1991
DOI: 10.1103/physrevb.44.5419
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Soft-x-ray-absorption studies of the location of extra charges induced by substitution in controlled-valence materials

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Cited by 197 publications
(153 citation statements)
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“…This value was consistent with x < 0.1 estimated from the Ti 2p XAS line-shape broadening [ Fig. 3(a)], which is a measure of the content of Ti 3+ component [22]. Since STO:Nb is a paramagnetic metal, we interpret that the valence of Ti is fluctuating between 3+ and 4+ with a time scale longer than that characteristic of a photoemission process (∼10 −16 s) [23], and PES provides a snapshot of this fluctuation to give a double-peaked Ti 2p spectrum.…”
supporting
confidence: 72%
“…This value was consistent with x < 0.1 estimated from the Ti 2p XAS line-shape broadening [ Fig. 3(a)], which is a measure of the content of Ti 3+ component [22]. Since STO:Nb is a paramagnetic metal, we interpret that the valence of Ti is fluctuating between 3+ and 4+ with a time scale longer than that characteristic of a photoemission process (∼10 −16 s) [23], and PES provides a snapshot of this fluctuation to give a double-peaked Ti 2p spectrum.…”
supporting
confidence: 72%
“…On a virgin pad the Ti L-edge spectra of the homogeneous film as well as the growth defect reveal the typical absorption characteristic of a Ti 4+ configuration in STO in good agreement with literature 21,22 (see Fig. 2(b)).…”
Section: © 2013 Author(s) All Article Content Except Where Otherwissupporting
confidence: 71%
“…Generally the observed shifts to lower photon energies indicate a lower valence and therefore the occurrence of Ti 3+ states. [25][26][27][28] The detailed line shape of our results can be compared to literature results of Abbate et al, 22 who presented Ti-XAS spectra for a systematic concentration series La 1-x Sr x TiO 3 with x = 0. . .…”
Section: © 2013 Author(s) All Article Content Except Where Otherwismentioning
confidence: 67%
“…No extra intensity was observed at ∼457 eV for any of these films, which would otherwise appear in the presence of Ti 3+ . 31,32 We thus confirm that virtually all Ti ions in the cobaltitetitanate films maintain the Ti 4+ oxidation state within an octahedral coordination environment, which in turn indicates that oxygen vacancies in the films are confined to the first coordination shell of Co. Given the persistent Ti 4+ O 6 octahedra and the corresponding localization of oxygen vacancies around Co, XAS was performed at the Co L 3,2 edge to probe simultaneously the oxygen coordination environment and oxidation state of the Co ions.…”
Section: -4supporting
confidence: 53%