Micelle-Assisted Formation of Self-Assembled Monolayers for Efficient and Stable Perovskite/Silicon Tandem Solar Cells

IF 24.4 1区 材料科学 Q1 CHEMISTRY, PHYSICAL
Linhui Liu, Zhiqin Ying, Xin Li, Haojiang Du, Meili Zhang, Jun Wu, Yihan Sun, Haofan Ma, Ziyu He, Yunyun Yu, Xuchao Guo, Jingsong Sun, Yuheng Zeng, Xi Yang, Jichun Ye
{"title":"Micelle-Assisted Formation of Self-Assembled Monolayers for Efficient and Stable Perovskite/Silicon Tandem Solar Cells","authors":"Linhui Liu, Zhiqin Ying, Xin Li, Haojiang Du, Meili Zhang, Jun Wu, Yihan Sun, Haofan Ma, Ziyu He, Yunyun Yu, Xuchao Guo, Jingsong Sun, Yuheng Zeng, Xi Yang, Jichun Ye","doi":"10.1002/aenm.202405675","DOIUrl":null,"url":null,"abstract":"Self-assembled monolayers (SAMs) are widely utilized in high-efficiency perovskite based solar cells due to their tunable energy alignment, minimal parasitic absorption, and compatibility with scalable processing. However, their performance on rough substrates and large-area devices is often hampered by SAMs self-clustering and poor perovskite wettability. In this study, these limitations are addressed with a straightforward micelle-assisted SAMs adsorption strategy. By incorporating a small amount of long-chain surfactants into the SAMs solution, the surfactants aggregate to form micelles that encapsulate SAMs molecules within their hydrophobic cores, significantly increasing the adsorption density of SAMs through micelle-admicelle interactions. Notably, the residual surfactants further improve perovskite wettability, enhance crystal quality, and facilitate hole transport across the buried interface. Consequently, the wide-bandgap single-junction perovskite solar cell achieves a notable power conversion efficiency (PCE) of 20.95% and enhances long-term stability compared to control devices. By integrating tunnel oxide passivated contact (TOPCon) silicon solar cells, a 1 cm<sup>2</sup> monolithic perovskite/silicon tandem device achieving a PCE of 29.8% is demonstrated, ranking among the highest reported efficiencies for perovskite/homojunction silicon tandem solar cells. Furthermore, the unencapsulated device maintains 92% of its initial performance after 300 h of maximum power point (MPP) tracking under unfiltered Xenon Lamp illumination.","PeriodicalId":111,"journal":{"name":"Advanced Energy Materials","volume":"69 1","pages":""},"PeriodicalIF":24.4000,"publicationDate":"2025-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Energy Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/aenm.202405675","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Self-assembled monolayers (SAMs) are widely utilized in high-efficiency perovskite based solar cells due to their tunable energy alignment, minimal parasitic absorption, and compatibility with scalable processing. However, their performance on rough substrates and large-area devices is often hampered by SAMs self-clustering and poor perovskite wettability. In this study, these limitations are addressed with a straightforward micelle-assisted SAMs adsorption strategy. By incorporating a small amount of long-chain surfactants into the SAMs solution, the surfactants aggregate to form micelles that encapsulate SAMs molecules within their hydrophobic cores, significantly increasing the adsorption density of SAMs through micelle-admicelle interactions. Notably, the residual surfactants further improve perovskite wettability, enhance crystal quality, and facilitate hole transport across the buried interface. Consequently, the wide-bandgap single-junction perovskite solar cell achieves a notable power conversion efficiency (PCE) of 20.95% and enhances long-term stability compared to control devices. By integrating tunnel oxide passivated contact (TOPCon) silicon solar cells, a 1 cm2 monolithic perovskite/silicon tandem device achieving a PCE of 29.8% is demonstrated, ranking among the highest reported efficiencies for perovskite/homojunction silicon tandem solar cells. Furthermore, the unencapsulated device maintains 92% of its initial performance after 300 h of maximum power point (MPP) tracking under unfiltered Xenon Lamp illumination.

Abstract Image

求助全文
约1分钟内获得全文 求助全文
来源期刊
Advanced Energy Materials
Advanced Energy Materials CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
41.90
自引率
4.00%
发文量
889
审稿时长
1.4 months
期刊介绍: Established in 2011, Advanced Energy Materials is an international, interdisciplinary, English-language journal that focuses on materials used in energy harvesting, conversion, and storage. It is regarded as a top-quality journal alongside Advanced Materials, Advanced Functional Materials, and Small. With a 2022 Impact Factor of 27.8, Advanced Energy Materials is considered a prime source for the best energy-related research. The journal covers a wide range of topics in energy-related research, including organic and inorganic photovoltaics, batteries and supercapacitors, fuel cells, hydrogen generation and storage, thermoelectrics, water splitting and photocatalysis, solar fuels and thermosolar power, magnetocalorics, and piezoelectronics. The readership of Advanced Energy Materials includes materials scientists, chemists, physicists, and engineers in both academia and industry. The journal is indexed in various databases and collections, such as Advanced Technologies & Aerospace Database, FIZ Karlsruhe, INSPEC (IET), Science Citation Index Expanded, Technology Collection, and Web of Science, among others.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信