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Enhanced Efficiency and Long-Term Stability of Perovskite Solar Cells by Synergistic Effect of Nonhygroscopic Doping in Conjugated Polymer-Based Hole-Transporting Layer

机译:通过在共轭聚合物基空穴输送层中的非特性掺杂的协同作用,增强钙钛矿太阳能电池的效率和长期稳定性

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摘要

A face-on oriented and p-doped semicrystalline conjugated polymer, poly[(2,5-bis(2-hexyldecyloxy)phenylene)-alt-(5,6-difluoro-4,7-di(thiophen-2-yl)benzo[c] [1,2,5]-thiadiazole) (PPDT2FBT), was studied as a hole transport layer (HTL) in methylammonium lead triioclidebased perovskite solar cells (PVSCs). PPDT2FBT exhibits a mid-band gap (1.7 eV), high vertical hole mobility (7.3 X 10(-3) cm(2)/V-s), and well-aligned frontier energy levels with a perovskite layer for efficient charge transfer/transport, showing a maximum power conversion efficiency (PCE) of 16.8%. Upon doping the PPDT2FBT HTL with a nonhygroscopic Lewis acid, tris(pentafluorophenyl)borane (BCF, 2-6 wt %), the vertical conductivity was improved by a factor of approximately 2, and the resulting PCE was further improved up to 17.7%, which is higher than that of standard PVSCs with 2,2',7,7'-tetralds(N,N-di-p-methoxyphenylamine)-9,9'-spirobilluorene (spiroOMeTAD) as an HTL. After BCF doping, the clearly enhanced carrier diffusion coefficient, diffusion length, and lifetime were measured using intensity-modulated photocurrent and photovoltage spectroscopy. Furthermore, compared to the standard PVSCs with spiro-OMeTAD, the temporal device stability was remarkably improved, preserving the similar to 60% of the original PCE for SOO h without encapsulation under light-soaking condition (1 sun AM 1.5G) at 85 degrees C and 85% humidity, which is mainly due to the highly crystalline conjugated backbone of PPDT2FBT and nonhygroscopic nature of BCF. In addition, formamidinium lead iodide/bromide (FAPbI(3-x)Br(x))-based PVSCs with the BCF-doped PPDT2FBT as an HTL was also prepared to show 18.8% PCE, suggesting a wide applicability of PPDT2FBT HTL for different types of PVSCs.,
机译:面向上定向和p掺杂的半晶缀合聚合物,聚[(2,5-双(2-己二烯)苯基苯基) - (5,6-二氟-4,7-di(噻吩-2-基)苯并[c] [1,2,5] - 硫唑)(PPDT2FBT)被研究作为甲基烷基铅三椰子基氏植物钙钛矿太阳能电池(PVSCs)的空穴传输层(HTL)。 PPDT2FBT展示中带隙(1.7eV),高垂直空穴迁移率(7.3×10(-3)厘米(2)/ vs),以及具有钙钛矿层的良好对准的前沿能量水平,用于高效电荷转移/运输,显示最大功率转换效率(PCE)为16.8%。在用非吸入式路易斯酸的PPDT2FBT HTL掺杂,TRIS(五氟苯基)硼烷(BCF,2-6wt%),垂直导电率提高了约2的因子,得到的PCE进一步提高了17.7%,其高于标准PVSC的标准PVSC,具有2,2',7,7'-Tetrals(N,N-Di-P-甲氧基甲氧基胺)-9,9'-螺呋喃(Spioometad)作为HTL。在BCF掺杂之后,使用强度调制的光电流和光电光谱测量明显增强的载体扩散系数,扩散长度和寿命。此外,与用螺欧比达的标准PVSC相比,时间器件稳定性显着提高,保持了与85度的光浸型条件(1 SUN 1.5G)下封装的原始PCE相似的60% C和85%的湿度,主要是由于PPDT2FBT的高晶缀合骨架和BCF​​的非从上学性质。此外,还制备了具有BCF掺杂PPDT2FBT作为HTL的基于甲酰胺铅碘化物/溴(Fapbi(3-X)Br(X))的PVSC,以显示18.8%的PCE,表明PPDT2FBT HTL的宽采适用于不同PVSC的类型。,

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