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

Dalton Transactions Pub Date: 2013-07-12 DOI: 10.1039/C3DT51416A

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, 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 [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.

Graphical abstract: Improving the photoresponse of copper(i) dyes in dye-sensitized solar cells by tuning ancillary and anchoring ligand modules
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