Synergistic Dimensional and Passivation Engineering via Blade Coating Enables Efficient and Stable Perovskite Solar Cells

IF 4.5 2区 化学 Q2 CHEMISTRY, PHYSICAL The Journal of Physical Chemistry Letters Pub Date : 2026-10-20 DOI:10.1021/acs.jpclett.6c02871
Junhao Geng,Yulu Liu,Xiao Zhou,Liu Yang,Shuang Li,Hongmei Zhan,Helong Zhu,Dezhong Zhang,Hui Tong,Zhipeng Wei,Chuanjiang Qin
{"title":"Synergistic Dimensional and Passivation Engineering via Blade Coating Enables Efficient and Stable Perovskite Solar Cells","authors":"Junhao Geng,Yulu Liu,Xiao Zhou,Liu Yang,Shuang Li,Hongmei Zhan,Helong Zhu,Dezhong Zhang,Hui Tong,Zhipeng Wei,Chuanjiang Qin","doi":"10.1021/acs.jpclett.6c02871","DOIUrl":null,"url":null,"abstract":"Upscaling perovskite solar cells (PSCs) for large-area industrial manufacturing urgently demands efficient and scalable surface passivation strategies. Although blade coating is highly promising for device upscaling, achieving comprehensive surface passivation remains a key challenge due to the abundant defects inherent in blade-coated perovskite films. Herein, we present a synergistic surface modification strategy combining dimensional engineering with passivation engineering for blade-coated PSCs. We introduce a multifunctional group Lewis base passivator, 5-bromobenzo[b]thiophen-3(2H)-one (BTO), to complement traditional dimensional engineering (e.g., phenethylammonium iodide (PEAI)), which typically struggles to passivate deep-level defects. In this dual strategy, PEAI constructs a robust 2D/3D heterojunction for interfacial energy level alignment, while BTO passivates uncoordinated Pb2+ defects via synergistic dual-site coordination. Consequently, blade-coated PSCs exhibit a power conversion efficiency of 25.15% and maintain 92.7% of their initial efficiency after 1500 h of air exposure (25 °C, 20–30% RH). Furthermore, this strategy mitigates efficiency roll-off upon scaling, yielding a high PCE of 22.02% for 14.7 cm2 minimodules.","PeriodicalId":62,"journal":{"name":"The Journal of Physical Chemistry Letters","volume":"13 1","pages":""},"PeriodicalIF":4.5000,"publicationDate":"2026-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry Letters","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.jpclett.6c02871","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Upscaling perovskite solar cells (PSCs) for large-area industrial manufacturing urgently demands efficient and scalable surface passivation strategies. Although blade coating is highly promising for device upscaling, achieving comprehensive surface passivation remains a key challenge due to the abundant defects inherent in blade-coated perovskite films. Herein, we present a synergistic surface modification strategy combining dimensional engineering with passivation engineering for blade-coated PSCs. We introduce a multifunctional group Lewis base passivator, 5-bromobenzo[b]thiophen-3(2H)-one (BTO), to complement traditional dimensional engineering (e.g., phenethylammonium iodide (PEAI)), which typically struggles to passivate deep-level defects. In this dual strategy, PEAI constructs a robust 2D/3D heterojunction for interfacial energy level alignment, while BTO passivates uncoordinated Pb2+ defects via synergistic dual-site coordination. Consequently, blade-coated PSCs exhibit a power conversion efficiency of 25.15% and maintain 92.7% of their initial efficiency after 1500 h of air exposure (25 °C, 20–30% RH). Furthermore, this strategy mitigates efficiency roll-off upon scaling, yielding a high PCE of 22.02% for 14.7 cm2 minimodules.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
通过叶片涂层的协同尺寸和钝化工程实现高效稳定的钙钛矿太阳能电池
大规模工业生产的钙钛矿太阳能电池迫切需要高效、可扩展的表面钝化策略。尽管叶片涂层在设备升级方面非常有前景,但由于叶片涂层钙钛矿薄膜固有的大量缺陷,实现全面的表面钝化仍然是一个关键挑战。在此,我们提出了一种结合尺寸工程和钝化工程的协同表面改性策略。我们引入了一种多功能基团刘易斯碱钝化剂,5-溴苯并[b]噻吩-3(2H)- 1 (BTO),以补充传统的尺寸工程(例如,苯乙基碘化铵(PEAI)),它通常难以钝化深层缺陷。在这种双重策略中,PEAI构建了一个强大的2D/3D异质结用于界面能级对准,而BTO通过协同的双位点配位来钝化未配位的Pb2+缺陷。因此,叶片涂层psc的功率转换效率为25.15%,在空气暴露1500小时(25°C, 20-30% RH)后保持其初始效率的92.7%。此外,这种策略减轻了扩展时的效率下降,14.7平方厘米的微型模块的PCE高达22.02%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
The Journal of Physical Chemistry Letters
The Journal of Physical Chemistry Letters CHEMISTRY, PHYSICAL-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
9.60
自引率
7.00%
发文量
1519
审稿时长
1.6 months
期刊介绍: The Journal of Physical Chemistry (JPC) Letters is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, chemical physicists, physicists, material scientists, and engineers. An important criterion for acceptance is that the paper reports a significant scientific advance and/or physical insight such that rapid publication is essential. Two issues of JPC Letters are published each month.
期刊最新文献
Spontaneous Ether Hydrolysis on Cryogenic Water Ice Surfaces Rate Coefficients for the OH Reaction with CF3SCF3: Atmospheric Lifetime and Global Warming Potential Synergistic Dimensional and Passivation Engineering via Blade Coating Enables Efficient and Stable Perovskite Solar Cells More Halogen-Localized, Yet More Strongly Electron Bound: Carbon Cage-Mediated Electron Stabilization in C60X– (X = F, Cl, Br, and I) Anions Remote Control of Excited-State Chemistry in Positive Reversibly Switchable Fluorescent Proteins
wanfang
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1