Zhou Yawei, Najar Adel, Zhang Jing, Feng Jiangshan, Cao Yang, Li Zhigang, Zhu Xuejie, Yang Dong, Liu Shengzhong Frank
Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education; School of Materials Science and Engineering; Shaanxi Key Laboratory for Advanced Energy Devices; Shaanxi Engineering Lab for Advanced Energy Technology; Institute for Advanced Energy Materials, Shaanxi Normal University, Xi'an 710119, Shaanxi, China.
Department of Physics, College of Science, United Arab Emirates University, Ain 12345, United Arab Emirates.
ACS Appl Mater Interfaces. 2022 Jun 29;14(25):28729-28737. doi: 10.1021/acsami.2c02525. Epub 2022 Jun 14.
Organic-inorganic Pb-based halide perovskite photoelectrical materials, especially perovskite solar cells (PSCs), have attracted attention due to the significant efforts in improving the power conversion efficiency (PCE) to above 25%. However, the stability issue of the PSCs restricts their further development for commercialization. Strategies are designed to keep moisture and oxygen out of the perovskite films, such as additive, surface passivation, and solvent engineering; however, usually, the corrosion of active films by the residual solvent is mostly ignored. Solvent residue is the paramount factor influencing the stability of the perovskite film prepared by the solution method, and most solvents can be easily absorbed and accelerate the perovskite film decomposition. Here, we studied the residual solvent effect on two kinds of perovskite films obtained by different annealing processes: hot air annealing and hot bench annealing. Several detection techniques were used to study the performance of two different annealing methods, including time-of-flight secondary ion mass spectrometry (ToF-SIMS), thermogravimetric analysis (TGA), and field-emission scanning electron microscopy (FESEM). The perovskite film obtained by hot air annealing shows less residual solvent and better device performance than the hot bench annealing method. This method is expected to provide insight into reducing solvent residue to improve the stability of the PSCs, especially for future commercialization.
有机-无机铅基卤化物钙钛矿光电材料,尤其是钙钛矿太阳能电池(PSC),由于在将功率转换效率(PCE)提高到25%以上方面所做的巨大努力而备受关注。然而,PSC的稳定性问题限制了它们在商业化方面的进一步发展。人们设计了各种策略来防止水分和氧气进入钙钛矿薄膜,如添加添加剂、进行表面钝化和溶剂工程;然而,通常活性薄膜被残留溶剂腐蚀的问题大多被忽视了。溶剂残留是影响溶液法制备的钙钛矿薄膜稳定性的首要因素,大多数溶剂很容易被吸收并加速钙钛矿薄膜的分解。在此,我们研究了残留溶剂对通过不同退火工艺获得的两种钙钛矿薄膜的影响:热风退火和热台退火。使用了几种检测技术来研究两种不同退火方法的性能,包括飞行时间二次离子质谱(ToF-SIMS)、热重分析(TGA)和场发射扫描电子显微镜(FESEM)。与热台退火方法相比,通过热风退火获得的钙钛矿薄膜显示出更少的残留溶剂和更好的器件性能。该方法有望为减少溶剂残留以提高PSC的稳定性提供见解,特别是对于未来的商业化应用。