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Open Circuit Potential Build-Up in Perovskite Solar Cells from Dark Conditions to 1 Sun
Author(s) -
Laxman Gouda,
Ronen Gottesman,
Adam Ginsburg,
David A. Keller,
Eynav Haltzi,
Jiangang Hu,
Shay Tirosh,
Assaf Y. Anderson,
Arie Zaban,
Pablo P. Boix
Publication year - 2015
Publication title -
the journal of physical chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.5b02014
Subject(s) - perovskite (structure) , open circuit voltage , oxide , materials science , optoelectronics , semiconductor , mesoporous material , short circuit , nanotechnology , voltage , chemical engineering , chemistry , electrical engineering , catalysis , biochemistry , engineering , metallurgy
The high open-circuit potential (Voc) achieved by perovskite solar cells (PSCs) is one of the keys to their success. The Voc analysis is essential to understand their working mechanisms. A large number of CH3NH3PbI3-xClx PSCs were fabricated on single large-area substrates and their Voc dependencies on illumination intensity, I0, 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 Voc in PSCs. The rise of Voc at low I0 is determined by the employed semiconductor n-type contact (TiO2 or MgO coated TiO2). In contrast, at I0 close to AM1.5G, the employed oxide does not affect the achieved voltage. Thus, a change of regime from an oxide-dominated EFn (as in the dye sensitized solar cells) to an EFn, directly determined by the CH3NH3PbI3-xClx absorber is suggested.

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