See all entries for this property (7 total)
Crystal system: cubic
| a: | 5.675 Å |
| b: | 5.675 Å |
| c: | 5.675 Å |
| α: | 90° |
| β: | 90° |
| γ: | 90° |
Starting materials: lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HCl
Product: Colorless MAPbCl3 crystals
Description: CH3NH3PbCI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HCl solution. The aqueous solution was cooled from l00°C to room temperature to obtain the colorless crystals.
Method: Temperature-dependent Guinier-Simon photograph
Description: Not specified.
See all entries for this property (7 total)
Crystal system: tetragonal
| a: | 5.656 Å |
| b: | 5.656 Å |
| c: | 5.63 Å |
| α: | 90° |
| β: | 90° |
| γ: | 90° |
Starting materials: lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HCl
Product: Colorless MAPbCl3 crystals
Description: CH3NH3PbCI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HCl solution. The aqueous solution was cooled from l00°C to room temperature to obtain the colorless crystals.
Method: Temperature-dependent Guinier-Simon photograph
Description: Not specified.
See all entries for this property (7 total)
Crystal system: orthorhombic
| a: | 5.673 Å |
| b: | 5.628 Å |
| c: | 11.182 Å |
| α: | 90° |
| β: | 90° |
| γ: | 90° |
Starting materials: lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HCl
Product: Colorless MAPbCl3 crystals
Description: CH3NH3PbCI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HCl solution. The aqueous solution was cooled from l00°C to room temperature to obtain the colorless crystals.
Method: Temperature-dependent Guinier-Simon photograph
Description: Not specified.
See all entries for this property (24 total)
Crystal system: cubic
| a: | 5.901 (±0.001) Å |
| b: | 5.901 (±0.001) Å |
| c: | 5.901 (±0.001) Å |
| α: | 90° |
| β: | 90° |
| γ: | 90° |
Starting materials: lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HBr
Product: Orange MAPbBr3 crystals
Description: CH3NH3PbBr3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HBr solution. The aqueous solution was cooled from l00°C to room temperature to obtain the orange crystals.
Method: temperature-dependent Guinier-Simon photograph
Description: No experimental details reported. Refer to Page 6374 Table I.
See all entries for this property (24 total)
Crystal system: tetragonal
| a: | 8.322 (±0.002) Å |
| b: | 8.322 (±0.002) Å |
| c: | 11.832 (±0.007) Å |
| α: | 90° |
| β: | 90° |
| γ: | 90° |
Starting materials: lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HBr
Product: Orange MAPbBr3 crystals
Description: CH3NH3PbBr3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HBr solution. The aqueous solution was cooled from l00°C to room temperature to obtain the orange crystals.
Method: temperature-dependent Guinier-Simon photograph
Description: No experimental details reported. Refer to Page 6374 Table I.
See all entries for this property (24 total)
Crystal system: tetragonal
| a: | 5.894 (±0.002) Å |
| b: | 5.894 (±0.002) Å |
| c: | 5.861 (±0.002) Å |
| α: | 90° |
| β: | 90° |
| γ: | 90° |
Starting materials: lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HBr
Product: Orange MAPbBr3 crystals
Description: CH3NH3PbBr3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HBr solution. The aqueous solution was cooled from l00°C to room temperature to obtain the orange crystals.
Method: temperature-dependent Guinier-Simon photograph
Description: No experimental details reported. Refer to Page 6374 Table I.
See all entries for this property (24 total)
Crystal system: orthorhombic
| a: | 7.979 (±0.001) Å |
| b: | 8.58 (±0.002) Å |
| c: | 11.849 (±0.002) Å |
| α: | 90° |
| β: | 90° |
| γ: | 90° |
Starting materials: lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HBr
Product: Orange MAPbBr3 crystals
Description: CH3NH3PbBr3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HBr solution. The aqueous solution was cooled from l00°C to room temperature to obtain the orange crystals.
Method: temperature-dependent Guinier-Simon photograph
Description: No experimental details reported. Refer to Page 6374 Table I.
See all entries for this property (35 total)
Crystal system: cubic
| a: | 6.3285 (±0.0004) Å |
| b: | 6.3285 (±0.0004) Å |
| c: | 6.3285 (±0.0004) Å |
| α: | 90° |
| β: | 90° |
| γ: | 90° |
Starting materials: lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HI
Product: Black MAPbI3 crystals
Description: CH3NH3PbI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in a concentrated HI solution. The aqueous solution was cooled from l00°C to 40°C to obtain the black crystals.
Method: temperature-dependent Guinier-Simon photograph
Description: No experimental details reported. Refer to Page 6374 Table I.
See all entries for this property (35 total)
Crystal system: tetragonal
| a: | 8.855 (±0.006) Å |
| b: | 8.855 (±0.006) Å |
| c: | 12.659 (±0.008) Å |
| α: | 90° |
| β: | 90° |
| γ: | 90° |
Starting materials: lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HI
Product: Black MAPbI3 crystals
Description: CH3NH3PbI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in a concentrated HI solution. The aqueous solution was cooled from l00°C to 40°C to obtain the black crystals.
Method: temperature-dependent Guinier-Simon photograph
Description: No experimental details reported. Refer to Page 6374 Table I.
See all entries for this property (35 total)
Crystal system: orthorhombic
| a: | 8.861 (±0.002) Å |
| b: | 8.581 (±0.002) Å |
| c: | 12.62 (±0.003) Å |
| α: | 90° |
| β: | 90° |
| γ: | 90° |
Starting materials: lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HI
Product: Black MAPbI3 crystals
Description: CH3NH3PbI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in a concentrated HI solution. The aqueous solution was cooled from l00°C to 40°C to obtain the black crystals.
Method: temperature-dependent Guinier-Simon photograph
Description: No experimental details reported. Refer to Page 6374 Table I.
See all entries for this property (5 total)
| Initial crystal system | orthorhombic |
| Final crystal system | tetragonal |
| Initial space group | P222_1 |
| Final space group | P4/mmm |
| Direction | Unknown |
| Phase transition temperature | 172.9 K |
Hysteresis: NIL
| Initial crystal system | tetragonal |
| Final crystal system | cubic |
| Initial space group | P4/mmm |
| Final space group | Pm3m |
| Direction | Unknown |
| Phase transition temperature | 178.8 K |
Hysteresis: NIL
Starting materials: lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HCl
Product: Colorless MAPbCl3 crystals
Description: CH3NH3PbCI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HCl solution. The aqueous solution was cooled from l00°C to room temperature to obtain the colorless crystals.
Method: Temperature-dependent Guinier-Simon photograph
Description: No method specified. Refer to Page 6374 Table I.
See all entries for this property (6 total)
| Initial crystal system | orthorhombic |
| Final crystal system | tetragonal |
| Initial space group | Pna2_1 |
| Final space group | P4/mmm |
| Direction | Unknown |
| Phase transition temperature | 144.5 K |
Hysteresis: NIL
| Initial crystal system | tetragonal |
| Final crystal system | tetragonal |
| Initial space group | P4/mmm |
| Final space group | I4/mcm |
| Direction | Unknown |
| Phase transition temperature | 155.1 K |
Hysteresis: NIL
| Initial crystal system | tetragonal |
| Final crystal system | cubic |
| Initial space group | I4/mcm |
| Final space group | Pm3m |
| Direction | Unknown |
| Phase transition temperature | 236.9 K |
Hysteresis: NIL
Starting materials: lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HBr
Product: Orange MAPbBr3 crystals
Description: CH3NH3PbBr3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HBr solution. The aqueous solution was cooled from l00°C to room temperature to obtain the orange crystals.
Method: Temperature-dependent Guinier-Simon photograph
Description: No method specified. Refer to Page 6374 Table I.
See all entries for this property (20 total)
| Initial crystal system | orthorhombic |
| Final crystal system | tetragonal |
| Initial space group | Pna2_1 |
| Final space group | I4/mcm |
| Direction | Unknown |
| Phase transition temperature | 162.2 K |
Hysteresis: NIL
| Initial crystal system | tetragonal |
| Final crystal system | cubic |
| Initial space group | I4/mcm |
| Final space group | Pm3m |
| Direction | Unknown |
| Phase transition temperature | 327.4 K |
Hysteresis: NIL
Starting materials: lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HI
Product: Black MAPbI3 crystals
Description: CH3NH3PbI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in a concentrated HI solution. The aqueous solution was cooled from l00°C to 40°C to obtain the black crystals.
Method: Temperature-dependent Guinier-Simon photograph
Description: No method specified. Refer to Page 6374 Table I.