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钌(II)-四唑配合物作为无硫氰酸盐染料敏化太阳能电池敏化剂的新实例。

New examples of Ru(II)-tetrazolato complexes as thiocyanate-free sensitizers for dye-sensitized solar cells.

作者信息

Fiorini Valentina, Marchini Edoardo, Averardi Mattia, Giorgini Loris, Muzzioli Sara, Dellai Angela, Argazzi Roberto, Sanson Alessandra, Sangiorgi Nicola, Caramori Stefano, Stagni Stefano

机构信息

Department of Industrial Chemistry "Toso Montanari", University of Bologna, Viale Risorgimento 4, I-40136 Bologna, Italy.

Department of Chemical and Pharmaceutical Sciences, University of Ferrara, via Luigi Borsari 46, I-44121 Ferrara, Italy.

出版信息

Dalton Trans. 2020 Oct 27;49(41):14543-14555. doi: 10.1039/d0dt02621b.

Abstract

A set of three new Ru(ii) polypyridyl complexes decorated with 5-aryl tetrazolato ligands (R-CN4)-, (D series, namely D1, D3 and D4), is presented herein. Whereas complex D1 represents the pyrazinyl tetrazolato analogue of a previously reported Ru(ii) complex (D2) with the general formula cis-[(dcbpy)2Ru(N^N)]+, in which dcbpy is 2,2'-bipyridine-4,4'-dicarboxylic acid and N^N is the chelating 2-pyridyl tetrazolato anion, the design of the unprecedented Ru(ii) species D3 and D4 relied upon a completely different architecture. More specifically, the molecular structure of thiocyanate-based species cis-[(dcbpy)2Ru(NCS)2], that is typically found in benchmark Ru(ii) dyes for dye sensitized solar cell (DSSCs), was modified with the replacement of two of the -NCS ligands in favour of the introduction of 5-aryl tetrazolato anions, such as the deprotonated form of 5-(4-bromophenyl)-1H-tetrazole, for complex D3 and 5-(4-cyanophenyl)-1H-tetrazole in the case of complex D4. To streamline the behavior of the D series of Ru(ii) complexes as photosensitizers for DSSCs, an in-depth analysis of the excited state properties of D1, D3 and D4 was performed through TDDFT calculations and TDAS (nanosecond transient difference absorption spectroscopy). The obtained results highlight a trend that was confirmed once D1, D3 and D4 were tested as photosensitizers for DSSC under different conditions. Along the series of the Ru(ii) complexes, the neutrally charged species D3 and D4 displayed the best photovoltaic performances.

摘要

本文介绍了一组由5-芳基四唑配体(R-CN4)-修饰的三种新型钌(II)多吡啶配合物(D系列,即D1、D3和D4)。配合物D1是先前报道的通式为顺式-[(dcbpy)2Ru(N^N)]+的钌(II)配合物(D2)的吡嗪基四唑类似物,其中dcbpy为2,2'-联吡啶-4,4'-二羧酸,N^N为螯合的2-吡啶基四唑阴离子,而前所未有的钌(II)物种D3和D4的设计则依赖于完全不同的结构。更具体地说,基于硫氰酸盐的物种顺式-[(dcbpy)2Ru(NCS)2]的分子结构,这种结构通常存在于染料敏化太阳能电池(DSSC)的基准钌(II)染料中,通过用5-芳基四唑阴离子取代两个-NCS配体进行了修饰,对于配合物D3,引入的是5-(4-溴苯基)-1H-四唑的去质子化形式,对于配合物D4则是5-(4-氰基苯基)-1H-四唑。为了简化D系列钌(II)配合物作为DSSC光敏剂的行为,通过TDDFT计算和TDAS(纳秒瞬态差分吸收光谱)对D1、D3和D4的激发态性质进行了深入分析。所得结果突出了一种趋势,当D1、D3和D4在不同条件下作为DSSC的光敏剂进行测试时,这一趋势得到了证实。在这一系列钌(II)配合物中,中性电荷物种D3和D4表现出最佳的光伏性能。

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