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用于锡铅钙钛矿太阳能电池的锚定电荷选择性自组装单分子层

Anchoring Charge Selective Self-Assembled Monolayers for Tin-Lead Perovskite Solar Cells.

作者信息

Zhang Zuhong, Zhu Rui, Tang Ying, Su Zhenhuang, Hu Shuaifeng, Zhang Xu, Zhang Junhan, Zhao Jinbo, Xue Yunchang, Gao Xingyu, Li Guixiang, Pascual Jorge, Abate Antonio, Li Meng

机构信息

Key Lab for Special Functional Materials of Ministry of Education, National & Local Joint Engineering Research Center for High-efficiency Display and Lighting Technology, School of Materials Science and Engineering, and Collaborative Innovation Center of Nano Functional Materials and Applications, Henan University, Kaifeng, 475004, P. R. China.

Shanghai Synchrotron Radiation Facility, Shanghai Advanced Research Institute, Chinese Academy of Sciences, 239 Zhangheng Road, Shanghai, 201204, P. R. China.

出版信息

Adv Mater. 2024 May;36(18):e2312264. doi: 10.1002/adma.202312264. Epub 2024 Feb 2.

Abstract

Self-assembled monolayers (SAMs) have displayed great potential for improving efficiency and stability in p-i-n perovskite solar cells (PSCs). The anchoring of SAMs at the conductiv metal oxide substrates and their interaction with perovskite materials must be rationally tailored to ensure efficient charge carrier extraction and improved quality of the perovskite films. Herein, SAMs molecules with different anchoring groups and spacers to control the interaction with perovskite in the p-i-n mixed Sn-Pb PSCs are selected. It is found that the monolayer with the carboxylate group exhibits appropriate interaction and has a more favorable orientation and arrangement than that of the phosphate group. This results in reduced nonradiative recombination and enhanced crystallinity. In addition, the short chain length leads to an improved energy level alignment of SAMs with perovskite, improving hole extraction. As a result, the narrow bandgap (≈1.25 eV) Sn-Pb PSCs show efficiencies of up to 23.1% with an open-circuit voltage of up to 0.89 V. Unencapsulated devices retain 93% of their initial efficiency after storage in N atmosphere for over 2500 h. Overall, this work highlights the underexplored potential of SAMs for perovskite photovoltaics and provides essential findings on the influence of their structural modification.

摘要

自组装单分子层(SAMs)在提高p-i-n钙钛矿太阳能电池(PSC)的效率和稳定性方面显示出巨大潜力。必须合理调整SAMs在导电金属氧化物衬底上的锚定及其与钙钛矿材料的相互作用,以确保有效的电荷载流子提取和提高钙钛矿薄膜的质量。在此,选择具有不同锚定基团和间隔基的SAMs分子,以控制其在p-i-n混合Sn-Pb PSC中与钙钛矿的相互作用。研究发现,含羧基的单分子层表现出适当的相互作用,并且比含磷酸基团的单分子层具有更有利的取向和排列。这导致非辐射复合减少,结晶度提高。此外,短链长度导致SAMs与钙钛矿的能级排列得到改善,从而改善空穴提取。结果,窄带隙(≈1.25 eV)的Sn-Pb PSC显示出高达23.1%的效率,开路电压高达0.89 V。未封装的器件在N2气氛中储存超过2500小时后,仍保留其初始效率的93%。总体而言,这项工作突出了SAMs在钙钛矿光伏领域尚未充分探索的潜力,并提供了关于其结构修饰影响的重要发现。

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