Gas-solid reaction based over one-micrometer thick stable perovskite films for efficient solar cells and modules

Besides high efficiency, the stability and reproducibility of perovskite solar cells (PSCs) are also key for their commercialization. Herein, we report a simple perovskite formation method to fabricate perovskite films with thickness over 1 μm in ambient condition on the basis of the fast gas−solid...

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Published inNature communications Vol. 9; no. 1; pp. 3880 - 11
Main Authors Liu, Zonghao, Qiu, Longbin, Juarez-Perez, Emilio J., Hawash, Zafer, Kim, Taehoon, Jiang, Yan, Wu, Zhifang, Raga, Sonia R., Ono, Luis K., Liu, Shengzhong (Frank), Qi, Yabing
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 24.09.2018
Nature Publishing Group
Nature Portfolio
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ISSN2041-1723
2041-1723
DOI10.1038/s41467-018-06317-8

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Abstract Besides high efficiency, the stability and reproducibility of perovskite solar cells (PSCs) are also key for their commercialization. Herein, we report a simple perovskite formation method to fabricate perovskite films with thickness over 1 μm in ambient condition on the basis of the fast gas−solid reaction of chlorine-incorporated hydrogen lead triiodide and methylamine gas. The resultant thick and smooth chlorine-incorporated perovskite films exhibit full coverage, improved crystallinity, low surface roughness and low thickness variation. The resultant PSCs achieve an average power conversion efficiency of 19.1 ± 0.4% with good reproducibility. Meanwhile, this method enables an active area efficiency of 15.3% for 5 cm × 5 cm solar modules. The un-encapsulated PSCs exhibit an excellent T 80 lifetime exceeding 1600 h under continuous operation conditions in dry nitrogen environment. Perovskite solar cells often suffer from poor uniformity and reproducibility especially in case of large area devices. Here Liu et al. developed a gas−solid reaction method that enables facile fabrication of over 1 µm thick perovskite films for solar modules with high efficiency, stability and reproducibility.
AbstractList Besides high efficiency, the stability and reproducibility of perovskite solar cells (PSCs) are also key for their commercialization. Herein, we report a simple perovskite formation method to fabricate perovskite films with thickness over 1 μm in ambient condition on the basis of the fast gas-solid reaction of chlorine-incorporated hydrogen lead triiodide and methylamine gas. The resultant thick and smooth chlorine-incorporated perovskite films exhibit full coverage, improved crystallinity, low surface roughness and low thickness variation. The resultant PSCs achieve an average power conversion efficiency of 19.1 ± 0.4% with good reproducibility. Meanwhile, this method enables an active area efficiency of 15.3% for 5 cm × 5 cm solar modules. The un-encapsulated PSCs exhibit an excellent T lifetime exceeding 1600 h under continuous operation conditions in dry nitrogen environment.
Perovskite solar cells often suffer from poor uniformity and reproducibility especially in case of large area devices. Here Liu et al. developed a gas−solid reaction method that enables facile fabrication of over 1 µm thick perovskite films for solar modules with high efficiency, stability and reproducibility.
Besides high efficiency, the stability and reproducibility of perovskite solar cells (PSCs) are also key for their commercialization. Herein, we report a simple perovskite formation method to fabricate perovskite films with thickness over 1 μm in ambient condition on the basis of the fast gas-solid reaction of chlorine-incorporated hydrogen lead triiodide and methylamine gas. The resultant thick and smooth chlorine-incorporated perovskite films exhibit full coverage, improved crystallinity, low surface roughness and low thickness variation. The resultant PSCs achieve an average power conversion efficiency of 19.1 ± 0.4% with good reproducibility. Meanwhile, this method enables an active area efficiency of 15.3% for 5 cm × 5 cm solar modules. The un-encapsulated PSCs exhibit an excellent T80 lifetime exceeding 1600 h under continuous operation conditions in dry nitrogen environment.Besides high efficiency, the stability and reproducibility of perovskite solar cells (PSCs) are also key for their commercialization. Herein, we report a simple perovskite formation method to fabricate perovskite films with thickness over 1 μm in ambient condition on the basis of the fast gas-solid reaction of chlorine-incorporated hydrogen lead triiodide and methylamine gas. The resultant thick and smooth chlorine-incorporated perovskite films exhibit full coverage, improved crystallinity, low surface roughness and low thickness variation. The resultant PSCs achieve an average power conversion efficiency of 19.1 ± 0.4% with good reproducibility. Meanwhile, this method enables an active area efficiency of 15.3% for 5 cm × 5 cm solar modules. The un-encapsulated PSCs exhibit an excellent T80 lifetime exceeding 1600 h under continuous operation conditions in dry nitrogen environment.
Besides high efficiency, the stability and reproducibility of perovskite solar cells (PSCs) are also key for their commercialization. Herein, we report a simple perovskite formation method to fabricate perovskite films with thickness over 1 μm in ambient condition on the basis of the fast gas−solid reaction of chlorine-incorporated hydrogen lead triiodide and methylamine gas. The resultant thick and smooth chlorine-incorporated perovskite films exhibit full coverage, improved crystallinity, low surface roughness and low thickness variation. The resultant PSCs achieve an average power conversion efficiency of 19.1 ± 0.4% with good reproducibility. Meanwhile, this method enables an active area efficiency of 15.3% for 5 cm × 5 cm solar modules. The un-encapsulated PSCs exhibit an excellent T 80 lifetime exceeding 1600 h under continuous operation conditions in dry nitrogen environment. Perovskite solar cells often suffer from poor uniformity and reproducibility especially in case of large area devices. Here Liu et al. developed a gas−solid reaction method that enables facile fabrication of over 1 µm thick perovskite films for solar modules with high efficiency, stability and reproducibility.
Besides high efficiency, the stability and reproducibility of perovskite solar cells (PSCs) are also key for their commercialization. Herein, we report a simple perovskite formation method to fabricate perovskite films with thickness over 1 μm in ambient condition on the basis of the fast gas−solid reaction of chlorine-incorporated hydrogen lead triiodide and methylamine gas. The resultant thick and smooth chlorine-incorporated perovskite films exhibit full coverage, improved crystallinity, low surface roughness and low thickness variation. The resultant PSCs achieve an average power conversion efficiency of 19.1 ± 0.4% with good reproducibility. Meanwhile, this method enables an active area efficiency of 15.3% for 5 cm × 5 cm solar modules. The un-encapsulated PSCs exhibit an excellent T 80 lifetime exceeding 1600 h under continuous operation conditions in dry nitrogen environment.
Besides high efficiency, the stability and reproducibility of perovskite solar cells (PSCs) are also key for their commercialization. Herein, we report a simple perovskite formation method to fabricate perovskite films with thickness over 1 mu m in ambient condition on the basis of the fast gas-solid reaction of chlorine-incorporated hydrogen lead triiodide and methylamine gas. The resultant thick and smooth chlorine-incorporated perovskite films exhibit full coverage, improved crystallinity, low surface roughness and low thickness variation. The resultant PSCs achieve an average power conversion efficiency of 19.1 +/- 0.4% with good reproducibility. Meanwhile, this method enables an active area efficiency of 15.3% for 5 cmx 5 cm solar modules. The un-encapsulated PSCs exhibit an excellent T-80 lifetime exceeding 1600 h under continuous operation conditions in dry nitrogen environment.
Besides high efficiency, the stability and reproducibility of perovskite solar cells (PSCs) are also key for their commercialization. Herein, we report a simple perovskite formation method to fabricate perovskite films with thickness over 1 μm in ambient condition on the basis of the fast gas−solid reaction of chlorine-incorporated hydrogen lead triiodide and methylamine gas. The resultant thick and smooth chlorine-incorporated perovskite films exhibit full coverage, improved crystallinity, low surface roughness and low thickness variation. The resultant PSCs achieve an average power conversion efficiency of 19.1 ± 0.4% with good reproducibility. Meanwhile, this method enables an active area efficiency of 15.3% for 5 cm × 5 cm solar modules. The un-encapsulated PSCs exhibit an excellent T80 lifetime exceeding 1600 h under continuous operation conditions in dry nitrogen environment.
ArticleNumber 3880
Author Liu, Zonghao
Raga, Sonia R.
Hawash, Zafer
Kim, Taehoon
Juarez-Perez, Emilio J.
Liu, Shengzhong (Frank)
Qiu, Longbin
Ono, Luis K.
Qi, Yabing
Jiang, Yan
Wu, Zhifang
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Snippet Besides high efficiency, the stability and reproducibility of perovskite solar cells (PSCs) are also key for their commercialization. Herein, we report a...
Perovskite solar cells often suffer from poor uniformity and reproducibility especially in case of large area devices. Here Liu et al. developed a gas−solid...
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SubjectTerms 147/135
147/3
639/301/299/946
639/4077/4072/4062
Chlorine
Commercialization
Efficiency
Energy conversion efficiency
Gas-solid reactions
Humanities and Social Sciences
Lead
Materials Engineering
Materialteknik
Methylamine
Modules
multidisciplinary
Perovskites
Photovoltaic cells
Reproducibility
Science
Science (multidisciplinary)
Solar cells
Surface roughness
Thick films
Thickness
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Title Gas-solid reaction based over one-micrometer thick stable perovskite films for efficient solar cells and modules
URI https://link.springer.com/article/10.1038/s41467-018-06317-8
https://www.ncbi.nlm.nih.gov/pubmed/30250031
https://www.proquest.com/docview/2111724469
https://www.proquest.com/docview/2112192695
https://pubmed.ncbi.nlm.nih.gov/PMC6155243
https://urn.kb.se/resolve?urn=urn:nbn:se:kau:diva-83181
https://doaj.org/article/158f4b2e5ec0442b92dcc0f8869fa4c8
Volume 9
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