材料科学
钙钛矿(结构)
能量转换效率
钝化
化学工程
光催化
电导率
介孔材料
铜
电子迁移率
二氧化钛
图层(电子)
光电子学
纳米技术
化学
催化作用
复合材料
冶金
工程类
物理化学
生物化学
作者
Alaa A. Zaky,Eleftherios Christopoulos,Konstantina Gkini,Michalis K. Arfanis,Labrini Sygellou,Andreas Kaltzoglou,Anastasios Stergiou,Nikos Tagmatarchis,Nikolaos Balis,Polycarpos Falaras
标识
DOI:10.1016/j.apcatb.2020.119714
摘要
The electron transport layer (ETL) plays a pivotal role in obtaining perovskite solar cells (PSCs) with high power conversion efficiency (PCE). Titanium dioxide is a widely used ETL, however it suffers from low electron mobility, poor conductivity and may act as a photocatalyst of chemical reactions leading to degradation of the perovskite. Herein, copper cations employed to modify the titania ETL of PSCs, mitigate the photocatalytic action of the compact layer, increase its conductivity and electron mobility, adjust favorably the energy levels, improve the ETL/perovskite interface, thus enhance perovskite’s light absorption and provoke passivation of the perovskite surface trap states. The investigation of structural and surface chemistry properties revealed the uniform distribution of Cu1+ in TiO2 and confirmed the determining role of copper in the fast extraction of the photogenerated charge carriers to the adjacent electrode. As a result, the champion planar PSCs based on the hydrophobic Cu-TiO2 ETL showed a 18.15 % PCE outperforming the reference devices (based on pristine TiO2 ETL) which showed a PCE equal to 15.78 %. The results followed the same trend also in the case of mesoporous PSCs, proving the universality of our approach. Finally, aging tests confirmed that the copper-modified devices showed higher stability in comparison with the non-modified ones retaining the 53 % of the initial PCE value after 51 days of storage in relative humidity (RH = 25 %) and dark conditions. Photostability experiments proved that the Cu-TiO2 based devices showed remarkable robustness and retained approximately 91 % of their initial PCE, even after 5 h under continuous UV stress. These results are associated with the suppression of the photocatalytic activity of the ETL and open new perspectives for improving the performance of TiO2-based PSCs.
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