Regulation of SnO2 ETL by Diphenylsulfone for highly efficient MAPbI3 based PSCs over 21.2% in open Air
Non-radiative recombination due to high-density defects at the bottom of the perovskite layer and in the SnO 2 ETL layer is not favourable for charge transfer. In this work, disodium diphenylsulfone-4,4′-dichloro-3,3′-disulfonate (SDCDPS) was introduced into SnO 2 solution to prepare a high-quality pinhole-free SnO 2 film. The sulfonate of SDCDPS collaborates with diphenylsulfone to passivate uncoordinated Sn 4+ in SnO 2 ETL, which will reduce the work function (W F ) in the SnO 2 , increasing the conduction of SnO 2 film and reducing the charge recombination of pre-buried interface. Besides, the sulfonate and diphenysulfone groups also passivate the uncoordinated Pb 2+ in perovskite to increase the crystallinity of perovskite and reduce non-radiative recombination. After SDCDPS modification, the power conversion efficiency of perovskite solar cells significantly increased from 18.2% to 21.2% with hysteresis factor decreasing from 10.4% to 3.35%. Also, the modified device shows well stability due to the enhancement of perovskite crystallization and the reducing defects. Under relative humidity of ∼60%, the PCE of the unencapsulated device modified by SDCDPS remains at 81% of the initial device after 720h. This work offers a dependable method for enhancing the quality of the buried interface in PSC and to pursue productive and consistent devices.
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