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通过调节辅助配体和锚定配体模块来提高染料敏化太阳能电池中铜(I)染料的光响应。

Improving the photoresponse of copper(I) dyes in dye-sensitized solar cells by tuning ancillary and anchoring ligand modules.

机构信息

Department of Chemistry, University of Basel, Spitalstrasse 51, CH4056 Basel, Switzerland.

出版信息

Dalton Trans. 2013 Sep 14;42(34):12293-308. doi: 10.1039/c3dt51416a. Epub 2013 Jul 12.

Abstract

The syntheses of five homoleptic copper(I) complexes [CuL2][PF6] are described in which L is a 4,4'-di(4-bromophenyl)-6,6'-dialkyl-2,2'-bipyridine ligand (compounds 1-4 with methyl, (n)butyl, (iso)butyl and hexyl substituents, respectively) or 4,4'-di(4-bromophenyl)-6,6'-diphenyl-2,2'-bipyridine (5). The new ligands 2-5 and copper(I) complexes [CuL2][PF6] (L = 1-5) have been fully characterized. The single crystal structures of 2{[Cu(1)2][PF6]}·3Me2CO, [Cu(2)2][PF6], 2{[Cu(3)2][PF6]}·Et2O and [Cu(5)2][PF6]·CH2Cl2 have been determined. The first three structures show similar distorted tetrahedral environments for the Cu(+) ions with angles between the least squares planes of the bpy domains of 85.6, 86.4 and 82.9°, respectively; in contrast, the Cu(+) ion in [Cu(5)2][PF6]·CH2Cl2 is in a flattened coordinate environment due to intra-cation face-to-face π-interactions. The solution absorption spectra of the complexes with ligands 1-4 are virtually identical with an MLCT band with values of λmax = 481-488 nm. In contrast, the absorption spectrum of [Cu(5)2][PF6] shows two broad bands in the visible region. Cyclic voltammetric data show that oxidation of the copper(I) centre occurs at a more positive potential in [Cu(2)2][PF6], [Cu(3)2][PF6] and [Cu(4)2][PF6] than in [Cu(1)2][PF6] or [Cu(5)2][PF6] with the latter being oxidized at the lowest potential. The complexes have been used to prepare dye-sensitized solar cells (DSCs) incorporating heteroleptic dyes of type Cu(L)(Lanchor) where L is 1-5 and Lanchor is a 6,6'-dimethyl-2,2'-bipyridine functionalized in the 4- and 4'-positions with phosphonic acid groups with (Lanchor = 7) and without (Lanchor = 6) a spacer between the metal-binding and anchoring domains. The presence of the spacer results in enhanced performances of the dyes, and the highest energy conversion efficiencies are observed for the dyes Cu(3)(7) (η = 2.43% compared to 5.96% for standard dye N719) and Cu(5)(7) (η = 2.89% compared to 5.96% for N719). Measurements taken periodically over the course of a week indicate that the cells undergo a ripening process (most clearly seen for Cu(5)(6) and Cu(5)(7)) before their optimum performances are achieved. IPCE (EQE) data are presented and confirm that, although the photo-to-current conversions are promising (37-49% for λmax≈ 480 nm), the copper(I) dyes do not realize the broad spectral response exhibited by N719.

摘要

描述了 5 种同核铜(I)配合物[CuL2][PF6]的合成,其中 L 是 4,4'-二(4-溴苯基)-6,6'-二取代-2,2'-联吡啶配体(化合物 1-4 分别具有甲基、(正)丁基、(异)丁基和己基取代基)或 4,4'-二(4-溴苯基)-6,6'-二苯基-2,2'-联吡啶(5)。新配体 2-5 和铜(I)配合物[CuL2][PF6](L=1-5)已被充分表征。确定了 2{[Cu(1)2][PF6]}·3Me2CO、[Cu(2)2][PF6]、2{[Cu(3)2][PF6]}·Et2O 和 [Cu(5)2][PF6]·CH2Cl2 的单晶结构。前三个结构显示 Cu(+)离子具有相似的扭曲四面体环境,bpy 域的最小二乘平面之间的角度分别为 85.6、86.4 和 82.9°;相比之下,[Cu(5)2][PF6]·CH2Cl2 中的 Cu(+)离子由于阳离子面-面π-相互作用而处于扁平的配位环境。配合物 1-4 的溶液吸收光谱几乎相同,具有 MLCT 带,λmax 值为 481-488nm。相比之下,[Cu(5)2][PF6]的吸收光谱在可见光区域显示两个宽带。循环伏安数据表明,在[Cu(2)2][PF6]、[Cu(3)2][PF6]和[Cu(4)2][PF6]中,铜(I)中心的氧化发生在更正的电位,而[Cu(1)2][PF6]或[Cu(5)2][PF6]的氧化电位更低。这些配合物已被用于制备染料敏化太阳能电池(DSC),其中包含杂配染料[Cu(L)(Lanchor)]+,其中 L 是 1-5,Lanchor 是 6,6'-二甲基-2,2'-联吡啶,在 4-和 4'-位用膦酸基团官能化,带有(Lanchor=7)和不带(Lanchor=6)金属结合和锚固结构域之间的间隔物。间隔物的存在导致染料性能得到增强,观察到染料[Cu(3)(7)]+(η=2.43%,而标准染料 N719 为 5.96%)和[Cu(5)(7)]+(η=2.89%,而标准染料 N719 为 5.96%)的最高能量转换效率。在一周的时间内定期进行的测量表明,在达到最佳性能之前,电池经历了一个成熟过程(在[Cu(5)(6)]+和[Cu(5)(7)]+中最为明显)。给出了 IPCE(EQE)数据,并证实尽管光电流转换很有希望(λmax≈480nm 时为 37-49%),但铜(I)染料并没有实现 N719 所展示的宽光谱响应。

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