Substituent engineering in tertiary phosphine oxides for passivating defects of perovskite solar cells

IF 10.7 Q1 CHEMISTRY, PHYSICAL EcoMat Pub Date : 2024-06-17 DOI:10.1002/eom2.12470
Sun-Ho Lee, Seong Chan Cho, Sang Uck Lee, Nam-Gyu Park
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Abstract

Defect passivation based on Lewis acid–base chemistry has been regarded as an effective strategy to improve the photovoltaic performance and stability of perovskite solar cells (PSCs). Here, we report on tertiary phosphine oxides (R3PO) as materials for defect passivation, where photovoltaic performance was investigated depending on the substituents R. Electron-donating ability of the substituents in R3PO was found to play an important role in passivation. Cyclohexyl substituent was better in achieving photovoltaic performance than linear hexyl substituent. The heterocyclic morpholine substituent bearing oxygen and nitrogen in cyclohexyl form further improved photovoltaic performance due to its enhanced electron-donating ability. Compared with an untreated PSC, the trimorpholinophosphine oxide (TMPPO)-treated PSC improved the power conversion efficiency from 21.95% to 23.72%. Additionally, the dark-storage stability test with an unencapsulated device showed that the TMPPO-treated device maintained 92.7% of its initial PCE after 1250 h, while 86.8% was maintained for the untreated device. Three hundred hour-light-soaking of the encapsulated devices revealed that the operational stability of the TMPPO-treated PSC was superior to the untreated device.

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用于钝化过氧化物太阳能电池缺陷的叔膦氧化物取代基工程
基于路易斯酸碱化学的缺陷钝化被认为是提高过氧化物太阳能电池(PSCs)光电性能和稳定性的有效策略。在此,我们报告了作为缺陷钝化材料的叔膦氧化物(R3PO),并根据取代基 R 的不同对其光伏性能进行了研究。在实现光伏性能方面,环己基取代基比直链己基取代基更好。环己基形式的杂环吗啉取代基中含有氧和氮,由于其电子负载能力增强,可进一步提高光伏性能。与未经处理的 PSC 相比,经过三吗啉氧化膦 (TMPPO) 处理的 PSC 可将功率转换效率从 21.95% 提高到 23.72%。此外,未封装器件的黑暗储存稳定性测试表明,经 TMPPO 处理的器件在 1250 小时后仍能保持 92.7% 的初始 PCE,而未经处理的器件则能保持 86.8%。对封装装置进行三百小时的光照浸泡表明,经 TMPPO 处理的 PSC 的操作稳定性优于未经处理的装置。
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审稿时长
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