Research output: Contribution to journal › Article › peer-review
Novel Non-Centrosymmetric NdSr4O(BO3)3 Borate and Nd(Ca1−xSrx)4O(BO3)3 Solid Solutions: Preparation, Crystal Structures, Thermal Expansion and Optical Properties. / Bubnova, Rimma; Yukhno, Valentina; Yurev, Artem; Povolotskiy, Alexey; Krzhizhanovskaya, Maria; Volkov, Sergey; Ugolkov, Valery; Filatov, Stanislav.
In: Crystals, Vol. 13, No. 9, 1395, 19.09.2023.Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - Novel Non-Centrosymmetric NdSr4O(BO3)3 Borate and Nd(Ca1−xSrx)4O(BO3)3 Solid Solutions: Preparation, Crystal Structures, Thermal Expansion and Optical Properties
AU - Bubnova, Rimma
AU - Yukhno, Valentina
AU - Yurev, Artem
AU - Povolotskiy, Alexey
AU - Krzhizhanovskaya, Maria
AU - Volkov, Sergey
AU - Ugolkov, Valery
AU - Filatov, Stanislav
PY - 2023/9/19
Y1 - 2023/9/19
N2 - A novel non-centrosymmetric NdSr4O(BO3)3 borate and solid solutions of Nd(Ca1−xSrx)4O(BO3)3 (x = 0.0, 0.1, 0.2, 0.3, 0.4, 0.5, 0.7, 1.0) were synthesized by solid-state reactions as well as crystallization from a melt. The crystal structures of the Nd(Ca1−xSrx)4O(BO3)3 solid solutions with x = 0.2, 0.5 and 1.0 were determined from single crystal X-ray diffraction data and refined in the monoclinic space group Cm to Robs = 0.028, 0.034 and 0.028, respectively. The thermal expansion of the samples with x = 0, 0.2 and 0.5 was investigated using powder high-temperature X-ray diffraction in the temperature range of 25–1000 °C. A similarity of the thermal and compositional (Ca-Sr substitution) deformations of Nd(Ca1−xSrx)4O(BO3)3 solid solutions is revealed: Heating of Nd(Ca0.5Sr0.5)4O(BO3)3 by 1 °C leads to the same deformations of the crystal structure as increasing the amount of Sr atoms in Nd(Ca0.5Sr0.5)4O(BO3)3 by 0.26 at% Sr. The SHG signal of the series of Nd(Ca1−xSrx)4O(BO3)3 solid solutions has a maximum at approximately x = 0.2.
AB - A novel non-centrosymmetric NdSr4O(BO3)3 borate and solid solutions of Nd(Ca1−xSrx)4O(BO3)3 (x = 0.0, 0.1, 0.2, 0.3, 0.4, 0.5, 0.7, 1.0) were synthesized by solid-state reactions as well as crystallization from a melt. The crystal structures of the Nd(Ca1−xSrx)4O(BO3)3 solid solutions with x = 0.2, 0.5 and 1.0 were determined from single crystal X-ray diffraction data and refined in the monoclinic space group Cm to Robs = 0.028, 0.034 and 0.028, respectively. The thermal expansion of the samples with x = 0, 0.2 and 0.5 was investigated using powder high-temperature X-ray diffraction in the temperature range of 25–1000 °C. A similarity of the thermal and compositional (Ca-Sr substitution) deformations of Nd(Ca1−xSrx)4O(BO3)3 solid solutions is revealed: Heating of Nd(Ca0.5Sr0.5)4O(BO3)3 by 1 °C leads to the same deformations of the crystal structure as increasing the amount of Sr atoms in Nd(Ca0.5Sr0.5)4O(BO3)3 by 0.26 at% Sr. The SHG signal of the series of Nd(Ca1−xSrx)4O(BO3)3 solid solutions has a maximum at approximately x = 0.2.
UR - https://www.mendeley.com/catalogue/2bc849e0-a2bc-3215-8f93-32fb0cce4f6a/
U2 - 10.3390/cryst13091395
DO - 10.3390/cryst13091395
M3 - Article
VL - 13
JO - Crystals
JF - Crystals
SN - 2073-4352
IS - 9
M1 - 1395
ER -
ID: 111863119