钝化
材料科学
钙钛矿(结构)
降级(电信)
开路电压
能量转换效率
离子
离子键合
碘化物
化学工程
铵
电流密度
光电子学
电压
无机化学
纳米技术
图层(电子)
电子工程
化学
电气工程
有机化学
工程类
物理
量子力学
作者
Biruk Alebachew Seid,Sercan Özen,Andrés‐Felipe Castro‐Mendez,Dieter Neher,Martin Stolterfoht,Felix Lang
标识
DOI:10.1002/adma.202501588
摘要
Abstract Bulky ammonium salt‐based passivation is an effective strategy for enhancing the performance and stability of perovskite solar cells (PSCs). Especially, phenethylammonium iodide (PEAI) is known to greatly improve open‐circuit voltage ( V OC ) and fill factor (FF). Despite these benefits, PEAI passivation leads to substantial short‐circuit current density ( J SC ) losses and rapid degradation under operational conditions. In this work, it is revealed that the J SC loss as well as the accelerated degradation in PEAI‐passivated devices is caused by an increased mobile ion density. To mitigate this performance and stability‐limiting mechanism, ultrathin layers of ammonium benzenesulfonate (ABS) and/or ethylenediammonium diiodide (EDAI 2 ) salts are then introduced between the PEAI and the perovskite, which stabilize the 2D perovskite layer and impede diffusion even under upon prolonged illumination. This leads to a reduced mobile ion density both in fresh devices and in the long term, lowering losses J SC , and thus enables power conversion efficiencies of ≈25% with enhanced stability. Overall, this study not only addresses the limitations of PEAI‐based 2D passivation but also paves the way for understanding 2D‐induced ionic J SC losses.
科研通智能强力驱动
Strongly Powered by AbleSci AI