钝化
材料科学
钙钛矿(结构)
能量转换效率
噻吩
光伏系统
化学工程
光电子学
纳米技术
化学
有机化学
图层(电子)
电气工程
工程类
作者
Jianxing Xia,Marco Cavazzini,Cansu Igci,Cristina Momblona,Simonetta Orlandi,Bin Ding,Yi Zhang,Hiroyuki Kanda,Nadja Klipfel,Sher Bahadar Khan,Abdullah M. Asiri,Paul J. Dyson,Gianluca Pozzi,Mohammad Khaja Nazeeruddin
出处
期刊:Solar RRL
[Wiley]
日期:2021-12-29
卷期号:6 (4)
被引量:5
标识
DOI:10.1002/solr.202100926
摘要
Organic hole‐transporting materials (HTMs) based on the Ullazine core yield so far only moderate power conversion efficiencies of up to 13.08% in perovskite solar cells (PSCs). Aiming to fabricate efficient and stable PSCs, novel Ullazine derivatives bearing thiophene units were designed and synthesized, allowing modulation of the electronic states of the HTMs and further providing defect passivation of the perovskite surface. Experimental and theoretical analysis show that thiophene units with ‐N( p ‐MeOC 6 H 4 ) 2 groups improve the conductivity of Ullazine HTMs, boosting the efficiency of PSCs to 20.21%. This value is the highest reported to date for Ullazine‐based HTMs, and is close to the performance of Spiro‐OMeTAD. In addition, unencapsulated PSCs based on the champion Ullazine exhibit superior stability with respect to Spiro‐OMeTAD, retaining nearly 90% of the initial efficiency following 1000 h aging, which is ascribed to a combination of higher water repellency and passivation of defects on the perovskite surface. This work demonstrates the high potential of HTMs based on Ullazine core as substitutes to Spiro‐OMeTAD.
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