1453263-40-5Relevant articles and documents
Improving the photoresponse of copper(i) dyes in dye-sensitized solar cells by tuning ancillary and anchoring ligand modules
Bozic-Weber, Biljana,Brauchli, Sven Y.,Constable, Edwin C.,Fuerer, Sebastian O.,Housecroft, Catherine E.,Malzner, Frederik J.,Wright, Iain A.,Zampese, Jennifer A.
, p. 12293 - 12308 (2013/09/02)
The syntheses of five homoleptic copper(i) complexes [CuL 2][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, nbutyl, isobutyl 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 [CuL 2][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)(L anchor)]+ 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.
