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Synthesis and characterization of novel thieno3,2-bthiophene based metal-free organic dyes with different heteroaromatic donor moieties as sensitizers for dye-sensitized solar cells

机译:具有不同杂芳族供体部分的新型噻吩并3,2-b噻吩基无金属有机染料的合成和表征,作为染料敏化太阳能电池的敏化剂

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摘要

Four novel heterocycle dyes 3a-d were synthesized in order to study the variations produced in the optical, electronic and photovoltaic properties by substitution of different electron-rich heterocyclic groups to the thieno[3,2-b]thiophene system. The final push-pull conjugated dyes 3a-d were synthesized by Suzuki-Miyaura coupling reaction followed by Knoevenagel condensation of the corresponding aldehyde precursors with cyanoacrylic acid 2a-d. These new push-pull systems are based on a thieno[3,2-b]thiophene spacer, a cyanoacetic acid anchoring group and several electron-rich heterocycles (thiophene, pyrrole and furan) as donor groups. The multidisciplinary study concerning the optical, redox and photovoltaic characterization of the dyes reveals that compound 3b bearing a hexyl-bithiophene donor group/heterocyclic spacer exhibits the best overall conversion efficiency (2.49%) as sensitizer in nanocrystalline TiO2 dye sensitized solar cells. Co-adsorption studies between N719 and 3b revealed that upon addition of N719 co-adsorbent, the optimized cell efficiencies were improved by 16–77%. The best efficiency was 4.40%, corresponding to 54% of the photovoltaic performance of the N719-based DSSC fabricated and measured under similar conditions.
机译:为了研究通过将不同的富电子杂环基团替换为噻吩并[3,2-b]噻吩系统而在光学,电子和光伏性质中产生的变化,合成了四种新颖的杂环染料3a-d。通过Suzuki-Miyaura偶联反应,然后将相应的醛前体与氰基丙烯酸2a-d进行Knoevenagel缩合,合成最终的推挽共轭染料3a-d。这些新的推挽系统基于噻吩并[3,2-b]噻吩间隔基,氰基乙酸锚定基团和几个富电子杂环(噻吩,吡咯和呋喃)作为供体基团。关于染料的光学,氧化还原和光伏表征的多学科研究表明,带有己基-联噻吩供体基团/杂环间隔基的化合物3b在纳米TiO2染料敏化的太阳能电池中作为敏化剂表现出最佳的总转化效率(2.49%)。 N719和3b之间的共吸附研究表明,添加N719共吸附剂后,优化的电池效率提高了16%至77%。最佳效率为4.40%,相当于在相似条件下制造和测量的基于N719的DSSC光伏性能的54%。

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