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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Real-Time Photodynamics of Squaraine-Based Dye-Sensitized Solar Cells with Iodide and Cobalt Electrolytes
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Real-Time Photodynamics of Squaraine-Based Dye-Sensitized Solar Cells with Iodide and Cobalt Electrolytes

机译:含碘化物和钴电解质的基于方胺的染料敏化太阳能电池的实时光动力学

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A series of dye-sensitized solar cells (DSSCs) has been prepared by using indole-based or quinoline-based squaraines (SQs) as the sensitizer and containing the commonly used I3~-/I~- redox pair or the lately employed cobalt complexes, [Co(dimethyIbipyridine)3]~(3+/2+), [Co-(bipyridine)3]~(3+/2+), and [Co(phenanfhroline)3]~(3+/2+) redox electrolytes. The photodynamics of the different electron transfer reactions have been investigated by means of the femto- to millisecond pump—probe techniques. In the femtosecond transient, absorption experiments, the electron injection rate constants and efficiencies, k_(ei) and φ_(ei) were determined for each cell. Larger values of k_(ei) and φ_(ei) for the indole-based (SQ.8,) compared to the quinoline-based (SQ.12) squaraines were obtained (13.2 × 10~(10) s~(-1) and 0.95 × 10~(10) vs 6.9 × 10~(10) s~(-1) and 0.81 for SQ 8 or SQ 12 with the I3~-/I~- pair, respectively), despite the similar values of the electron injection driving forces (~ΔG_(ei)~0 = 0.75 vs 0.76 eV). This is due to the lower electron density in the lowest unoccupied molecular orbital at the anchoring group (-COOH) in SQ 12 compared to SQ 8. However, the type of electrolyte did not affect the kinetics of the electron injection processes. In the flash photolysis experiments, the kinetic parameters of the electron recombination via dye or electrolyte and the cation regeneration were calculated from the decays of the transient absorption signals of the electrons (1550 nm) or the SQ cation (570 nm), It was found that the electron recombination with the oxidized redox species is faster with the Co-based compared to the I3~-/I~- electrolytes for both SQs, τ_(rec) = 3 versus ~0.5-1 ms. This proves that the steric hindrance in these SQs is not sufficient to avoid the approach of the Co~(3+) species to the surface of the TiO2 nanoparticle. Moreover, the regeneration rate constants and efficiencies, k_(,eg) and φ_(reg), are considerably smaller for the cells with the different Co-based electrolytes compared to those with the I3~-/I~- pair (i.e, k_(reg) = 30 × 104 vs 8 × 10~4 M~(-1) s~(-1) and φ_(reg) = 0.96 vs 0.75 with the [Co(dmb)3]~(3+/2+) for SQ 8). This is explained by the lower regeneration driving force, -ΔG_(reg), in the Co-based electrolytes (0.3-0.1 eV). Thus, the use of Co-based electrolytes in these two SQs is detrimental to the overall efficiency of the cell, since -ΔG_(reg) values below 0.4 eV do not give complete regeneration efficiency. Finally, we have compared the measured photocurrent with the calculated electron injection and regeneration efficiencies, and we found a good correlation between both parameters.
机译:染料敏化太阳能电池(DSSC)的制备是通过使用吲哚基或喹啉基方晶(SQs)作为敏化剂,并包含常用的I3-I- / I-氧化还原对或最近使用的钴配合物。 ,[Co(dimethyIbipyridine)3]〜(3 + / 2 +),[Co-(bipyridine)3]〜(3 + / 2 +)和[Co(phenanfhroline)3]〜(3 + / 2 +)氧化还原电解质。已经通过飞秒至毫秒泵浦探针技术研究了不同电子转移反应的光动力学。在飞秒瞬态吸收实验中,确定了每个单元的电子注入速率常数和效率k_(ei)和φ_(ei)。与基于喹啉的(SQ.12)相比,基于吲哚的(SQ.8)的k_(ei)和φ_(ei)更大(13.2×10〜(10)s〜(-1) )和0.95×10〜(10)对比6.9×10〜(10)s〜(-1)和0.81(对于带有I3〜-/ I〜-对的SQ 8或SQ 12),尽管电子注入驱动力(〜ΔG_(ei)〜0 = 0.75 vs 0.76 eV)。这是由于与SQ 8相比,SQ 12中锚定基团(-COOH)的最低未占据分子轨道的电子密度较低。但是,电解质的类型并未影响电子注入过程的动力学。在闪速光解实验中,通过电子或SQ阳离子(57050 nm)的瞬态吸收信号的衰减来计算通过染料或电解质进行电子重组和阳离子再生的动力学参数,发现相对于I3〜-/ I〜-电解质,对于SQs,τ_(rec)= 3相对于〜0.5-1 ms,与Co相比,Co-基与氧化还原物种的电子复合更快。这证明了这些SQ中的空间位阻不足以避免Co〜(3+)种类接近TiO2纳米粒子的表面。而且,与具有I3〜-/ I〜-对的电池相比,具有不同Co基电解质的电池的再生速率常数和效率k_(例如)和φ_(reg)要小得多。 (reg)= 30×104 vs 8×10〜4 M〜(-1)s〜(-1),φ_(reg)= 0.96 vs 0.75,[Co(dmb)3]〜(3 + / 2 + )用于SQ 8)。这由Co基电解质(0.3-0.1eV)中较低的再生驱动力-ΔG_(reg)来解释。因此,在这两个SQ中使用Co基电解质会损害电池的整体效率,因为低于0.4 eV的-ΔG_(reg)值不能提供完全的再生效率。最后,我们将测得的光电流与计算出的电子注入和再生效率进行了比较,发现这两个参数之间具有良好的相关性。

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