无机材料学报

• 研究论文 •    

反式钙钛矿太阳能电池中乙酰丙酮铈界面缓冲层的研究

解鑫倩1,2, 洪祥1,2, 杨松旺1,2   

  1. 1.中国科学院 上海硅酸盐研究所,中国科学院能量转换材料重点实验室,上海 201899;
    2.中国科学院大学 材料科学与光电工程中心,北京 100049
  • 收稿日期:2026-03-13 修回日期:2026-05-20
  • 作者简介:解鑫倩(2002-), 女, 硕士研究生. E-mail: xiexinqian23@mails.ucas.ac.cn
  • 基金资助:
    上海市科委关键技术研发计划项目(25DZ3001903); 中国载人航天工程空间应用系统项目(KJZ-YY-WCL0502)

Cerium Acetylacetonate Interfacial Buffer Layer for Inverted Perovskite Solar Cells

XIE Xinqian1,2, HONG Xiang1,2, YANG Songwang1,2   

  1. 1. CAS Key Laboratory of Materials for Energy Conversion, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 201899, China;
    2. Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing 100049, China
  • Received:2026-03-13 Revised:2026-05-20
  • About author:XIE Xinqian (2002-), female, Master candidate. E-mail: xiexinqian23@mails.ucas.ac.cn
  • Supported by:
    Shanghai Science and Technology Commission Program (25DZ3001903); Space Application System of China Manned Space Program (KJZ-YY-WCL0502)

摘要: 反式钙钛矿太阳能电池(PSCs)因快速增长的效率、低温制备工艺以及低成本等特点备受关注,但溶液法制备的氧化锡(SnO2)电子传输层(ETL)往往存在表面孔洞和界面接触不佳等问题,导致界面非辐射复合加剧,限制了器件性能的进一步提升。本研究在溶液法制备的SnO2 ETL与银电极之间引入乙酰丙酮铈(Ce(acac)3)作为界面缓冲层。实验结果表明,Ce(acac)3能够有效覆盖并平整SnO2表面,构建连续致密的界面层。同时,改进后的SnO2薄膜表面功函数降低,界面电子提取势垒减小,非辐射复合受到抑制,载流子提取和传输性能得到优化。最终,PSCs的光电转换效率(PCE)从20.33%提升至22.85%,优于传统浴铜灵(BCP)缓冲层器件的20.95%;此外,未封装器件在空气环境中放置1000 h后仍能保持初始效率的85%以上。本研究通过引入Ce(acac)3作为无机界面缓冲层,实现了界面形貌和化学特性的共同优化,为全溶液法制备高效稳定反式钙钛矿太阳能电池奠定了基础。

关键词: 反式钙钛矿太阳能电池, 乙酰丙酮铈, SnO2电子传输层, 界面缓冲层

Abstract: Inverted perovskite solar cells (PSCs) have garnered significant attention due to their rapidly increasing efficiency, low-temperature fabrication process, and low cost. However, solution-processed tin oxide (SnO2) electron transport layers (ETLs) often suffer from surface pinholes and poor interfacial contact, which aggravate interfacial non-radiative recombination and limit further performance improvement. In this work, cerium acetylacetonate (Ce(acac)3) was introduced as an interfacial buffer layer between the solution-processed SnO2 ETL and the Ag electrode. Ce(acac)3 effectively covers and planarizes the SnO2 surface, forming a continuous and dense interfacial layer. Furthermore, the modified SnO2 films exhibit a decreased work function, leading to a reduced electron extraction barrier at the interface. This effectively suppresses non-radiative recombination and optimizes charge carrier extraction and transport. Consequently, the power conversion efficiency (PCE) of the PSC is enhanced from 20.33% to 22.85%, outperforming the conventional bathocuproine (BCP) buffer layer-based device (20.95%). Moreover, unencapsulated devices retain over 85% of the initial efficiency after 1000 h of storage in ambient air. This work demonstrates that introducing Ce(acac)3 as an inorganic interfacial buffer layer enables optimization of interfacial morphology and chemical properties, paving the way for fabricating fully solution‑processed, highly efficient and stable inverted PSCs.

Key words: inverted perovskite solar cell, cerium acetylacetonate, SnO2 electron transport layer, interfacial buffer layer

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