Volume 126, Issue 42 pp. 11414-11417
Zuschrift

A Layered Hybrid Perovskite Solar-Cell Absorber with Enhanced Moisture Stability

Ian C. Smith

Ian C. Smith

Department of Chemistry, Stanford University, Stanford, CA 94305 (USA)

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Dr. Eric T. Hoke

Dr. Eric T. Hoke

Department of Materials Science and Engineering, Stanford University, Stanford, CA 94305 (USA)

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Dr. Diego Solis-Ibarra

Dr. Diego Solis-Ibarra

Department of Chemistry, Stanford University, Stanford, CA 94305 (USA)

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Prof. Michael D. McGehee

Prof. Michael D. McGehee

Department of Materials Science and Engineering, Stanford University, Stanford, CA 94305 (USA)

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Prof. Hemamala I. Karunadasa

Corresponding Author

Prof. Hemamala I. Karunadasa

Department of Chemistry, Stanford University, Stanford, CA 94305 (USA)

Department of Chemistry, Stanford University, Stanford, CA 94305 (USA)Search for more papers by this author
First published: 01 September 2014
Citations: 626

This research was funded by the Global Climate and Energy Project. X-ray diffraction studies were performed at the Stanford Nanocharacterization Laboratory. We thank William Nguyen and Greyson Christoforo for experimental assistance.

Abstract

Two-dimensional hybrid perovskites are used as absorbers in solar cells. Our first-generation devices containing (PEA)2(MA)2[Pb3I10] (1; PEA=C6H5(CH2)2NH3+, MA=CH3NH3+) show an open-circuit voltage of 1.18 V and a power conversion efficiency of 4.73 %. The layered structure allows for high-quality films to be deposited through spin coating and high-temperature annealing is not required for device fabrication. The 3D perovskite (MA)[PbI3] (2) has recently been identified as a promising absorber for solar cells. However, its instability to moisture requires anhydrous processing and operating conditions. Films of 1 are more moisture resistant than films of 2 and devices containing 1 can be fabricated under ambient humidity levels. The larger bandgap of the 2D structure is also suitable as the higher bandgap absorber in a dual-absorber tandem device. Compared to 2, the layered perovskite structure may offer greater tunability at the molecular level for material optimization.

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