TY - JOUR
T1 - Defect Passivation in Perovskite Solar Cells by Cyano-Based π-Conjugated Molecules for Improved Performance and Stability
AU - Wang, Kai
AU - Liu, Jiang
AU - Yin, Jun
AU - Aydin, Erkan
AU - Harrison, George T.
AU - Liu, Wenzhu
AU - Chen, Shanyong
AU - Mohammed, Omar F.
AU - De Wolf, Stefaan
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: This work was supported by the King Abdullah University of Science and Technology (KAUST) Office of Sponsored Research (OSR) under award no. KAUST OSR-CARF URF/1/ 3079-33-01.
PY - 2020/7/9
Y1 - 2020/7/9
N2 - Defects at the surface and grain boundaries of metal–halide perovskite films lead to performance losses of perovskite solar cells (PSCs). Here, organic cyano-based π-conjugated molecules composed of indacenodithieno[3,2-b]thiophene (IDTT) are reported and it is found that their cyano group can effectively passivate such defects. To achieve a homogeneous distribution, these molecules are dissolved in the antisolvent, used to initiate the perovskite crystallization. It is found that these molecules are self-anchored at the grain boundaries due to their strong binding to undercoordinated Pb2+. On a device level, this passivation scheme enhances the charge separation and transport at the grain boundaries due to the well-matched energetic levels between the passivant and the perovskite. Consequently, these benefits contribute directly to the achievement of power conversion efficiencies as high as 21.2%, as well as the improved environmental and thermal stability of the PSCs. The surface treatment provides a new strategy to simultaneously passivate defects and enhance charge extraction/transport at the device interface by manipulating the anchoring groups of the molecules.
AB - Defects at the surface and grain boundaries of metal–halide perovskite films lead to performance losses of perovskite solar cells (PSCs). Here, organic cyano-based π-conjugated molecules composed of indacenodithieno[3,2-b]thiophene (IDTT) are reported and it is found that their cyano group can effectively passivate such defects. To achieve a homogeneous distribution, these molecules are dissolved in the antisolvent, used to initiate the perovskite crystallization. It is found that these molecules are self-anchored at the grain boundaries due to their strong binding to undercoordinated Pb2+. On a device level, this passivation scheme enhances the charge separation and transport at the grain boundaries due to the well-matched energetic levels between the passivant and the perovskite. Consequently, these benefits contribute directly to the achievement of power conversion efficiencies as high as 21.2%, as well as the improved environmental and thermal stability of the PSCs. The surface treatment provides a new strategy to simultaneously passivate defects and enhance charge extraction/transport at the device interface by manipulating the anchoring groups of the molecules.
UR - http://hdl.handle.net/10754/664141
UR - https://onlinelibrary.wiley.com/doi/abs/10.1002/adfm.202002861
UR - http://www.scopus.com/inward/record.url?scp=85087714065&partnerID=8YFLogxK
U2 - 10.1002/adfm.202002861
DO - 10.1002/adfm.202002861
M3 - Article
SN - 1616-301X
SP - 2002861
JO - Advanced Functional Materials
JF - Advanced Functional Materials
ER -