甲脒
钙钛矿(结构)
串联
能量转换效率
铷
光伏
材料科学
带隙
光致发光
钙钛矿太阳能电池
量子效率
光电子学
纳米技术
光伏系统
化学
结晶学
钾
冶金
复合材料
生物
生态学
作者
Shahriyar Safat Dipta,Ashraful Hossain Howlader,Walia Binte Tarique,Ashraf Uddin
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2024-06-10
卷期号:29 (12): 2758-2758
被引量:10
标识
DOI:10.3390/molecules29122758
摘要
The solar energy market is predicted to be shared between Si solar cells and third-generation photovoltaics in the future. Perovskite solar cells (PSCs) show the greatest potential to capture a share there as a single junction or in tandem with silicon. Researchers worldwide are looking to optimize the composition of the perovskite film to achieve an optimal bandgap, performance, and stability. Traditional perovskites have a mixture of formamidinium and methyl ammonium as the A-site cation in their ABX3 structure. However, in recent times, the use of cesium and rubidium has become popular for making highly efficient PSCs. A thorough analysis of the performance and stability of double-, triple-, and quadruple-cation PSCs under different environmental conditions was performed in this study. The performance of the device and the films was analyzed by electrical measurements (J–V, dark J–V, EQE), scanning electron microscopy, atomic force microscopy, photoluminescence, and X-ray diffraction. The quadruple-cation device with the formula Cs0.07Rb0.03FA0.77MA0.13PbI2.8Br0.2 showed the highest power conversion efficiency (PCE) of 21.7%. However, this device had the least stability under all conditions. The triple-cation device with the formula Cs0.1FA0.6MA0.3PbI2.8Br0.2, with a slightly lower PCE (21.2%), was considerably more stable, resulting in about 30% more energy harvested than that using the other two devices during their life cycle.
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