Co‐Self‐Assembled Monolayers Modified NiOx for Stable Inverted Perovskite Solar Cells

[4‐(3,6‐dimethyl‐9H‐carbazol‐9yl)butyl]phosphonic acid (Me‐4PACz) self‐assembled molecules (SAM) are an effective method to solve the problem of the buried interface of NiOx in inverted perovskite solar cells (PSCs). However, the Me‐4PACz end group (carbazole core) cannot forcefully passivate defect...

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Published inAdvanced materials (Weinheim) Vol. 36; no. 16; pp. e2311970 - n/a
Main Authors Cao, Qi, Wang, Tianyue, Pu, Xingyu, He, Xilai, Xiao, Mingchao, Chen, Hui, Zhuang, Lvchao, Wei, Qi, Loi, Hok‐Leung, Guo, Peng, Kang, Bochun, Feng, Guangpeng, Zhuang, Jing, Feng, Guitao, Li, Xuanhua, Yan, Feng
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LanguageEnglish
Published Weinheim Wiley Subscription Services, Inc 01.04.2024
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Abstract [4‐(3,6‐dimethyl‐9H‐carbazol‐9yl)butyl]phosphonic acid (Me‐4PACz) self‐assembled molecules (SAM) are an effective method to solve the problem of the buried interface of NiOx in inverted perovskite solar cells (PSCs). However, the Me‐4PACz end group (carbazole core) cannot forcefully passivate defects at the bottom of the perovskite film. Here, a Co‐SAM strategy is employed to modify the buried interface of PSCs. Me‐4PACz is doped with phosphorylcholine chloride (PC) to form a Co‐SAM to improve the monolayer coverage and reduce leakage current. The phosphate group and chloride ions (Cl−) in PC can inhibit NiOx surface defects. Meantime, the quaternary ammonium ions and Cl− in PC can fill organic cations and halogen vacancies in the perovskite film to enable defects passivation. Moreover, Co‐SAM can promote the growth of perovskite crystals, collaboratively solve the problem of buried defects, suppress nonradiative recombination, accelerate carrier transmission, and relieve the residual stress of the perovskite film. Consequently, the Co‐SAM modified devices show power conversion efficiencies as high as 25.09% as well as excellent device stability with 93% initial efficiency after 1000 h of operation under one‐sun illumination. This work demonstrates the novel approach for enhancing the performance and stability of PSCs by modifying Co‐SAM on NiOx. Phosphorylcholine chloride and Me‐4PACz are used to form Co‐SAM on the NiOx surface to optimize the buried interface in PSCs. Co‐SAM can promote the growth of perovskite crystals, passivate buried defects, optimize the energy band alignment, and relieve the residual stress of the perovskite film, leading to power conversion efficiencies as high as 25.09% and excellent device stability.
AbstractList [4-(3,6-dimethyl-9H-carbazol-9yl)butyl]phosphonic acid (Me-4PACz) self-assembled molecules (SAM) are an effective method to solve the problem of the buried interface of NiOx in inverted perovskite solar cells (PSCs). However, the Me-4PACz end group (carbazole core) cannot forcefully passivate defects at the bottom of the perovskite film. Here, a Co-SAM strategy is employed to modify the buried interface of PSCs. Me-4PACz is doped with phosphorylcholine chloride (PC) to form a Co-SAM to improve the monolayer coverage and reduce leakage current. The phosphate group and chloride ions (Cl-) in PC can inhibit NiOx surface defects. Meantime, the quaternary ammonium ions and Cl- in PC can fill organic cations and halogen vacancies in the perovskite film to enable defects passivation. Moreover, Co-SAM can promote the growth of perovskite crystals, collaboratively solve the problem of buried defects, suppress nonradiative recombination, accelerate carrier transmission, and relieve the residual stress of the perovskite film. Consequently, the Co-SAM modified devices show power conversion efficiencies as high as 25.09% as well as excellent device stability with 93% initial efficiency after 1000 h of operation under one-sun illumination. This work demonstrates the novel approach for enhancing the performance and stability of PSCs by modifying Co-SAM on NiOx.[4-(3,6-dimethyl-9H-carbazol-9yl)butyl]phosphonic acid (Me-4PACz) self-assembled molecules (SAM) are an effective method to solve the problem of the buried interface of NiOx in inverted perovskite solar cells (PSCs). However, the Me-4PACz end group (carbazole core) cannot forcefully passivate defects at the bottom of the perovskite film. Here, a Co-SAM strategy is employed to modify the buried interface of PSCs. Me-4PACz is doped with phosphorylcholine chloride (PC) to form a Co-SAM to improve the monolayer coverage and reduce leakage current. The phosphate group and chloride ions (Cl-) in PC can inhibit NiOx surface defects. Meantime, the quaternary ammonium ions and Cl- in PC can fill organic cations and halogen vacancies in the perovskite film to enable defects passivation. Moreover, Co-SAM can promote the growth of perovskite crystals, collaboratively solve the problem of buried defects, suppress nonradiative recombination, accelerate carrier transmission, and relieve the residual stress of the perovskite film. Consequently, the Co-SAM modified devices show power conversion efficiencies as high as 25.09% as well as excellent device stability with 93% initial efficiency after 1000 h of operation under one-sun illumination. This work demonstrates the novel approach for enhancing the performance and stability of PSCs by modifying Co-SAM on NiOx.
[4‐(3,6‐dimethyl‐9H‐carbazol‐9yl)butyl]phosphonic acid (Me‐4PACz) self‐assembled molecules (SAM) are an effective method to solve the problem of the buried interface of NiOx in inverted perovskite solar cells (PSCs). However, the Me‐4PACz end group (carbazole core) cannot forcefully passivate defects at the bottom of the perovskite film. Here, a Co‐SAM strategy is employed to modify the buried interface of PSCs. Me‐4PACz is doped with phosphorylcholine chloride (PC) to form a Co‐SAM to improve the monolayer coverage and reduce leakage current. The phosphate group and chloride ions (Cl−) in PC can inhibit NiOx surface defects. Meantime, the quaternary ammonium ions and Cl− in PC can fill organic cations and halogen vacancies in the perovskite film to enable defects passivation. Moreover, Co‐SAM can promote the growth of perovskite crystals, collaboratively solve the problem of buried defects, suppress nonradiative recombination, accelerate carrier transmission, and relieve the residual stress of the perovskite film. Consequently, the Co‐SAM modified devices show power conversion efficiencies as high as 25.09% as well as excellent device stability with 93% initial efficiency after 1000 h of operation under one‐sun illumination. This work demonstrates the novel approach for enhancing the performance and stability of PSCs by modifying Co‐SAM on NiOx. Phosphorylcholine chloride and Me‐4PACz are used to form Co‐SAM on the NiOx surface to optimize the buried interface in PSCs. Co‐SAM can promote the growth of perovskite crystals, passivate buried defects, optimize the energy band alignment, and relieve the residual stress of the perovskite film, leading to power conversion efficiencies as high as 25.09% and excellent device stability.
[4‐(3,6‐dimethyl‐9H‐carbazol‐9yl)butyl]phosphonic acid (Me‐4PACz) self‐assembled molecules (SAM) are an effective method to solve the problem of the buried interface of NiOx in inverted perovskite solar cells (PSCs). However, the Me‐4PACz end group (carbazole core) cannot forcefully passivate defects at the bottom of the perovskite film. Here, a Co‐SAM strategy is employed to modify the buried interface of PSCs. Me‐4PACz is doped with phosphorylcholine chloride (PC) to form a Co‐SAM to improve the monolayer coverage and reduce leakage current. The phosphate group and chloride ions (Cl−) in PC can inhibit NiOx surface defects. Meantime, the quaternary ammonium ions and Cl− in PC can fill organic cations and halogen vacancies in the perovskite film to enable defects passivation. Moreover, Co‐SAM can promote the growth of perovskite crystals, collaboratively solve the problem of buried defects, suppress nonradiative recombination, accelerate carrier transmission, and relieve the residual stress of the perovskite film. Consequently, the Co‐SAM modified devices show power conversion efficiencies as high as 25.09% as well as excellent device stability with 93% initial efficiency after 1000 h of operation under one‐sun illumination. This work demonstrates the novel approach for enhancing the performance and stability of PSCs by modifying Co‐SAM on NiOx.
Author Xiao, Mingchao
Wang, Tianyue
Cao, Qi
Pu, Xingyu
Zhuang, Jing
Yan, Feng
Loi, Hok‐Leung
Chen, Hui
Wei, Qi
Guo, Peng
Feng, Guangpeng
Feng, Guitao
Li, Xuanhua
He, Xilai
Kang, Bochun
Zhuang, Lvchao
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  surname: Yan
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Snippet [4‐(3,6‐dimethyl‐9H‐carbazol‐9yl)butyl]phosphonic acid (Me‐4PACz) self‐assembled molecules (SAM) are an effective method to solve the problem of the buried...
[4-(3,6-dimethyl-9H-carbazol-9yl)butyl]phosphonic acid (Me-4PACz) self-assembled molecules (SAM) are an effective method to solve the problem of the buried...
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SubjectTerms buried interface
Carbazoles
Carrier recombination
Chloride ions
Cobalt
Crystal defects
Crystal growth
Energy conversion efficiency
inverted perovskite solar cells
Leakage current
Monolayers
Perovskites
Phosphonic acids
Phosphorylcholine
Photovoltaic cells
Residual stress
Self-assembly
self‐assembled monolayer
Solar cells
Stability
Surface defects
Title Co‐Self‐Assembled Monolayers Modified NiOx for Stable Inverted Perovskite Solar Cells
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fadma.202311970
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