TY - JOUR
T1 - Fully Conjugated Co-Self-Assembled Monolayers for Efficient and Stable Inverted Perovskite Solar Cells
AU - Liu, Yuanzhong
AU - Yang, Xin
AU - Ding, Xinliang
AU - Wang, Jiarong
AU - Xu, Weitai
AU - Wang, Xiaoting
AU - Zhang, Liujiang
AU - Yan, Yiran
AU - Wang, Jia
AU - Hou, Yanna
AU - Yang, Lin
AU - Chu, Tianjiao
AU - Jiang, Qinglong
AU - Zhu, Xiangrong
AU - Hu, Ziyang
AU - Kan, Bin
AU - Gao, Xingyu
AU - Fu, Qiang
AU - Yang, Liyou
AU - Chen, Zhicai
AU - Shao, Shiyang
AU - Lu, Linfeng
AU - Ji, Xiaofei
PY - 2025/4/28
Y1 - 2025/4/28
N2 - [4-(3,6-dimethyl-9H-carbazol-9-yl)butyl]phosphonic acid (Me-4PACz) consistently exhibits inhomogeneous distribution on the substrate, which makes it a challenge for the growth of high-quality perovskite film, resulting in undesired interfacial losses at buried interfaces. Moreover, the flexible alkyl chains of Me-4PACz are not conducive to intermolecular interactions and hinder charge flow. Here, a novel molecule with 4-Methoxy-N-(4-methoxyphenyl)-N-phenylaniline (TPA) and carbazole backbone, named CzTPA is designed, which constituted Co-SAM with Me-4PACz. The two carboxyls on the end of carbazole will act as an anchoring group to cover the inadequate coverage of Me-4PACz on the NiOx. The methoxy group on the TPA can passivation the uncoordinated Pb2+ at the perovskite buried interface by the interaction of Pb─O. Additionally, the Me-4PACz can be restrained self-aggregation by interacting with the TPA group of CzTPA. The cooperation of CzTPA realizes the more homogeneous distribution of Me-4PACz on the NiOx, efficient charge transport, and minimize buried interfacial defects. Accordingly, the CzTPA modification can significantly enhance the efficiency of 1.54-eV PSCs from 23.53% to 25.66% and sustain 91.4% of its original efficiency after 1992 h under continuous illumination at 65 °C. More importantly, a 1.68 eV of wide-bandgap PSC achieved a PCE of 22.75% with good photostability. © 2025 Wiley-VCH GmbH.
AB - [4-(3,6-dimethyl-9H-carbazol-9-yl)butyl]phosphonic acid (Me-4PACz) consistently exhibits inhomogeneous distribution on the substrate, which makes it a challenge for the growth of high-quality perovskite film, resulting in undesired interfacial losses at buried interfaces. Moreover, the flexible alkyl chains of Me-4PACz are not conducive to intermolecular interactions and hinder charge flow. Here, a novel molecule with 4-Methoxy-N-(4-methoxyphenyl)-N-phenylaniline (TPA) and carbazole backbone, named CzTPA is designed, which constituted Co-SAM with Me-4PACz. The two carboxyls on the end of carbazole will act as an anchoring group to cover the inadequate coverage of Me-4PACz on the NiOx. The methoxy group on the TPA can passivation the uncoordinated Pb2+ at the perovskite buried interface by the interaction of Pb─O. Additionally, the Me-4PACz can be restrained self-aggregation by interacting with the TPA group of CzTPA. The cooperation of CzTPA realizes the more homogeneous distribution of Me-4PACz on the NiOx, efficient charge transport, and minimize buried interfacial defects. Accordingly, the CzTPA modification can significantly enhance the efficiency of 1.54-eV PSCs from 23.53% to 25.66% and sustain 91.4% of its original efficiency after 1992 h under continuous illumination at 65 °C. More importantly, a 1.68 eV of wide-bandgap PSC achieved a PCE of 22.75% with good photostability. © 2025 Wiley-VCH GmbH.
KW - buried interface
KW - defect passivation
KW - perovskite solar cells
KW - self-assembled monolayer
KW - suppressed phase separation
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UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-105003763939&origin=recordpage
U2 - 10.1002/smll.202502367
DO - 10.1002/smll.202502367
M3 - RGC 21 - Publication in refereed journal
SN - 1613-6810
VL - 21
JO - Small
JF - Small
IS - 17
M1 - 2502367
ER -