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Chemical approach to neutral–ionic valence instability,quantum phase transition,and relaxor ferroelectricity in organic charge-transfer complexes
Authors:Sachio Horiuchi  Reiji Kumai  Yoichi Okimoto  Yoshinori Tokura
Affiliation:1. Correlated Electron Research Center (CERC), National Institute of Advanced Industrial Science and Technology (AIST), Higashi 1-1-1, Tsukuba, Ibaraki 305-8562, Japan;2. Spin Superstructure Project (SSS), ERATO, JST, c/o AIST, Tsukuba 305-8562, Japan;3. Department of Applied Physics, The University of Tokyo, Tokyo 113-8656, Japan
Abstract:Neutral–ionic (NI) phase transition is a reversible switching of organic charge-transfer complexes between distinct valence states by external stimuli. This phase transformation in the low-dimensional system is demonstrated to provide a variety of novel dielectric, structural, and electronic properties. Importantly, ionization of the electron donor–acceptor pairs is usually accompanied by a ferroelectric or antiferroelectric order of the molecular lattice, leading to huge dielectric response near the transition point. Although these characteristics are potentially useful for future electronic and optical applications, the thermally accessible NI transition (TINIT) is still an extremely rare case. The TINIT compounds including some new materials are overviewed in order to provide convenient guides to their design and experimental identifications. The phase transition and dielectric properties can be closely controlled in various ways depending on chemical and physical modifications of the crystals. Among them, a quantum phase transition and relaxor ferroelectricity, both of which are currently attracting subjects from both scientific and practical perspectives, are highlighted as the first achievements in organic charge-transfer complexes.
Keywords:Neutral&ndash  ionic phase transition   Charge-transfer complex   Ferroelectricity   Relaxor   Quantum phase transition
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