Open Circuit Potential Build-Up in Perovskite Solar Cells from Dark Conditions to 1 Sun

• Published in: The journal of physical chemistry letters 2015-11, Vol.6 (22), p.4640-4645
• Main Authors: Gouda, Laxman, Gottesman, Ronen, Ginsburg, Adam, Keller, David A, Haltzi, Eynav, Hu, Jiangang, Tirosh, Shay, Anderson, Assaf Y, Zaban, Arie, Boix, Pablo P
• Format: Article
• Language: English
• ISSN: 1948-7185; 1948-7185
• DOI: 10.1021/acs.jpclett.5b02014

The high open-circuit potential (V oc) achieved by perovskite solar cells (PSCs) is one of the keys to their success. The V oc analysis is essential to understand their working mechanisms. A large number of CH3NH3PbI3–x Cl x PSCs were fabricated on single large-area substrates and their V oc dependencies on illumination intensity, I 0, were measured showing three distinctive regions. Similar results obtained in Al2O3 based PSCs relate the effect to the compact TiO2 rather than the mesoporous oxide. We propose that two working mechanisms control the V oc in PSCs. The rise of V oc at low I 0 is determined by the employed semiconductor n-type contact (TiO2 or MgO coated TiO2). In contrast, at I 0 close to AM1.5G, the employed oxide does not affect the achieved voltage. Thus, a change of regime from an oxide-dominated E Fn (as in the dye sensitized solar cells) to an E Fn, directly determined by the CH3NH3PbI3–x Cl x absorber is suggested.