基于紫外可见光谱的快速绿色 FCF 染料-果糖-十二烷基硫酸钠-NaOH 电解质光电池长期光稳定性的探索性研究

Pooran Koli
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引用次数: 0

摘要

光电耦合电池是一种以有机-无机化学为基础的设备。这些电池使用光敏剂、还原剂、表面活性剂、碱、溶剂和电极等化学物质。化学材料的光衰和牺牲迫在眉睫,导致这些电池的电力输出、效率和寿命有限。为了实现实际应用,这些设备的电输出可扩展性和稳定性至关重要。因此,本研究对基于快速绿色 FCF 染料-果糖-十二烷基硫酸钠(SLS)-NaOH 电解质的电池的长期光稳定性进行了研究。对电池的电输出进行了长期监测。此外,还对电解液的光稳定性进行了测定和光谱分析。据观察,即使在电解质衰变后,Fast Green FCF 染料-果糖-SLS-NaOH 光电池装置仍能产生电能。在 24 小时内,观察到约 90.54 % 的染料降解。即使不使用浓度为 0.2 × 10-4 M(即初始浓度的 9.46%)的敏化剂,该电池也能产生电流。此外,FCF 染料和 SLS 的光降解产物(有机磺酸盐)也是产生电流的潜在候选物质。在阳光下充电的电池即使在切断电解质照明后也能产生电流。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
UV–visible spectroscopic exploratory insight into the long term photo-stability of the fast green FCF dye-fructose-sodium lauryl sulphate-NaOH electrolyte based photogalvanic cell

Photo-galvanic cells are organo-inorganic chemical based devices. These cells use chemicals like photo-sensitizer(s), reductant(s), surfactant(s), alkali, solvent, and electrodes. Photo-decay and sacrifice of the chemical materials is imminent leading to the limited electrical output, efficiency and life of these cells. For realizing practical applications, the scalability of electrical output and stability of these devices is of utmost importance. Therefore, the long term photo-stability of Fast Green FCF dye-Fructose-Sodium lauryl sulphate (SLS)-NaOH electrolyte based cells has been studied in present work. The electrical output of the cell has been monitored over long period of time. Further, the photo-stability of electrolyte has been determined and analyzed spectroscopically. It has been observed that the Fast Green FCF dye-Fructose-SLS-NaOH photogalvanic cell device is capable of producing power even after decay of electrolyte. In early 24 h, about 90.54 % of dye degradation is observed. The cell is capable of giving current with even left out concentration ∼0.2 × 10−4 M (i.e., 9.46 % of initial concentration) of sensitizer. Further, the photo-degradation products (organic sulfonates) of FCF dye and SLS are also potential candidates for current generation. Cell charged in sunlight is capable of generating current even after cutting-off the illumination of electrolyte.

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