Thermodynamically stabilized β-CsPbI₃–based perovskite solar cells with efficiencies >18

Although β-CsPbI₃ has a bandgap favorable for application in tandem solar cells, depositing and stabilizing β-CsPbI₃ experimentally has remained a challenge.We obtained highly crystalline β-CsPbI₃ films with an extended spectral response and enhanced phase stability. Synchrotron-based x-ray scatteri...

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Published inScience (American Association for the Advancement of Science) Vol. 365; no. 6453; pp. 591 - 595
Main Authors Wang, Yong, Dar, M. Ibrahim, Ono, Luis K., Zhang, Taiyang, Kan, Miao, Li, Yawen, Zhang, Lijun, Wang, Xingtao, Yang, Yingguo, Gao, Xingyu, Qi, Yabing, Grätzel, Michael, Zhao, Yixin
Format Journal Article
LanguageEnglish
Published Washington American Association for the Advancement of Science 09.08.2019
The American Association for the Advancement of Science
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Abstract Although β-CsPbI₃ has a bandgap favorable for application in tandem solar cells, depositing and stabilizing β-CsPbI₃ experimentally has remained a challenge.We obtained highly crystalline β-CsPbI₃ films with an extended spectral response and enhanced phase stability. Synchrotron-based x-ray scattering revealed the presence of highly oriented β-CsPbI₃ grains, and sensitive elemental analyses—including inductively coupled plasma mass spectrometry and time-of-flight secondary ion mass spectrometry—confirmed their all-inorganic composition. We further mitigated the effects of cracks and pinholes in the perovskite layer by surface treating with choline iodide, which increased the charge-carrier lifetime and improved the energy-level alignment between the β-CsPbI₃ absorber layer and carrier-selective contacts. The perovskite solar cells made from the treated material have highly reproducible and stable efficiencies reaching 18.4% under 45 ± 5°C ambient conditions.
AbstractList Although β-CsPbI3 has a bandgap favorable for application in tandem solar cells, depositing and stabilizing β-CsPbI3 experimentally has remained a challenge. We obtained highly crystalline β-CsPbI3 films with an extended spectral response and enhanced phase stability. Synchrotron-based x-ray scattering revealed the presence of highly oriented β-CsPbI3 grains, and sensitive elemental analyses-including inductively coupled plasma mass spectrometry and time-of-flight secondary ion mass spectrometry-confirmed their all-inorganic composition. We further mitigated the effects of cracks and pinholes in the perovskite layer by surface treating with choline iodide, which increased the charge-carrier lifetime and improved the energy-level alignment between the β-CsPbI3 absorber layer and carrier-selective contacts. The perovskite solar cells made from the treated material have highly reproducible and stable efficiencies reaching 18.4% under 45 ± 5°C ambient conditions.Although β-CsPbI3 has a bandgap favorable for application in tandem solar cells, depositing and stabilizing β-CsPbI3 experimentally has remained a challenge. We obtained highly crystalline β-CsPbI3 films with an extended spectral response and enhanced phase stability. Synchrotron-based x-ray scattering revealed the presence of highly oriented β-CsPbI3 grains, and sensitive elemental analyses-including inductively coupled plasma mass spectrometry and time-of-flight secondary ion mass spectrometry-confirmed their all-inorganic composition. We further mitigated the effects of cracks and pinholes in the perovskite layer by surface treating with choline iodide, which increased the charge-carrier lifetime and improved the energy-level alignment between the β-CsPbI3 absorber layer and carrier-selective contacts. The perovskite solar cells made from the treated material have highly reproducible and stable efficiencies reaching 18.4% under 45 ± 5°C ambient conditions.
Although β-CsPbI₃ has a bandgap favorable for application in tandem solar cells, depositing and stabilizing β-CsPbI₃ experimentally has remained a challenge.We obtained highly crystalline β-CsPbI₃ films with an extended spectral response and enhanced phase stability. Synchrotron-based x-ray scattering revealed the presence of highly oriented β-CsPbI₃ grains, and sensitive elemental analyses—including inductively coupled plasma mass spectrometry and time-of-flight secondary ion mass spectrometry—confirmed their all-inorganic composition. We further mitigated the effects of cracks and pinholes in the perovskite layer by surface treating with choline iodide, which increased the charge-carrier lifetime and improved the energy-level alignment between the β-CsPbI₃ absorber layer and carrier-selective contacts. The perovskite solar cells made from the treated material have highly reproducible and stable efficiencies reaching 18.4% under 45 ± 5°C ambient conditions.
Orthorhombic phases for perovskite solar cellsThe power conversion efficiencies (PCEs) of all-inorganic perovskites are lower than those of materials with organic cations. This is in part because these materials have larger bandgaps. The cubic crystal phases of these materials also exhibit poor stability. Wang et al. synthesized the orthorhombic β-phase of CsPbI3 from HPbI3 and CsI. The material exhibited higher stability and a more favorable bandgap, which allowed for PCEs of 15%. Passivation of the surface trap state with choline iodide boosted PCEs to 18%.Science, this issue p. 591Although β-CsPbI3 has a bandgap favorable for application in tandem solar cells, depositing and stabilizing β-CsPbI3 experimentally has remained a challenge. We obtained highly crystalline β-CsPbI3 films with an extended spectral response and enhanced phase stability. Synchrotron-based x-ray scattering revealed the presence of highly oriented β-CsPbI3 grains, and sensitive elemental analyses—including inductively coupled plasma mass spectrometry and time-of-flight secondary ion mass spectrometry—confirmed their all-inorganic composition. We further mitigated the effects of cracks and pinholes in the perovskite layer by surface treating with choline iodide, which increased the charge-carrier lifetime and improved the energy-level alignment between the β-CsPbI3 absorber layer and carrier-selective contacts. The perovskite solar cells made from the treated material have highly reproducible and stable efficiencies reaching 18.4% under 45 ± 5°C ambient conditions.
Author Wang, Xingtao
Gao, Xingyu
Grätzel, Michael
Dar, M. Ibrahim
Li, Yawen
Wang, Yong
Yang, Yingguo
Zhao, Yixin
Zhang, Taiyang
Ono, Luis K.
Zhang, Lijun
Qi, Yabing
Kan, Miao
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Copyright Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works
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Snippet Although β-CsPbI₃ has a bandgap favorable for application in tandem solar cells, depositing and stabilizing β-CsPbI₃ experimentally has remained a challenge.We...
Orthorhombic phases for perovskite solar cellsThe power conversion efficiencies (PCEs) of all-inorganic perovskites are lower than those of materials with...
Although β-CsPbI3 has a bandgap favorable for application in tandem solar cells, depositing and stabilizing β-CsPbI3 experimentally has remained a challenge....
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SubjectTerms Beta phase
Carrier lifetime
Cations
Choline
Cracks
Current carriers
Energy conversion efficiency
Energy gap
Inductively coupled plasma mass spectrometry
Iodides
Ions
Mass spectrometry
Mass spectroscopy
Perovskites
Phase stability
Photovoltaic cells
Pinholes
Scientific imaging
Secondary ion mass spectrometry
Solar cells
Spectral sensitivity
Spectroscopy
X-ray scattering
Title Thermodynamically stabilized β-CsPbI₃–based perovskite solar cells with efficiencies >18
URI https://www.jstor.org/stable/26762406
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