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Halos show the path to perfection : peripheral iodo-substituents improve the efficiencies of bis(diimine)copper(I) dyes in dye-sensitized solar cells

机译:Halos显示了完美的途径:外周碘取代基提高了染料敏化太阳能电池中双(二亚胺)铜(I)染料的效率

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摘要

The homoleptic copper(I) complexes [CuL2][PF6] (L = 4,4′-bis(4-halophenyl)-6,6′-dimethyl-2,2′-bipyridine with halogen = F (2) and Cl (3)) have been prepared and characterized, and their absorption spectroscopic and electrochemical properties compared to that with L = 4,4′-bis(4-bromophenyl)-6,6′-dimethyl-2,2′-bipyridine (4). The synthesis of [CuL2][PF6] (L = 4,4′-bis(4-iodophenyl)-6,6′-dimethyl-2,2′-bipyridine, 5) resulted in a mixture of [Cu(5)2][PF6] and [Cu(5)(MeCN)2][PF6]; variable temperature 1H NMR spectroscopy confirmed that the complexes are in equilibrium in CD3CN solution. The structure of [Cu(5)(MeCN)2][PF6] was determined by single crystal X-ray crystallography, and confirms a distorted tetrahedral geometry for the copper(I) centre. The heteroleptic dyes [Cu(1)(2)]+, [Cu(1)(3)]+, [Cu(1)(4)]+ and [Cu(1)(5)]+ (1 = ((6,6′-dimethyl-[2,2′-bipyridine]-4,4′-diyl)bis(4,1-phenylene))bis(phosphonic acid)) have been assembled by ligand exchange between [CuL2]+ and TiO2 functionalized with the anchoring ligand 1, and the performances of the dyes in fully masked dye-sensitized solar cells (DSCs) have been measured and compared. On the day of DSC fabrication, the trend for the global efficiencies, η, depends on the halo-substituent in the order I > F ≈ Br > Cl. Ripening of the DSCs occurs and after 7 days, the dependence of η on the halo-atom is in the order I > Cl ≈ F ≈ Br; the highest η is 3.16% for [Cu(1)(5)]+ compared to 7.63% for N719. Compared to the other halo-functionalized dyes, [Cu(1)(5)]+ shows an extended spectral response to longer wavelength, with enhanced electron injection. The results of DFT calculations suggest that the better dye performance of [Cu(1)(5)]+ may be associated with improved electron transfer over the halogen of the aryl substituent from the reduced electrolyte. The assembly of anchored dye [Cu(1)(5)]+ by treating functionalized-TiO2 with a 1 : 1 mixture of [Cu(MeCN)4]+ and 5, yields a dye which gives a DSC performance that matches that made by ligand exchange using [Cu(5)2][PF6] and [Cu(5)(MeCN)2][PF6].
机译:均相铜(I)配合物[CuL2] [PF6](L = 4,4'-双(4-卤代苯基)-6,6'-二甲基-2,2'-联吡啶与卤素= F(2)和Cl (3))的制备和表征,与L = 4,4'-双(4-溴苯基)-6,6'-二甲基-2,2'-联吡啶(4)相比,它们的吸收光谱和电化学性质)。 [CuL2] [PF6](L = 4,4'-双(4-碘苯基)-6,6'-二甲基-2,2'-联吡啶,5)的合成产生了[Cu(5) 2] [PF6]和[Cu(5)(MeCN)2] [PF6];可变温度1H NMR光谱证实,络合物在CD3CN溶液中处于平衡状态。 [Cu(5)(MeCN)2] [PF6]的结构是通过单晶X射线晶体学确定的,证实了铜(I)中心的四面体几何形状失真。杂合染料[Cu(1)(2)] +,[Cu(1)(3)] +,[Cu(1)(4)] +和[Cu(1)(5)] +(1 =( (6,6'-二甲基-[2,2'-联吡啶] -4,4'-二基)双(4,1-亚苯基))双(膦酸)已通过[CuL2] +之间的配体交换组装和用锚定配体1功能化的TiO2,已经测量并比较了染料在完全掩盖的染料敏化太阳能电池(DSC)中的性能。在DSC制造的那天,整体效率的趋势η取决于卤素取代基的顺序,即I> F≈Br> Cl。 DSCs发生成熟,并且在7天后,η对卤原子的依赖性为I> Cl≈F≈Br; [Cu(1)(5)] +的最高η为3.16%,而N719为7.63%。与其他卤素官能化的染料相比,[Cu(1)(5)] +显示出对更长波长的扩展光谱响应,并增强了电子注入。 DFT计算的结果表明,[Cu(1)(5)] +的更好的染料性能可能与还原的电解质上芳基取代基的卤素上电子转移的改善有关。通过用[Cu(MeCN)4] +和5的1:1混合物处理官能化的TiO2来组装锚固染料[Cu(1)(5)] +,所得到的染料的DSC性能可与通过使用[Cu(5)2] [PF6]和[Cu(5)(MeCN)2] [PF6]进行配体交换。

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