Highly stable inverted perovskite solar cells with all-inorganic selective contact using iron-doped zinc oxide

钝化 钙钛矿(结构) 材料科学 能量转换效率 兴奋剂 氧化物 光电流 化学工程 氧化镍 钙钛矿太阳能电池 开路电压 纳米技术 光电子学 图层(电子) 冶金 电压 电气工程 工程类
作者
Long Wang,Yufang Li,Honglie Shen,Lei Wang,Qichen Zhao,Jinjie Zheng,Hechao Li,Zhihong Xie,Andi Chen,Sijia Miao,Haibin Huang
出处
期刊:Journal of Chemical Physics [American Institute of Physics]
卷期号:162 (9) 被引量:2
标识
DOI:10.1063/5.0246664
摘要

Perovskite solar cells (PSCs) have achieved remarkable performance advancements over the past decade. In inverted p-i-n PSCs, commonly utilized electron transport layers (ETL), such as C60 and PCBM, are associated with notable stability challenges and high production costs. This study reports on a novel and highly stable perovskite solar cell that employs iron-doped zinc oxide (FZO) nanoparticles as the ETL and nickel oxide (NiOx) as the hole transport layer, demonstrating a power conversion efficiency (PCE) of ∼12%. In comparison with PSCs that utilize zinc oxide (ZnO) as the ETL, those incorporating FZO demonstrated a maximum PCE enhancement of 18.3%. The incorporation of iron doping mitigates the basicity of the ZnO ETL, thereby reducing the deprotonation at the FZO/perovskite interface and enhancing the stability of the PSCs. The unpackaged FZO device maintained an initial PCE of 90% after 400 h at a relative humidity of 45% ± 5%. (2-(9H-carbazol-9-yl)ethyl)phosphonic acid and 2-phenylethylamine hydroiodide were used to passivate the NiOx/perovskite and perovskite/ZnO(FZO) interfaces, respectively, which further improved the PSC performance. Ultimately, FZO-based PSCs with a PCE of 13.65%, an open-circuit voltage (Voc) of 1.04 V, a short-circuit current density (Jsc) of 20.79, and a fill factor (FF) of 63.1% were obtained, and the PCE demonstrated a notable increase of over 35% compared to pristine ZnO-based devices. Results indicate that high device performance, low fabrication costs, and excellent stability can be attained through the use of simple chemically synthesized oxides as inorganic selective charge transport layers in PSCs.
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