Performance Enhancement of Hole Transport Layer-Free Carbon-Based CsPbIBr 2 Solar Cells through the Application of Perovskite Quantum Dots
CsPbIBr , with its suitable bandgap, shows great potential as the top cell in tandem solar cells. Nonetheless, its further development is hindered by a high defect density, severe carrier recombination, and poor stability. In this study, CsPbI Br quantum dots were utilized as an additive in the ethy...
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Veröffentlicht in: | Nanomaterials (Basel, Switzerland) Switzerland), 2024-10, Vol.14 (20) |
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creator | Yu, Qi Sun, Wentian Tang, Shu |
description | CsPbIBr
, with its suitable bandgap, shows great potential as the top cell in tandem solar cells. Nonetheless, its further development is hindered by a high defect density, severe carrier recombination, and poor stability. In this study, CsPbI
Br
quantum dots were utilized as an additive in the ethyl acetate anti-solvent, while a layer of CsPbBr
QDs was introduced between the ETL and the CsPbIBr
light-harvester film. The combined effect of these two QDs enhanced the nucleation, crystallization, and growth of CsPbIBr
perovskite, yielding high-quality films characterized by an enlarged crystal size, reduced grain boundaries, and smooth surfaces. And a wider absorption range and better energy band alignment were achieved owing to the nano-size effect of QDs. These improvements led to a decreased defect density and the suppression of non-radiative recombination. Additionally, the presence of long-chain organic molecules in the QD solution promoted the formation of a hydrophobic surface, significantly enhancing the long-term stability of CsPbIBr
PSCs. Consequently, the devices achieved a PCE of 9.20% and maintained an initial efficiency of 85% after 60 days of storage in air. Thus, this strategy proves to be an effective approach for the preparation of efficient and stable CsPbIBr
PSCs. |
doi_str_mv | 10.3390/nano14201651 |
format | Article |
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, with its suitable bandgap, shows great potential as the top cell in tandem solar cells. Nonetheless, its further development is hindered by a high defect density, severe carrier recombination, and poor stability. In this study, CsPbI
Br
quantum dots were utilized as an additive in the ethyl acetate anti-solvent, while a layer of CsPbBr
QDs was introduced between the ETL and the CsPbIBr
light-harvester film. The combined effect of these two QDs enhanced the nucleation, crystallization, and growth of CsPbIBr
perovskite, yielding high-quality films characterized by an enlarged crystal size, reduced grain boundaries, and smooth surfaces. And a wider absorption range and better energy band alignment were achieved owing to the nano-size effect of QDs. These improvements led to a decreased defect density and the suppression of non-radiative recombination. Additionally, the presence of long-chain organic molecules in the QD solution promoted the formation of a hydrophobic surface, significantly enhancing the long-term stability of CsPbIBr
PSCs. Consequently, the devices achieved a PCE of 9.20% and maintained an initial efficiency of 85% after 60 days of storage in air. Thus, this strategy proves to be an effective approach for the preparation of efficient and stable CsPbIBr
PSCs.</description><identifier>ISSN: 2079-4991</identifier><identifier>EISSN: 2079-4991</identifier><identifier>DOI: 10.3390/nano14201651</identifier><identifier>PMID: 39452987</identifier><language>eng</language><publisher>Switzerland</publisher><ispartof>Nanomaterials (Basel, Switzerland), 2024-10, Vol.14 (20)</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0009-0005-1689-3581</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39452987$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Qi</creatorcontrib><creatorcontrib>Sun, Wentian</creatorcontrib><creatorcontrib>Tang, Shu</creatorcontrib><title>Performance Enhancement of Hole Transport Layer-Free Carbon-Based CsPbIBr 2 Solar Cells through the Application of Perovskite Quantum Dots</title><title>Nanomaterials (Basel, Switzerland)</title><addtitle>Nanomaterials (Basel)</addtitle><description>CsPbIBr
, with its suitable bandgap, shows great potential as the top cell in tandem solar cells. Nonetheless, its further development is hindered by a high defect density, severe carrier recombination, and poor stability. In this study, CsPbI
Br
quantum dots were utilized as an additive in the ethyl acetate anti-solvent, while a layer of CsPbBr
QDs was introduced between the ETL and the CsPbIBr
light-harvester film. The combined effect of these two QDs enhanced the nucleation, crystallization, and growth of CsPbIBr
perovskite, yielding high-quality films characterized by an enlarged crystal size, reduced grain boundaries, and smooth surfaces. And a wider absorption range and better energy band alignment were achieved owing to the nano-size effect of QDs. These improvements led to a decreased defect density and the suppression of non-radiative recombination. Additionally, the presence of long-chain organic molecules in the QD solution promoted the formation of a hydrophobic surface, significantly enhancing the long-term stability of CsPbIBr
PSCs. Consequently, the devices achieved a PCE of 9.20% and maintained an initial efficiency of 85% after 60 days of storage in air. Thus, this strategy proves to be an effective approach for the preparation of efficient and stable CsPbIBr
PSCs.</description><issn>2079-4991</issn><issn>2079-4991</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFjk9Lw0AUxBdRbNHePMv7AtFsNrHdo40tFTxU7L28tC8mun_C243Qr-CnbgoK3pzLbw7DzAhxI9M7pXR679B5mWepfCjkmRhn6VQnudby_I8fiUkIH-kgLdWsUJdipHReZHo2HYvvNXHt2aLbESxcc6IlF8HXsPKGYMPoQuc5wgseiJMlE0GJXHmXzDHQHsqwrp7nDBm8eYMMJRkTIDbs-_dmIMFj15l2h7H17tQ7TPqv8NlGgtceXewtPPkYrsVFjSbQ5IdX4na52JSrpOsrS_ttx61FPmx_z6t_A0fRHFhK</recordid><startdate>20241014</startdate><enddate>20241014</enddate><creator>Yu, Qi</creator><creator>Sun, Wentian</creator><creator>Tang, Shu</creator><scope>NPM</scope><orcidid>https://orcid.org/0009-0005-1689-3581</orcidid></search><sort><creationdate>20241014</creationdate><title>Performance Enhancement of Hole Transport Layer-Free Carbon-Based CsPbIBr 2 Solar Cells through the Application of Perovskite Quantum Dots</title><author>Yu, Qi ; Sun, Wentian ; Tang, Shu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_394529873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yu, Qi</creatorcontrib><creatorcontrib>Sun, Wentian</creatorcontrib><creatorcontrib>Tang, Shu</creatorcontrib><collection>PubMed</collection><jtitle>Nanomaterials (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Qi</au><au>Sun, Wentian</au><au>Tang, Shu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Performance Enhancement of Hole Transport Layer-Free Carbon-Based CsPbIBr 2 Solar Cells through the Application of Perovskite Quantum Dots</atitle><jtitle>Nanomaterials (Basel, Switzerland)</jtitle><addtitle>Nanomaterials (Basel)</addtitle><date>2024-10-14</date><risdate>2024</risdate><volume>14</volume><issue>20</issue><issn>2079-4991</issn><eissn>2079-4991</eissn><abstract>CsPbIBr
, with its suitable bandgap, shows great potential as the top cell in tandem solar cells. Nonetheless, its further development is hindered by a high defect density, severe carrier recombination, and poor stability. In this study, CsPbI
Br
quantum dots were utilized as an additive in the ethyl acetate anti-solvent, while a layer of CsPbBr
QDs was introduced between the ETL and the CsPbIBr
light-harvester film. The combined effect of these two QDs enhanced the nucleation, crystallization, and growth of CsPbIBr
perovskite, yielding high-quality films characterized by an enlarged crystal size, reduced grain boundaries, and smooth surfaces. And a wider absorption range and better energy band alignment were achieved owing to the nano-size effect of QDs. These improvements led to a decreased defect density and the suppression of non-radiative recombination. Additionally, the presence of long-chain organic molecules in the QD solution promoted the formation of a hydrophobic surface, significantly enhancing the long-term stability of CsPbIBr
PSCs. Consequently, the devices achieved a PCE of 9.20% and maintained an initial efficiency of 85% after 60 days of storage in air. Thus, this strategy proves to be an effective approach for the preparation of efficient and stable CsPbIBr
PSCs.</abstract><cop>Switzerland</cop><pmid>39452987</pmid><doi>10.3390/nano14201651</doi><orcidid>https://orcid.org/0009-0005-1689-3581</orcidid></addata></record> |
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source | Open Access: PubMed Central; MDPI - Multidisciplinary Digital Publishing Institute; DOAJ Directory of Open Access Journals; EZB Electronic Journals Library; PubMed Central Open Access |
title | Performance Enhancement of Hole Transport Layer-Free Carbon-Based CsPbIBr 2 Solar Cells through the Application of Perovskite Quantum Dots |
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