新型吡咯胺偶氮吡唑酮的合成、热行为、光谱、计算及其在敏化太阳能电池中的应用。

IF 3.1 4区 化学 Q2 BIOCHEMICAL RESEARCH METHODS
Yousif K Zyara, Hussain J Mohammed
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引用次数: 0

摘要

以吡啶-2-基甲胺和(3-(3-甲基-5-氧-2,5-二氢- 1h -吡唑-1-基)苯基)氨基磺酸为原料合成了一种新的2-吡啶胺-偶氮-3-甲基-1-(3-氨基磺酰胺苯基)-5-吡唑酮(2PAMP)染料,并探索了其在染料敏化太阳能电池中的应用可能性。通过紫外可见光谱、红外光谱、核磁共振光谱和热分析对染料的结构进行了确定。考察了2PAMP在各种溶剂中的可见吸收性能,并对其溶剂致变色行为进行了评价。此外,利用密度泛函理论(DFT)方法,结合混合B3LYP泛函和6-311G(d, p)基集,研究了化学反应性建模。该染料2PAMP被用作染料敏化太阳能电池(DSSCs)的替代敏化剂。根据从电流电压曲线中得到的效率参数Voc、Jsc、FF和%来描述太阳能电池。2PAMP对DSSC的最大效率为0.3600%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New Picolylamine Azo Pyrazolone Synthesis, Thermal Behavior, Spectroscopic, Computational and its Application in Sensitized Solar Cells.

A new 2-picolylamine-azo-3-methyl-1-(3-sulfoamidophenyl)-5-pyrazolone (2PAMP) dye was synthesized from pyridin-2-ylmethanamine and (3-(3-methyl-5-oxo-2,5-dihydro-1H-pyrazol-1-yl)phenyl)sulfamic acid and searched for the possibilities of its employment in Dye-Sensitized Solar Cells. The structure of the dyes was certain by UV-visible and FT-IR, 1H-NMR spectroscopic techniques, and thermal analysis. The solvatochromic behavior of the 2PAMP was evaluated concerning its visible absorption properties in various solvents. Moreover, chemical reactivity modeling using the Density Functional Theory (DFT) method with the hybrid B3LYP functional in conjunction with the 6-311G(d, p) basis set has been investigated. This dye, 2PAMP, was utilized as an alternative sensitizer for Dye-Sensitized Solar Cells (DSSCs). The solar cells were depicted according to their efficiency parameters Voc, Jsc, FF, and ƞ%, gained from the current vs. voltage curves. The maximum efficiency of DSSC with 2PAMP was 0.3600%.

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来源期刊
Journal of Fluorescence
Journal of Fluorescence 化学-分析化学
CiteScore
4.60
自引率
7.40%
发文量
203
审稿时长
5.4 months
期刊介绍: Journal of Fluorescence is an international forum for the publication of peer-reviewed original articles that advance the practice of this established spectroscopic technique. Topics covered include advances in theory/and or data analysis, studies of the photophysics of aromatic molecules, solvent, and environmental effects, development of stationary or time-resolved measurements, advances in fluorescence microscopy, imaging, photobleaching/recovery measurements, and/or phosphorescence for studies of cell biology, chemical biology and the advanced uses of fluorescence in flow cytometry/analysis, immunology, high throughput screening/drug discovery, DNA sequencing/arrays, genomics and proteomics. Typical applications might include studies of macromolecular dynamics and conformation, intracellular chemistry, and gene expression. The journal also publishes papers that describe the synthesis and characterization of new fluorophores, particularly those displaying unique sensitivities and/or optical properties. In addition to original articles, the Journal also publishes reviews, rapid communications, short communications, letters to the editor, topical news articles, and technical and design notes.
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