钙钛矿(结构)
材料科学
光伏
光电子学
氧化铈
辐照
能量转换效率
氧化物
辐射
光伏系统
晶界
太阳能
氧化锡
能量转换
质子
铈
辐射损伤
卤化物
化学工程
电离辐射
纳米技术
纳米颗粒
光热治疗
电致发光
吸收剂量
钙钛矿太阳能电池
碘化物
开路电压
抗辐射性
原子层沉积
天线效应
作者
Minwoo Lee,George Kwesi Asare,Kaiwen Sun,Siwon Yun,Jongchul Lim,Dong Han Seo,Hongjae Shim,Martin A. Green,Charles W. Chandler,Mark Baker,Jihoo Lim,Xiaojing Hao,Helen Hejin Park,Jae Sung Yun
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-12-12
卷期号:11 (1): 389-400
被引量:1
标识
DOI:10.1021/acsenergylett.5c02116
摘要
Halide perovskite solar cells (HPSCs) hold strong potential for next-generation photovoltaics owing to their high efficiency and defect-tolerant structure. Yet, achieving long-term stability under operational stressors such as heat, prolonged illumination, and ionizing radiation remains a key challenge, particularly for applications in space and other harsh environments. Here, we report a dual-passivation approach that incorporates cerium oxide (CeOx) nanoparticles into the perovskite absorber layer using an n-octylammonium iodide (OAI)-assisted post-treatment. CeOx, a redox-active oxide widely used in radiation shielding, improves crystallinity, reduces defect density, and enhances interfacial energy alignment. The resulting devices exhibit a power conversion efficiency (PCE) of 24.9%, the highest reported for n-i-p HPSCs employing poly(bis(4-phenyl)(2,4,6-trimethylphenyl)amine) as the hole transport layer. Under 0.05 MeV proton irradiation at fluences up to 2 × 1014 protons cm–2, the treated devices retained 91% of their open-circuit voltage and 81% of their initial PCE. Spectroscopic and electrical analyses revealed suppressed nonradiative recombination, preserved grain boundary potential, and improved photothermal stability. These results demonstrate that CeOx incorporation offers an effective strategy for enhancing the durability of perovskite solar cells under simultaneous environmental and radiation exposure, paving the way toward reliable deployment in both terrestrial and aerospace energy technologies.
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