Improved environmental stability of organic lead trihalide perovskite-based photoactive-layers in the presence of mesoporous TiO2

被引:118
作者
O'Mahony, Flannan T. F. [1 ,2 ]
Lee, Yong Hui [3 ]
Jellett, Cameron [1 ,2 ]
Dmitrov, Stoichko [1 ,2 ]
Bryant, Daniel T. J. [1 ,2 ]
Durrant, James R. [1 ,2 ]
O'Regan, Brian C. [1 ,2 ]
Graetzel, Michael [3 ]
Nazeeruddin, Mohammad K. [3 ]
Haque, Saif A. [1 ,2 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AZ, England
[2] Univ London Imperial Coll Sci Technol & Med, Ctr Plast Elect, London SW7 2AZ, England
[3] Ecole Polytech Fed Lausanne, Swiss Fed Inst Technol, Lab Photon & Interfaces, Stn 6, CH-1015 Lausanne, Switzerland
基金
英国工程与自然科学研究理事会;
关键词
SOLAR-CELLS; PERFORMANCE; EFFICIENCY; DEPOSITION; LENGTHS;
D O I
10.1039/c5ta01221j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Impressive hybrid photovoltaic device performances have been realised with the methylammonium lead triiodide (MAPbI(3)) perovskite absorber in a wide range of device architectures. However, the question as to which of these systems represents the most commercially viable long-term prospect is yet to be answered conclusively. Here, we report on the photoinduced charge transfer processes in MAPbI(3) based films measured under inert and ambient conditions. When exposed to ambient conditions, the coated mesoporous Al2O3 and bilayer systems show a rapid and significant degradation in the yield of long-lived charge separation. This process, which does not affect sensitized-mesoporous TiO2 films, is only found to occur when both light and oxygen are present. These observations indicate that the presence of a mesostructured TiO2 electron acceptor to rapidly extract the photoexcited electron from the perovskite sensitizer may be crucial for fundamental photovoltaic stability and significantly increases innate tolerance to environmental conditions. This work highlights a significant advantage of retaining mesoscale morphological control in the design of perovskite photovoltaics.
引用
收藏
页码:7219 / 7223
页数:5
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