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Heteroleptic copper(I) sensitizers with one versus two hole-transporting units in functionalized 2,9-dimethyl-1,10-phenanthroline ancillary ligands

机译:在功能化的2,9-二甲基-1,10-菲咯啉辅助配体中具有一对二空穴传输单元的异质铜(I)敏化剂

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摘要

A series of homoleptic [Cu(L)2][PF6] complexes in which L is a 2,9-dimethyl-1,10-phenanthroline fused at the 5,6-positions with a 2′-functionalized imidazole (ligands 1–4), or substituted at the 4,7-positions with electron-donating 4-(diphenylamino)phenyl groups (ligand 5) is described; the imidazole 2′-functionality in 1 is 4-bromophenyl, in 2 is 4-(diphenylamino)phenyl, in 3 is 4-(bis(4-n-butoxy)phenylamino)phenyl, and in 4 is 4-(carbazol-9-yl)phenyl. The copper complexes were characterized by mass spectrometry, NMR and absorption spectroscopies and cyclic voltammetry; the single crystal structure of ligand 4 has been determined. Compared to the solution absorption spectra of [Cu(1)2][PF6], [Cu(2)2][PF6], [Cu(3)2][PF6] and [Cu(4)2][PF6], that of [Cu(5)2][PF6] shows increased absorbance at wavelengths >375 nm. An on-surface strategy was used to assemble heteroleptic [Cu(6)(L)]+ dyes on TiO2 electrodes where 6 is ((6,6′-dimethyl-[2,2′-bipyridine]-4,4′-diyl)bis(4,1-phenylene))bis(phosphonic acid); solid-state absorption spectra confirmed enhanced light-harvesting between 375 and 600 nm for [Cu(6)(5)]+ with respect to [Cu(6)(1)]+, [Cu(6)(2)]+, [Cu(6)(3)]+ and [Cu(6)(4)]+. Comparison of the performances of dye-sensitized solar cells (DSCs) containing [Cu(6)(2)]+, [Cu(6)(3)]+ and [Cu(6)(4)]+ with those with [Cu(6)(1)]+ indicate only a marginal influence of the diphenylamine or carbazole hole-transporting domains in 5,6-substituted phenanthroline dyes. The introduction of the 4-(diphenylamino)phenyl hole-transporting units in the 4- and 7-positions of the phen unit in 5 proves to be beneficial, with DSCs containing [Cu(6)(5)]+ performing better than those with the other four dyes; duplicate DSCs were tested for each dye to validate the results. While the values of the maximum external quantum efficiencies (EQEmax) for [Cu(6)(1)]+ and [Cu(6)(4)]+ are greater than for [Cu(6)(5)]+, the extension of the EQE spectrum for [Cu(6)(5)]+ to longer wavelengths results in higher short-circuit current densities (JSC) compared to DSCs with [Cu(6)(1)]+, [Cu(6)(2)]+, [Cu(6)(3)]+ and [Cu(6)(4)]+.ud
机译:一系列均一的[Cu(L)2] [PF6]配合物,其中L是在5,6位与2'-官能化的咪唑融合的2,9-二甲基-1,10-菲咯啉(配体1–描述了4)或在4,7-位被供电子的4-(二苯基氨基)苯基(配体5)取代; 1中的咪唑2'-官能团是4-溴苯基,2是4-(二苯基氨基)苯基,3是4-(双(4-正丁氧基)苯基氨基)苯基,4是4-(咔唑- 9-基)苯基。铜配合物通过质谱,NMR和吸收光谱法以及循环伏安法进行表征。已经确定了配体4的单晶结构。与[Cu(1)2] [PF6],[Cu(2)2] [PF6],[Cu(3)2] [PF6]和[Cu(4)2] [PF6]的溶液吸收光谱相比,[Cu(5)2] [PF6]的波长在大于375 nm的波长处显示出增加的吸光度。使用表面上的策略在TiO2电极上组装杂配[Cu(6)(L)] +染料,其中6为(((6,6'-二甲基-[2,2'-联吡啶] -4,4'-二基)双(4,1-亚苯基))双(膦酸);固态吸收光谱证实,相对于[Cu(6)(1)] +,[Cu(6)(2)] +,[Cu(6)(5)] +在375至600 nm之间增强了光捕获,[Cu(6)(3)] +和[Cu(6)(4)] +。含有[Cu(6)(2)] +,[Cu(6)(3)] +和[Cu(6)(4)] +的染料敏化太阳能电池(DSC)与具有[ Cu(6)(1)] +仅表示5,6-取代的菲咯啉染料中二苯胺或咔唑空穴传输域的边缘影响。事实证明,在5中的phen单元的4和7位上引入4-(二苯氨基)苯基空穴传输单元是有益的,其中包含[Cu(6)(5)] +的DSC的性能要优于那些。与其他四种染料;测试每种染料的重复DSC,以验证结果。尽管[Cu(6)(1)] +和[Cu(6)(4)] +的最大外部量子效率(EQEmax)值大于[Cu(6)(5)] +,但是与具有[Cu(6)(1)] +,[Cu(6)]的DSC相比,[Cu(6)(5)] +的EQE谱扩展到更长的波长会导致更高的短路电流密度(JSC) (2)] +,[Cu(6)(3)] +和[Cu(6)(4)] +。 ud

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