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Energy level diagram of HC(NH2)2PbI3 single crystal evaluated by electrical and optical analyses

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Abstract

Recently, organic–inorganic halide perovskites have received attention for applications in solar cells. Measurements of high-quality single crystals reveal lower defect densities and longer carrier lifetimes than those of conventional thin films, which result in improved electrical and optical properties. However, single crystal surfaces are sensitive to exposure to ambient conditions, and degrade under long-term storage in air. The surface also shows differences from the bulk in terms of its optical and electronic characteristics. For a heterojunction device, the interface at the single crystal is important. Understanding the difference between the surface and bulk properties offers insights into device design. Here, we prepared non-sliced and sliced formamidinium lead iodide (FAPbI3; FA+ = HC(NH2)2+) single crystals with a bandgap of 1.4 eV, which matches well with the requirements for solar cell photoabsorption layers. We evaluate the energy level diagrams of the surface and bulk regions, respectively. Our data indicate that the valence band maximum of the surface region is at a higher energy level than that of the bulk region. We also discuss hypotheses for the well-known and unexplained phenomena (multiple bandgaps and bandgap narrowing) seen in the absorption and photoluminescence spectra of single crystals. We conclude that these effects are likely caused by a combination of the degraded surface, Rashba-splitting in bulk, and self-absorption by the single crystal itself.

Graphical abstract: Energy level diagram of HC(NH2)2PbI3 single crystal evaluated by electrical and optical analyses

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Publication details

The article was received on 06 Nov 2017, accepted on 04 Dec 2017 and first published on 22 Dec 2017


Article type: Paper
DOI: 10.1039/C7CP07477H
Citation: Phys. Chem. Chem. Phys., 2018, Advance Article
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    Energy level diagram of HC(NH2)2PbI3 single crystal evaluated by electrical and optical analyses

    T. Sekimoto, M. Suzuka, T. Yokoyama, R. Uchida, S. Machida, T. Sekiguchi and K. Kawano, Phys. Chem. Chem. Phys., 2018, Advance Article , DOI: 10.1039/C7CP07477H

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