Abstract
Compared to three-dimensional (3D) organic-inorganic hybrid perovskites, two-dimensional (2D) ones possess great possibilities to realize stable cost-effective perovskite solar cells (PSCs). However, studies indicated that PSCs with 2D perovskites exhibited poor power conversion efficiencies (PCEs). In this study, we report novel propargylamine cation (PPA+)-based quasi-2D perovskites. PPA+ employed as an organic spacer is for enhancing charge-carrier transport of quasi-2D (PPA)2(CH3NH3)2Pb3I10 thin films, consequently boosting PCEs of PSCs. To further boost PCEs of PSCs with quasi-2D (PPA)2(CH3NH3)2Pb3I10 thin films, a quasi-2D (PPA)2(CH3NH3)2Pb3I10 thin film is processed with Pb(SCN)2 additives. Systematical studies indicate that the quasi-2D (PPA)2(CH3NH3)2Pb3I10 thin film processed with Pb(SCN)2 additives exhibits superior film morphology and crystallinity, larger crystals, reduced nonradiative charge-carrier recombination, and enhanced and balanced charge-carrier mobilities compared to the pristine quasi-2D (PPA)2(CH3NH3)2Pb3I10 thin film. As a result, PSCs with the quasi-2D (PPA)2(CH3NH3)2Pb3I10 thin film processed with Pb(SCN)2 additives exhibit a PCE of 15.20%, which is an over 25% enhancement compared to those (12.16%) with a pristine quasi-2D (PPA)2(CH3NH3)2Pb3I10 thin film. In addition, PSCs with the quasi-2D (PPA)2(CH3NH3)2Pb3I10 thin film processed with Pb(SCN)2 additives possess dramatically suppressed photocurrent hysteresis and significantly boosted stability. All these results indicate that we have developed a facile way to synthesize novel 2D perovskite thin films for realizing stable and efficient PSCs with dramatically suppressed photocurrent hysteresis.
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