Loading…
Chemical Reaction of FA Cations Enables Efficient and Stable Perovskite Solar Cells
Organometal halide perovskite solar cells (PSCs) have received great attention owing to a rapid increase in power conversion efficiency (PCE) over the last decade. However, the deficit of long‐term stability is a major obstacle to the implementation of PSCs in commercialization. The defects in perov...
Saved in:
Published in: | Small (Weinheim an der Bergstrasse, Germany) Germany), 2024-08, Vol.20 (35), p.e2310455-n/a |
---|---|
Main Authors: | , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c3285-10c0fa7c4959c3e063afafedbe9067218fae7b248ba60bf4d8a54f3a0f0dd48d3 |
container_end_page | n/a |
container_issue | 35 |
container_start_page | e2310455 |
container_title | Small (Weinheim an der Bergstrasse, Germany) |
container_volume | 20 |
creator | Wang, Baohua Hui, Wei Zhao, Qiangqiang Zhang, Yuezhou Kang, Xinxin Li, Maoxin Gu, Lei Bao, Yaqi Su, Jiacheng Zhang, Jie Gao, Xingyu Pang, Shuping Song, Lin |
description | Organometal halide perovskite solar cells (PSCs) have received great attention owing to a rapid increase in power conversion efficiency (PCE) over the last decade. However, the deficit of long‐term stability is a major obstacle to the implementation of PSCs in commercialization. The defects in perovskite films are considered as one of the primary causes. To address this issue, isocyanic acid (HNCO) is introduced as an additive into the perovskite film, in which the added molecules form covalent bonds with FA cations via a chemical reaction. This chemical reaction gives rise to an efficient passivation on the perovskite film, resulting in an improved film quality, a suppressed non‐radiation recombination, a facilitated carrier transport, and optimization of energy band levels. As a result, the HNCO‐based PSCs achieve a high PCE of 24.41% with excellent storage stability both in an inert atmosphere and in air. Different from conventional passivation methods based on coordination effects, this work presents an alternative chemical reaction for defect passivation, which opens an avenue toward defect‐mitigated PSCs showing enhanced performance and stability.
The covalent bonds between the FA cations and the HNCO additives give rise to an efficient passivation on the perovskite films, resulting in an improved film quality, a suppressed non‐radiation recombination, a facilitated carrier transport, and a better energy band levels alignment. Consequently, the modified devices show excellent power conversion efficiency and stability. |
doi_str_mv | 10.1002/smll.202310455 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3048768467</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3097818942</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3285-10c0fa7c4959c3e063afafedbe9067218fae7b248ba60bf4d8a54f3a0f0dd48d3</originalsourceid><addsrcrecordid>eNqF0M1LwzAYBvAgis6Pq0cJePGy-eajbXocZVNhojg9lzR9g51pq02n7L83Y3OCF09vEn55eHkIOWcwYgD82tfOjThwwUBG0R4ZsJiJYax4ur87Mzgix94vAATjMjkkR0IFEaXxgMyzV6wrox19Qm36qm1oa-l0TDO9vng6aXThMExrK1Nh01PdlHTer1_pI3btp3-reqTz1umOZuicPyUHVjuPZ9t5Ql6mk-fsdjh7uLnLxrOhEVxFQwYGrE6MTKPUCIRYaKstlgWmECecKasxKbhUhY6hsLJUOpJWaLBQllKV4oRcbXLfu_Zjib7P68qbsIFusF36XIBUSaxknAR6-Ycu2mXXhO2CShPFVCp5UKONMl3rfYc2f--qWnernEG-rjtf153v6g4fLraxy6LGcsd_-g0g3YCvyuHqn7h8fj-b_YZ_A_fhi4c</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3097818942</pqid></control><display><type>article</type><title>Chemical Reaction of FA Cations Enables Efficient and Stable Perovskite Solar Cells</title><source>Wiley</source><creator>Wang, Baohua ; Hui, Wei ; Zhao, Qiangqiang ; Zhang, Yuezhou ; Kang, Xinxin ; Li, Maoxin ; Gu, Lei ; Bao, Yaqi ; Su, Jiacheng ; Zhang, Jie ; Gao, Xingyu ; Pang, Shuping ; Song, Lin</creator><creatorcontrib>Wang, Baohua ; Hui, Wei ; Zhao, Qiangqiang ; Zhang, Yuezhou ; Kang, Xinxin ; Li, Maoxin ; Gu, Lei ; Bao, Yaqi ; Su, Jiacheng ; Zhang, Jie ; Gao, Xingyu ; Pang, Shuping ; Song, Lin</creatorcontrib><description>Organometal halide perovskite solar cells (PSCs) have received great attention owing to a rapid increase in power conversion efficiency (PCE) over the last decade. However, the deficit of long‐term stability is a major obstacle to the implementation of PSCs in commercialization. The defects in perovskite films are considered as one of the primary causes. To address this issue, isocyanic acid (HNCO) is introduced as an additive into the perovskite film, in which the added molecules form covalent bonds with FA cations via a chemical reaction. This chemical reaction gives rise to an efficient passivation on the perovskite film, resulting in an improved film quality, a suppressed non‐radiation recombination, a facilitated carrier transport, and optimization of energy band levels. As a result, the HNCO‐based PSCs achieve a high PCE of 24.41% with excellent storage stability both in an inert atmosphere and in air. Different from conventional passivation methods based on coordination effects, this work presents an alternative chemical reaction for defect passivation, which opens an avenue toward defect‐mitigated PSCs showing enhanced performance and stability.
The covalent bonds between the FA cations and the HNCO additives give rise to an efficient passivation on the perovskite films, resulting in an improved film quality, a suppressed non‐radiation recombination, a facilitated carrier transport, and a better energy band levels alignment. Consequently, the modified devices show excellent power conversion efficiency and stability.</description><identifier>ISSN: 1613-6810</identifier><identifier>ISSN: 1613-6829</identifier><identifier>EISSN: 1613-6829</identifier><identifier>DOI: 10.1002/smll.202310455</identifier><identifier>PMID: 38682596</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Carrier recombination ; Carrier transport ; Cations ; Chemical bonds ; Chemical reactions ; Commercialization ; Covalent bonds ; defect passivation ; Defects ; Energy bands ; Energy conversion efficiency ; HNCO ; in situ chemical reaction ; Inert atmospheres ; Passivity ; perovskite solar cells ; Perovskites ; Photovoltaic cells ; Solar cells ; Storage stability</subject><ispartof>Small (Weinheim an der Bergstrasse, Germany), 2024-08, Vol.20 (35), p.e2310455-n/a</ispartof><rights>2024 Wiley‐VCH GmbH</rights><rights>2024 Wiley‐VCH GmbH.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3285-10c0fa7c4959c3e063afafedbe9067218fae7b248ba60bf4d8a54f3a0f0dd48d3</cites><orcidid>0000-0003-4971-6301</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38682596$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Baohua</creatorcontrib><creatorcontrib>Hui, Wei</creatorcontrib><creatorcontrib>Zhao, Qiangqiang</creatorcontrib><creatorcontrib>Zhang, Yuezhou</creatorcontrib><creatorcontrib>Kang, Xinxin</creatorcontrib><creatorcontrib>Li, Maoxin</creatorcontrib><creatorcontrib>Gu, Lei</creatorcontrib><creatorcontrib>Bao, Yaqi</creatorcontrib><creatorcontrib>Su, Jiacheng</creatorcontrib><creatorcontrib>Zhang, Jie</creatorcontrib><creatorcontrib>Gao, Xingyu</creatorcontrib><creatorcontrib>Pang, Shuping</creatorcontrib><creatorcontrib>Song, Lin</creatorcontrib><title>Chemical Reaction of FA Cations Enables Efficient and Stable Perovskite Solar Cells</title><title>Small (Weinheim an der Bergstrasse, Germany)</title><addtitle>Small</addtitle><description>Organometal halide perovskite solar cells (PSCs) have received great attention owing to a rapid increase in power conversion efficiency (PCE) over the last decade. However, the deficit of long‐term stability is a major obstacle to the implementation of PSCs in commercialization. The defects in perovskite films are considered as one of the primary causes. To address this issue, isocyanic acid (HNCO) is introduced as an additive into the perovskite film, in which the added molecules form covalent bonds with FA cations via a chemical reaction. This chemical reaction gives rise to an efficient passivation on the perovskite film, resulting in an improved film quality, a suppressed non‐radiation recombination, a facilitated carrier transport, and optimization of energy band levels. As a result, the HNCO‐based PSCs achieve a high PCE of 24.41% with excellent storage stability both in an inert atmosphere and in air. Different from conventional passivation methods based on coordination effects, this work presents an alternative chemical reaction for defect passivation, which opens an avenue toward defect‐mitigated PSCs showing enhanced performance and stability.
The covalent bonds between the FA cations and the HNCO additives give rise to an efficient passivation on the perovskite films, resulting in an improved film quality, a suppressed non‐radiation recombination, a facilitated carrier transport, and a better energy band levels alignment. Consequently, the modified devices show excellent power conversion efficiency and stability.</description><subject>Carrier recombination</subject><subject>Carrier transport</subject><subject>Cations</subject><subject>Chemical bonds</subject><subject>Chemical reactions</subject><subject>Commercialization</subject><subject>Covalent bonds</subject><subject>defect passivation</subject><subject>Defects</subject><subject>Energy bands</subject><subject>Energy conversion efficiency</subject><subject>HNCO</subject><subject>in situ chemical reaction</subject><subject>Inert atmospheres</subject><subject>Passivity</subject><subject>perovskite solar cells</subject><subject>Perovskites</subject><subject>Photovoltaic cells</subject><subject>Solar cells</subject><subject>Storage stability</subject><issn>1613-6810</issn><issn>1613-6829</issn><issn>1613-6829</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqF0M1LwzAYBvAgis6Pq0cJePGy-eajbXocZVNhojg9lzR9g51pq02n7L83Y3OCF09vEn55eHkIOWcwYgD82tfOjThwwUBG0R4ZsJiJYax4ur87Mzgix94vAATjMjkkR0IFEaXxgMyzV6wrox19Qm36qm1oa-l0TDO9vng6aXThMExrK1Nh01PdlHTer1_pI3btp3-reqTz1umOZuicPyUHVjuPZ9t5Ql6mk-fsdjh7uLnLxrOhEVxFQwYGrE6MTKPUCIRYaKstlgWmECecKasxKbhUhY6hsLJUOpJWaLBQllKV4oRcbXLfu_Zjib7P68qbsIFusF36XIBUSaxknAR6-Ycu2mXXhO2CShPFVCp5UKONMl3rfYc2f--qWnernEG-rjtf153v6g4fLraxy6LGcsd_-g0g3YCvyuHqn7h8fj-b_YZ_A_fhi4c</recordid><startdate>20240801</startdate><enddate>20240801</enddate><creator>Wang, Baohua</creator><creator>Hui, Wei</creator><creator>Zhao, Qiangqiang</creator><creator>Zhang, Yuezhou</creator><creator>Kang, Xinxin</creator><creator>Li, Maoxin</creator><creator>Gu, Lei</creator><creator>Bao, Yaqi</creator><creator>Su, Jiacheng</creator><creator>Zhang, Jie</creator><creator>Gao, Xingyu</creator><creator>Pang, Shuping</creator><creator>Song, Lin</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4971-6301</orcidid></search><sort><creationdate>20240801</creationdate><title>Chemical Reaction of FA Cations Enables Efficient and Stable Perovskite Solar Cells</title><author>Wang, Baohua ; Hui, Wei ; Zhao, Qiangqiang ; Zhang, Yuezhou ; Kang, Xinxin ; Li, Maoxin ; Gu, Lei ; Bao, Yaqi ; Su, Jiacheng ; Zhang, Jie ; Gao, Xingyu ; Pang, Shuping ; Song, Lin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3285-10c0fa7c4959c3e063afafedbe9067218fae7b248ba60bf4d8a54f3a0f0dd48d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Carrier recombination</topic><topic>Carrier transport</topic><topic>Cations</topic><topic>Chemical bonds</topic><topic>Chemical reactions</topic><topic>Commercialization</topic><topic>Covalent bonds</topic><topic>defect passivation</topic><topic>Defects</topic><topic>Energy bands</topic><topic>Energy conversion efficiency</topic><topic>HNCO</topic><topic>in situ chemical reaction</topic><topic>Inert atmospheres</topic><topic>Passivity</topic><topic>perovskite solar cells</topic><topic>Perovskites</topic><topic>Photovoltaic cells</topic><topic>Solar cells</topic><topic>Storage stability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Baohua</creatorcontrib><creatorcontrib>Hui, Wei</creatorcontrib><creatorcontrib>Zhao, Qiangqiang</creatorcontrib><creatorcontrib>Zhang, Yuezhou</creatorcontrib><creatorcontrib>Kang, Xinxin</creatorcontrib><creatorcontrib>Li, Maoxin</creatorcontrib><creatorcontrib>Gu, Lei</creatorcontrib><creatorcontrib>Bao, Yaqi</creatorcontrib><creatorcontrib>Su, Jiacheng</creatorcontrib><creatorcontrib>Zhang, Jie</creatorcontrib><creatorcontrib>Gao, Xingyu</creatorcontrib><creatorcontrib>Pang, Shuping</creatorcontrib><creatorcontrib>Song, Lin</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Small (Weinheim an der Bergstrasse, Germany)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Baohua</au><au>Hui, Wei</au><au>Zhao, Qiangqiang</au><au>Zhang, Yuezhou</au><au>Kang, Xinxin</au><au>Li, Maoxin</au><au>Gu, Lei</au><au>Bao, Yaqi</au><au>Su, Jiacheng</au><au>Zhang, Jie</au><au>Gao, Xingyu</au><au>Pang, Shuping</au><au>Song, Lin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chemical Reaction of FA Cations Enables Efficient and Stable Perovskite Solar Cells</atitle><jtitle>Small (Weinheim an der Bergstrasse, Germany)</jtitle><addtitle>Small</addtitle><date>2024-08-01</date><risdate>2024</risdate><volume>20</volume><issue>35</issue><spage>e2310455</spage><epage>n/a</epage><pages>e2310455-n/a</pages><issn>1613-6810</issn><issn>1613-6829</issn><eissn>1613-6829</eissn><abstract>Organometal halide perovskite solar cells (PSCs) have received great attention owing to a rapid increase in power conversion efficiency (PCE) over the last decade. However, the deficit of long‐term stability is a major obstacle to the implementation of PSCs in commercialization. The defects in perovskite films are considered as one of the primary causes. To address this issue, isocyanic acid (HNCO) is introduced as an additive into the perovskite film, in which the added molecules form covalent bonds with FA cations via a chemical reaction. This chemical reaction gives rise to an efficient passivation on the perovskite film, resulting in an improved film quality, a suppressed non‐radiation recombination, a facilitated carrier transport, and optimization of energy band levels. As a result, the HNCO‐based PSCs achieve a high PCE of 24.41% with excellent storage stability both in an inert atmosphere and in air. Different from conventional passivation methods based on coordination effects, this work presents an alternative chemical reaction for defect passivation, which opens an avenue toward defect‐mitigated PSCs showing enhanced performance and stability.
The covalent bonds between the FA cations and the HNCO additives give rise to an efficient passivation on the perovskite films, resulting in an improved film quality, a suppressed non‐radiation recombination, a facilitated carrier transport, and a better energy band levels alignment. Consequently, the modified devices show excellent power conversion efficiency and stability.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38682596</pmid><doi>10.1002/smll.202310455</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-4971-6301</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1613-6810 |
ispartof | Small (Weinheim an der Bergstrasse, Germany), 2024-08, Vol.20 (35), p.e2310455-n/a |
issn | 1613-6810 1613-6829 1613-6829 |
language | eng |
recordid | cdi_proquest_miscellaneous_3048768467 |
source | Wiley |
subjects | Carrier recombination Carrier transport Cations Chemical bonds Chemical reactions Commercialization Covalent bonds defect passivation Defects Energy bands Energy conversion efficiency HNCO in situ chemical reaction Inert atmospheres Passivity perovskite solar cells Perovskites Photovoltaic cells Solar cells Storage stability |
title | Chemical Reaction of FA Cations Enables Efficient and Stable Perovskite Solar Cells |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T16%3A15%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Chemical%20Reaction%20of%20FA%20Cations%20Enables%20Efficient%20and%20Stable%20Perovskite%20Solar%20Cells&rft.jtitle=Small%20(Weinheim%20an%20der%20Bergstrasse,%20Germany)&rft.au=Wang,%20Baohua&rft.date=2024-08-01&rft.volume=20&rft.issue=35&rft.spage=e2310455&rft.epage=n/a&rft.pages=e2310455-n/a&rft.issn=1613-6810&rft.eissn=1613-6829&rft_id=info:doi/10.1002/smll.202310455&rft_dat=%3Cproquest_cross%3E3097818942%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3285-10c0fa7c4959c3e063afafedbe9067218fae7b248ba60bf4d8a54f3a0f0dd48d3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3097818942&rft_id=info:pmid/38682596&rfr_iscdi=true |