Gao Xiao-Xin, Luo Wen, Zhang Yi, Hu Ruiyuan, Zhang Bao, Züttel Andreas, Feng Yaqing, Nazeeruddin Mohammad Khaja
School of Chemical Engineering and Technology, Tianjin University, 135 Yaguan Road, Tianjin, 300350, China.
Institute of Chemical Sciences and Engineering, École Polytechnique Fédérale de Lausanne (EPFL Valais Wallis), CH-1951, Sion, Switzerland.
Adv Mater. 2020 Mar;32(9):e1905502. doi: 10.1002/adma.201905502. Epub 2020 Jan 27.
Organic-inorganic metal halide perovskite solar cells (PSCs) have achieved certified power conversion efficiency (PCE) of 25.2% with complex compositional and bandgap engineering. However, the thermal instability of methylammonium (MA) cation can cause the degradation of the perovskite film, remaining a risk for the long-term stability of the devices. Herein, a unique method is demonstrated to fabricate highly phase-stable perovskite film without MA by introducing cesium chloride (CsCl) in the double cation (Cs, formamidinium) perovskite precursor. Moreover, due to the suboptimal bandgap of bromide (Br ), the amount of Br is regulated, leading to high power conversion efficiency. As a result, MA-free perovskite solar cells achieve remarkable long-term stability and a PCE of 20.50%, which is one of the best results for MA-free PSCs. Moreover, the unencapsulated device retains about 80% of the original efficiencies after a 1000 h aging study. These results provide a feasible approach to enhance solar cell stability and performance simultaneously, paving the way for commercializing PSCs.
通过复杂的成分和带隙工程,有机-无机金属卤化物钙钛矿太阳能电池(PSC)已实现25.2%的认证功率转换效率(PCE)。然而,甲铵(MA)阳离子的热不稳定性会导致钙钛矿薄膜降解,这仍然是器件长期稳定性的一个风险。在此,展示了一种独特的方法,通过在双阳离子(铯、甲脒)钙钛矿前驱体中引入氯化铯(CsCl)来制备不含MA的高度相稳定的钙钛矿薄膜。此外,由于溴化物(Br)的带隙不理想,对Br的量进行了调节,从而实现了高功率转换效率。结果,不含MA的钙钛矿太阳能电池实现了显著的长期稳定性和20.50%的PCE,这是不含MA的PSC的最佳结果之一。此外,经过1000小时老化研究后,未封装的器件保留了约80%的原始效率。这些结果为同时提高太阳能电池稳定性和性能提供了一种可行的方法,为PSC商业化铺平了道路。