Please use this identifier to cite or link to this item:
|Title:||Key role of Bismuth in the magnetoelastic transitions of Ba3BiIr2O9 and Ba3BiRu2O9 as revealed by chemical doping|
|Publisher:||America Chemical Society|
|Citation:||Blanchard, P. E. R., Huang, Z., Kennedy, B. J., Liu, S., Miiller, W., Reynolds, E., Zhou, Q., Avdeev. M., Zhang, Z., Aitken, J. B., Cowie, B. C. C., Jang, L. Y., Tan T. T., Li. S., & Ling, C. D. (2014). Key Role of Bismuth in the Magnetoelastic Transitions of Ba3BiIr2O9 and Ba3BiRu2O9 As Revealed by Chemical Doping. Inorganic Chemistry, 53(2), 952-960. doi:10.1021/ic4023745|
|Abstract:||The key role played by bismuth in an average intermediate oxidation state in the magnetoelastic spin-gap compounds Ba3BiRu2O9 and Ba3BiIr2O9 has been confirmed by systematically replacing bismuth with La3+ and Ce4+. Through a combination of powder diffraction (neutron and synchrotron), X-ray absorption spectroscopy, and magnetic properties measurements, we show that Ru/Ir cations in Ba3BiRu2O9 and Ba3BiIr2O9 have oxidation states between +4 and +4.5, suggesting that Bi cations exist in an unusual average oxidation state intermediate between the conventional +3 and +5 states (which is confirmed by the Bi L3-edge spectrum of Ba3BiRu2O9). Precise measurements of lattice parameters from synchrotron diffraction are consistent with the presence of intermediate oxidation state bismuth cations throughout the doping ranges. We find that relatively small amounts of doping (∼10 at%) on the bismuth site suppress and then completely eliminate the sharp structural and magnetic transitions observed in pure Ba3BiRu2O9 and Ba3BiIr2O9, strongly suggesting that the unstable electronic state of bismuth plays a critical role in the behavior of these materials. © 2013, American Chemical Society.|
|Gov't Doc #:||6720|
|Appears in Collections:||Journal Articles|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.