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首页> 外文期刊>Electrochimica Acta >Use of lithium iodide and tetrapropylammonium iodide in gel electrolytes for improved performance of quasi-solid-state dye-sensitized solar cells: Recording an efficiency of 6.40%
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Use of lithium iodide and tetrapropylammonium iodide in gel electrolytes for improved performance of quasi-solid-state dye-sensitized solar cells: Recording an efficiency of 6.40%

机译:在凝胶电解质中使用碘化锂和四丙基碘化铵,以改善准固态染料敏化太阳能电池的性能:记录效率为6.40%

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摘要

Use of gel electrolytes in place of liquid electrolytes in DSCs is one of the proposed alternatives to circumvent some of the problems suffered by the liquid electrolyte-based DSCs such as electrolyte leakage, solvent evaporation and reaction of I ions with atmospheric oxygen due to sealing imperfections. Even though the use of gel electrolytes sacrifices the cell efficiency up to some extent due to their low ion mobility, there are promising properties of gel electrolytes such as thermal stability, lower flammability and environmental friendliness. Use of Li+ and tetrapropylammonium (Pr4N+)-based iodide salts in gel electrolytes is quite common. However, the effects of Li+ and Pr4N+ on vital processes such as recombination and diffusion of I-3 through the device have not been fully understood. In this study we have attempted to examine the influence of Li+ and Pr4N+ cations present in the electrolyte on the cell performance. The general structure of the devices used was FTO/TiO2 working electrode/dye (N719)/gel electrolyte/lightly platinized FTO counter electrode. As a first step, devices based on two types of electrolytes were prepared using only LiI salt in one set and only Pr4N+I salt in the other. The salt concentrations were optimized independently for best cell performance in each case. Then a composite salt was prepared using a mixture of LiI and Pr4N+I and the relative proportions of the two salts were varied until the efficiency reached a maximum. The reason for this choice was the fact that the bulk cations such as Pr4N+ have high dissociation constant resulting in easy release of I to the electrolyte whereas Li+ ions tend to increase the amorphous nature of the electrolyte supporting the hopping mechanism of transport of I-3 through the electrolyte. A best efficiency of 6.40% was obtained for the composite salt having a molar ratio of 1:3 of Pr4N+I to LiI, while the individual salts gave efficiencies 5.36% and 6.10%, respectively under identical conditions. We have employed XRD, FTIR, LSV and AC impedance measurements along with the literature support to explain the observed performance of the DSC devices fabricated with different salt compositions. (C) 2016 Elsevier Ltd. All rights reserved.
机译:在DSC中使用凝胶电解质代替液体电解质是解决基于液体电解质的DSC所遇到的一些问题(例如电解质泄漏,溶剂蒸发以及由于密封缺陷而导致的I离子与大气氧反应)的替代方案之一。 。即使使用凝胶电解质由于其低的离子迁移率而在某种程度上牺牲了电池效率,但是凝胶电解质还是有希望的性质,例如热稳定性,较低的可燃性和环境友好性。 Li +和四丙基铵(Pr4N +)基碘化物盐在凝胶电解质中的使用非常普遍。然而,人们还没有完全了解Li +和Pr4N +对生命过程的影响,例如I-3的重组和通过装置的扩散。在这项研究中,我们试图检查电解质中存在的Li +和Pr4N +阳离子对电池性能的影响。所用设备的一般结构是FTO / TiO2工作电极/染料(N719)/凝胶电解质/轻镀FTO对电极。第一步,仅使用一组LiI盐,使用另一组Pr4N + I盐制备基于两种电解质的器件。分别对盐浓度进行了优化,以实现最佳的电池性能。然后使用LiI和Pr4N + I的混合物制备复合盐,并且改变两种盐的相对比例直至效率达到最大。选择该离子的原因是这样的事实,即大量阳离子(例如Pr4N +)具有较高的解离常数,导致I易于释放到电解质中,而Li +离子则倾向于增加电解质的无定形性质,从而支持I-3的跃迁机制。通过电解质。 Pr4N + I与LiI摩尔比为1:3的复合盐的最佳效率为6.40%,而在相同条件下,各个盐的效率分别为5.36%和6.10%。我们已经使用XRD,FTIR,LSV和AC阻抗测量以及文献支持来解释用不同盐成分制造的DSC器件的观察性能。 (C)2016 Elsevier Ltd.保留所有权利。

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