Jialin Wang, Likai Zheng, Hak-Beom Kim*, Han He, Sanlong Wang, Felix T. Eickemeyer, Yimhyun Jo, Ying Zhao, Mingyang Wei*, Jaeki Jeong*, Michael Grätzel* and Xiaodan Zhang*,
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引用次数: 0
摘要
铵钝化钙钛矿太阳能电池(PSCs)具有优异的器件性能和稳定性。除了典型的化学钝化作用外,铵盐还控制着钙钛矿表面的电子结构,但其分子结构与性质的关系需要进一步了解,特别是偶极子效应。在这里,我们使用咔唑和它的卤化对应物作为铵盐的官能团。具有刚性共轭分子结构的2-氯咔唑-9-乙基碘化铵(CzCl-EAI)进一步提供了化学钝化并增强了钙钛矿的环境稳定性。此外,我们发现卤化增强了分子内电荷转移,使分子偶极矩更大,导致钙钛矿薄膜的耗尽区比PDAI2条件宽三倍。在准稳态(QSS)测量下,基于混合钝化的反向PSCs的功率转换效率(PCE)达到25.16%,经认证为24.35%。在iso - d -2条件下,未封装的器件在1100小时内保持了91%以上的初始PCE,在50-60%相对湿度(RH)的环境空气中连续光照500小时后保持了80%的初始性能。
Dipolar Carbazole Ammonium for Broadened Electric Field Distribution in High-Performance Perovskite Solar Cells
Perovskite solar cells (PSCs) with ammonium passivation exhibit superior device performance and stability. Beyond typical chemical passivation, ammonium salts control the electronic structure of perovskite surfaces, yet the molecular structure–property relationship requires further understanding, especially the dipole effect. Here, we employed carbazole and its halogenated counterpart as the functional group of ammonium salts. 2-Chloro-carbazol-9-ethylammonium iodide (CzCl-EAI) with a rigid, conjugated molecular structure further provides chemical passivation and enhances the ambient stability of perovskites. In addition, we found that halogenation enhances the intramolecular charge transfer for a larger molecular dipole moment, leading to the depletion region of perovskite films threefold wider than that of the PDAI2 condition. The power conversion efficiency (PCE) of inverted PSCs based on mixed passivation reached 25.16% and certified 24.35% under the quasi-steady-state (QSS) measurement. Unencapsulated devices retained over 91% of initial PCE under ISOS-D-2 conditions over 1100 h and maintained 80% of their initial performance after 500 h of continuous light illumination in ambient air with a 50–60% relative humidity (RH).
期刊介绍:
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