Water-Accelerated Photooxidation of CH3NH3PbI3 Perovskite

Timothy D Siegler; Wiley A Dunlap-Shohl; Yuhuan Meng; Yuhang Yang; Wylie F Kau; Preetham P Sunkari; Chang En Tsai; Zachary J Armstrong; Yu-Chia Chen; David A C Beck; Marina Meilă; Hugh W Hillhouse

doi:10.1021/jacs.2c00391

Water-Accelerated Photooxidation of CH₃NH₃PbI₃ Perovskite

J Am Chem Soc. 2022 Mar 30;144(12):5552-5561. doi: 10.1021/jacs.2c00391. Epub 2022 Mar 17.

Authors

Timothy D Siegler^{1

2}, Wiley A Dunlap-Shohl^{1

2}, Yuhuan Meng^{2

3}, Yuhang Yang⁴, Wylie F Kau^{1

2}, Preetham P Sunkari^{1

2}, Chang En Tsai^{1

2}, Zachary J Armstrong^{1

2}, Yu-Chia Chen^{5

6}, David A C Beck^{1

3

6}, Marina Meilă^{6

7}, Hugh W Hillhouse^{1

2

3}

Affiliations

¹ Department of Chemical Engineering, University of Washington, Seattle, Washington 98195-0005, United States.
² Clean Energy Institute, University of Washington, Seattle, Washington 98195-0005, United States.
³ Molecular Engineering and Sciences Institute, University of Washington, Seattle, Washington 98195-0005, United States.
⁴ Department of Materials Science and Engineering, University of Washington, Seattle, Washington 98195-0005, United States.
⁵ Department of Electrical and Computer Engineering, University of Washington, Seattle, Washington 98195-0005, United States.
⁶ eScience Institute, University of Washington, Seattle, Washington 98195-0005, United States.
⁷ Department of Statistics, University of Washington, Seattle, Washington 98195-0005, United States.

PMID: 35296136
DOI: 10.1021/jacs.2c00391

Abstract

Halide perovskites have the potential to disrupt the photovoltaics market based on their high performance and low cost. However, the decomposition of perovskites under moisture, oxygen, and light raises concerns about service lifetime, especially because degradation mechanisms and the corresponding rate laws that fit the observed data have thus far eluded researchers. Here, we report a water-accelerated photooxidation mechanism dominating the degradation kinetics of archetypal perovskite CH₃NH₃PbI₃ in air under >1% relative humidity at 25 °C. From this mechanism, we develop a kinetic model that quantitatively predicts the degradation rate as a function of temperature, ambient O₂ and H₂O levels, and illumination. Because water is a possible product of dry photooxidation, these results highlight the need for encapsulation schemes that rigorously block oxygen ingress, as product water may accumulate beneath the encapsulant and initiate the more rapid water-accelerated photooxidative decomposition.