Initial crystal system | unknown |
Final crystal system | unknown |
Initial space group | unknown |
Final space group | unknown |
Direction | both |
Phase transition temperature | 150.0 K |
Hysteresis: NIL
Initial crystal system | unknown |
Final crystal system | unknown |
Initial space group | unknown |
Final space group | unknown |
Direction | both |
Phase transition temperature | 233.0 K |
Hysteresis: NIL
Starting materials: HBr, CH3NH2, Pb(NO3)2
Product: N-deuterated MAPbBr3 single crystals
Description: Add concentrated HBr to neutralize 20 g of 40% CH3NH2 aqueous solution (D2O-H2O mixture). Add 7.1 g (0.021 mol) of Pb(NO3)2 solution drop-wise under vigorous stirring at 100°C to the concentrated CH3NH3Br solution. Red organic crystals form while dripping in the solution. Cool the solution to room temperature and filter out the crystals. Wash crystals firstly with n-butanol and then with benzene; subsequently dry crystals in vacuum.
Comment: Synthesis references: [1] D. Weber, Z. Naturforsch. 33b, 1443 (1978).
Method: 2H and 14N NMR
Description: 2H and 14N NMR spectra were recorded at 55.4257 and 26.083 MHz, respectively, on a Nicolet 360 NB spectrometer (B0 = 8.48 T). Refer to Page 581.