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Photovoltage Behavior in Perovskite Solar Cells under Light-Soaking Showing Photoinduced Interfacial Changes

机译:光浸泡下钙钛矿太阳能电池的光电压特性显示光致界面变化

摘要

The photovoltage of perovskite solar cells (PSCs) was studied over a wide range of light intensities, showing changes from pristine to light-soaking (LS) conditions, explained using a specific model of spatial charge distribution. Migration of ions and vacancies under photovoltage conditions results in localized charge redistribution manifested as positive charge accumulation at the TiO2 or TiO2–MgO interlayer–perovskite interface, signifying photoinduced interfacial upward band bending. Consequentially, generation of an electrostatic potential (Velec) and an increase in interfacial recombination rate are confirmed. The magnitude and effect of Velec and interfacial recombination on the photovoltage depend on the illumination intensity and on the LS duration. PSCs with mesoporous Al2O3 showed similar changes, validating the role of the compact TiO2. Faster generation and a gradual increase of Velec are apparent under LS, which expresses the constant migration of ions and vacancies toward the interface. The nonrigid TiO2–perovskite interface calls for a vital perspective change of PSCs.
机译:钙钛矿型太阳能电池(PSC)的光电压在很宽的光强度范围内进行了研究,显示了从原始到浸透(LS)的变化,并使用空间电荷分布的特定模型进行了解释。离子和空位在光电压条件下的迁移导致局部电荷再分布,表现为在TiO2或TiO2-MgO层间-钙钛矿界面上的正电荷累积,表明光诱导的界面向上带弯曲。因此,证实了静电势(Velec)的产生和界面复合率的增加。 Velec和界面复合对光电压的大小和影响取决于照明强度和LS持续时间。具有介孔Al2O3的PSC表现出相似的变化,证实了致密TiO2的作用。在LS下,Velec的生成速度更快且逐渐增加,这表明离子和空位向界面不断迁移。非刚性的TiO2-钙钛矿界面要求对PSC进行重要的视角改变。

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