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由于具有适合的带隙和较高的稳定性, CsPbIBr 2无机钙钛矿被认为是一种较有前景的太阳能电池光吸收材料. 但是目前报道的CsPbIBr 2钙钛矿太阳能电池效率还偏低, 主要原因是制备的CsPbIBr 2钙钛矿膜质量差、缺陷多. 本文通过将醋酸纤维素(CA)加入CsPbIBr 2钙钛矿前驱体溶液中改善CsPbIBr 2钙钛矿结晶过程, 从而制备高质量的CsPbIBr 2钙钛矿膜. 实验结果表明, CA中的C=O基团与前驱体溶液中的Pb 2+间存在明显的相互作用, 这种相互作用结合CA加入引起的前驱体溶液粘度增加, 使CsPbIBr 2钙钛矿的结晶速率明显降低, 从而制备了致密、结晶度高、晶粒尺寸大、晶界和缺陷少的高质量CsPbIBr 2钙钛矿膜. 同时, CA的保护作用显著提高了CsPbIBr 2钙钛矿膜的稳定性. 用碳材料层作为空穴传输层和背电极, 制备结构为FTO/TiO 2/CsPbIBr 2钙钛矿膜/碳层的碳基CsPbIBr 2钙钛矿太阳能电池. 在100 mW/cm 2光照下, CA-CsPbIBr 2钙钛矿太阳能电池的效率达到7.52%, 比未加CA的CsPbIBr 2钙钛矿电池提高了40%. 同时, 将CA-CsPbIBr 2钙钛矿太阳能电池在空气环境中贮存800 h, 其效率仍保持初始值的90%以上, 表明具有较高的长期稳定性.
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关键词:
- 醋酸纤维素/
- CsPbIBr2钙钛矿/
- 稳定性/
- 钙钛矿太阳能电池
CsPbIBr 2perovskite has been considered as a promising candidate for the light-harvesting material of perovskite solar cells (PSCs) due to its acceptable band gap and high stability. Nevertheless, the efficiency of CsPbIBr 2-based PSC still lags behind that of its homologs and is far away from the theoretical value. This can be attributed to the poor quality of CsPbIBr 2perovskite film. Therefore, it is highly desirable to improve the quality of CsPbIBr 2perovskite film for enhancing the photovoltaic performance of CsPbIBr 2PSCs. In this work, cellulose acetate (CA) is used as a polymer additive that is introduced into CsPbIBr 2precursor solution for improving the quality of CsPbIBr 2perovskite film via controlling crystallization process. The interaction between the C=O group of CA and Pb 2+in the precursor solution and the enhanced viscosity of precursor solution induced by CA addition reduce the crystallization rate of CsPbIBr 2perovskite. As a result, a compact CsPbIBr 2perovskite film with high crystallinity, large grain size, and low density of defect is prepared. The remarkably improved quality of CsPbIBr 2perovskite film upon CA addition can be attributed to the relatively slow crystallization rate. The slow crystallization rate allows the perovskite film to have enough time to form perfect perovskite crystal structure with large-size crystal grain and low density of defects. Furthermore, the oxygen functional groups of CA can passivate the undercoordinated Pb 2+, which effectively suppresses the defects and traps induced by Pb 2+in CsPbIBr 2perovskite film. The stability of CsPbIBr 2perovskite film is also greatly improved by CA addition. The added CA does not participate into the CsPbIBr 2perovskite crystal but distributes at the grain boundaries and, or, interfaces area and forms a moisture barrier around perovskite grains, which obviously enhances the stability of CsPbIBr 2perovskite film in the ambient air. The carbon-based CsPbIBr 2perovskite solar cells with a configuration of FTO/TiO 2/perovskite film/ carbon are fabricated by using the carbon layer as both the hole-transport layer and the back electrode. Under the illumination of 100 mW/cm 2, the PSC based on CA-CsPbIBr 2perovskite film delivers a high conversion efficiency of 7.52%, which is increased by 40% compared with the efficiency of the device based on the pure CsPbIBr 2perovskite film. In addition, the PSC based on CA-CsPbIBr 2perovskite film shows a hysteresis index (HI) of 7%, while the device based on pure CsPbIBr 2film displays a higher HI of 22%. This result demonstrates that the CA addition can effectively suppress the hysteresis effect of inorganic PSCs. The stability of the PSC based on CA-CsPbIBr 2perovskite film is investigated by tracking the variation of the efficiency with time in the ambient condition. The fabricated PSCs without any encapsulation are stored in the air. The photovoltaic performance is measured once a day. The efficiency of the PSC based on CA-CsPbIBr 2perovskite remains more than 90% of its initial value after being stored in the air for 800 h, showing an excellent long-term stability. Therefore, this work provides a facile and effective method of improving the quality of CsPbIBr 2perovskite films, which is expected to be helpful in developing high-efficiency and stable carbon-based inorganic PSCs. [1] [2] [3] [4] [5] [6] [7] [8] [9] [10] [11] [12] [13] [14] [15] [16] [17] [18] [19] [20] [21] [22] [23] [24] [25] [26] [27] [28] [29] -
电池 扫描方向 Voc/V Jsc/(mA·cm2) FF PCE/% HIa Rrec/Ω CsPbIBr2 正向 平均 0.96 ± 0.05 9.89 ± 0.39 0.33 ± 0.4 3.13 ± 0.72 22% 1448 最高 1.03 10.35 0.39 4.16 反向 平均 1.01 ± 0.03 10.21 ± 0.42 0.45 ± 0.02 4.64 ± 0.56 最高 1.07 10.62 0.47 5.34 CA
-CsPbIBr2正向 平均 1.02 ± 0.03 10.52 ± 0.37 0.57 ± 0.02 6.12 ± 0.67 7% 2269 最高 1.06 10.91 0.60 6.94 反向 平均 1.05 ± 0.03 10.55 ± 0.27 0.62 ± 0.02 6.87 ± 0.38 最高 1.08 10.88 0.64 7.52 aHI = (PCE反向–PCE正向)/PCE反向 
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[1] [2] [3] [4] [5] [6] [7] [8] [9] [10] [11] [12] [13] [14] [15] [16] [17] [18] [19] [20] [21] [22] [23] [24] [25] [26] [27] [28] [29]
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