Low-temperature deposition of TiO2 compact layers for metal-organic perovskite solar cells on plastic
Thomas M. Brown a, Aldo Di Carlo a, Fabio Matteocci a, Stefano Razza a, Francesco Di Giacomo a, Maria Luisa Grilli b, Andrea Capasso b, Nicola Lisi b, Wilhelmus M.M. Kessels c, Valerio Zardetto c, Mariadriana Creatore c, Silvia Licoccia d, Alessandra D'Epifanio d
a CHOSE - Centre for Hybrid and Organic Solar Energy, University of Rome ‘‘Tor Vergata’’, Via del Politecnico, 1, Roma, Italy
b Department of Materials and New Technologies, ENEA, Casaccia Research Centre, Via Anguillarese 301, 00123, Rome
c Eindhoven University of Technology, Department of Applied Physics, 5600MB, Eindhoven, Netherlands
d University of Rome Tor Vergata, Department of Chemical Science and Technologies, Italy, Via della Ricerca Scientifica, 1, Roma, Italy
Poster, Andrea Capasso, 084
Publication date: 1st July 2014

Organic-inorganic perovskites demonstrated to be a potentially disruptive material for photovoltaics. Power conversion efficiencies (PCE) in the order of 18% and 10% have been recently reached on glass and plastic substrates, respectively[1, 2]. Plastic solar cells are attractive in many technological areas, but their fabrication poses more strict constrains in terms of processing temperatures. In perovskite-based cell, an electron-transporting layer on top of the cathode appears necessary to correctly collect the charges at the electrode without inducing recombination. A TiO2 compact layer is usually deposited on glass electrodes by spray pyrolysis to this end. However, such process implies temperatures exceeding 400°C which are unsuitable for plastic substrates. Here we present a comparison of low-temperature TiO2 compact layers on PET/ITO/TiO2/CH3NH3PbI3-xClx/Spiro-O-MeTAD/Au structures (with and without mesoporous TiO2). The TiO2 compact layers were deposited by two techniques under 150°C: sputtering and plasma enhanced atomic layer deposition (PE-ALD).The planar architecture exhibited a very high VOC (970 mV for 40 nm of sputtered TiO2 and 880 mV for 11 nm of PE-ALD TiO2)  but with current densities below 1.5 mA cm-2. When a UV-sintered TiO2 mesoporous scaffold was used to guide the perovskite growth and increase the charge injection, an increase of the PCE of one order of magnitude was obtained (from 0.3 to 5.8% for sputtering and from 0.8 to 7.4 for PE-ALD). As a further proof of the importance of the compact TiO2, mesostructured devices without compact layer were realized; as expected, the high recombination rate between the perovskite and the ITO limited the VOC below 50 mV. In summary, three new low-temperature TiO2 processing techniques (i.e., sputtering, PE-ALD, and UV-sintering) were successfully adopted to fabricate efficient flexible metal-organic perovskite solar cells with efficiency up to 7.4%.

References

[1] NREL, http://www.nrel.gov/ncpv/images/efficiency_chart.jpg 2014.

[2] D. Liu, T. L. Kelly, Nature Photonics 2013, 8, 133.



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