S-2-methylbutylammonium lead bromide: atomic structure

Atomic structure
H_relaxed_structure
Origin: computational
Space group: P 2₁
Lattice parameters

Crystal system: monoclinic

a:15.31429958 Å
b:8.22050953 Å
c:8.172200204 Å
α:90°
β:100.7149963°
γ:90°
Y. Xie, R. Song, A. Singh, M. Jana, V. Blum, and D. Mitzi, Kinetically Controlled Structural Transitions in Layered Halide-Based Perovskites: An Approach to Modulate Spin Splitting, Journal of the American Chemical Society 144 (33), 15223‑15235 (2022). doi: https://doi.org/10.1021/jacs.2c05574.
System description
Dimensionality: 2D n: 1
Sample type: single crystal
Related data
This data set is directly linked to other data sets: See all related data

Starting materials: S-2-MeBA, PbBr2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether

Product: yellow flaky single crystals (S-2-MeBA)2PbBr4

Description: Add (S-2-MeBA) (0.25 mmol) and PbBr2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbBr4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbBr4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbBr4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).

Comment: Differential scanning calorimetry (DSC):A TA Discovery DSC 2500 was used to carry out low-temperature conventional differential scanning calorimetry (DSC) measurements. The instrument was under helium purge with a 5 K/min ramp from 298 K to 124 K and back to 298 K (with use of an LN2P cooler). Sample powder was loaded into a Tzero Hermetic aluminum pan, with temperature and enthalpy calibrated in advance.A similar instrument was used to perform high-temperature DSC measurements under nitrogen purge. The ramp rate was 5 K/min from 298 K to 603 K. An aluminum pan was hermetically sealed to contain samples.

Method: Differential scanning calorimetry (DSC)

Description: A TA Discovery DSC 2500 was used to carry out low-temperature conventional differential scanning calorimetry (DSC) measurements. The instrument was under helium purge with a 5 K/min ramp from 298 K to 124 K and back to 298 K (with use of an LN2P cooler). Sample powder was loaded into a Tzero Hermetic aluminum pan, with temperature and enthalpy calibrated in advance. A similar instrument was used to perform high-temperature DSC measurements under nitrogen purge. The ramp rate was 5 K/min from 298 K to 603 K. An aluminum pan was hermetically sealed to contain samples.

Code: FHI-aims

Level of theory: Density Functional Theory (DFT)

Exchange-correlation functional: PBE-TS

K-point grid: 3X5X5

Level of relativity: atomic ZORA

Basis set definition: intermediate

Y. Xie, R. Song, A. Singh, M. Jana, V. Blum, and D. Mitzi, Kinetically Controlled Structural Transitions in Layered Halide-Based Perovskites: An Approach to Modulate Spin Splitting, Journal of the American Chemical Society 144 (33), 15223‑15235 (2022). doi: https://doi.org/10.1021/jacs.2c05574.

Entry added on: May 8, 2025, 1:36 p.m.
Entry added by: Chunyu Chen Mat. Sci Duke University
Last updated on: May 8, 2025, 1:36 p.m.
Last updated by: Chunyu Chen Mat. Sci Duke University

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Atomic coordinates



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