Top and Bottom Perovskite Interface Engineering by Fullerene Surface Modification of Titanium Dioxide as Electron Transport Layer

被引:16
作者
Ciro, John [1 ]
Mesa, Santiago [1 ]
Felipe Montoya, Juan [1 ]
Ignacio Uribe, Jose [1 ,2 ]
Betancur, Rafael [1 ]
Jaramillo, Franklin [1 ]
机构
[1] Univ Antioquia UdeA, Fac Ingn, Ctr Invest Innovat & Desarrollo Mat CIDEMAT, Calle 70 52-21, Medellin 050010, Colombia
[2] Univ Antioquia UdeA, Inst Fis, Grp Estado Solido, Calle 70 52-21, Medellin 050010, Colombia
关键词
electron transport layer; interface engineering; TiO2; modification; n-i-p planar perovskite solar cell; fullerene; HETEROJUNCTION SOLAR-CELLS; CHARGE INJECTION; EFFICIENCY; HYSTERESIS; TIO2; DEPOSITION; LIFETIME; BEHAVIOR;
D O I
10.1021/acsami.7b06343
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Optimization of the interface between the electron transport layer (ETL) and the hybrid perovskite is crucial to achieve high-performance perovskite solar cell (PSC) devices. Fullerene-based compounds have attracted attention as modifiers on the surface properties of TiO2, the archetypal ETL in regular n-i-p PSCs. However, the partial solubility of fullerenes in the aprotic solvents used for perovskite deposition hinders its application to low temperature solution-processed PSCs. In this work, we introduce a new method for fullerene modification of TiO2 layers derived from nanoparticles (NPs) inks. Atomic force microscopy characterization reveals that the resulting ETL is a network of TiO2-NPs interconnected by fullerenes. Interestingly, this surface modification enhances the bottom interface of the perovskite by improving the charge transfer as well as the top perovskite interface by reducing surface trap states enhancing the contact with the p-type buffer layer. As a result, rigid PSCs reached a 17.2% power conversion efficiency (PCE), while flexible PSCs exhibited a remarkable stabilized PCE of 12.2% demonstrating the potential application of this approach for further scale-up of PSC devices.
引用
收藏
页码:29654 / 29659
页数:6
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