材料科学
制作
钙钛矿(结构)
磁滞
光电子学
化学浴沉积
光活性层
纳米技术
图层(电子)
热稳定性
光伏系统
能量转换效率
薄膜
化学工程
聚合物太阳能电池
电气工程
工程类
物理
病理
医学
替代医学
量子力学
作者
Bo Yang,Ming Wang,Xiaofei Hu,Tingwei Zhou,Zhigang Zang
出处
期刊:Nano Energy
[Elsevier BV]
日期:2019-01-02
卷期号:57: 718-727
被引量:235
标识
DOI:10.1016/j.nanoen.2018.12.097
摘要
Inorganic perovskite solar cells (IPSCs) with CsPbIBr2 as the light harvester have attracted tremendous attention owing to its thermal stability, low cost and facile manufacture, where electron transport layer (ETL) plays indispensable roles of charge separation, electron transportation and hole-blocking. Although TiO2 is widely used as an ETL, its high-temperature fabrication and low electron mobility hinder the performance and application of IPSCs. Herein, we have proposed a low-temperature (70 °C) chemical bath deposition (CBD) method with different time to prepare In2S3 films as the ETL of IPSCs. By regulating the deposition time of In2S3 films to 85 min, our best-performing device has obtained a high PCE of 5.59% with reduced hysteresis, which is a relative high efficiency for CsPbIBr2 IPSCs by low-temperature fabrication at present. However, the TiO2-based device shows a low efficiency of 5.02% and serious hysteresis. Meanwhile, the In2S3-based devices exhibit improved stability under ambient conditions without encapsulation. Experimental results precisely clarify that this enhanced photovoltaic performance is attributed to the suitable band alignment, low resistance, low recombination of photo-generated carriers at the interface of ETL/perovskite. Promisingly, our low temperature fabricated perovskite and ETL layers might broaden new insights for solution-processed flexible devices.
科研通智能强力驱动
Strongly Powered by AbleSci AI