钝化
材料科学
钙钛矿(结构)
介孔材料
纳米技术
再现性
混合太阳能电池
光伏系统
聚合物
光电子学
图层(电子)
太阳能电池
化学工程
聚合物太阳能电池
复合材料
化学
电气工程
色谱法
工程类
生物化学
催化作用
作者
Jose M. Obrero‐Perez,Lidia Contreras-Bernal,Fernando Nuñez‐Galvez,Javier Castillo‐Seoane,Karen Valadez‐Villalobos,Francisco J. Aparicio,Juan A. Anta,Ana Borras,Juan R. Sanchez-Valencia,Angel Barranco
标识
DOI:10.1002/aenm.202200812
摘要
Despite the youthfulness of hybrid halide perovskite solar cells, their efficiencies are currently comparable to commercial silicon and have surpassed quantum-dots solar cells. Yet, the scalability of these devices is a challenge due to their low reproducibility and stability under environmental conditions. However, the techniques reported to date to tackle such issues recurrently involve the use of solvent methods that would further complicate their transfer to industry. Herein a reliable alternative relaying in the implementation of an ultrathin plasma polymer as a passivation interface between the electron transport layer and the hybrid perovskite layer is presented. Such a nanoengineered interface provides solar devices with increased long-term stability under ambient conditions. Thus, without involving any additional encapsulation step, the cells retain more than 80% of their efficiency after being exposed to the ambient atmosphere for more than 1000 h. Moreover, this plasma polymer passivation strategy significantly improves the coverage of the mesoporous scaffold by the perovskite layer, providing the solar cells with enhanced performance, with a champion efficiency of 19.2%, a remarkable value for Li-free standard mesoporous n-i-p architectures, as well as significantly improved reproducibility.
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