FITC低约30倍,这表明将FITC掺入纤维素主链会显著降低荧光效率。FLC溶液的[公式:见正文]比其对应的FITC溶液低六倍,但[公式:见正文]高10 - 20倍。据推测,这是因为纤维素主链与荧光素部分相互作用较弱,这表明除了如传统分子中观察到的荧光素分子内非辐射过程引起的荧光淬灭外,还存在一种可称为准静态的淬灭机制,对应于荧光素部分与纤维素主链之间的静态淬灭。使用斯特里克勒 - 伯格公式,我们推导出分析辐射衰减速率常数[公式:见正文],最终估计了每个单个荧光荧光素部分中极短寿命荧光素部分的数量,这与静态淬灭非常吻合。