Starting materials: (PMA)2PbI4 crystals, DMF, glass substrates
Product: Thin-film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.
Starting materials: (PMA)2PbBr4 crystals, DMF, glass substrates
Product: Thin film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.
Starting materials: (PMA)2PbCl4 crystals, DMF, quartz substrates
Product: Thin film on quartz
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.
See all entries for this property (3 total)
Starting materials: (PEA)2PbI4 crystals, DMF, glass substrates
Product: Thin film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.
See all entries for this property (2 total)
Starting materials: (PEA)2PbBr4 crystals, DMF, glass substrates
Product: Thin film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.
Starting materials: (PEA)2PbCl4 crystals, DMF, quartz substrates
Product: Thin film on quartz
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.
Starting materials: (NMA)2PbBr4 crystals, DMF, glass substrates
Product: Thin-film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He−Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.
Starting materials: (NMA)2PbCl4 crystals, DMF, quartz substrates
Product: Thin film on quartz
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He−Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.
Starting materials: (NEA)2PbI4 crystals, DMF, glass substrates
Product: Thin film on glass
Description: Dissolve the 2D single crystal into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He−Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.
Starting materials: (NEA)2PbBr4 crystals, DMF, glass substrates
Product: Thin film on glass
Description: Dissolve the 2D single crystal into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He−Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.
Crystal system: monoclinic
| a: | 12.266 (±0.005) Å |
| b: | 12.276 (±0.005) Å |
| c: | 38.651 (±0.018) Å |
| α: | 90° |
| β: | 98.867 (±0.014)° |
| γ: | 90° |
Starting materials: PbI2 (99.999% trace metal basis), HI (57 wt % in H2O, with hypophosphorous acid as stabilizer, assay 99.95%), CH3OH (>99.9%), 2-(2-naphthyl)ethanamine (NEA, 95%)
Product: Red and laminar crystals.
Description: Dissolve PbI2 (27.0 mg) in 0.5 mL of HI (57%). Place CH3OH (1 ml) on top of the PbI2 solution. Add 0.020 mL of NEA liquid into the CH3OH layer. Crystals would form in the solution overnight.
Method: Single-crystal X-ray diffraction
Description: Single-crystal X-ray diffraction data were collected using a Bruker D8 ADVANCE Series II at room temperature. The crystal structures were solved and refined by Shelxl and Olex software.
See all entries for this property (2 total)
Crystal system: orthorhombic
| a: | 41.3314 (±0.0011) Å |
| b: | 8.0801 (±0.0002) Å |
| c: | 8.0836 (±0.0002) Å |
| α: | 90° |
| β: | 90° |
| γ: | 90° |
Starting materials: HBr (48 wt % in H2O, assay >99.99%), 1-(2-Naphthyl)methanamine (95+%) in methanol, PbBr2 (99.999% trace metal basis), DMF
Product: Colorless and laminar crystals.
Description: Add a stoichiometric amount of 48% concentrated HBr into the NMA methanol solution to prepare NMA·HBr. Evaporate methanol to form colorless NMA·HBr crystals. Separate the crystals. Dissolve NMA·HBr (9.5 mg) and PbBr2 (7.3 mg) into DMF (0.2 mL). Separate the crystals after the partial evaporation of DMF.
Method: Single-crystal X-ray diffraction
Description: Single-crystal X-ray diffraction data were collected using a Bruker D8 ADVANCE Series II at room temperature. The crystal structures were solved and refined by Shelxl and Olex software.
See all entries for this property (2 total)
Crystal system: orthorhombic
| a: | 33.3529 (±0.0007) Å |
| b: | 8.1466 (±0.0002) Å |
| c: | 8.1232 (±0.0002) Å |
| α: | 90° |
| β: | 90° |
| γ: | 90° |
Starting materials: PbBr2 (99.999% trace metal basis), phenylmethylamine (PMA, >99.0%), HBr (48 wt % in H2O, assay >99.99%), CH3OH (>99.9%)
Product: Colorless and laminar crystals.
Description: Dissolve PbBr2 (50.3 mg) in 0.5 mL of HBr (48%). Place CH3OH (1 ml) on the top of the PbBr2 solution. Add 0.030 mL of PMA liquid into the CH3OH layer. Expect to form crystals in the solution overnight.
Method: Single-crystal X-ray diffraction
Description: Single-crystal X-ray diffraction data were collected using a Bruker D8 ADVANCE Series II at room temperature. The crystal structures were solved and refined by Shelxl and Olex software.
See all entries for this property (27 total)
Crystal system: triclinic
| a: | 8.7389 (±0.0002) Å |
| b: | 8.7403 (±0.0002) Å |
| c: | 32.9952 (±0.0006) Å |
| α: | 84.646 (±0.001)° |
| β: | 84.657 (±0.001)° |
| γ: | 89.643 (±0.001)° |
Starting materials: PbI2 (99.999% trace metal basis), HI (57 wt % in H2O, with hypophosphorous acid as stabilizer, assay 99.95%), CH3OH (>99.9%), 2-phenylethylamine (PEA, 99%)
Product: Red and laminar crystals.
Description: Dissolve PbI2 (54.6 mg) in 0.5 mL of HI (57%). Place CH3OH (1 ml) on the top of the PbI2 solution. Add 0.030 mL of PEA liquid into the CH3OH layer. Crystals would form in the solution overnight.
Method: Single-crystal X-ray diffraction
Description: Single-crystal X-ray diffraction data were collected using a Bruker D8 ADVANCE Series II at room temperature. The crystal structures were solved and refined by Shelxl and Olex software.
Comment: This is the experimentally resolved structure, which contains a statistical (disordered) representation of the equatorial iodine atoms in the original refinement. This structure is our recommended "best" published experimental structure for phenethylammonium lead iodide at room temperature, supported by a computational comparison of the total energies of various published structures after full structure optimization in Chemistry of Materials, Vol. 34, issue 7, 3109-3122 (2022), https://doi.org/10.1021/acs.chemmater.1c04213. The computationally relaxed (PEA)2PbI4 structure with resolved disorder (i.e., no overlapping iodine positions), optimized using the PBE+Tkatchenko-Scheffler approach, is also available in the HybriD3 database (see datasets linked to the present one.)
Crystal system: triclinic
| a: | 8.2989 (±0.0004) Å |
| b: | 8.2986 (±0.0004) Å |
| c: | 19.8768 (±0.0009) Å |
| α: | 92.827 (±0.001)° |
| β: | 99.124 (±0.001)° |
| γ: | 90.142 (±0.001)° |
Starting materials: PbBr2 (99.999% trace metal basis), HBr (48 wt % in H2O, assay >99.99%), CH3OH (>99.9%), 2-(2-naphthyl)ethanamine (NEA, 95%)
Product: Colorless and laminar crystals.
Description: Dissolve PbBr2 (21.5 mg) in 0.5 mL of HBr (48%). Place CH3OH (1 ml) on top of the PbBr2 solution. Add 0.020 mL of NEA liquid into the CH3OH layer. Crystals would form in the solution overnight.
Method: Single-crystal X-ray diffraction
Description: Single-crystal X-ray diffraction data were collected using a Bruker D8 ADVANCE Series II at room temperature. The crystal structures were solved and refined by Shelxl and Olex software.
Crystal system: triclinic
| Photoluminescence peak position, nm |
|---|
Starting materials: (PEA)2PbCl4 crystals, DMF, quartz substrates
Product: Thin film on quartz
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.
Crystal system: monoclinic
| Photoluminescence peak position, nm |
|---|
Starting materials: (NEA)2PbI4 crystals, DMF, glass substrates
Product: Thin-film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He−Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.
Crystal system: orthorhombic
| Photoluminescence peak position, nm |
|---|
Starting materials: (NMA)2PbBr4 crystals, DMF, glass substrates
Product: Thin-film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He−Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.
Crystal system: orthorhombic
| Photoluminescence peak position, nm |
|---|
Starting materials: (PMA)2PbBr4 crystals, DMF, glass substrates
Product: Thin film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.
Crystal system: triclinic
| Photoluminescence peak position, nm |
|---|
Starting materials: (PEA)2PbI4 crystals, DMF, glass substrates
Product: Thin film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.
Crystal system: triclinic
| Photoluminescence peak position, nm |
|---|
Starting materials: (NEA)2PbBr4 crystals, DMF, glass substrates
Product: Thin film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.
Crystal system: triclinic
| Photoluminescence peak position, nm |
|---|
Starting materials: (PEA)2PbBr4 crystals, DMF, glass substrates
Product: Thin film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.
Crystal system: orthorhombic
| Photoluminescence peak position, nm |
|---|
Starting materials: (PMA)2PbI4 crystals, DMF, glass substrates
Product: Thin film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.
Crystal system: orthorhombic
| Photoluminescence peak position, nm |
|---|
Starting materials: (PMA)2PbCl4 crystals, DMF, quartz substrates
Product: Thin film on quartz
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.
Crystal system: orthorhombic
| Photoluminescence peak position, nm |
|---|
Starting materials: (NMA)2PbCl4 crystals, DMF, quartz substrates
Product: Thin film on quartz
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: Photoluminescence
Description: The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.
See all entries for this property (2 total)
Starting materials: (PEA)2PbCl4 crystals, DMF, quartz substrates
Product: Thin film on quartz
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: UV-Vis absorption
Description: Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.
Starting materials: (PMA)2PbCl4 crystals, DMF, quartz substrates
Product: Thin film on quartz
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: UV-Vis absorption
Description: Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.
Starting materials: (NMA)2PbCl4 crystals, DMF, quartz substrates
Product: Thin film on quartz
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: UV-Vis absorption
Description: Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.
See all entries for this property (2 total)
Starting materials: (PEA)2PbBr4 crystals, DMF, glass substrates
Product: Thin film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: UV-Vis absorption
Description: Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.
See all entries for this property (2 total)
Starting materials: (PMA)2PbBr4 crystals, DMF, glass substrates
Product: Thin film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: UV-Vis absorption
Description: Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.
Starting materials: (NEA)2PbBr4 crystals, DMF, glass substrates
Product: Thin film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: UV-Vis absorption
Description: Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.
Starting materials: (NMA)2PbBr4 crystals, DMF, glass substrates
Product: Thin-film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: UV-vis absorption
Description: Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.
See all entries for this property (4 total)
Starting materials: (PEA)2PbI4 crystals, DMF, glass substrates
Product: Thin film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: UV-Visible absorption
Description: Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.
Starting materials: (PMA)2PbI4 crystals, DMF, glass substrates
Product: Thin film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: UV-Visible absorption
Description: Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.
Starting materials: (NEA)2PbI4 crystals, DMF, glass substrates
Product: Thin-film on glass
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: UV-Vis absorption
Description: Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.
See all entries for this property (2 total)
Starting materials: (PEA)2PbCl4 crystals, DMF, quartz substrates
Product: Thin film on quartz
Description: Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.
Method: UV-Vis absorption
Description: Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.