Ferroelectric Domain Wall Induced Band Gap Reduction and Charge Separation in Organometal Halide Perovskites

• Published in: The journal of physical chemistry letters Vol. 6; no. 4; pp. 693 - 699
• Main Authors: Liu, Shi, Zheng, Fan, Koocher, Nathan Z, Takenaka, Hiroyuki, Wang, Fenggong, Rappe, Andrew M
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 19.02.2015
• Subjects: electron−hole separation; domain engineering; perovskite solar cells; density functional theory; electronic structure
• ISSN: 1948-7185; 1948-7185
• DOI: 10.1021/jz502666j

Organometal halide perovskites have been intensely studied in the past 5 years, inspired by their certified high photovoltaic power conversion efficiency. Some of these materials are room-temperature ferroelectrics. The presence of switchable ferroelectric domains in methylammonium lead triiodide, CH3NH3PbI3, has recently been observed via piezoresponse force microscopy. Here, we focus on the structural and electronic properties of ferroelectric domain walls in CH3NH3PbX3 (X = Cl, Br, I). We find that organometal halide perovskites can form both charged and uncharged domain walls due to the flexible orientational order of the organic molecules. The electronic band gaps for domain structures possessing 180 and 90° walls are estimated with density functional theory. It is found that the presence of charged domain walls will significantly reduce the band gap by 20–40%, while the presence of uncharged domain walls has no substantial impact on the band gap. We demonstrate that charged domain walls can serve as segregated channels for the motions of charge carriers. These results highlight the importance of ferroelectric domain walls in hybrid perovskites for photovoltaic applications and suggest a possible avenue for device optimization through domain patterning.