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Highly efficient IR to NIR upconversion in Gd2O2S: Er3+ for photovoltaic applications

: Martín-Rodríguez, R.; Fischer, S.; Ivaturi, A.; Froehlich, B.; Krämer, K.W.; Goldschmidt, J.C.; Richards, B.S.; Meijerink, A.


Chemistry of Materials 25 (2013), No.9, pp.1912-1921
ISSN: 0897-4756
ISSN: 1520-5002
Journal Article
Fraunhofer ISE ()
Solarzellen - Entwicklung und Charakterisierung; Silicium-Photovoltaik; Farbstoff; Organische und Neuartige Solarzellen; Alternative Photovoltaik-Technologien; Herstellung und Analyse von hocheffizienten Solarzellen; Photonenmanagement; Industrielle und neuartige Solarzellenstrukturen; Neuartige Konzepte; cells; Upconversion; Luminescence; Yield

Upconversion (UC) is a promising option to enhance the efficiency of solar cells by conversion of sub-bandgap infrared photons to higher energy photons that can be utilized by the solar cell. The UC quantum yield is a key parameter for a successful application. Here the UC luminescence properties of Er 3+-doped Gd2O2S are investigated by means of luminescence spectroscopy, quantum yield measurements, and excited state dynamics experiments. Excitation into the maximum of the 4I 15/2 4I13/2 Er3+ absorption band around 1500 nm induces very efficient UC emission from different Er 3+ excited states with energies above the silicon bandgap, in particular, the emission originating from the 4I11/2 state around 1000 nm. Concentration dependent studies reveal that the highest UC quantum yield is realized for a 10% Er3+-doping concentration. The UC luminescence is compared to the well-known Er3+-doped -NaYF4 UC material for which the highest UC quantum yield has been reported for 25% Er3+. The UC internal quantum yields were measured in this work for Gd2O2S: 10%Er3+ and -NaYF4: 25%Er3+ to be 12 ± 1% and 8.9 ± 0.7%, respectively, under monochromatic excitation around 1500 nm at a power of 700 W/m2. The UC quantum yield reported here for Gd 2O2S: 10%Er3+ is the highest value achieved so far under monochromatic excitation into the 4I13/2 Er 3+ level. Power dependence and lifetime measurements were performed to understand the mechanisms responsible for the efficient UC luminescence. We show that the main process yielding 4I11/2 UC emission is energy transfer UC.