Stabilization of Sn2+ in FA0.75MA0.25SnI3 perovskite thin films using electron doner polymer PCDTBT and an improvement in charge transport properties for perovskite solar cells

Ashok Vishwakarma, Pankaj Kumar, Anand Pandey, Lokendra Kumar
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Abstract

Lead free tin halide perovskites for the fabrication of perovskite solar cells have been attracted much attention owing to their outstanding optoelectronic and eco-friendly properties. These materials face severe issues like poor environmental stability, low formation energy, and faster oxidation of tin from Sn2+ to Sn4+ state leading to poor film quality and self-doping. In this work, we have fabricated FA0.75MA0.25SnI3 perovskite thin films via solution processing method and studied conjugated polymer Poly[N-9′-hepta-decanyl-2,7-carbazole-alt-5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadia-zole)] (PCDTBT) induced effects in perovskite thin films. Micro-strain of PCDTBT doped FA0.75MA0.25SnI3 perovskite reduced without any change in the crystal structure. Reduction in electron trap density have been observed owing to improved film quality and enlarged perovskite grains. We have observed that Sn4+ content in 0.050wt% PCDTBT doped FA0.75MA0.25SnI3 perovskite film get reduced as shown in X-ray Photoelectron Spectroscopy (XPS) results. The reduction in Sn4+ (cause of self-doping) content shows that PCDTBT doping, maintains the stability of Sn2+ in FA0.75MA0.25SnI3 perovskite thin film. A decrement in hole density from 3.2x1018 cm-3 for pristine to 1.3x1017 cm-3 for 0.050wt% PCDTBT doped FA0.75MA0.25SnI3 perovskite has been observed from C-V measurement which is consistent with XPS results. Thus, PCDTBT doping in perovskite films can effectively tackle the severe issues of tin oxidation and defects in lead-free tin halide perovskite photoactive layer for solar cell application.
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使用电子捐献者聚合物 PCDTBT 稳定 FA0.75MA0.25SnI3 包晶体薄膜中的 Sn2+ 并改善包晶体太阳能电池的电荷传输特性
用于制造过氧化锡太阳能电池的无铅卤化锡过氧化物因其出色的光电和环保特性而备受关注。这些材料面临着环境稳定性差、形成能低、锡从 Sn2+ 到 Sn4+ 状态的氧化速度快等严重问题,导致薄膜质量差和自掺杂。在这项工作中,我们制备了 FA0.75MA0.25SnI3 包晶薄膜,并研究了共轭聚合物 Poly[N-9′-hepta-decanyl-2,7-carbazole-alt-5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadia-zole)] (PCDTBT) 在包晶薄膜中的诱导效应。掺杂了 PCDTBT 的 FA0.75MA0.25SnI3 包晶的微应变减小了,而晶体结构没有发生任何变化。由于薄膜质量的提高和包晶晶粒的增大,电子陷阱密度也有所降低。我们观察到,从 X 射线光电子能谱(XPS)结果可以看出,掺杂了 0.050wt% PCDTBT 的 FA0.75MA0.25SnI3 包晶薄膜中的 Sn4+ 含量降低了。Sn4+(自掺杂的原因)含量的降低表明,PCDTBT 掺杂保持了 FA0.75MA0.25SnI3 包晶薄膜中 Sn2+ 的稳定性。通过 C-V 测量观察到,空穴密度从原始的 3.2x1018 cm-3 下降到 0.050wt% PCDTBT 掺杂的 FA0.75MA0.25SnI3 包晶石的 1.3x1017 cm-3,这与 XPS 测量结果一致。因此,在包晶体薄膜中掺杂 PCDTBT 能有效解决无铅卤化锡包晶体光活性层中严重的锡氧化和缺陷问题,从而应用于太阳能电池。
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