Fabrication of Efficient Perovskite Solar Cells and Module by a Solution Process Using a CH3NH3PbI3·DMF as a Key Precursor
Masashi Ozaki a, Ai Shimazaki a, Naoki Maruyama a, Mina Jung a, Alwani Rafiehm a, Yumi Nakaike a, Tomoko Aharen a, Takahiro Sasamori a, Norihiro Tokitoh a, Yasujiro Murata a, Atsushi Wakamiya a
a Kyoto University, Japan, Goryo-Ohara, Nishikyo-ku, Kyoto 615-8245, Japan
Asia-Pacific International Conference on Perovskite, Organic Photovoltaics and Optoelectronics
Proceedings of International Conference Asia-Pacific Hybrid and Organic Photovoltaics 2018 (AP-HOPV18)
Kitakyūshū-shi, Japan, 2018 January 28th - 30th
Organizers: Shuzi Hayase, Juan Bisquert and Hiroshi Segawa
Poster, Masashi Ozaki, 095
Publication date: 27th October 2017

Perovskite solar cells have attracted much attention as a promising printable photovoltaic device with high power conversion efficiency (PCE). The performance of perovskite solar cells highly depends on the quality of the perovskite layer, and thus the development of the fabrication technology to obtain a dense and flat perovskite layer is one of crucial issues in this field. We have recently optimized our solution method with solvent engineering using a mixed solvent of N,N-dimethylformamide (DMF) and dimethyl sulfoxide (DMSO), which gave a high PCE ~20% even in the cells composed of pure CH3NH3PbI3 perovskite as a photo-absorber. In this method, the higher volatility of DMF relative to DMSO needs a rather narrow process window during spin-coating. For a larger scale device, the development of fabrication method for perovskite layer with a wider process window and high reproducibility is strongly required.

We isolated the complex of CH3NH3PbI3·DMF from a mixture of PbI2 and CH3NH3I in DMF, in which a solvent molecule of DMF is intercalated between the perovskite components. This complex shows higher solubility in DMSO (within 10 min at room temperature) than that of PbI2 and CH3NH3I mixture (1:1) in DMSO (60 min), suggesting its utility as a highly purified precursor for perovskite layer in the solution method using DMSO with a wider process window.

Whereas, the lower saturated concentration of PbI2 and CH3NH3I mixture (1:1) in DMSO (1.2 M) limits the concentration of the precursor solution to 1.1 M, the higher saturated concentration of CH3NH3PbI3·DMF (2.0 M) allows us to use the higher concentration of 1.4 M in DMSO for spin-coating. Using a 1.1 M DMSO solution of PbI2 and CH3NH3I mixture resulted in the formation of thin perovskite with the thickness of ca. 180 nm, which gave the moderate JSC and PCE (JSC = 21.8 mA/cm2, VOC = 1.15 V, FF = 0.70, PCE = 17.6%). In contrast, the use of 1.4 M DMSO solution of the complex successfully provided a dense and thicker perovskite layer with the thickness of ca. 350 nm, which improved JSC and PCE (JSC = 22.7 mA/cm2, VOC = 1.15 V, FF = 0.76, PCE = 19.8%). Furthermore, this method is an easily applicable to large-area module. We further demonstrate large-area perovskite solar module of 22 cm2 with 14.2% stabilized active-area efficiency output.

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