Abstract
As the oldest known magnetic material, magnetite (Fe3O4) has fascinated mankind for millennia. As the first oxide in which a relationship between electrical conductivity and fluctuating/localized electronic order was shown1, magnetite represents a model system for understanding correlated oxides in general. Nevertheless, the exact mechanism of the insulator–metal, or Verwey, transition has long remained inaccessible2,3,4,5,6,7,8. Recently, three-Fe-site lattice distortions called trimerons were identified as the characteristic building blocks of the low-temperature insulating electronically ordered phase9. Here we investigate the Verwey transition with pump–probe X-ray diffraction and optical reflectivity techniques, and show how trimerons become mobile across the insulator–metal transition. We find this to be a two-step process. After an initial 300 fs destruction of individual trimerons, phase separation occurs on a 1.5±0.2 ps timescale to yield residual insulating and metallic regions. This work establishes the speed limit for switching in future oxide electronics10.
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References
Verwey, E. J. W. Electronic conduction of magnetite (Fe3O4) and its transition point at low temperatures. Nature 144, 327–328 (1939).
Nazarenko, E. et al. Resonant X-ray diffraction studies on the charge ordering in magnetite. Phys. Rev. Lett. 97, 056403 (2006).
Lorenzo, J. E. et al. Charge and orbital correlations at and above the Verwey phase transition in magnetite. Phys. Rev. Lett. 101, 226401 (2008).
Garcia, J. et al. Reexamination of the temperature dependences of resonant reflections in highly stoichiometric magnetite. Phys. Rev. Lett. 102, 176405 (2009).
Piekarz, P., Parlinski, K. & Oles, A. M. Origin of the Verwey transition in magnetite: Group theory, electronic structure, and lattice dynamics study. Phys. Rev. B 76, 165124 (2007).
Uzu, H. & Tanaka, A. Complex-orbital order in Fe3O4 and mechanism of the Verwey transition. J. Phys. Soc. Jpn 77, 074711 (2008).
Garcia, J. & Subias, G. The Verwey transition—a new perspective. J. Phys. 16, R145 (2004).
Weng, S-C. et al. Direct observation of charge ordering in magnetite using resonant multiwave X-ray diffraction. Phys. Rev. Lett. 108, 146404 (2012).
Senn, M. S., Wright, J. P. & Attfield, J. P. Charge order and three-site distortions in the Verwey structure of magnetite. Nature 481, 173–176 (2012).
Yang, Z., Ko, C. & Ramanatha, S. Oxide electronics utilizing ultrafast metal-insulator transitions. Annu. Rev. Mater. Res. 41, 337–367 (2011).
Fujii, Y., Shirane, G. & Yamada, Y. Study of the 123-K phase transition of magnetite by critical neutron scattering. Phys. Rev. B 11, 2036–2041 (1975).
Shapiro, S. M., Iizumi, M. & Shirane, G. Neutron scattering study of the diffuse critical scattering associated with the Verwey transition in magnetite. Phys. Rev. B 14, 200–207 (1976).
Weber, F. et al. Signature of checkerboard fluctuations in the phonon spectra of a possible polaronic metal La1.2Sr1.8Mn2O7 . Nature Mater. 8, 798–802 (2009).
Imada, M., Fujimori, A. & Tokura, Y. Metal insulator transitions. Rev. Mod. Phys. 70, 1039–1263 (1998).
Uehara, M., Mori, S., Chen, C. H. & Cheong, S-W. Percolative phase separation underlies colossal magnetoresistance in mixed valent mangatite. Nature 399, 560–563 (1999).
Lai, K. et al. Mesoscopic percolating resistance network in a strained manganite thin film. Science 329, 190–193 (2010).
Massee, F. et al. Bilayer manganites: Polarons on the verge of a metallic breakdown. Nature Phys. 7, 978–982 (2011).
Pontius, N. et al. Time-resolved resonant soft x-ray diffraction with free-electron lasers: Femtosecond dynamics across the Verwey transition in magnetite. Appl. Phys. Lett. 98, 182504 (2011).
Park, S. K., Ishikawa, T. & Tokura, Y. Charge-gap formation upon the Verwey transition in Fe3O4 . Phys. Rev. B 58, 3717–3720 (1998).
Novelli, F. et al. Ultrafast optical spectroscopy of the lowest energy excitations in the Mott insulator compound YVO3: Evidence for Hubbard-type excitons. Phys. Rev. B 86, 165135 (2012).
Emma, P. et al. First lasing and operation of an Ångstrom-wavelength free-electron laser. Nature Photon. 4, 641–647 (2010).
Blasco, J., Garcia, J. & Subias, G. Structural transformation in magnetite below the Verwey transition. Phys. Rev. B 83, 104105 (2011).
Huang, D. J. et al. Charge-orbital ordering and Verwey transition in magnetite measured by resonant soft X-ray scattering. Phys. Rev. Lett. 96, 096401 (2006).
Schlappa, J. et al. Direct observation of t2g orbital ordering in magnetite. Phys. Rev. Lett. 100, 026406 (2008).
Tanaka, A. et al. Symmetry of orbital order in Fe3O4 studied by Fe L2,3 resonant X-ray diffraction. Phys. Rev. Lett. 108, 227203 (2012).
Lee, W. S. et al. Phase fluctuations and the absence of topological defects in a photo-excited charge-ordered nickelate. Nature Commun. 3, 838 (2012).
Samuelson, E. J. & Steinsvoll, O. Low-energy phonons in magnetite. Phys. Status Solidi B 61, 615–620 (1974).
Wu, Y. et al. High frequency scaled graphene transistors on diamond-like carbon. Nature 472, 74–78 (2011).
Heimann, P. et al. Linac Coherent Light Source soft x-ray materials science instrument optical design and monochromator commissioning. Rev. Sci. Instrum. 82, 093104 (2011).
Doering, D. et al. Development of a compact fast CCD camera and resonant soft X-ray scattering endstation for time-resolved pump–probe experiments. Rev. Sci. Instrum. 82, 073303 (2011).
Acknowledgements
Research at Stanford was supported through the Stanford Institute for Materials and Energy Sciences (SIMES) under contract DE-AC02-76SF00515 and the LCLS by the US Department of Energy, Office of Basic Energy Sciences. Portions of this research were carried out on the SXR Instrument at the LCLS, a division of SLAC National Accelerator Laboratory and an Office of Science user facility operated by Stanford University for the US Department of Energy. The SXR Instrument is funded by a consortium whose membership includes the LCLS, Stanford University through the Stanford Institute for Materials Energy Sciences (SIMES), Lawrence Berkeley National Laboratory (LBNL, contract number DE-AC02-05CH11231), University of Hamburg through the BMBF priority programme FSP 301, and the Center for Free Electron Laser Science (CFEL). The stay of M.S.G. at SLAC was made possible by support from FOM/NWO and the Helmholtz Virtual Institute Dynamic Pathways in Multidimensional Landscapes. The Cologne team was supported by the DFG through SFB 608 and by the BMBF (contract 05K10PK2). The University of Hamburg team was supported by the SFB 925 ‘Light induced dynamics and control of correlated quantum systems’. The Elettra-Sincrotrone Trieste and University of Trieste team was supported by European Union Seventh Framework Programme [FP7/2007–2013] under grant agreement number 280555 and by the Italian Ministry of University and Research under grant numbers: FIRB-RBAP045JF2 and FIRB-RBAP06AWK3. D.F., F.N., M.E. and F.P. thank F. Cilento and F. Randi for technical support.
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H.A.D., A.F., C.S-L. and W.W. conceived and planned the experiments. All authors except M.S.G. carried out the experiments. W.F.S., J.J.T., O.K., M.T. and P.K. provided excellent experimental guidance for using the SXR beamline and the LCLS optical laser system. W.S.L., Y.D.C., D.H.L., R.G.M., M.Y. and L.P. provided excellent support for the RSXS endstation. S.d.J. and R.K. performed the data analysis. D.F., F.N., M.E. and F.P. performed the time-resolved optical experiments and interpreted the optical data. S.d.J., R.K., M.S.G., C.S-L. and H.A.D. wrote the manuscript with help and input from all authors.
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de Jong, S., Kukreja, R., Trabant, C. et al. Speed limit of the insulator–metal transition in magnetite. Nature Mater 12, 882–886 (2013). https://doi.org/10.1038/nmat3718
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DOI: https://doi.org/10.1038/nmat3718
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