Saivineeth Penukula, Favian Tippin, Muzhi Li, K. Khawaja, Feng Yan, Nicholas Rolston
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引用次数: 0
摘要
离子迁移是金属卤化物包光体太阳能电池(PSCs)快速降解的主要原因之一,我们报告了一种利用瞬态暗电流测量来量化移动离子浓度(No)的方法。我们对 PSC 进行了原位和原位测量,并研究了一系列温度条件下薄膜和器件中 No 的演变情况。我们还研究了器件结构、顶部电极化学以及金属卤化物包晶成分和尺寸对 No 的影响。研究表明,二维包晶与不与卤化物发生反应的惰性 C 电极一起可将离子浓度降低约 99%,同时还可将机械可靠性提高约 250%。我们相信,这项工作可以为开发稳定的 PSC 提供设计指南,即从最大限度地减少移动离子及其在运行条件下随时间演变的角度出发。
Use of carbon electrodes to reduce mobile ion concentration and improve reliability of metal halide perovskite photovoltaics
Ion migration is one of the prime reasons for the rapid degradation of metal halide perovskite solar cells (PSCs), and we report on a method for quantifying mobile ion concentration (No) using a transient dark current measurement. We perform both ex-situ and in-situ measurements on PSCs and study the evolution of No in films and devices under a range of temperatures. We also study the effect of device architecture, top electrode chemistry, and metal halide perovskite composition and dimensionality on No. Two-dimensional perovskites are shown to reduce the ion concentration along with inert C electrodes that do not react with halides by ~99% while also improving mechanical reliability by ~250%. We believe this work can provide design guidelines for the development of stable PSCs through the lens of minimizing mobile ions and their evolution over time under operational conditions.