Tuning the chemical properties of europium complexes as downshifting agents for copper indium gallium selenide solar cells

摘要

New europium(III) beta-diketonate based complexes with the general formula [Eu(beta-Dik)(3)(NL)(x)], where beta-Dik = 2-thenoyltrifluoroacetonate, 4,4,4-trifluoro-1-phenyl-1,3-butanedione, 4,4,4-trifluoro-1-(2-naphthyl)-1,3- butanedione, NL = diphenyl sulfoxide (x = 2), bis[2-(diphenylphosphino) phenyl] ether oxide (x = 1), triphenylphosphine oxide (x = 2), 5,6-epoxy-5,6-dihydro-[1,10] phenanthroline (x = 1), are designed and synthesized. The coordination complexes are comprehensively characterized by elemental analysis, infrared and H-1, C-13 and F-19 NMR spectroscopy. The complexes are embedded into poly(ethylene-co-vinyl acetate) (EVA), poly(methyl methacrylate) (PMMA) or poly(vinyl butyral-co-vinyl alcohol-co-vinyl acetate) (PVB) matrices. Photoluminescence behavior is investigated in detail and it exhibits the characteristic D-5(0) -> F-7(0-4) emission bands with quantum yields of 55-83% in the solid state and 34-86% in the polymers. Encapsulation of CIGS solar cells with luminescent downshifting (LDS) layers results in an important improvement of external quantum efficiency (EQE) in the UV region, from 14% and up to 58% at 360 nm for the best compound. The short circuit current density (J(sc)) in the range of 300-400 nm increases up to 0.77 mA cm(-2) for the best LDS which corresponds to 71% of the J(sc) enhancement of an ideal downshifter. I-V measurements follow the spectral response data with an absolute increase in conversion efficiency of up to 0.8%.