Tuning the chemical properties of europium complexes as downshifting agents for copper indium gallium selenide solar cells
Résumé
New europium(III) β-diketonate based complexes with the general formula [Eu(β-Dik)3(NL)x], where β-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 1 H, 13 C, 19 F 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 exhibits the characteristic 5 D0→ 7 F0-4 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) layer 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 (Jsc) 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 Jsc 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 %.
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