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Monovalent Cation Doping of CH3NH3PbI3 for Efficient Perovskite Solar Cells
Published on: March 19, 2017
Buried Interface Modification Toward Efficient CsPbI2.2Br0.8 Based Monolithic Perovskite/Organic Tandem Solar Cells
Xin-Yi Li1, Zhuxia Wu2, Qin Yao3
1Institute of Functional Nano & Soft Materials (FUNSOM), Joint International Research Laboratory of Carbon-Based Functional Materials and Devices, Soochow University, Suzhou, Jiangsu, 215123, P. R. China.
Abstract:
Wide-bandgap perovskite sub-cells (WPSCs), one of the most crucial components of perovskite-based tandem solar cells (PTSCs), play a critical role in determining the performance of tandem devices. However, confined by the compromised crystallization properties of wide-bandgap perovskites, WPSCs exhibit significantly lower efficiency than their theoretical limit. In particular, for n-i-p structured all-inorganic WPSCs (AIWPSCs), severe nonradiative recombination due to the buried interface defects severely decreases the photovoltaic performance. Herein, an efficient propionate group (PA-) based ionic liquid, methylamine propionate (MAPA), is introduced into the perovskite/electron-transport layer (ETL) interface to passivate the buried interface of AIWPSCs. The intense interaction between the PA- and Pb-Pb dimer effectively heals the defects at the buried interface and facilitates a more homogeneous elemental distribution in the perovskite film. As a result, CsPbI2.2Br0.8-based AIWPSCs with a high power conversion efficiency (PCE) of 18.29% and open-circuit voltage (VOC) of 1.33 V are obtained, which illustrates the superiority of MAPA in optimizing the performance of AIWPSCs. Moreover, by integrating these AIWPSCs with small-bandgap organic solar cells (SOSCs), high performance n-i-p structured all-inorganic perovskite/organic tandem solar cells (AIPOTSCs) with a high PCE of 23.19% and VOC of 2.08 V are also achieved.

