碳电极掺杂MAPbI3钙钛矿太阳能电池的合成与表征

D. A. Yusra, N. Mufti, E. Latifah
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引用次数: 0

摘要

基于有机金属钙钛矿三卤化物(MAPbI3)的太阳能电池因其具有高效率、柔韧性和透明性的第三代太阳能电池的潜力而引起了许多研究者的关注。然而,这种钙钛矿太阳能电池对环境敏感,稳定性较差。本研究在MAPbI3合成工艺和碳电极的使用下,对钙钛矿太阳能电池添加醋酸镁的性能进行了研究。总的来说,本研究中的钙钛矿太阳能电池排列由ITO/TiO2 mp/MAPbI3/碳糊组成。介孔TiO2 (mp)涂层采用丝网印刷的方法进行,MAPbI3涂层采用两段自旋涂层,在PbI2涂层后加入醋酸镁进行。然后用x射线衍射仪(XRD)对所得样品进行表征。利用太阳模拟器测量了太阳能电池的I-V和光响应,分析了太阳能电池的性能。XRD结果表明,在PbI2杂质存在的情况下,MAPbI3薄膜已经形成。所得太阳能电池的性能值为Voc = 3.45 V, Jsc = 0.04,效率约为0.09%。在响应照片的测量中,时间值的增加为7.29 s,衰减时间为34.38 s。低效率值可能是由于缺少一层空穴转移材料(HTM)和PbI2杂质的存在。然而,即使响应增加或衰减缓慢,光响应模式随时间的稳定性也显示出相当好的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and Characterization of Magnesium Acetate Doped MAPbI3 Perovskite Solar Cells with Carbon Electrodes
The organometal perovskite trihalide (MAPbI3) based solar cell has attracted the attention of many researchers because it has the potential to be a third-generation solar cell that has high efficiency, flexibility and transparency. However, this perovskite solar cell is sensitive to the environment and less stable. In this study, a performance study of perovskite solar cells with the addition of magnesium acetate was carried out in the MAPbI3 synthesis process and the use of carbon electrodes. In general, the perovskite solar cell arrangement in this study consisted of ITO/TiO2 mp/MAPbI3/carbon paste. Mesoporous TiO2 (mp) coating was carried out using the screen printing method, while MAPbI3 coating was carried out with a two-stage spin coating with the addition of magnesium acetate after PbI2 coating in the first stage. The samples obtained were then characterized using an X-Ray Diffractometer (XRD). Analysis of the performance of solar cells was carried out by measuring I-V and photoresponses using a solar simulator. XRD results show that MAPbI3 film has been formed even though there is still impurity of PbI2. The resulting solar cell performance has a value of Voc equals 3.45 V and Jsc equals 0.04 with an efficiency of around 0.09 per cent. In the measurement of the response photo, the increase in time value was 7.29 s and the decay time was 34.38 s. The low-efficiency value is probably due to the absence of a layer of hole transfer materials (HTM) and the presence of PbI2 impurities. However, the stability of the photoresponse pattern against time has shown quite good results even though the response is increased or the decay is slow.
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