Kian Sing Low, Jacqueline M Cole, Xiaolan Zhou, Nataliya Yufa
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Results show that the metal (M) core exhibits a distorted octahedral environment with M-N π-backbonding effects affording the propensity of the metal ion towards oxidation. The same characteristics are observed in iron-based analogues. The role of carboxylic groups in this series of dyes is assessed by comparing complexes which contain or are devoid of COOH groups. Space-group variation and large molecular conformational differences occur when COOH groups are present, while such structural features are very similar in their absence. The nature of the anion is also shown to influence the structure of COOH-containing complexes. These structural findings are corroborated by solution-based UV-vis absorption spectroscopy and DSC device performance tests. The presence of COOH groups in this series of compounds is shown to be mandatory for dye-uptake in TiO(2) in the DSC fabrication process. Throughout this study, results are compared with those of the world's most famous DSC dye, N3 (N719 in its fully protonated form): cis-bis(isothiocyanato)bis(2,2'-bipyridyl-4,4'-dicarboxylato)ruthenium(II). Overall, the molecular origins of charge-transfer in these complexes are ascertained. 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引用次数: 20
摘要
作为为染料敏化太阳能电池(dsc)设计更高效染料的努力的一部分,在世界上性能最好的化学染料系列:2,2'-联吡啶-4,4'-羧酸钌(II)配合物中建立了结构-性能关系。统计分析基于剑桥结构数据库的晶体学数据,用于确定共同的结构特征和结构变化对其显著分子成分的影响。此外,还报道了三(2,2′-联吡啶基)二氯钌(II)六水化合物和三(2,2′-联吡啶基)铁(II)二硫氰酸酯的两种新晶体结构;这些增加了这一统计调查。结果表明,金属(M)芯呈现出扭曲的八面体环境,M- n π-背键效应使金属离子具有氧化倾向。在铁基类似物中观察到相同的特性。羧基在这一系列染料中的作用是通过比较含有或不含羧基的配合物来评估的。当COOH基团存在时,会发生空间基团变化和较大的分子构象差异,而当COOH基团不存在时,这些结构特征非常相似。阴离子的性质也会影响含羧基配合物的结构。这些结构发现被基于溶液的紫外-可见吸收光谱和DSC器件性能测试证实。在DSC制造过程中,羧基的存在对TiO(2)的染料摄取是必需的。在整个研究中,结果与世界上最著名的DSC染料N3 (N719完全质子化形式):顺式-双(异硫氰酸酯)双(2,2'-联吡啶-4,4'-二羧酸)钌(II)进行了比较。总的来说,确定了这些复合物中电荷转移的分子起源。这些发现对DSC技术中更高效染料的材料发现具有重要意义。
Rationalizing the molecular origins of Ru- and Fe-based dyes for dye-sensitized solar cells.
As part of an effort to design more efficient dyes for dye-sensitized solar cells (DSCs), structure-property relationships are established in the world's best-performing chemical series of dyes: 2,2'-bipyridyl-4,4'-carboxylatoruthenium(II) complexes. Statistical analysis, based on crystallographic data from the Cambridge Structural Database, is used to determine common structural features and the effects of structural change to its salient molecular constituents. Also included is the report of two new crystal structures for tris(2,2'-bipyridyl)dichlororuthenium(II)hexahydrate and tris(2,2'-bipyridyl)iron(II)dithiocyanate; these add to this statistical enquiry. Results show that the metal (M) core exhibits a distorted octahedral environment with M-N π-backbonding effects affording the propensity of the metal ion towards oxidation. The same characteristics are observed in iron-based analogues. The role of carboxylic groups in this series of dyes is assessed by comparing complexes which contain or are devoid of COOH groups. Space-group variation and large molecular conformational differences occur when COOH groups are present, while such structural features are very similar in their absence. The nature of the anion is also shown to influence the structure of COOH-containing complexes. These structural findings are corroborated by solution-based UV-vis absorption spectroscopy and DSC device performance tests. The presence of COOH groups in this series of compounds is shown to be mandatory for dye-uptake in TiO(2) in the DSC fabrication process. Throughout this study, results are compared with those of the world's most famous DSC dye, N3 (N719 in its fully protonated form): cis-bis(isothiocyanato)bis(2,2'-bipyridyl-4,4'-dicarboxylato)ruthenium(II). Overall, the molecular origins of charge-transfer in these complexes are ascertained. The findings have important implications to the materials discovery of more efficient dyes for DSC technology.
期刊介绍:
Acta Crystallographica Section B: Structural Science, Crystal Engineering and Materials publishes scientific articles related to the structural science of compounds and materials in the widest sense. Knowledge of the arrangements of atoms, including their temporal variations and dependencies on temperature and pressure, is often the key to understanding physical and chemical phenomena and is crucial for the design of new materials and supramolecular devices. Acta Crystallographica B is the forum for the publication of such contributions. Scientific developments based on experimental studies as well as those based on theoretical approaches, including crystal-structure prediction, structure-property relations and the use of databases of crystal structures, are published.