Robert Bosch GmbH, Gerlingen, Germany.
Langmuir. 2012 Aug 7;28(31):11354-63. doi: 10.1021/la302197z. Epub 2012 Jul 25.
Processing dye-sensitized solar cells gains more and more importance as interest in industrial applications grows daily. For large-scale processing and optimizing manufacturing in terms of environmental acceptability as well as time and material saving, a detailed knowledge of certain process steps is crucial. In this paper we concentrate on the sensitizing step of production, i.e., the anchoring of the dye molecules onto the TiO(2) semiconductor. A vacuum-tight attentuated total reflection infrared (ATR-IR) flow-through cell was developed, thus allowing measurements using a vacuum spectrometer to monitor infiltration of dye molecules into the porous TiO(2) film in situ at high sensitivity. In particular, the influence of the anchor and backbone of perylene dye molecules as well as the influence of solvents on the adsorption process was investigated. The experiments clearly show that an anhydride group reacts much slower than an acid group. A significantly lower amount of anhydride dye can be adsorbed on the films. Ex situ transmission experiments furthermore indicate that the availability of OH groups on the TiO(2) surface may limit dye adsorption. Also the backbone and base frame of the dye can influence the adsorption time drastically. Electrical cell characteristics correlate with the amount of adsorbed dye molecules determined by in situ ATR-IR measurements. The latter is also sensitive toward the diffusion of the dye through the porous layer. To gain a deeper understanding of the interplay between diffusion and adsorption, simulations were performed that allowed us to extract diffusion and adsorption constants. Again it was demonstrated that the anchoring group has a strong effect on the adsorption rate. The influence of the solvent was also studied, and it was found that both adsorption and desorption are affected by the solvent. Protic polar solvents are able to remove bound dye molecules, which is a possible pathway of cell degradation. Most importantly, the analysis shows the potential of this approach for the evaluation of molecules or additives concerning their characteristics important for cell processing.
染料敏化太阳能电池的处理越来越受到重视,因为人们对工业应用的兴趣与日俱增。为了实现大规模处理和优化制造,使其在环境可接受性、时间和材料节约方面达到最佳状态,详细了解某些工艺步骤至关重要。本文集中研究生产中的敏化步骤,即染料分子固定在 TiO(2)半导体上。为此,我们开发了一种密闭衰减全反射红外(ATR-IR)流通池,从而可以使用真空光谱仪进行测量,以高灵敏度原位监测染料分子渗透到多孔 TiO(2)薄膜中。特别是,研究了苝染料分子的锚定基和主链以及溶剂对吸附过程的影响。实验清楚地表明,酸基的反应速度比酐基快得多。薄膜上吸附的酐基染料量要少得多。此外,体外传输实验表明,TiO(2)表面的 OH 基团的可用性可能会限制染料的吸附。染料的主链和基本框架也会极大地影响吸附时间。电池的电特性与通过原位 ATR-IR 测量确定的吸附染料分子的数量相关。后者还对染料通过多孔层的扩散敏感。为了更深入地了解扩散和吸附之间的相互作用,进行了模拟,从而可以提取扩散和吸附常数。再次证明,锚定基团对吸附速率有很强的影响。溶剂的影响也进行了研究,发现吸附和脱附都受到溶剂的影响。质子极性溶剂能够去除结合的染料分子,这是电池降解的一种可能途径。最重要的是,分析表明这种方法具有评估对电池处理很重要的分子或添加剂的特性的潜力。