Transient photoinduced ‘hidden’ phase in a manganite

The control over phase transitions in complex oxides offers the possibility to control their electronic and structural properties. The discovery of a new route to ultrafast photoswitching of manganites via high-energy ‘hidden’ excited states offers the possibility of phase transitions free from ther...

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Published in:Nature materials Vol. 10; no. 2; pp. 101 - 105
Main Authors: Ichikawa, Hirohiko, Nozawa, Shunsuke, Sato, Tokushi, Tomita, Ayana, Ichiyanagi, Kouhei, Chollet, Matthieu, Guerin, Laurent, Dean, Nicky, Cavalleri, Andrea, Adachi, Shin-ichi, Arima, Taka-hisa, Sawa, Hiroshi, Ogimoto, Yasushi, Nakamura, Masao, Tamaki, Ryo, Miyano, Kenjiro, Koshihara, Shin-ya
Format: Journal Article
Language:English
Published: London Nature Publishing Group UK 01.02.2011
Nature Publishing Group
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ISSN:1476-1122, 1476-4660, 1476-4660
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Abstract The control over phase transitions in complex oxides offers the possibility to control their electronic and structural properties. The discovery of a new route to ultrafast photoswitching of manganites via high-energy ‘hidden’ excited states offers the possibility of phase transitions free from thermal effects. Photoinduced phase transitions are of special interest in condensed matter physics 1 , 2 because they can be used to change complex macroscopic material properties on the ultrafast timescale. Cooperative interactions between microscopic degrees of freedom greatly enhance the number and nature of accessible states, making it possible to switch electronic, magnetic or structural properties in new ways 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 . Photons with high energies, of the order of electron volts, in particular are able to access electronic states that may differ greatly from states produced with stimuli close to equilibrium 10 . In this study we report the photoinduced change in the lattice structure of a charge and orbitally ordered Nd 0.5 Sr 0.5 MnO 3 thin film using picosecond time-resolved X-ray diffraction. The photoinduced state is structurally ordered, homogeneous, metastable and has crystallographic parameters different from any thermodynamically accessible state. A femtosecond time-resolved spectroscopic study shows the formation of an electronic gap in this state. In addition, the threshold-like behaviour and high efficiency in photo-generation yield of this gapped state highlight the important role of cooperative interactions in the formation process. These combined observations point towards a ‘hidden insulating phase’ distinct from that found in the hitherto known phase diagram.
AbstractList The control over phase transitions in complex oxides offers the possibility to control their electronic and structural properties. The discovery of a new route to ultrafast photoswitching of manganites via high-energy ‘hidden’ excited states offers the possibility of phase transitions free from thermal effects. Photoinduced phase transitions are of special interest in condensed matter physics 1 , 2 because they can be used to change complex macroscopic material properties on the ultrafast timescale. Cooperative interactions between microscopic degrees of freedom greatly enhance the number and nature of accessible states, making it possible to switch electronic, magnetic or structural properties in new ways 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 . Photons with high energies, of the order of electron volts, in particular are able to access electronic states that may differ greatly from states produced with stimuli close to equilibrium 10 . In this study we report the photoinduced change in the lattice structure of a charge and orbitally ordered Nd 0.5 Sr 0.5 MnO 3 thin film using picosecond time-resolved X-ray diffraction. The photoinduced state is structurally ordered, homogeneous, metastable and has crystallographic parameters different from any thermodynamically accessible state. A femtosecond time-resolved spectroscopic study shows the formation of an electronic gap in this state. In addition, the threshold-like behaviour and high efficiency in photo-generation yield of this gapped state highlight the important role of cooperative interactions in the formation process. These combined observations point towards a ‘hidden insulating phase’ distinct from that found in the hitherto known phase diagram.
Photoinduced phase transitions are of special interest in condensed matter physics because they can be used to change complex macroscopic material properties on the ultrafast timescale. Cooperative interactions between microscopic degrees of freedom greatly enhance the number and nature of accessible states, making it possible to switch electronic, magnetic or structural properties in new ways. Photons with high energies, of the order of electron volts, in particular are able to access electronic states that may differ greatly from states produced with stimuli close to equilibrium. In this study we report the photoinduced change in the lattice structure of a charge and orbitally ordered Nd(0.5)Sr(0.5)MnO(3) thin film using picosecond time-resolved X-ray diffraction. The photoinduced state is structurally ordered, homogeneous, metastable and has crystallographic parameters different from any thermodynamically accessible state. A femtosecond time-resolved spectroscopic study shows the formation of an electronic gap in this state. In addition, the threshold-like behaviour and high efficiency in photo-generation yield of this gapped state highlight the important role of cooperative interactions in the formation process. These combined observations point towards a 'hidden insulating phase' distinct from that found in the hitherto known phase diagram.Photoinduced phase transitions are of special interest in condensed matter physics because they can be used to change complex macroscopic material properties on the ultrafast timescale. Cooperative interactions between microscopic degrees of freedom greatly enhance the number and nature of accessible states, making it possible to switch electronic, magnetic or structural properties in new ways. Photons with high energies, of the order of electron volts, in particular are able to access electronic states that may differ greatly from states produced with stimuli close to equilibrium. In this study we report the photoinduced change in the lattice structure of a charge and orbitally ordered Nd(0.5)Sr(0.5)MnO(3) thin film using picosecond time-resolved X-ray diffraction. The photoinduced state is structurally ordered, homogeneous, metastable and has crystallographic parameters different from any thermodynamically accessible state. A femtosecond time-resolved spectroscopic study shows the formation of an electronic gap in this state. In addition, the threshold-like behaviour and high efficiency in photo-generation yield of this gapped state highlight the important role of cooperative interactions in the formation process. These combined observations point towards a 'hidden insulating phase' distinct from that found in the hitherto known phase diagram.
Photoinduced phase transitions are of special interest in condensed matter physics because they can be used to change complex macroscopic material properties on the ultrafast timescale. Cooperative interactions between microscopic degrees of freedom greatly enhance the number and nature of accessible states, making it possible to switch electronic, magnetic or structural properties in new ways. Photons with high energies, of the order of electron volts, in particular are able to access electronic states that may differ greatly from states produced with stimuli close to equilibrium. In this study we report the photoinduced change in the lattice structure of a charge and orbitally ordered Nd(0.5)Sr(0.5)MnO(3) thin film using picosecond time-resolved X-ray diffraction. The photoinduced state is structurally ordered, homogeneous, metastable and has crystallographic parameters different from any thermodynamically accessible state. A femtosecond time-resolved spectroscopic study shows the formation of an electronic gap in this state. In addition, the threshold-like behaviour and high efficiency in photo-generation yield of this gapped state highlight the important role of cooperative interactions in the formation process. These combined observations point towards a 'hidden insulating phase' distinct from that found in the hitherto known phase diagram.
Photoinduced phase transitions are of special interest in condensed matter physics because they can be used to change complex macroscopic material properties on the ultrafast timescale. Cooperative interactions between microscopic degrees of freedom greatly enhance the number and nature of accessible states, making it possible to switch electronic, magnetic or structural properties in new ways. Photons with high energies, of the order of electron volts, in particular are able to access electronic states that may differ greatly from states produced with stimuli close to equilibrium. In this study we report the photoinduced change in the lattice structure of a charge and orbitally ordered Nd0.5Sr0.5MnO3 thin film using picosecond time-resolved X-ray diffraction. The photoinduced state is structurally ordered, homogeneous, metastable and has crystallographic parameters different from any thermodynamically accessible state. A femtosecond time-resolved spectroscopic study shows the formation of an electronic gap in this state. In addition, the threshold-like behaviour and high efficiency in photo-generation yield of this gapped state highlight the important role of cooperative interactions in the formation process. These combined observations point towards a "hidden insulating phase" distinct from that found in the hitherto known phase diagram. [PUBLICATION ABSTRACT]
Author Chollet, Matthieu
Tamaki, Ryo
Adachi, Shin-ichi
Dean, Nicky
Arima, Taka-hisa
Guerin, Laurent
Sato, Tokushi
Ichiyanagi, Kouhei
Miyano, Kenjiro
Nakamura, Masao
Koshihara, Shin-ya
Sawa, Hiroshi
Tomita, Ayana
Ichikawa, Hirohiko
Nozawa, Shunsuke
Ogimoto, Yasushi
Cavalleri, Andrea
Author_xml – sequence: 1
  givenname: Hirohiko
  surname: Ichikawa
  fullname: Ichikawa, Hirohiko
  organization: JST, ERATO
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  givenname: Shunsuke
  surname: Nozawa
  fullname: Nozawa, Shunsuke
  organization: JST, ERATO, Photon Factory, Institute of Materials Structure Science, High Energy Accelerator Research Organization
– sequence: 3
  givenname: Tokushi
  surname: Sato
  fullname: Sato, Tokushi
  organization: JST, ERATO, Photon Factory, Institute of Materials Structure Science, High Energy Accelerator Research Organization, CREST & Department of Materials Science, JST, Tokyo Institute of Technology
– sequence: 4
  givenname: Ayana
  surname: Tomita
  fullname: Tomita, Ayana
  organization: JST, ERATO, CREST & Department of Materials Science, JST, Tokyo Institute of Technology
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  givenname: Kouhei
  surname: Ichiyanagi
  fullname: Ichiyanagi, Kouhei
  organization: JST, ERATO, Present addresses: #609(7A2) Kiban Bldg., 5-1-5 Kashiwanoha, Kashiwa City, 277-8561, Chiba, Japan (K.I.); X-ray Science Division, Argonne National Lab., Argonne, Illinois 60439, USA (M.C.); European Synchrotron Radiation Facility (ESRF), 6 rue Jules Horowitz, BP220, 38043 Grenoble, France (L.G.); Department of Applied Physics, Nagoya University, Nagoya 464-8603, Japan (H.S.); Cross-Correlated Materials Research Group (CMRG), ASI, RIKEN, Wako, Saitama 351-0198, Japan (M.N.)
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  givenname: Matthieu
  surname: Chollet
  fullname: Chollet, Matthieu
  organization: CREST & Department of Materials Science, JST, Tokyo Institute of Technology, Present addresses: #609(7A2) Kiban Bldg., 5-1-5 Kashiwanoha, Kashiwa City, 277-8561, Chiba, Japan (K.I.); X-ray Science Division, Argonne National Lab., Argonne, Illinois 60439, USA (M.C.); European Synchrotron Radiation Facility (ESRF), 6 rue Jules Horowitz, BP220, 38043 Grenoble, France (L.G.); Department of Applied Physics, Nagoya University, Nagoya 464-8603, Japan (H.S.); Cross-Correlated Materials Research Group (CMRG), ASI, RIKEN, Wako, Saitama 351-0198, Japan (M.N.)
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  givenname: Laurent
  surname: Guerin
  fullname: Guerin, Laurent
  organization: JST, ERATO, Present addresses: #609(7A2) Kiban Bldg., 5-1-5 Kashiwanoha, Kashiwa City, 277-8561, Chiba, Japan (K.I.); X-ray Science Division, Argonne National Lab., Argonne, Illinois 60439, USA (M.C.); European Synchrotron Radiation Facility (ESRF), 6 rue Jules Horowitz, BP220, 38043 Grenoble, France (L.G.); Department of Applied Physics, Nagoya University, Nagoya 464-8603, Japan (H.S.); Cross-Correlated Materials Research Group (CMRG), ASI, RIKEN, Wako, Saitama 351-0198, Japan (M.N.)
– sequence: 8
  givenname: Nicky
  surname: Dean
  fullname: Dean, Nicky
  organization: Department of Physics, University of Oxford, Clarendon Laboratory
– sequence: 9
  givenname: Andrea
  surname: Cavalleri
  fullname: Cavalleri, Andrea
  organization: Department of Physics, University of Oxford, Clarendon Laboratory, Max Planck Research Group for Structural Dynamics, University of Hamburg, Center For Free Electron Laser Science
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  fullname: Arima, Taka-hisa
  organization: Institute of Multidisciplinary Research for Advanced Materials, Tohoku University
– sequence: 12
  givenname: Hiroshi
  surname: Sawa
  fullname: Sawa, Hiroshi
  organization: Photon Factory, Institute of Materials Structure Science, High Energy Accelerator Research Organization, Present addresses: #609(7A2) Kiban Bldg., 5-1-5 Kashiwanoha, Kashiwa City, 277-8561, Chiba, Japan (K.I.); X-ray Science Division, Argonne National Lab., Argonne, Illinois 60439, USA (M.C.); European Synchrotron Radiation Facility (ESRF), 6 rue Jules Horowitz, BP220, 38043 Grenoble, France (L.G.); Department of Applied Physics, Nagoya University, Nagoya 464-8603, Japan (H.S.); Cross-Correlated Materials Research Group (CMRG), ASI, RIKEN, Wako, Saitama 351-0198, Japan (M.N.)
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  givenname: Masao
  surname: Nakamura
  fullname: Nakamura, Masao
  organization: JST, CREST & Research Center for Advanced Science and Technology, University of Tokyo, Present addresses: #609(7A2) Kiban Bldg., 5-1-5 Kashiwanoha, Kashiwa City, 277-8561, Chiba, Japan (K.I.); X-ray Science Division, Argonne National Lab., Argonne, Illinois 60439, USA (M.C.); European Synchrotron Radiation Facility (ESRF), 6 rue Jules Horowitz, BP220, 38043 Grenoble, France (L.G.); Department of Applied Physics, Nagoya University, Nagoya 464-8603, Japan (H.S.); Cross-Correlated Materials Research Group (CMRG), ASI, RIKEN, Wako, Saitama 351-0198, Japan (M.N.)
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  givenname: Ryo
  surname: Tamaki
  fullname: Tamaki, Ryo
  organization: JST, CREST & Research Center for Advanced Science and Technology, University of Tokyo
– sequence: 16
  givenname: Kenjiro
  surname: Miyano
  fullname: Miyano, Kenjiro
  organization: JST, CREST & Research Center for Advanced Science and Technology, University of Tokyo
– sequence: 17
  givenname: Shin-ya
  surname: Koshihara
  fullname: Koshihara, Shin-ya
  email: skoshi@cms.titech.ac.jp
  organization: JST, ERATO, CREST & Department of Materials Science, JST, Tokyo Institute of Technology
BackLink https://www.ncbi.nlm.nih.gov/pubmed/21240287$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright Springer Nature Limited 2010
Copyright Nature Publishing Group Feb 2011
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Snippet The control over phase transitions in complex oxides offers the possibility to control their electronic and structural properties. The discovery of a new route...
Photoinduced phase transitions are of special interest in condensed matter physics because they can be used to change complex macroscopic material properties...
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SubjectTerms Biomaterials
Chemistry and Materials Science
Condensed Matter Physics
Diffraction
Electronics
letter
Materials Science
Nanotechnology
Optical and Electronic Materials
Particle physics
Phase transitions
Physics
Thin films
X-ray diffraction
Title Transient photoinduced ‘hidden’ phase in a manganite
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https://www.ncbi.nlm.nih.gov/pubmed/21240287
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Volume 10
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