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Universal Approach for Managing Iodine Migration in Inverted Single-Junction and Tandem Perovskite Solar Cells
Advanced Materials ( IF 27.4 ) Pub Date : 2024-11-18 , DOI: 10.1002/adma.202410779
Zhenhua Song, Kexuan Sun, Yuanyuan Meng, Zewei Zhu, Yaohua Wang, Weifu Zhang, Yang Bai, Xiaoyi Lu, Ruijia Tian, Chang Liu, Ziyi Ge

Despite significant progress in the power-conversion efficiency (PCE) of perovskite solar cells (PSCs), the instability of devices remains a considerable obstacle for commercial applications. This instability primarily originates from the migration of halide ions—particularly iodide ions (I). Under light exposure and thermal stress, I migrates and transforms into I2, leading to irreversible degradation and performance loss. To address this issue, we introduced the additive 2,1,3-benzothiadiazole,5,6-difluoro-4,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) (BT2F-2B) into the perovskite. The strong coordination between the unhybridized p orbital and lone-pair electrons from I inhibits the deprotonation of MAI/FAI and the subsequent conversion of I to I₂. The highly electronegative fluorine enhances its electrostatic interaction with I. Consequently, the synergistic effect of BT2F-2B effectively suppresses the decomposition of perovskite and the defect density of the iodide vacancies. This approach delivers a PCE over 26% for inverted single-junction PSCs, with exceptional operational stability. According to the ISOS-L-3 testing protocol (maximum power point tracking at 85 °C and 50% relative humidity), treated PSCs retain 85% of their original PCE after 1000 h of aging. When the BT2F-2B is applied to a wide-bandgap (1.77 eV) perovskite system, the PCE of all-perovskite tandem solar cells reaches 27.8%, confirming the universality of the proposed strategy.

中文翻译:


管理倒置单结和叠层钙钛矿太阳能电池中碘迁移的通用方法



尽管钙钛矿太阳能电池 (PSC) 的功率转换效率 (PCE) 取得了重大进展,但器件的不稳定性仍然是商业应用的巨大障碍。这种不稳定性主要源于卤化物离子的迁移,尤其是碘离子 (I)。在光照和热应力下,I 迁移并转化为 I2,导致不可逆的降解和性能损失。为了解决这个问题,我们在钙钛矿中引入了添加剂 2,1,3-苯并噻二唑,5,6-二氟-4,7-双(4,4,5,5-四甲基-1,3,2-二氧杂硼-2-基)(BT2F-2B)。来自 I 的未杂化 p 轨道电子和孤对电子之间的强配位抑制了 MAI/FAI 的去质子化以及随后 I 向 I₂ 的转化。高电负性氟增强了它与 I 的静电相互作用。因此,BT2F-2B 的协同作用有效抑制了钙钛矿的分解和碘化物空位的缺陷密度。这种方法为倒置单液接 PSC 提供了超过 26% 的 PCE,具有出色的操作稳定性。根据 ISOS-L-3 测试方案(在 85 °C 和 50% 相对湿度下的最大功率点跟踪),处理过的 PSC 在老化 1000 小时后仍保留其 85% 的原始 PCE。当 BT2F-2B 应用于宽带隙 (1.77 eV) 钙钛矿系统时,全钙钛矿叠层太阳能电池的 PCE 达到 27.8%,证实了所提策略的普遍性。
更新日期:2024-11-18
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