Inorganic alkali lead iodide semiconducting APbI3 (A = Li, Na, K, Cs) and NH4PbI3 films prepared from solution: Structure, morphology, and electronic structure

Lucangelo Dimesso; Michael Wussler; Thomas Mayer; Eric Mankel; Wolfram Jaegermann; Lucangelo Dimesso; Michael Wussler; Thomas Mayer; Eric Mankel; Wolfram Jaegermann

doi:10.3934/matersci.2016.3.737

AIMS Materials Science

2016, Volume 3, Issue 3: 737-755. doi: 10.3934/matersci.2016.3.737

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Inorganic alkali lead iodide semiconducting APbI₃ (A = Li, Na, K, Cs) and NH₄PbI₃ films prepared from solution: Structure, morphology, and electronic structure

Materials Science Department, Technische Universitaet Darmstadt, Jovanka-Bontschits-Strasse 2, D-64287, Darmstadt, Germany

Received: 18 March 2016 Accepted: 21 June 2016 Published: 28 June 2016

APbI₃ alkali lead iodides were prepared from aqueous (A= Na, Cs, ammonium NH₄⁺, and methylammonium CH₃NH₃⁺) and acetone (A= Li, K) solutions by a self-organization low temperature process. Diffraction analysis revealed that the methylammonium-containing system (MAPbI₃) crystallizes into a tetragonal perovskite structure, whereas the alkali and NH₄⁺ systems adopt orthorhombic structures. Morphological inspection confirmed the influence of the cation on the growth mechanism: for A = Cs and NH₄⁺, needle-like crystallites with lengths up to 3–4 mm; for A = K, thin stripes with lengths up to 5–6 mm; and for A = MA⁺, dodecahedral crystallites were observed. For A = Li and Na, the APbI₃ systems typically resulted in polycrystalline aggregates. Optical absorption measurements demonstrated large energy band gaps for the alkali and ammonium systems with values between 2.19 and 2.40 eV. For electronic and chemical characterization by photoelectron spectroscopy, the as-prepared powders were dissolved in di-methylformamide and re-crystallized as thin films on F:SnO₂ substrates by spin-coating. The binding energy differences between Pb4f and I3d core levels are highly similar in the investigated systems and close to the value measured for PbI₂, indicating similar relative partial charges and formal oxidation states. The binding energies of the alkali ions are in accordance with oxidation state +1. The X-ray excited valence band spectra of the investigated APbI₃ systems exhibited similar line shapes in the region between the valence band maximum and 4.5 eV higher binding energy due to common PbI₆ octahedra which dominate the electronic structure. While the ionization energy values are quite similar (6.15 ±
0.25 eV), the Fermi-level positions of the unintentionally doped materials vary for different cations and different batches of the same material, which indicates that the position of the Fermi level can be influenced by changing the process parameters.
- solution process,
- alkali lead iodide,
- ammonium lead iodide,
- X-ray photoelectron spectroscopy,
- ultra-violet photoelectron spectroscopy
Citation: Lucangelo Dimesso, Michael Wussler, Thomas Mayer, Eric Mankel, Wolfram Jaegermann. Inorganic alkali lead iodide semiconducting APbI3 (A = Li, Na, K, Cs) and NH4PbI3 films prepared from solution: Structure, morphology, and electronic structure[J]. AIMS Materials Science, 2016, 3(3): 737-755. doi: 10.3934/matersci.2016.3.737

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Abstract

APbI₃ alkali lead iodides were prepared from aqueous (A= Na, Cs, ammonium NH₄⁺, and methylammonium CH₃NH₃⁺) and acetone (A= Li, K) solutions by a self-organization low temperature process. Diffraction analysis revealed that the methylammonium-containing system (MAPbI₃) crystallizes into a tetragonal perovskite structure, whereas the alkali and NH₄⁺ systems adopt orthorhombic structures. Morphological inspection confirmed the influence of the cation on the growth mechanism: for A = Cs and NH₄⁺, needle-like crystallites with lengths up to 3–4 mm; for A = K, thin stripes with lengths up to 5–6 mm; and for A = MA⁺, dodecahedral crystallites were observed. For A = Li and Na, the APbI₃ systems typically resulted in polycrystalline aggregates. Optical absorption measurements demonstrated large energy band gaps for the alkali and ammonium systems with values between 2.19 and 2.40 eV. For electronic and chemical characterization by photoelectron spectroscopy, the as-prepared powders were dissolved in di-methylformamide and re-crystallized as thin films on F:SnO₂ substrates by spin-coating. The binding energy differences between Pb4f and I3d core levels are highly similar in the investigated systems and close to the value measured for PbI₂, indicating similar relative partial charges and formal oxidation states. The binding energies of the alkali ions are in accordance with oxidation state +1. The X-ray excited valence band spectra of the investigated APbI₃ systems exhibited similar line shapes in the region between the valence band maximum and 4.5 eV higher binding energy due to common PbI₆ octahedra which dominate the electronic structure. While the ionization energy values are quite similar (6.15 ±
0.25 eV), the Fermi-level positions of the unintentionally doped materials vary for different cations and different batches of the same material, which indicates that the position of the Fermi level can be influenced by changing the process parameters.

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