Ternary hybrid perovskite solid solution single crystals: growth, composition determination and phase stability in highly moist atmosphere

Author(s):  
Kezheng Tao ◽  
Lei Gao ◽  
Qingfeng Yan
RSC Advances ◽  
2018 ◽  
Vol 8 (6) ◽  
pp. 2900-2905 ◽  
Author(s):  
C. Wu ◽  
K. Chen ◽  
D. Y. Guo ◽  
S. L. Wang ◽  
P. G. Li

Cations size induced phase tuning in hybrid perovskite single crystals: interplay of lattice distortion and strain relaxation.


2002 ◽  
Vol 75 (7) ◽  
pp. 327-329 ◽  
Author(s):  
Seisaku OHSHIRO ◽  
Mitsunobu IWASAKI ◽  
Masayoshi HARA ◽  
Seishiro ITO

2001 ◽  
Vol 222 (1-2) ◽  
pp. 194-201 ◽  
Author(s):  
M. Berkowski ◽  
J. Fink-Finowicki ◽  
P. Byszewski ◽  
R. Diduszko ◽  
E. Kowalska ◽  
...  

2018 ◽  
Vol 74 (7) ◽  
pp. 1010-1012 ◽  
Author(s):  
Emil Stoyanov ◽  
Kurt Leinenweber ◽  
Thomas L. Groy ◽  
Abds-Sami Malik

Single crystals of a GeO2–TiO2 solid solution with the corresponding composition Ge0.57Ti0.43O2 (germanium titanium tetraoxide) were obtained by devitrification of germania-titania glass at high pressure and temperature. The new compound crystallizes in the rutile structure type (space group P42/mnm), where Ge and Ti share the same position M (site symmetry m.mm), with occupancy values of 0.57 (3) and 0.43 (3), respectively, and one O-atom position (m.2m). The M site is in a sixfold O-atom coordination and, as in the original TiO2 rutile structure, an elongation of the O—M—O bonds along the c-axis direction of the coordination polyhedron and deviation of the angles from 90° lead to a decrease in the coordination symmetry from octahedral to tetragonal. The Ge and Ti atoms are fully disordered in the structure, which indicates that the rutile structure is surprisingly pliant given the differing sizes of the two cations.


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