Elhorst Fransien D, Sebastián Alonso Javier E, Bolink Henk J, Koster L Jan Anton
Zernike Institute for Advanced Materials, University of Groningen, Nijenborgh 3, 9747 AG Groningen, The Netherlands.
Instituto de Ciencia Molecular, Universidad de Valencia, C/Catedrático J. Beltrán 2, 46980 Paterna, Spain.
ACS Energy Lett. 2025 Aug 26;10(9):4574-4579. doi: 10.1021/acsenergylett.5c01690. eCollection 2025 Sep 12.
Mobile ions in metal halide perovskites are found to degrade perovskite solar cells (PSCs). Therefore, characterizing their density and mobility is crucial for improving the long-term performance of PSCs. We introduce a formula to determine the mobility directly from impedance spectroscopy. The validity of the formula is confirmed through extensive drift-diffusion simulations varying 38 parameters including mobilities, ion densities, layer thicknesses, and trap densities. All in all, these simulations describe a wide variety of PSCs. Alternative formulas from the literature are also tested but are found to be suboptimal. After validation, we experimentally determine the ion mobility of a methylammonium lead iodide PSC to be 4 × 10 m V s. This new formula, which depends on the low-frequency feature of the impedance spectrum, facilitates the precise and straightforward determination of the ion mobility in PSCs.
人们发现金属卤化物钙钛矿中的移动离子会使钙钛矿太阳能电池(PSC)性能退化。因此,表征它们的密度和迁移率对于提高PSC的长期性能至关重要。我们引入了一个直接从阻抗谱确定迁移率的公式。通过广泛的漂移扩散模拟,在改变包括迁移率、离子密度、层厚度和陷阱密度在内的38个参数的情况下,证实了该公式的有效性。总而言之,这些模拟描述了各种各样的PSC。还测试了文献中的其他公式,但发现它们并不理想。经过验证后,我们通过实验确定了甲基碘化铅PSC的离子迁移率为4×10 m V s。这个依赖于阻抗谱低频特征的新公式,有助于精确且直接地确定PSC中的离子迁移率。