AVS 66th International Symposium & Exhibition | |
Thin Films Division | Thursday Sessions |
Session TF+SS-ThA |
Session: | Metal Halide Perovskites, Other Organic/Inorganic Hybrid Thin Films |
Presenter: | Mingzhen Liu, UESTC, China |
Correspondent: | Click to Email |
In recent years, organic lead halide perovskite materials have attracted much attention due to their outstanding optoelectric properties and low manufacturing cost. To improve the stability of perovskite solar cells, inorganic CsPbI3 perovskite has been demonstrated as promising material for solar cells owing to the superb photoelectronic property and composition stability. However, the low stability of perovskite phase CsPbI3 (α-phase) with an appropriate band gap under ambient environment hinders its practical application.
Here, we investigate new ways of synthesizing inorganic perovskite materials and optimizing the device stability through dimensional engineering. we tailor the three-dimension CsPbI3 perovskite into quasi-two-dimensional CsxPEA1-xPbI3 perovskite, where an optimal CsxPEA1-xPbI3 film remains stable in α phase up to 250℃. Moreover, we further present an in-depth investigation of the so-called stable ‘α-CsPbI3,’ especially the starting material hydrogen lead trihalide (HPbI3, also known as PbI2∙xHI) that is usually used for synthesizing α-CsPbI3. We notice that the “mythical” HPbI3, the often-assumed reaction product of HI and PbI2, does not actually exist. Instead, adding acid to DMF is known to generate a weak base dimethylamine (DMA) through hydrolysis, and with the presence of PbI2 the actual final product is believed to be a compound of DMAPbI3. Our findings offer new insights into producing inorganic perovskite materials, and lead to further understanding in perovskite materials for solar cells with improved efficiency and stability.