The effect of the CH3NH3PbClxI3-x perovskite layer thickness and grain size on its electrophysical and optical properties

IF 0.3 Q4 PHYSICS, MULTIDISCIPLINARY
T.M. Mukametkali, X.S. Rozhkova, A.K. Aimukhanov, K. Apshe, A.K. Zeinidenov, B.R. Ilyassov
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Abstract

Lead halide perovskite CH3NH3PbClx I3-x thin films are widely used as photoactive layers in perovskite solar cells. CH3NH3PbClx I3-x is a low band gap semiconductor with a broad absorption spectrum and a high conductivity showing excellent compatibility with exciting hole and electron selective layers in terms of electronic energy alignment, which provide efficient charge generation, separation and transport in perovskite solar cells. In this paper, CH3NH3PbClx I3-x layers were deposited on the TiO2 surface by one step spin-coating technique from a methylammonium iodide (MAI) and lead chloride (PbCl2 ) solution. To prepare the perovskite solution, PbCl2 (Sigma-Aldrich)230 mg of PbCl2 and 394 mg of MAI were dissolved in 1 ml of N, N-Dimethylformamide (Sigma-Aldrich) solvent. As expected, the elevation of the spin-coating rate resulted in CH3NH3PbClx I3-x thickness reduction, which should lead to a decrease in the R3 resistance in CH3NH3PbClx I3-x. However, the impedance spectroscopy revealed that with thickness reduction from 955 nm to 753 nm, the R3 resistance of CH3NH3PbClx I3-x declines from about 2590 Ώ to 2258 Ώ reaching the minimum value at 505 nm. The further decrease in CH3NH3PbClx I3-x thickness increased CH3NH3PbClx I3-x film resistance. The study of CH3NH3PbClx I3-x absorbance and luminescence spectra showed that the change in CH3NH3PbClx I3-x defect density occurred, which explains the decrease in CH3NH3PbClx I3-x resistance. According to the absorbance and luminescence spectroscopy study, the CH3NH3PbClx I3-x thickness reduction led to a decrease in the density of interstitial CH3NH3PbClx I3-x + defects. CH3NH3PbClx I3-x + species form deep levels trapping free electrons and as a result, increasing CH3NH3PbClx I3-x resistance. The PSCs based on a 505 nm thick CH3NH3PbClx I3-x layer showed the highest performance with the improved short current density and fill factor. The champion device had a power conversion efficiency of 9.92 %.
CH3NH3PbClxI3-x钙钛矿层厚度和晶粒尺寸对其电物理和光学性能的影响
卤化铅钙钛矿CH3NH3PbClx I3-x薄膜作为光活性层广泛应用于钙钛矿太阳能电池中。CH3NH3PbClx I3-x是一种低带隙半导体,具有广泛的吸收光谱和高导电性,在电子能量排列方面与激发空穴和电子选择层具有良好的兼容性,可在钙钛矿太阳能电池中提供高效的电荷产生、分离和传输。本文以甲基碘化铵(MAI)和氯化铅(PbCl2)溶液为原料,采用一步自旋镀膜技术在TiO2表面沉积了CH3NH3PbClx I3-x层。将PbCl2 (Sigma-Aldrich)230 mg的PbCl2和394 mg的MAI溶于1ml的N, N-二甲基甲酰胺(Sigma-Aldrich)溶剂中制备钙钛矿溶液。正如预期的那样,自旋涂覆速率的提高导致CH3NH3PbClx I3-x的厚度减少,这将导致CH3NH3PbClx I3-x中的R3电阻降低。然而,阻抗谱分析表明,随着厚度从955 nm减小到753 nm, CH3NH3PbClx I3-x的R3电阻从2590 Ώ左右下降到2258 Ώ,在505 nm处达到最小值。CH3NH3PbClx I3-x厚度的进一步降低增加了CH3NH3PbClx I3-x膜电阻。对CH3NH3PbClx I3-x吸光度和发光光谱的研究表明,CH3NH3PbClx I3-x缺陷密度发生了变化,这解释了CH3NH3PbClx I3-x电阻降低的原因。根据吸光度和发光光谱研究,CH3NH3PbClx I3-x厚度的减小导致间隙CH3NH3PbClx I3-x +缺陷密度的降低。CH3NH3PbClx I3-x +形成深能级捕获自由电子,从而增加CH3NH3PbClx I3-x电阻。505 nm厚ch3nh3pbclxi3 -x层制备的PSCs在短电流密度和填充系数提高的情况下性能最好。冠军装置的功率转换效率为9.92%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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