Department of Mechanical and Materials Engineering, University of Nebraska-Lincoln , Lincoln, Nebraska 68588-0656, United States.
Acc Chem Res. 2016 Feb 16;49(2):286-93. doi: 10.1021/acs.accounts.5b00420. Epub 2016 Jan 28.
Organometal trihalide perovskites (OTPs) are emerging as very promising photovoltaic materials because the power conversion efficiency (PCE) of OTP solar cells quickly rises and now rivals with that of single crystal silicon solar cells after only five-years research. Their prospects to replace silicon photovoltaics to reduce the cost of renewable clean energy are boosted by the low-temperature solution processing as well as the very low-cost raw materials and relative insensitivity to defects. The flexibility, semitransparency, and vivid colors of perovskite solar cells are attractive for niche applications such as built-in photovoltaics and portable lightweight chargers. However, the low stability of current hybrid perovskite solar cells remains a serious issue to be solved before their broad application. Among all those factors that affect the stability of perovskite solar cells, ion migration in OTPs may be intrinsic and cannot be taken away by device encapsulation. The presence of ion migration has received broad attention after the report of photocurrent hysteresis in OTP based solar cells. As suggested by much direct and indirect experimental evidence, the ion migration is speculated to be the origin or an important contributing factor for many observed unusual phenomenon in OTP materials and devices, such as current-voltage hysteresis, switchable photovoltaic effect, giant dielectric constant, diminished transistor behavior at room temperature, photoinduced phase separation, photoinduced self-poling effect, and electrical-field driven reversible conversion between lead iodide (PbI2) and methylammonium lead triiodide (MAPbI3). Undoubtedly thorough insight into the ion-migration mechanism is highly desired for the development of OTP based devices to improve intrinsic stability in the dark and under illumination. In this Account, we critically review the recent progress in understanding the fundamental science on ion migration in OTP based solar cells. We look into both theoretical and experiment advances in answering these basic questions: Does ion migration occur and cause the photocurrent hysteresis in perovskite solar cells? What are the migrating ion species? How do ions migrate? How does ion migration impact the device efficiency and stability? How can ion migration be mitigated or eliminated? We also raise some questions that need to be understood and addressed in the future.
有机金属卤化物钙钛矿(OTP)作为极具前景的光伏材料崭露头角,因为 OTP 太阳能电池的光电转换效率(PCE)仅经过五年的研究便迅速提升,如今已可与单晶硅太阳能电池相媲美。低温溶液处理工艺,以及低廉的原材料成本和对缺陷相对不敏感等特性,使 OTP 有望取代硅光伏技术,降低可再生清洁能源的成本。钙钛矿太阳能电池的柔韧性、半透明性和丰富色彩使其在一些特定应用中具有吸引力,例如内置光伏和便携式轻量级充电器。然而,当前混合钙钛矿太阳能电池的稳定性低仍是其广泛应用前需要解决的一个严重问题。在影响钙钛矿太阳能电池稳定性的所有因素中,OTP 中的离子迁移可能是固有存在的,无法通过器件封装去除。在基于 OTP 的太阳能电池中光电流滞后现象的报告公布后,离子迁移的存在受到了广泛关注。大量直接和间接的实验证据表明,离子迁移可能是 OTP 材料和器件中许多观察到的异常现象的起源或重要贡献因素,例如电流-电压滞后、可切换光伏效应、巨大介电常数、室温下晶体管性能下降、光致相分离、光致自极化效应以及电场所驱动的 lead iodide (PbI2) 和 methylammonium lead triiodide (MAPbI3) 之间的可逆转换。毫无疑问,深入了解离子迁移机制对于开发基于 OTP 的器件以提高暗态和光照下的固有稳定性非常重要。在本综述中,我们批判性地回顾了在理解基于 OTP 的太阳能电池中离子迁移的基本科学方面的最新进展。我们探讨了回答以下基本问题的理论和实验进展:离子迁移是否发生并导致钙钛矿太阳能电池的光电流滞后?迁移离子的种类是什么?离子如何迁移?离子迁移如何影响器件效率和稳定性?如何减轻或消除离子迁移?我们还提出了一些需要在未来理解和解决的问题。