Light-activated tautomeric transition enhanced buried heterointerface for highly efficient and ultraviolet robust perovskite solar cells

IF 10.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Sheng Jiang, Shaobing Xiong, Shuaifei Mao, Yefan Zhang, Dongyang Zhao, Xiaomeng You, Vladimir Gaishun, Dmitry Kovalenk, Qinye Bao
{"title":"Light-activated tautomeric transition enhanced buried heterointerface for highly efficient and ultraviolet robust perovskite solar cells","authors":"Sheng Jiang, Shaobing Xiong, Shuaifei Mao, Yefan Zhang, Dongyang Zhao, Xiaomeng You, Vladimir Gaishun, Dmitry Kovalenk, Qinye Bao","doi":"10.1007/s11426-024-2194-0","DOIUrl":null,"url":null,"abstract":"<p>The buried heterointerface of perovskite solar cells (PSCs) suffers from serious nonradiative recombination and ultraviolet (UV) light stress, relentlessly limiting further increase in their power conversion efficiency and operational stability. Herein, we develop an emerging strategy of incorporating a thin UV-activated tautomeric transition layer onto underlying charge transport layer and then depositing perovskite layer to construct an efficient hole-selective buried heterojunction. It is revealed that the UV-activated tautomeric transition interlayer not only improves upper perovskite crystallinity, diminishes thermionic loss for collecting hole and passivates defect site at such buried contact that significantly promote charge transport and suppress nonradiative recombination, but also effectively protects adjacent perovskite from UV degradation through “UV sunscreen” effect. As a result, we report a remarkably enhanced efficiency of 24.76% compared to 22.02% of the control device. More importantly, the achieved high-efficiency PSC features excellent resistance against UV radiation at 365 nm of 100 and 850 mW cm<sup>−2</sup>, which are approximately 21 and 184 times of UV flux (4.6 mW cm<sup>−2</sup>) under AM 1.5G solar illumination. This work provides a promising approach of strengthening buried heterointerface for simultaneous realization of highly efficient and UV robust PSCs.</p>","PeriodicalId":772,"journal":{"name":"Science China Chemistry","volume":"3 1","pages":""},"PeriodicalIF":10.4000,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science China Chemistry","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1007/s11426-024-2194-0","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

The buried heterointerface of perovskite solar cells (PSCs) suffers from serious nonradiative recombination and ultraviolet (UV) light stress, relentlessly limiting further increase in their power conversion efficiency and operational stability. Herein, we develop an emerging strategy of incorporating a thin UV-activated tautomeric transition layer onto underlying charge transport layer and then depositing perovskite layer to construct an efficient hole-selective buried heterojunction. It is revealed that the UV-activated tautomeric transition interlayer not only improves upper perovskite crystallinity, diminishes thermionic loss for collecting hole and passivates defect site at such buried contact that significantly promote charge transport and suppress nonradiative recombination, but also effectively protects adjacent perovskite from UV degradation through “UV sunscreen” effect. As a result, we report a remarkably enhanced efficiency of 24.76% compared to 22.02% of the control device. More importantly, the achieved high-efficiency PSC features excellent resistance against UV radiation at 365 nm of 100 and 850 mW cm−2, which are approximately 21 and 184 times of UV flux (4.6 mW cm−2) under AM 1.5G solar illumination. This work provides a promising approach of strengthening buried heterointerface for simultaneous realization of highly efficient and UV robust PSCs.

光激活同分异构转换增强型埋藏异质界面,用于高效和紫外线稳健型过氧化物太阳能电池
过氧化物太阳能电池(PSCs)的埋藏异质界面存在严重的非辐射重组和紫外线(UV)应力,这无情地限制了其功率转换效率和运行稳定性的进一步提高。在此,我们开发了一种新兴战略,即在底层电荷传输层上加入一层薄的紫外激活同素异构过渡层,然后沉积包晶层,从而构建高效的空穴选择性埋藏异质结。结果表明,紫外激活同分异构过渡夹层不仅提高了上层包晶的结晶度,减少了收集空穴的热离子损耗,而且钝化了埋入接触处的缺陷位点,从而显著促进了电荷传输并抑制了非辐射重组,同时还通过 "紫外线防晒霜 "效应有效地保护了相邻的包晶免受紫外线降解。因此,与对照器件的 22.02% 相比,我们报告的效率显著提高了 24.76%。更重要的是,所获得的高效 PSC 在 365 纳米波长下具有出色的抗紫外线辐射能力,抗紫外线辐射能力分别为 100 和 850 mW cm-2,约为 AM 1.5G 太阳能照明下紫外线通量(4.6 mW cm-2)的 21 和 184 倍。这项工作为同时实现高效、抗紫外线的 PSC 提供了一种很有前景的强化埋藏异质界面的方法。
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 求助全文
来源期刊
Science China Chemistry
Science China Chemistry CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
14.40
自引率
7.30%
发文量
3787
审稿时长
2.2 months
期刊介绍: Science China Chemistry, co-sponsored by the Chinese Academy of Sciences and the National Natural Science Foundation of China and published by Science China Press, publishes high-quality original research in both basic and applied chemistry. Indexed by Science Citation Index, it is a premier academic journal in the field. Categories of articles include: Highlights. Brief summaries and scholarly comments on recent research achievements in any field of chemistry. Perspectives. Concise reports on thelatest chemistry trends of interest to scientists worldwide, including discussions of research breakthroughs and interpretations of important science and funding policies. Reviews. In-depth summaries of representative results and achievements of the past 5–10 years in selected topics based on or closely related to the research expertise of the authors, providing a thorough assessment of the significance, current status, and future research directions of the field.
×
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