Accelerated aging of all-inorganic, interface-stabilized perovskite solar cells

Author:

Zhao Xiaoming1ORCID,Liu Tianran12ORCID,Burlingame Quinn C.3ORCID,Liu Tianjun4ORCID,Holley Rudolph1ORCID,Cheng Guangming5ORCID,Yao Nan5ORCID,Gao Feng4ORCID,Loo Yueh-Lin1ORCID

Affiliation:

1. Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ 08544, USA.

2. Department of Electrical and Computer Engineering, Princeton University, Princeton, NJ 08544, USA.

3. Andlinger Center for Energy and the Environment, Princeton University, Princeton, NJ 08544, USA.

4. Department of Physics, Chemistry, and Biology (IFM), Linköping University, SE-58183 Linköping, Sweden.

5. Princeton Institute for the Science and Technology of Materials, Princeton University, Princeton, NJ 08544, USA.

Abstract

To understand degradation routes and improve the stability of perovskite solar cells (PSCs), accelerated aging tests are needed. Here, we use elevated temperatures (up to 110°C) to quantify the accelerated degradation of encapsulated CsPbI 3 PSCs under constant illumination. Incorporating a two-dimensional (2D) Cs 2 PbI 2 Cl 2 capping layer between the perovskite active layer and hole-transport layer stabilizes the interface while increasing power conversion efficiency of the all-inorganic PSCs from 14.9 to 17.4%. Devices with this 2D capping layer did not degrade at 35°C and required >2100 hours at 110°C under constant illumination to degrade by 20% of their initial efficiency. Degradation acceleration factors based on the observed Arrhenius temperature dependence predict intrinsic lifetimes of 51,000 ± 7000 hours (>5 years) operating continuously at 35°C.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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