TY - JOUR
T1 - Highly improved efficiency and stability of planar perovskite solar cells via bifunctional phytic acid dipotassium anchored SnO2 electron transport layer
AU - Liu, Congcong
AU - Guo, Min
AU - Su, Haijun
AU - Zhai, Peng
AU - Xie, Keyu
AU - Liu, Zhike
AU - Zhang, Jun
AU - Liu, Lin
AU - Fu, Hengzhi
N1 - Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/6/30
Y1 - 2022/6/30
N2 - The defects at the interface of SnO2 electron transport layers (ETLs) /perovskite layer hinder extraction and transfer of charge, which restrict the further improvement of the photoelectric conversion efficiency (PCE) of SnO2-based perovskite solar cells (PSCs). Herein, an effective bifunctional anchoring strategy is developed to passivate SnO2/perovskite interface defects by adequate chelate sites in polydentate phytic acid dipotassium (PAD) to anchor SnO2 colloids. It is confirmed that polydentate PAD anchoring can form new Sn-O-P bonds with uncoordinated Sn2+, which can efficiently passivate the SnO2 surface defects and alleviate the interfacial charge recombination between SnO2 and perovskite layer. The reduction of SnO2 surface defects enhances the electron transport efficiency and increases the conductivity of the PAD-SnO2 ETLs to 2.1 times that of SnO2 ETLs. Meanwhile, the anchoring group potassium ions (K+) in PAD can promote the in-plane growth of perovskite grains and increase the average grain size of perovskite from 560 nm to 850 nm. As a consequence, the PCE of the PAD-SnO2-based PSCs increased sharply to 21.61%, which is 10.7% higher than that of the PSCs made with SnO2 ETLs (19.52%). The unencapsulated PSCs deposited on PAD-SnO2 ETLs can remain 99.5% of their initial efficiency after 60 days under 25–30% humidity.
AB - The defects at the interface of SnO2 electron transport layers (ETLs) /perovskite layer hinder extraction and transfer of charge, which restrict the further improvement of the photoelectric conversion efficiency (PCE) of SnO2-based perovskite solar cells (PSCs). Herein, an effective bifunctional anchoring strategy is developed to passivate SnO2/perovskite interface defects by adequate chelate sites in polydentate phytic acid dipotassium (PAD) to anchor SnO2 colloids. It is confirmed that polydentate PAD anchoring can form new Sn-O-P bonds with uncoordinated Sn2+, which can efficiently passivate the SnO2 surface defects and alleviate the interfacial charge recombination between SnO2 and perovskite layer. The reduction of SnO2 surface defects enhances the electron transport efficiency and increases the conductivity of the PAD-SnO2 ETLs to 2.1 times that of SnO2 ETLs. Meanwhile, the anchoring group potassium ions (K+) in PAD can promote the in-plane growth of perovskite grains and increase the average grain size of perovskite from 560 nm to 850 nm. As a consequence, the PCE of the PAD-SnO2-based PSCs increased sharply to 21.61%, which is 10.7% higher than that of the PSCs made with SnO2 ETLs (19.52%). The unencapsulated PSCs deposited on PAD-SnO2 ETLs can remain 99.5% of their initial efficiency after 60 days under 25–30% humidity.
KW - Bifunctional anchoring strategy
KW - Passivate defects
KW - Perovskite solar cells
KW - Phytic acid dipotassium
UR - http://www.scopus.com/inward/record.url?scp=85125771668&partnerID=8YFLogxK
U2 - 10.1016/j.apsusc.2022.152943
DO - 10.1016/j.apsusc.2022.152943
M3 - 文章
AN - SCOPUS:85125771668
SN - 0169-4332
VL - 588
JO - Applied Surface Science
JF - Applied Surface Science
M1 - 152943
ER -