钙钛矿(结构)
材料科学
结晶度
甲脒
钝化
溴化物
溴化铵
化学工程
卤化物
纳米技术
无机化学
化学
复合材料
图层(电子)
肺表面活性物质
工程类
作者
Yang Li,Lixin Zhang,Junming Xia,Tanghao Liu,Kaiyang Wang
出处
期刊:Small
[Wiley]
日期:2023-05-16
卷期号:19 (28)
被引量:12
标识
DOI:10.1002/smll.202208243
摘要
Inverted perovskite solar cells (IPSCs) have witnessed an impressive development in recent years. However, their efficiency is still significantly behind theoretical limits, and device instabilities hinder their commercialization. Two main obstacles to further enhancing their performance via one-step deposition are: 1) the unsatisfactory film quality of perovskite and 2) the poor surface contact. To address the above issues, 4-butanediol ammonium Bromide (BD) is utilized to passivate Pb2+ defects by forming PbN bonds and fill vacancies of formamidinium ions at the buried surface of perovskite. The wettability of poly [bis (4-phenyl) (2,4,6-triMethylphenyl) amine] films is also improved due to the formation of hydrogen bonds between PTAA and BD molecules, resulting in better surface contacts and enhanced perovskite crystallinity. As a result, BD-modified perovskite thin films show a significant increase in the mean grain size, as well as a dramatic enhancement in the PL decay lifetime. The BD-treated device exhibits an efficiency of up to 21.26%, considerably higher than the control device. Moreover, the modified devices show dramatically enhanced thermal and ambient stability compared to the control ones. This methodology paves the way to obtain high-quality perovskite films for fabricating high-performance IPSCs.
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