Kinetic Stabilization of the Sol–Gel State in Perovskites Enables Facile Processing of High‐Efficiency Solar Cells
Perovskite solar cells increasingly feature mixed‐halide mixed‐cation compounds (FA1−x−yMAxCsyPbI3−zBrz) as photovoltaic absorbers, as they enable easier processing and improved stability. Here, the underlying reasons for ease of processing are revealed. It is found that halide and cation engineerin...
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| Published in | Advanced materials (Weinheim) Vol. 31; no. 32; pp. e1808357 - n/a |
|---|---|
| Main Authors | , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Germany
Wiley Subscription Services, Inc
01.08.2019
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| Abstract | Perovskite solar cells increasingly feature mixed‐halide mixed‐cation compounds (FA1−x−yMAxCsyPbI3−zBrz) as photovoltaic absorbers, as they enable easier processing and improved stability. Here, the underlying reasons for ease of processing are revealed. It is found that halide and cation engineering leads to a systematic widening of the anti‐solvent processing window for the fabrication of high‐quality films and efficient solar cells. This window widens from seconds, in the case of single cation/halide systems (e.g., MAPbI3, FAPbI3, and FAPbBr3), to several minutes for mixed systems. In situ X‐ray diffraction studies reveal that the processing window is closely related to the crystallization of the disordered sol–gel and to the number of crystalline byproducts; the processing window therefore depends directly on the precise cation/halide composition. Moreover, anti‐solvent dripping is shown to promote the desired perovskite phase with careful formulation. The processing window of perovskite solar cells, as defined by the latest time the anti‐solvent drip yields efficient solar cells, broadened with the increasing complexity of cation/halide content. This behavior is ascribed to kinetic stabilization of sol–gel state through cation/halide engineering. This provides guidelines for designing new formulations, aimed at formation of the perovskite phase, ultimately resulting in high‐efficiency perovskite solar cells produced with ease and with high reproducibility.
The role of cation and halide mixing is revealed using in situ X‐ray scattering measurements during spin‐coating. Modulating the cation/halide composition directly impacts the lifetime of the sol–gel precursor film and its easy and reproducible conversion to the perovskite phase to yield solar cells with 20% power conversion efficiency. |
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| AbstractList | Perovskite solar cells increasingly feature mixed-halide mixed-cation compounds (FA1- x - y MAx Csy PbI3- z Brz ) as photovoltaic absorbers, as they enable easier processing and improved stability. Here, the underlying reasons for ease of processing are revealed. It is found that halide and cation engineering leads to a systematic widening of the anti-solvent processing window for the fabrication of high-quality films and efficient solar cells. This window widens from seconds, in the case of single cation/halide systems (e.g., MAPbI3 , FAPbI3 , and FAPbBr3 ), to several minutes for mixed systems. In situ X-ray diffraction studies reveal that the processing window is closely related to the crystallization of the disordered sol-gel and to the number of crystalline byproducts; the processing window therefore depends directly on the precise cation/halide composition. Moreover, anti-solvent dripping is shown to promote the desired perovskite phase with careful formulation. The processing window of perovskite solar cells, as defined by the latest time the anti-solvent drip yields efficient solar cells, broadened with the increasing complexity of cation/halide content. This behavior is ascribed to kinetic stabilization of sol-gel state through cation/halide engineering. This provides guidelines for designing new formulations, aimed at formation of the perovskite phase, ultimately resulting in high-efficiency perovskite solar cells produced with ease and with high reproducibility.Perovskite solar cells increasingly feature mixed-halide mixed-cation compounds (FA1- x - y MAx Csy PbI3- z Brz ) as photovoltaic absorbers, as they enable easier processing and improved stability. Here, the underlying reasons for ease of processing are revealed. It is found that halide and cation engineering leads to a systematic widening of the anti-solvent processing window for the fabrication of high-quality films and efficient solar cells. This window widens from seconds, in the case of single cation/halide systems (e.g., MAPbI3 , FAPbI3 , and FAPbBr3 ), to several minutes for mixed systems. In situ X-ray diffraction studies reveal that the processing window is closely related to the crystallization of the disordered sol-gel and to the number of crystalline byproducts; the processing window therefore depends directly on the precise cation/halide composition. Moreover, anti-solvent dripping is shown to promote the desired perovskite phase with careful formulation. The processing window of perovskite solar cells, as defined by the latest time the anti-solvent drip yields efficient solar cells, broadened with the increasing complexity of cation/halide content. This behavior is ascribed to kinetic stabilization of sol-gel state through cation/halide engineering. This provides guidelines for designing new formulations, aimed at formation of the perovskite phase, ultimately resulting in high-efficiency perovskite solar cells produced with ease and with high reproducibility. Perovskite solar cells increasingly feature mixed‐halide mixed‐cation compounds (FA1−x−yMAxCsyPbI3−zBrz) as photovoltaic absorbers, as they enable easier processing and improved stability. Here, the underlying reasons for ease of processing are revealed. It is found that halide and cation engineering leads to a systematic widening of the anti‐solvent processing window for the fabrication of high‐quality films and efficient solar cells. This window widens from seconds, in the case of single cation/halide systems (e.g., MAPbI3, FAPbI3, and FAPbBr3), to several minutes for mixed systems. In situ X‐ray diffraction studies reveal that the processing window is closely related to the crystallization of the disordered sol–gel and to the number of crystalline byproducts; the processing window therefore depends directly on the precise cation/halide composition. Moreover, anti‐solvent dripping is shown to promote the desired perovskite phase with careful formulation. The processing window of perovskite solar cells, as defined by the latest time the anti‐solvent drip yields efficient solar cells, broadened with the increasing complexity of cation/halide content. This behavior is ascribed to kinetic stabilization of sol–gel state through cation/halide engineering. This provides guidelines for designing new formulations, aimed at formation of the perovskite phase, ultimately resulting in high‐efficiency perovskite solar cells produced with ease and with high reproducibility. The role of cation and halide mixing is revealed using in situ X‐ray scattering measurements during spin‐coating. Modulating the cation/halide composition directly impacts the lifetime of the sol–gel precursor film and its easy and reproducible conversion to the perovskite phase to yield solar cells with 20% power conversion efficiency. Perovskite solar cells increasingly feature mixed‐halide mixed‐cation compounds (FA 1− x − y MA x Cs y PbI 3− z Br z ) as photovoltaic absorbers, as they enable easier processing and improved stability. Here, the underlying reasons for ease of processing are revealed. It is found that halide and cation engineering leads to a systematic widening of the anti‐solvent processing window for the fabrication of high‐quality films and efficient solar cells. This window widens from seconds, in the case of single cation/halide systems (e.g., MAPbI 3 , FAPbI 3 , and FAPbBr 3 ), to several minutes for mixed systems. In situ X‐ray diffraction studies reveal that the processing window is closely related to the crystallization of the disordered sol–gel and to the number of crystalline byproducts; the processing window therefore depends directly on the precise cation/halide composition. Moreover, anti‐solvent dripping is shown to promote the desired perovskite phase with careful formulation. The processing window of perovskite solar cells, as defined by the latest time the anti‐solvent drip yields efficient solar cells, broadened with the increasing complexity of cation/halide content. This behavior is ascribed to kinetic stabilization of sol–gel state through cation/halide engineering. This provides guidelines for designing new formulations, aimed at formation of the perovskite phase, ultimately resulting in high‐efficiency perovskite solar cells produced with ease and with high reproducibility. Perovskite solar cells increasingly feature mixed‐halide mixed‐cation compounds (FA1−x−yMAxCsyPbI3−zBrz) as photovoltaic absorbers, as they enable easier processing and improved stability. Here, the underlying reasons for ease of processing are revealed. It is found that halide and cation engineering leads to a systematic widening of the anti‐solvent processing window for the fabrication of high‐quality films and efficient solar cells. This window widens from seconds, in the case of single cation/halide systems (e.g., MAPbI3, FAPbI3, and FAPbBr3), to several minutes for mixed systems. In situ X‐ray diffraction studies reveal that the processing window is closely related to the crystallization of the disordered sol–gel and to the number of crystalline byproducts; the processing window therefore depends directly on the precise cation/halide composition. Moreover, anti‐solvent dripping is shown to promote the desired perovskite phase with careful formulation. The processing window of perovskite solar cells, as defined by the latest time the anti‐solvent drip yields efficient solar cells, broadened with the increasing complexity of cation/halide content. This behavior is ascribed to kinetic stabilization of sol–gel state through cation/halide engineering. This provides guidelines for designing new formulations, aimed at formation of the perovskite phase, ultimately resulting in high‐efficiency perovskite solar cells produced with ease and with high reproducibility. Perovskite solar cells increasingly feature mixed-halide mixed-cation compounds (FA MA Cs PbI Br ) as photovoltaic absorbers, as they enable easier processing and improved stability. Here, the underlying reasons for ease of processing are revealed. It is found that halide and cation engineering leads to a systematic widening of the anti-solvent processing window for the fabrication of high-quality films and efficient solar cells. This window widens from seconds, in the case of single cation/halide systems (e.g., MAPbI , FAPbI , and FAPbBr ), to several minutes for mixed systems. In situ X-ray diffraction studies reveal that the processing window is closely related to the crystallization of the disordered sol-gel and to the number of crystalline byproducts; the processing window therefore depends directly on the precise cation/halide composition. Moreover, anti-solvent dripping is shown to promote the desired perovskite phase with careful formulation. The processing window of perovskite solar cells, as defined by the latest time the anti-solvent drip yields efficient solar cells, broadened with the increasing complexity of cation/halide content. This behavior is ascribed to kinetic stabilization of sol-gel state through cation/halide engineering. This provides guidelines for designing new formulations, aimed at formation of the perovskite phase, ultimately resulting in high-efficiency perovskite solar cells produced with ease and with high reproducibility. |
| Author | Tang, Ming‐Chun Smilgies, Detlef‐M. Munir, Rahim Aydin, Erkan Barrit, Dounya De Bastiani, Michele Wang, Kai Dang, Hoang X. Wolf, Stefaan Amassian, Aram |
| Author_xml | – sequence: 1 givenname: Kai surname: Wang fullname: Wang, Kai organization: Division of Physical Science and Engineering, and KAUST Solar Center – sequence: 2 givenname: Ming‐Chun surname: Tang fullname: Tang, Ming‐Chun organization: Division of Physical Science and Engineering, and KAUST Solar Center – sequence: 3 givenname: Hoang X. surname: Dang fullname: Dang, Hoang X. organization: North Carolina State University – sequence: 4 givenname: Rahim orcidid: 0000-0002-6029-3760 surname: Munir fullname: Munir, Rahim organization: Division of Physical Science and Engineering, and KAUST Solar Center – sequence: 5 givenname: Dounya surname: Barrit fullname: Barrit, Dounya organization: Division of Physical Science and Engineering, and KAUST Solar Center – sequence: 6 givenname: Michele surname: De Bastiani fullname: De Bastiani, Michele organization: Division of Physical Science and Engineering, and KAUST Solar Center – sequence: 7 givenname: Erkan surname: Aydin fullname: Aydin, Erkan organization: Division of Physical Science and Engineering, and KAUST Solar Center – sequence: 8 givenname: Detlef‐M. surname: Smilgies fullname: Smilgies, Detlef‐M. organization: Cornell University – sequence: 9 givenname: Stefaan surname: Wolf fullname: Wolf, Stefaan email: stefaan.dewolf@kaust.edu.sa organization: Division of Physical Science and Engineering, and KAUST Solar Center – sequence: 10 givenname: Aram orcidid: 0000-0002-5734-1194 surname: Amassian fullname: Amassian, Aram email: aamassi@ncsu.edu organization: North Carolina State University |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31206857$$D View this record in MEDLINE/PubMed |
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| Keywords | in situ GIWAXS hybrid perovskite solar cells mixed-cation mixed-halide perovskites kinetic stabilization anti-solvent drip |
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| Snippet | Perovskite solar cells increasingly feature mixed‐halide mixed‐cation compounds (FA1−x−yMAxCsyPbI3−zBrz) as photovoltaic absorbers, as they enable easier... Perovskite solar cells increasingly feature mixed‐halide mixed‐cation compounds (FA 1− x − y MA x Cs y PbI 3− z Br z ) as photovoltaic absorbers, as they... Perovskite solar cells increasingly feature mixed-halide mixed-cation compounds (FA MA Cs PbI Br ) as photovoltaic absorbers, as they enable easier processing... Perovskite solar cells increasingly feature mixed-halide mixed-cation compounds (FA1- x - y MAx Csy PbI3- z Brz ) as photovoltaic absorbers, as they enable... |
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| SubjectTerms | anti‐solvent drip Cations Crystallization Formulations hybrid perovskite solar cells in situ GIWAXS kinetic stabilization Materials science mixed‐cation mixed‐halide perovskites Perovskites Photovoltaic cells Sol-gel processes Solar cells Solvents Stabilization Windows (intervals) |
| Title | Kinetic Stabilization of the Sol–Gel State in Perovskites Enables Facile Processing of High‐Efficiency Solar Cells |
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