2005
DOI: 10.1016/j.elspec.2005.01.129
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High-resolution photoemission study of Nd1−xSrxMnO3

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Cited by 6 publications
(6 citation statements)
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“…Whereas the Auger contributions are mainly seen in the range of 3-4 eV and 8-9 eV with SB069-3 linear energy shifts with hν, the spectral weight near E F is confirmed to be derived from the Mn 3d components. The sharp peak at 2.0 eV originates from the Mn 3d t 2g states reflecting the localized character, and the hump structure from E F to 1.5 eV is due to the Mn 3d e g states [13]. Figure 2(b) shows the enlarged view of the Mn 3d e g states near E F excited at E for x = 0.38 and 0.40 samples in the metallic phase.…”
Section: Resultsmentioning
confidence: 99%
“…Whereas the Auger contributions are mainly seen in the range of 3-4 eV and 8-9 eV with SB069-3 linear energy shifts with hν, the spectral weight near E F is confirmed to be derived from the Mn 3d components. The sharp peak at 2.0 eV originates from the Mn 3d t 2g states reflecting the localized character, and the hump structure from E F to 1.5 eV is due to the Mn 3d e g states [13]. Figure 2(b) shows the enlarged view of the Mn 3d e g states near E F excited at E for x = 0.38 and 0.40 samples in the metallic phase.…”
Section: Resultsmentioning
confidence: 99%
“…However, the occurrence of dynamic phase segregation within the FM phase has been proposed for NSMO47 based on Mn 2p resonance photoemission results 18 . A phase separation model in which AFM droplets lie in a conducting FM host was also proposed for Nd 0.55 Sr 0.45 MnO 3 19,20 , a sample with Sr content and macroscopic properties that are similar to NSMO47.…”
Section: Resultsmentioning
confidence: 99%
“…In Fig. 2(a), the peak at about 2.0 eV originates from the Mn 3d t 2g state and the spectral weight from the Fermi level ðE F Þ to 1.5 eV is derived from the Mn 3d e g state [4][5][6]. The temperature dependence of the Mn 3d spectra near E F is shown in Fig.…”
Section: Methodsmentioning
confidence: 99%
“…The sample surface was obtained by in situ fracturing near room temperature. A possible Auger contribution is clarified to be negligible at hn ¼ 643 eV within the energy region from E F to $3 eV [3,4]. The position of E F was calibrated by the Fermi edge of an evaporated Au film in electrical contact with manganese crystals.…”
Section: Methodsmentioning
confidence: 99%