Control of bond-strain-induced electronic phase transitions in iron perovskites

Ikuya Yamada, Hidenobu Etani, Kazuki Tsuchida, Shohei Marukawa, Naoaki Hayashi, Takateru Kawakami, Masaichiro Mizumaki, Kenya Ohgushi, Yoshihiro Kusano, Jungeun Kim, Naruki Tsuji, Ryoji Takahashi, Norimasa Nishiyama, Toru Inoue, Tetsuo Irifune, Mikio Takano

研究成果: Article査読

39 被引用数 (Scopus)

抄録

Unusual electronic phase transitions in the A-site ordered perovskites LnCu3Fe4O12 (Ln: trivalent lanthanide ion) are investigated. All LnCu3Fe4O12 compounds are in identical valence states of Ln3+Cu2+3Fe 3.75+4O12 at high temperature. LnCu 3Fe4O12 with larger Ln ions (Ln = La, Pr, Nd, Sm, Eu, Gd, Tb) show an intersite charge transfer transition (3Cu2+ + 4Fe3.75+ → 3Cu3+ + 4Fe3+) in which the transition temperature decreases from 360 to 240 K with decreasing Ln ion size. In contrast, LnCu3Fe4O12 with smaller Ln ions (Ln = Dy, Ho, Er, Tm Yb, Lu) transform into a charge-disproportionated (8Fe 3.75+ → 5Fe3+ + 3Fe5+) and charge-ordered phase below ∼250-260 K. The former series exhibits metal-to-insulator, antiferromagnetic, and isostructural volume expansion transitions simultaneously with intersite charge transfer. The latter shows metal-to-semiconductor, ferrimagnetic, and structural phase transitions simultaneously with charge disproportionation. Bond valence calculation reveals that the metal-oxygen bond strains in these compounds are classified into two types: overbonding or compression stress (underbonding or tensile stress) in the Ln-O (Fe-O) bond is dominant in the former series, while the opposite stresses or bond strains are found in the latter. Intersite charge transfer transition temperatures are strongly dependent upon the global instability indices that represent the structural instability calculated from the bond valence sum, whereas the charge disproportionation occurs at almost identical temperatures, regardless of the magnitude of structural instability. These findings provide a new aspect of the structure-property relationship in transition metal oxides and enable precise control of electronic states by bond strains.

本文言語English
ページ(範囲)13751-13761
ページ数11
ジャーナルInorganic chemistry
52
23
DOI
出版ステータスPublished - 2013 12 2
外部発表はい

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Inorganic Chemistry

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