In Situ Bonding Regulation of Surface Ligands for Efficient and Stable FAPbI3 Quantum Dot Solar Cells

Quantum dots (QDs) of formamidinium lead triiodide (FAPbI3) perovskite hold great potential, outperforming their inorganic counterparts in terms of phase stability and carrier lifetime, for high‐performance solar cells. However, the highly dynamic nature of FAPbI3 QDs, which mainly originates from t...

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Published inAdvanced science Vol. 9; no. 35; pp. e2204476 - n/a
Main Authors Ding, Shanshan, Hao, Mengmeng, Fu, Changkui, Lin, Tongen, Baktash, Ardeshir, Chen, Peng, He, Dongxu, Zhang, Chengxi, Chen, Weijian, Whittaker, Andrew K., Bai, Yang, Wang, Lianzhou
Format Journal Article
LanguageEnglish
Published Weinheim John Wiley & Sons, Inc 01.12.2022
John Wiley and Sons Inc
Wiley
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Online AccessGet full text
ISSN2198-3844
2198-3844
DOI10.1002/advs.202204476

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Abstract Quantum dots (QDs) of formamidinium lead triiodide (FAPbI3) perovskite hold great potential, outperforming their inorganic counterparts in terms of phase stability and carrier lifetime, for high‐performance solar cells. However, the highly dynamic nature of FAPbI3 QDs, which mainly originates from the proton exchange between oleic acid and oleylamine (OAm) surface ligands, is a key hurdle that impedes the fabrication of high‐efficiency solar cells. To tackle such an issue, here, protonated‐OAm in situ to strengthen the ligand binding at the surface of FAPbI3 QDs, which can effectively suppress the defect formation during QD synthesis and purification processes is selectively introduced. In addition, by forming a halide‐rich surface environment, the ligand density in a broader range for FAPbI3 QDs without compromising their structural integrity, which significantly improves their optoelectronic properties can be modulated. As a result, the power conversion efficiency of FAPbI3 QD solar cells (QDSCs) is enhanced from 7.4% to 13.8%, a record for FAPbI3 QDSCs. Furthermore, the suppressed proton exchange and reduced surface defects in FAPbI3 QDs also enhance the stability of QDSCs, which retain 80% of the initial efficiency upon exposure to ambient air for 3000 hours. An in situ surface ligand regulation strategy for deliberately controlling protonated‐oleylamine (OAm) dominated surface binding of formamidinium lead triiodide quantum dots (FAPbI3 QDs) is demonstrated. The QDs present reduced long‐chain insulating ligand density without compromising their structural integrity, leading to the corresponding QD solar cell a record power conversion efficiency of 13.8% for FAPbI3 QDSCs.
AbstractList Abstract Quantum dots (QDs) of formamidinium lead triiodide (FAPbI3) perovskite hold great potential, outperforming their inorganic counterparts in terms of phase stability and carrier lifetime, for high‐performance solar cells. However, the highly dynamic nature of FAPbI3 QDs, which mainly originates from the proton exchange between oleic acid and oleylamine (OAm) surface ligands, is a key hurdle that impedes the fabrication of high‐efficiency solar cells. To tackle such an issue, here, protonated‐OAm in situ to strengthen the ligand binding at the surface of FAPbI3 QDs, which can effectively suppress the defect formation during QD synthesis and purification processes is selectively introduced. In addition, by forming a halide‐rich surface environment, the ligand density in a broader range for FAPbI3 QDs without compromising their structural integrity, which significantly improves their optoelectronic properties can be modulated. As a result, the power conversion efficiency of FAPbI3 QD solar cells (QDSCs) is enhanced from 7.4% to 13.8%, a record for FAPbI3 QDSCs. Furthermore, the suppressed proton exchange and reduced surface defects in FAPbI3 QDs also enhance the stability of QDSCs, which retain 80% of the initial efficiency upon exposure to ambient air for 3000 hours.
Quantum dots (QDs) of formamidinium lead triiodide (FAPbI3) perovskite hold great potential, outperforming their inorganic counterparts in terms of phase stability and carrier lifetime, for high‐performance solar cells. However, the highly dynamic nature of FAPbI3 QDs, which mainly originates from the proton exchange between oleic acid and oleylamine (OAm) surface ligands, is a key hurdle that impedes the fabrication of high‐efficiency solar cells. To tackle such an issue, here, protonated‐OAm in situ to strengthen the ligand binding at the surface of FAPbI3 QDs, which can effectively suppress the defect formation during QD synthesis and purification processes is selectively introduced. In addition, by forming a halide‐rich surface environment, the ligand density in a broader range for FAPbI3 QDs without compromising their structural integrity, which significantly improves their optoelectronic properties can be modulated. As a result, the power conversion efficiency of FAPbI3 QD solar cells (QDSCs) is enhanced from 7.4% to 13.8%, a record for FAPbI3 QDSCs. Furthermore, the suppressed proton exchange and reduced surface defects in FAPbI3 QDs also enhance the stability of QDSCs, which retain 80% of the initial efficiency upon exposure to ambient air for 3000 hours.
Quantum dots (QDs) of formamidinium lead triiodide (FAPbI 3 ) perovskite hold great potential, outperforming their inorganic counterparts in terms of phase stability and carrier lifetime, for high‐performance solar cells. However, the highly dynamic nature of FAPbI 3 QDs, which mainly originates from the proton exchange between oleic acid and oleylamine (OAm) surface ligands, is a key hurdle that impedes the fabrication of high‐efficiency solar cells. To tackle such an issue, here, protonated‐OAm in situ to strengthen the ligand binding at the surface of FAPbI 3 QDs, which can effectively suppress the defect formation during QD synthesis and purification processes is selectively introduced. In addition, by forming a halide‐rich surface environment, the ligand density in a broader range for FAPbI 3 QDs without compromising their structural integrity, which significantly improves their optoelectronic properties can be modulated. As a result, the power conversion efficiency of FAPbI 3 QD solar cells (QDSCs) is enhanced from 7.4% to 13.8%, a record for FAPbI 3 QDSCs. Furthermore, the suppressed proton exchange and reduced surface defects in FAPbI 3 QDs also enhance the stability of QDSCs, which retain 80% of the initial efficiency upon exposure to ambient air for 3000 hours. An in situ surface ligand regulation strategy for deliberately controlling protonated‐oleylamine (OAm) dominated surface binding of formamidinium lead triiodide quantum dots (FAPbI 3 QDs) is demonstrated. The QDs present reduced long‐chain insulating ligand density without compromising their structural integrity, leading to the corresponding QD solar cell a record power conversion efficiency of 13.8% for FAPbI 3 QDSCs.
Quantum dots (QDs) of formamidinium lead triiodide (FAPbI3 ) perovskite hold great potential, outperforming their inorganic counterparts in terms of phase stability and carrier lifetime, for high-performance solar cells. However, the highly dynamic nature of FAPbI3 QDs, which mainly originates from the proton exchange between oleic acid and oleylamine (OAm) surface ligands, is a key hurdle that impedes the fabrication of high-efficiency solar cells. To tackle such an issue, here, protonated-OAm in situ to strengthen the ligand binding at the surface of FAPbI3 QDs, which can effectively suppress the defect formation during QD synthesis and purification processes is selectively introduced. In addition, by forming a halide-rich surface environment, the ligand density in a broader range for FAPbI3 QDs without compromising their structural integrity, which significantly improves their optoelectronic properties can be modulated. As a result, the power conversion efficiency of FAPbI3 QD solar cells (QDSCs) is enhanced from 7.4% to 13.8%, a record for FAPbI3 QDSCs. Furthermore, the suppressed proton exchange and reduced surface defects in FAPbI3 QDs also enhance the stability of QDSCs, which retain 80% of the initial efficiency upon exposure to ambient air for 3000 hours.Quantum dots (QDs) of formamidinium lead triiodide (FAPbI3 ) perovskite hold great potential, outperforming their inorganic counterparts in terms of phase stability and carrier lifetime, for high-performance solar cells. However, the highly dynamic nature of FAPbI3 QDs, which mainly originates from the proton exchange between oleic acid and oleylamine (OAm) surface ligands, is a key hurdle that impedes the fabrication of high-efficiency solar cells. To tackle such an issue, here, protonated-OAm in situ to strengthen the ligand binding at the surface of FAPbI3 QDs, which can effectively suppress the defect formation during QD synthesis and purification processes is selectively introduced. In addition, by forming a halide-rich surface environment, the ligand density in a broader range for FAPbI3 QDs without compromising their structural integrity, which significantly improves their optoelectronic properties can be modulated. As a result, the power conversion efficiency of FAPbI3 QD solar cells (QDSCs) is enhanced from 7.4% to 13.8%, a record for FAPbI3 QDSCs. Furthermore, the suppressed proton exchange and reduced surface defects in FAPbI3 QDs also enhance the stability of QDSCs, which retain 80% of the initial efficiency upon exposure to ambient air for 3000 hours.
Quantum dots (QDs) of formamidinium lead triiodide (FAPbI3) perovskite hold great potential, outperforming their inorganic counterparts in terms of phase stability and carrier lifetime, for high‐performance solar cells. However, the highly dynamic nature of FAPbI3 QDs, which mainly originates from the proton exchange between oleic acid and oleylamine (OAm) surface ligands, is a key hurdle that impedes the fabrication of high‐efficiency solar cells. To tackle such an issue, here, protonated‐OAm in situ to strengthen the ligand binding at the surface of FAPbI3 QDs, which can effectively suppress the defect formation during QD synthesis and purification processes is selectively introduced. In addition, by forming a halide‐rich surface environment, the ligand density in a broader range for FAPbI3 QDs without compromising their structural integrity, which significantly improves their optoelectronic properties can be modulated. As a result, the power conversion efficiency of FAPbI3 QD solar cells (QDSCs) is enhanced from 7.4% to 13.8%, a record for FAPbI3 QDSCs. Furthermore, the suppressed proton exchange and reduced surface defects in FAPbI3 QDs also enhance the stability of QDSCs, which retain 80% of the initial efficiency upon exposure to ambient air for 3000 hours. An in situ surface ligand regulation strategy for deliberately controlling protonated‐oleylamine (OAm) dominated surface binding of formamidinium lead triiodide quantum dots (FAPbI3 QDs) is demonstrated. The QDs present reduced long‐chain insulating ligand density without compromising their structural integrity, leading to the corresponding QD solar cell a record power conversion efficiency of 13.8% for FAPbI3 QDSCs.
Author Zhang, Chengxi
Wang, Lianzhou
Ding, Shanshan
Chen, Peng
Baktash, Ardeshir
Bai, Yang
Fu, Changkui
Lin, Tongen
Chen, Weijian
He, Dongxu
Whittaker, Andrew K.
Hao, Mengmeng
AuthorAffiliation 1 Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia Brisbane QLD 4072 Australia
3 Australian Centre for Advanced Photovoltaics School of Photovoltaics and Renewable Energy Engineering University of New South Wales Sydney NSW 2052 Australia
4 Faculty of Materials Science and Engineering/Institute of Technology for Carbon Neutrality Shenzhen Institute of Advanced Technology Chinese Academy of Sciences Shenzhen 518055 P. R. China
5 Shenzhen Key Laboratory of Energy Materials for Carbon Neutrality Shenzhen 518055 P. R. China
2 School of Chemical Engineering The University of Queensland St Lucia Brisbane QLD 4072 Australia
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References_xml – volume: 4
  start-page: 1954
  year: 2019
  publication-title: ACS Energy Lett.
– volume: 29
  start-page: 7088
  year: 2017
  publication-title: Chem. Mater.
– volume: 69
  start-page: 626
  year: 2022
  publication-title: J. Energy Chem.
– volume: 67
  year: 2020
  publication-title: Nano Energy
– volume: 12
  year: 2020
  publication-title: ACS Appl. Mater. Interfaces
– volume: 57
  start-page: 9083
  year: 2018
  publication-title: Angew. Chem., Int. Ed.
– volume: 139
  start-page: 5309
  year: 2017
  publication-title: J. Am. Chem. Soc.
– volume: 5
  start-page: 3322
  year: 2020
  publication-title: ACS Energy Lett.
– volume: 3
  start-page: 5620
  year: 2020
  publication-title: ACS Appl. Energy Mater.
– volume: 28
  start-page: 8718
  year: 2016
  publication-title: Adv. Mater.
– volume: 110
  start-page: 671
  year: 2006
  publication-title: J. Phys. Chem. B
– volume: 29
  start-page: 5168
  year: 2017
  publication-title: Chem. Mater.
– volume: 8
  start-page: 4988
  year: 2017
  publication-title: J. Phys. Chem. Lett.
– volume: 4
  start-page: 2571
  year: 2019
  publication-title: ACS Energy Lett.
– volume: 26
  start-page: 2435
  year: 2016
  publication-title: Adv. Funct. Mater.
– volume: 12
  year: 2018
  publication-title: ACS Nano
– volume: 31
  year: 2019
  publication-title: Adv. Mater.
– volume: 34
  year: 2022
  publication-title: Adv. Mater.
– volume: 6
  start-page: 419
  year: 2021
  publication-title: Nat. Energy
– volume: 26
  start-page: 8757
  year: 2016
  publication-title: Adv. Funct. Mater.
– volume: 2
  start-page: 1866
  year: 2018
  publication-title: Joule
– volume: 32
  start-page: 1089
  year: 2020
  publication-title: Chem. Mater.
– volume: 11
  year: 2017
  publication-title: ACS Nano
– volume: 10
  start-page: 2071
  year: 2016
  publication-title: ACS Nano
– volume: 16
  year: 2020
  publication-title: Small
– volume: 8
  start-page: 489
  year: 2017
  publication-title: J. Phys. Chem. Lett.
– volume: 58
  start-page: 5552
  year: 2019
  publication-title: Angew. Chem., Int. Ed.
– volume: 30
  year: 2020
  publication-title: Adv. Funct. Mater.
– volume: 358
  start-page: 745
  year: 2017
  publication-title: Science
– volume: 29
  year: 2019
  publication-title: Adv. Funct. Mater.
– volume: 9
  start-page: 1994
  year: 2016
  publication-title: Nano Res.
– volume: 2
  start-page: 2450
  year: 2018
  publication-title: Joule
– volume: 5
  start-page: 79
  year: 2020
  publication-title: Nat. Energy
– volume: 32
  year: 2020
  publication-title: Adv. Mater.
– volume: 11
  start-page: 3119
  year: 2017
  publication-title: ACS Nano
– volume: 57
  start-page: 7906
  year: 2021
  publication-title: ChemComm
– volume: 12
  start-page: 1878
  year: 2021
  publication-title: Nat. Commun.
– volume: 3
  year: 2017
  publication-title: Sci. Adv.
– volume: 12
  start-page: 1704
  year: 2018
  publication-title: ACS Nano
– volume: 28
  year: 2018
  publication-title: Adv. Funct. Mater.
– volume: 28
  start-page: 2253
  year: 2016
  publication-title: Adv. Mater.
– volume: 11
  year: 2019
  publication-title: Nanoscale
– volume: 26
  start-page: 4991
  year: 2014
  publication-title: Adv. Mater.
– volume: 8
  start-page: 8104
  year: 2020
  publication-title: J. Mater. Chem. A
– volume: 9
  year: 2021
  publication-title: J. Mater. Chem. A
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Snippet Quantum dots (QDs) of formamidinium lead triiodide (FAPbI3) perovskite hold great potential, outperforming their inorganic counterparts in terms of phase...
Quantum dots (QDs) of formamidinium lead triiodide (FAPbI3 ) perovskite hold great potential, outperforming their inorganic counterparts in terms of phase...
Quantum dots (QDs) of formamidinium lead triiodide (FAPbI 3 ) perovskite hold great potential, outperforming their inorganic counterparts in terms of phase...
Abstract Quantum dots (QDs) of formamidinium lead triiodide (FAPbI3) perovskite hold great potential, outperforming their inorganic counterparts in terms of...
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SubjectTerms Efficiency
Ligands
Morphology
Optical properties
perovskites
photovoltaic performance
proton exchange control
Quantum dots
stability
surface ligands
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Title In Situ Bonding Regulation of Surface Ligands for Efficient and Stable FAPbI3 Quantum Dot Solar Cells
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fadvs.202204476
https://www.proquest.com/docview/2755550834
https://www.proquest.com/docview/2731056471
https://pubmed.ncbi.nlm.nih.gov/PMC9762318
https://doaj.org/article/fe932799cf9544f4ba4b75abfa1e042b
Volume 9
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