The crystal structures of PdBi modifications from in-situ high-temperature single-crystal X-ray diffraction

封面

如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

The transformation of PdBi compound at high temperatures was studied using in-situ high-temperature single-crystal X-ray diffraction. The new data about crystal structure of high temperature PdBi modification is obtained. The structure of PdBi at T = 293, 373, 423 and 473 К, is orthorhombic, space group Cmc21, unit cell parameters: a = 8.7160(3), b = 7.2031(3), c = 10.6631(4) Å, V = 669.45(4) Å3, Z = 16 (293 К). Upon further heating, a phase transition to the high-temperature modification occurs. The structure of PdBi at T = 523 and 573 К was solved in orthorhombic space group Cmcm, a = 3.6162(3), b = 10.6446(8), c = 4.4208(4) Å, V = 170.17(3) Å3, Z = 4 (523 К).

全文:

受限制的访问

作者简介

O. Кarimova

Institute of Geology of Ore Deposits RAS

编辑信件的主要联系方式.
Email: oxana.karimova@gmail.com
俄罗斯联邦, Moscow

A. Zolotarev

St. Petersburg State University

Email: oxana.karimova@gmail.com

Institute of Earth Sciences, St. Petersburg State University

俄罗斯联邦, St. Petersburg

A. Mezhueva

Institute of Geology of Ore Deposits RAS

Email: oxana.karimova@gmail.com
俄罗斯联邦, Moscow

L. Ivanova

Institute of Geology of Ore Deposits RAS

Email: oxana.karimova@gmail.com
俄罗斯联邦, Moscow

D. Chareev

Institute of Experimental Mineralogy RAS; Ural Federal University; Dubna State University

Email: oxana.karimova@gmail.com
俄罗斯联邦, Moscow region, Chernogolovka; Ekaterinburg; Moscow region, Dubna

参考

  1. Алексеевский Н.Е. // ЖЭТФ. 1952. Т. 23. С. 484.
  2. Журавлев Н.Н., Жданов Г.С. // ЖЭТФ. 1953. Т. 25. С. 485.
  3. Хейкер Д.М., Жданов Г.С., Журавлев Н.Н. // ЖЭТФ. 1953. Т. 25. № 5. С. 621.
  4. Bahtt Y.C., Schubert K. // J. Less-Comon. Met. 1979. V. 64. P. P17. https://doi.org/10.1016/0022-5088(79)90184-X
  5. Ионов В.М., Томилин Н.А., Прозоровский А.Е. и др. // Кристаллография. 1989. Т. 34. № 4. С. 829.
  6. Okamoto H. // J. Phase Equilibria. 1994. V. 15. № 2. P. 191. https://doi.org/10.1007/BF02646366
  7. Rigaku Oxford Diffraction, CrysAlisPro Software System, version 41.104a. Rigaku Oxford Diffraction, Yarnton, England, 2021.
  8. Sheldrick G.M. // Acta Cryst. A. 2015. V. 71. P. 3. https://doi.org/10.1107/S2053273314026370
  9. Sheldrick G.M. // Acta Cryst. C. 2015. V. 71. P. 3. https://dx.doi.org/10.1107/S2053229614024218
  10. Farrugia L.J. // J. Appl. Cryst. 1999. V. 32. P. 837. https://doi.org/10.1107/S0021889899006020
  11. Pennington W.T. // J. Appl. Cryst. 1999. V. 32. P. 1028. https://doi.org/10.1107/S0021889899011486
  12. Cambridge Crystallographic Data Centre (CCDC). Inorganic Crystal Structure Data Base – ICSD. https://www.ccdc.cam.ac.uk/, http://www.fizkarlsruhe.de
  13. Бюргер М.Дж. // Кристаллография. 1971. Т. 16. С. 1084.
  14. Филатов С.К., Пауфлер П. // Зап. Рос. минерал. о-ва. 2019. Т. 148. № 5. С. 1.

补充文件

附件文件
动作
1. JATS XML
2. Fig. 1. SEM image of a PdBi crystal obtained in the backscattered electron detection mode.

下载 (128KB)
3. Fig. 2. Coordination polyhedra of palladium in the structure of the β-modification of PdBi.

下载 (412KB)
4. Fig. 3. Projection of the crystal structure of β-PdBi onto the plane: a – (101), b – (011).

下载 (349KB)
5. Fig. 4. Coordination polyhedron of palladium in the structure of the γ-modification of PdBi.

下载 (212KB)
6. Fig. 5. Projection of the crystal structure of γ-PdBi onto the plane: a – (101), b – (011).

下载 (136KB)
7. Fig. 6. Schematic representation of chains of palladium atoms in the structure of the PdBi compound at different temperatures, changes in the lengths of Pd–Pd bonds and the angles between them in the process of converting β-PdBi (293 and 473 K) into γ-PdBi (573 K).

下载 (134KB)

版权所有 © Russian Academy of Sciences, 2025