TY - JOUR
T1 - Passivation agent with dipole moment for surface modification towards efficient and stable perovskite solar cells
AU - Wang, Ge
AU - Wang, Chen
AU - Gao, Yajun
AU - Wen, Shanpeng
AU - MacKenzie, Roderick C.I.
AU - Guo, Liuxing
AU - Dong, Wei
AU - Ruan, Shengping
N1 - KAUST Repository Item: Exported on 2021-08-06
Acknowledgements: This work was supported by the National Natural Science Foundation of China (Grant Nos. 52073115, 61874048, 12073009), the Project of Science and Technology Development Plan of Jilin Province (Grant No. 20200201085JC).
PY - 2021/4/23
Y1 - 2021/4/23
N2 - Recently, there has been renewed interest in interface engineering as a means to further push the performance of perovskite solar cells closer to the Schockly-Queisser limit. Herein, for the first time we employ a multi-functional 4-chlorobenzoic acid to produce a self-assembled monolayer on a perovskite surface. With this interlayer we observe passivation of perovskite surface defects and a significant suppression of non-radiative charge recombination. Furthermore, at the surface of the interlayer we observe, charge dipoles which tune the energy level alignment, enabling a larger energetic driving force for hole extraction. The perovskite surface becomes more hydrophilic due to the presence of the interlayer. Consequently, we observe an improvement in open-circuit voltage from 1.08 to 1.16 V, a power conversion efficiency improvement from 18% to 21% and an improved stability under ambient conditions. Our work highlights the potential of SAMs to engineer the photo-electronic properties and stability of perovskite interfaces to achieve high-performance light harvesting devices.
AB - Recently, there has been renewed interest in interface engineering as a means to further push the performance of perovskite solar cells closer to the Schockly-Queisser limit. Herein, for the first time we employ a multi-functional 4-chlorobenzoic acid to produce a self-assembled monolayer on a perovskite surface. With this interlayer we observe passivation of perovskite surface defects and a significant suppression of non-radiative charge recombination. Furthermore, at the surface of the interlayer we observe, charge dipoles which tune the energy level alignment, enabling a larger energetic driving force for hole extraction. The perovskite surface becomes more hydrophilic due to the presence of the interlayer. Consequently, we observe an improvement in open-circuit voltage from 1.08 to 1.16 V, a power conversion efficiency improvement from 18% to 21% and an improved stability under ambient conditions. Our work highlights the potential of SAMs to engineer the photo-electronic properties and stability of perovskite interfaces to achieve high-performance light harvesting devices.
UR - http://hdl.handle.net/10754/670439
UR - https://linkinghub.elsevier.com/retrieve/pii/S2095495621002278
UR - http://www.scopus.com/inward/record.url?scp=85111076427&partnerID=8YFLogxK
U2 - 10.1016/j.jechem.2021.04.023
DO - 10.1016/j.jechem.2021.04.023
M3 - Article
SN - 2095-4956
VL - 64
SP - 55
EP - 61
JO - Journal of Energy Chemistry
JF - Journal of Energy Chemistry
ER -