1. Regulate excess PbI2 distribution on perovskite film via amphiphilic surfactant for efficient and stable device.
- Author
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Duan, Gongtao, Zhang, Wenfeng, Huang, Yuelong, Yu, Wei, Zhou, Xiangqing, Wen, Fang, Shang, Yanbo, Chen, Qian, Yu, Lang, Hu, Xin, Zhang, Yuchen, Bobba, Raja Sekhar, Mabrouk, Sally, Yang, Shangfeng, Liu, Fengguang, and Qiao, Quinn
- Subjects
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MOTION picture distribution , *PEROVSKITE , *SURFACE active agents , *SURFACE energy , *THIN films , *SOLAR cells - Abstract
Lead iodide (PbI 2) as a defect passivation in perovskite thin films can reduce halide vacancies and improve the performance of perovskite solar cells. However, excess PbI 2 can hurt the device's performance. In the case of perovskite films prepared by two-step sequential deposition, excess PbI 2 is distributed on the surface of perovskite film. The photo-decomposition of PbI 2 and the formation of surface energy barriers can hinder charge transfer in the device, leading to reduced device performance and accelerated device degradation. Inspired by the use of surfactants to control the morphology of perovskite nanocrystals, a dual-functional surfactant (oleamide) was introduced to control the distribution of excess PbI 2 on perovskite films. By adding oleamide, the aggregation distribution of PbI 2 was successfully achieved at the perovskite grain boundaries (GBs), forming a Type-I band alignment and reducing the trap density, thereby prolonging the carrier lifetime. The results show that the power conversion efficiency (PCE) of the device increased from 21.23% to 23.12% after the introduction of oleamide. Compared with the control and oleamide-modified devices, the deep-level defects were reduced by about five orders of magnitude due to the Lewis-base nature of amide groups in oleamide. In addition, due to the aggregation distribution of excess PbI 2 at GBs and the hydrophobicity of oleamide, the modified device showed better stability, maintaining 83% of its initial performance after 1000 h in air. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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