Crystallization of non-fullerene acceptor might cause catastrophic failure in ductile organic solar cells (Conference Presentation)

Masoud Ghasemi, Huawei Hu, Nrup Balar, B. O’Connor, H. Ade
{"title":"Crystallization of non-fullerene acceptor might cause catastrophic failure in ductile organic solar cells (Conference Presentation)","authors":"Masoud Ghasemi, Huawei Hu, Nrup Balar, B. O’Connor, H. Ade","doi":"10.1117/12.2321996","DOIUrl":null,"url":null,"abstract":"Organic solar cell (OSC) technology has recently achieved over 13% efficiency through the synthesis of novel non-fullerene small molecule acceptors (NFAs), which can be processed from benign solvents as low-cost third generation photovoltaics[1,2]. Of critical importance to OSCs is understanding the morphological and thermal stability of the active layers governed by thermodynamics and kinetics as an intrinsic stability process which cannot be controlled by encapsulation[3,4]. Here we highlight the importance of ductility of donor polymers on nucleation and growth of micro-size small molecule crystals which leads to the catastrophic failure of the solar cells in the long-term operating condition We consider three high performance polymers P3HT, PBnDBT-FTAZ, and PffBT4T-C9C13 blended with EH-IDTBR as the model systems to investigate the thermal stability of state of the art non-fullerene OSCs, where elevated temperatures were used to accelerate the crystal formation and imitate the long-term operation conditions of OCSs. We also propose an easy accessible method using differential scanning calorimetry (DSC) to investigate the thermal behavior of NFA in the blends. Although non-fullerene solar cells have shown to have better overall morphological stability compared to their fullerene counterparts, our results suggest that catastrophic failure due to micro-size crystal formation in non-fullerene systems can happen at a rate similar to fullerene systems unless the right donor polymer is chosen to suppress the crystallization of small molecule. It is also shown and argued that the growth rate of small molecule crystals can be reduced upon mixing of NFAs with semi-crystalline polymers, such as P3HT with a higher overall density compared to amorphous donor polymers, i.e. PBnDT-FTAZ. Our findings may pave a way to understand and predict the morphological stability of non-fullerene OSCs.\n\nReferences\n[1] L. Ye, Y. Xiong, Q. Zhang, S. Li, C. Wang, Z. Jiang, J. Hou, W. You, H. Ade, Adv. Mater. 2017, DOI: 10.1002/adma.201705485.\n[2] S. Holliday, R. S. Ashraf, A. Wadsworth, D. Baran, S. A. Yousaf, C. B. Nielsen, C.-H. Tan, S. D. Dimitrov, Z. Shang, N. Gasparini, M. Alamoudi, F. Laquai, C. J. Brabec, A. Salleo, J. R. Durrant, I. McCulloch, Nat. Commun. 2016, 7, 11585.\n[3] M. Ghasemi, L. Ye, Q. Zhang, L. Yan, J. H. Kim, O. Awartani, W. You, A. Gadisa, H. Ade, Adv. Mater. 2017, 29, 1604603.\n[4] L. Ye, H. Hu, M. Ghasemi, T. Wang, B. A. Collins, J.-H. Kim, K. Jiang, J. Carpenter, H. Li, Z. Li, T. McAfee, J. Zhao, X. K. Chen, J. Y. L. Lai, T. Ma, J.-L. Bredas, H. Yan, H. Ade, Nat. Mater. 2018, DOI: 10.1038/s41563-017-0005-1.","PeriodicalId":122801,"journal":{"name":"Organic, Hybrid, and Perovskite Photovoltaics XIX","volume":"55 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic, Hybrid, and Perovskite Photovoltaics XIX","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1117/12.2321996","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Organic solar cell (OSC) technology has recently achieved over 13% efficiency through the synthesis of novel non-fullerene small molecule acceptors (NFAs), which can be processed from benign solvents as low-cost third generation photovoltaics[1,2]. Of critical importance to OSCs is understanding the morphological and thermal stability of the active layers governed by thermodynamics and kinetics as an intrinsic stability process which cannot be controlled by encapsulation[3,4]. Here we highlight the importance of ductility of donor polymers on nucleation and growth of micro-size small molecule crystals which leads to the catastrophic failure of the solar cells in the long-term operating condition We consider three high performance polymers P3HT, PBnDBT-FTAZ, and PffBT4T-C9C13 blended with EH-IDTBR as the model systems to investigate the thermal stability of state of the art non-fullerene OSCs, where elevated temperatures were used to accelerate the crystal formation and imitate the long-term operation conditions of OCSs. We also propose an easy accessible method using differential scanning calorimetry (DSC) to investigate the thermal behavior of NFA in the blends. Although non-fullerene solar cells have shown to have better overall morphological stability compared to their fullerene counterparts, our results suggest that catastrophic failure due to micro-size crystal formation in non-fullerene systems can happen at a rate similar to fullerene systems unless the right donor polymer is chosen to suppress the crystallization of small molecule. It is also shown and argued that the growth rate of small molecule crystals can be reduced upon mixing of NFAs with semi-crystalline polymers, such as P3HT with a higher overall density compared to amorphous donor polymers, i.e. PBnDT-FTAZ. Our findings may pave a way to understand and predict the morphological stability of non-fullerene OSCs. References [1] L. Ye, Y. Xiong, Q. Zhang, S. Li, C. Wang, Z. Jiang, J. Hou, W. You, H. Ade, Adv. Mater. 2017, DOI: 10.1002/adma.201705485. [2] S. Holliday, R. S. Ashraf, A. Wadsworth, D. Baran, S. A. Yousaf, C. B. Nielsen, C.-H. Tan, S. D. Dimitrov, Z. Shang, N. Gasparini, M. Alamoudi, F. Laquai, C. J. Brabec, A. Salleo, J. R. Durrant, I. McCulloch, Nat. Commun. 2016, 7, 11585. [3] M. Ghasemi, L. Ye, Q. Zhang, L. Yan, J. H. Kim, O. Awartani, W. You, A. Gadisa, H. Ade, Adv. Mater. 2017, 29, 1604603. [4] L. Ye, H. Hu, M. Ghasemi, T. Wang, B. A. Collins, J.-H. Kim, K. Jiang, J. Carpenter, H. Li, Z. Li, T. McAfee, J. Zhao, X. K. Chen, J. Y. L. Lai, T. Ma, J.-L. Bredas, H. Yan, H. Ade, Nat. Mater. 2018, DOI: 10.1038/s41563-017-0005-1.
非富勒烯受体结晶可能导致韧性有机太阳能电池的灾难性失效(会议报告)
有机太阳能电池(OSC)技术最近通过合成新型非富勒烯小分子受体(nfa)实现了超过13%的效率,这种非富勒烯小分子受体可以从良性溶剂中加工成低成本的第三代光伏电池[1,2]。对osc至关重要的是理解由热力学和动力学控制的活性层的形态和热稳定性是一个不能被封装控制的内在稳定性过程[3,4]。本文以三种高性能聚合物P3HT、PBnDBT-FTAZ和PffBT4T-C9C13与h - idtbr共混为模型体系,研究了当前非富勒烯OSCs的热稳定性。其中,使用高温来加速晶体形成,并模拟OCSs的长期运行条件。我们还提出了一种简单易行的方法,使用差示扫描量热法(DSC)来研究NFA在共混物中的热行为。尽管与富勒烯相比,非富勒烯太阳能电池具有更好的整体形态稳定性,但我们的研究结果表明,除非选择合适的供体聚合物来抑制小分子的结晶,否则非富勒烯系统中由于微尺寸晶体形成而导致的灾难性故障可能以与富勒烯系统相似的速率发生。研究还表明,在将nfa与半晶聚合物混合后,小分子晶体的生长速度可以降低,例如与非晶给体聚合物(即PBnDT-FTAZ)相比,P3HT具有更高的总密度。我们的发现可能为理解和预测非富勒烯osc的形态稳定性铺平了道路。[1]叶磊,熊艳,张强,李树生,王超,姜志强,侯军,游伟,阿德华,adma.2017, DOI: 10.1002/adma.201705485.[2]S. Holliday, R. S. Ashraf, A. Wadsworth, D. Baran, S. A. Yousaf, C. B. Nielsen, c - h。陈志强,尚志强,陈志强,陈志强,陈志强,陈志强,陈志强,陈志强,陈志强,陈志强,陈志强,陈志强。[3]叶莉,张强,闫丽丽,金金辉,欧·阿瓦塔尼,尤伟,a·加迪萨,阿德,adh .高分子学报,2017,29,1604603.[4]叶丽玲,胡洪辉,M. Ghasemi,王涛,b.a. Collins, j.h。金,江锴,J.卡彭特,李洪辉,李正志,T. McAfee,赵杰,陈新康,赖家勇,马涛,j.l l。布雷达斯,阎竑,艾德竑,自然科学学报。2018,DOI: 10.1038/s41563-017-0005-1。
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
自引率
0.00%
发文量
0
×
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:604180095
Book学术官方微信