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 in | Advanced science Vol. 9; no. 35; pp. e2204476 - n/a |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
John Wiley & Sons, Inc
01.12.2022
John Wiley and Sons Inc Wiley |
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Online Access | Get full text |
ISSN | 2198-3844 2198-3844 |
DOI | 10.1002/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. |
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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 | 2021; 9 2017; 8 2018; 28 2021; 6 2019; 4 2017; 3 2019; 31 2019; 11 2019; 58 2016; 10 2014; 26 2020; 16 2022; 69 2006; 110 2020; 12 2017; 29 2020; 32 2017; 358 2017; 139 2020; 8 2021; 57 2020; 5 2018; 2 2020; 3 2021; 12 2020; 30 2017; 11 2022; 34 2019; 29 2020; 67 2018; 12 2016; 28 2016; 26 2016; 9 2018; 57 |
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 |
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