钝化
钙钛矿(结构)
材料科学
能量转换效率
磁滞
带隙
载流子寿命
化学工程
钙钛矿太阳能电池
纳米技术
光电子学
图层(电子)
硅
量子力学
物理
工程类
作者
Shuyue Xue,Jing Wang,Haibo Liu,Jinzhan Su
标识
DOI:10.1002/solr.202400443
摘要
CsPbIBr 2 has garnered significant interest due to its ideal bandgap and good stability. However, defects formed at the interface between the electron transport layer and the perovskite can lead to increased non‐radiative recombination, which negatively impacts both the power conversion efficiency (PCE) of perovskite solar cells and the long‐term stability of the cells. Herein, the TiO 2 /perovskite interface is modified by adding sodium silicate to passivate the defects on the interface. The introduction of Na + partially reduces Ti 4+ to Ti 3+ in TiO 2 , thereby passivating trap states caused by oxygen vacancy defects and adjusting the energy level alignment between TiO 2 and the perovskite film, enhancing the carrier transport efficiency. Additionally, SiO 3 2− can form SiOPb (and Cs) bonds with the undercoordinated Pb 2+ and Cs + on the surface of the perovskite layer, effectively passivating surface defects of the perovskite film and thereby improving the efficiency of the devices. Ultimately, the carbon‐based all‐inorganic CsPbIBr 2 perovskite solar cells treated with Na 2 SiO 3 exhibit a significantly improved PCE of 10.85% compared to 8.62% of the control sample and achieve a high open‐circuit voltage of 1.31 V. With this modification, the devices also demonstrate reduced hysteresis effects and enhanced stability.
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