2017
DOI: 10.1134/s1087659617020092
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Electron exchange between dopant iron sites in glass films of arsenic selenide

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Cited by 2 publications
(8 citation statements)
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“…10), and the relative area under the spectrum corresponding to Fe 2+ sites is decreased (Fig. 11) (Marchenko, Luzhkov, Rasnyuk et al 2017). for an iron concentration of (1) 2 and (2) 4 at.%, and (3) of Fe 2+ sites for an iron concentration of 4 at.%; the dashed lines correspond to the temperature dependences of the central shifts of the Mössbauer spectra of the (I) Fe 3+ and (II) Fe 2+ sites, which are determined from the temperature dependences of the squared Doppler shifts in the 57 Fe Mössbauer spectra Fig.…”
Section: Electronic Exchange Between Centres Of Ironmentioning
confidence: 97%
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“…10), and the relative area under the spectrum corresponding to Fe 2+ sites is decreased (Fig. 11) (Marchenko, Luzhkov, Rasnyuk et al 2017). for an iron concentration of (1) 2 and (2) 4 at.%, and (3) of Fe 2+ sites for an iron concentration of 4 at.%; the dashed lines correspond to the temperature dependences of the central shifts of the Mössbauer spectra of the (I) Fe 3+ and (II) Fe 2+ sites, which are determined from the temperature dependences of the squared Doppler shifts in the 57 Fe Mössbauer spectra Fig.…”
Section: Electronic Exchange Between Centres Of Ironmentioning
confidence: 97%
“…It is obvious that when the Fermi level is close to the level of iron, the electron exchange between the two oxidation states of iron (Fe 2+ and Fe 3+ ) is possible, which should give rise to the convergence of the central shift values of the Mössbauer spectra of the Fe 2+ and Fe3+ sites. In the limit of fast electron exchange, when the lifetimes of the Fe 2+ and Fe 3+ states are much shorter than the lifetime of the 57 mFe nuclear isomer (~10 -7 s), the Mössbauer spectrum of the averaged state of iron with the following central shift should be (Marchenko, Luzhkov, Rasnyuk et al 2017):…”
Section: Electronic Exchange Between Centres Of Ironmentioning
confidence: 99%
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