Photoinduced phase transition in strongly electron-lattice and electron-electron correlated molecular crystals

Tadahiko Ishikawa, Ken Onda, Shin Ya Koshihara

Research output: Contribution to journalReview articlepeer-review

1 Citation (Scopus)

Abstract

Strongly electron-lattice- and electron-electron-correlated molecular crystals, such as charge transfer (CT) complexes, are often sensitive to external stimuli, e.g., photoexcitation, due to the cooperative or competitive correlation of various interactions present in the crystals. These crystals are thus productive targets for studying photoinduced phase transitions (PIPTs). Recent advancements in research on the PIPT of CT complexes, especially Et2Me2Sb[Pd(dmit)2]2 and (EDO-TTF)2PF6, are reviewed in this report. The former exhibits a photoinduced insulator-to-insulator phase transition with clearly assigned spectral change. We demonstrate how to find the dynamics of PIPT using this system. The latter exhibits a photoinduced hidden state as an initial PIPT process. Wide energy ranged time-resolved spectroscopy can probe many kinds of photo-absorption processes, i.e., intra-molecular and inter-molecular electron excitations and intramolecular and electron-molecular vibrations. The photoinduced spectral changes in these photo-absorption processes reveal various aspects of the dynamics of PIPT, including electronic structural changes, lattice structural changes, and molecular deformations. The complexities of the dynamics of the latter system were revealed by our measurements.

Original languageEnglish
Pages (from-to)1067-1083
Number of pages17
JournalCrystals
Volume2
Issue number3
DOIs
Publication statusPublished - Jul 27 2012
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Chemical Engineering(all)
  • Materials Science(all)
  • Condensed Matter Physics
  • Inorganic Chemistry

Fingerprint

Dive into the research topics of 'Photoinduced phase transition in strongly electron-lattice and electron-electron correlated molecular crystals'. Together they form a unique fingerprint.

Cite this