Appearance of pentavalent Fe ion as a result of a charge disproportionation in Fe-substituted Li2MnO3. (March 2021)
- Record Type:
- Journal Article
- Title:
- Appearance of pentavalent Fe ion as a result of a charge disproportionation in Fe-substituted Li2MnO3. (March 2021)
- Main Title:
- Appearance of pentavalent Fe ion as a result of a charge disproportionation in Fe-substituted Li2MnO3
- Authors:
- Tabuchi, Mitsuharu
Kobayashi, Yasuhiro - Abstract:
- Abstract: 20% Fe substituted Li2 MnO3 (Li1+ x (Fe0.2 Mn0.8 )1- x O2, 0 < x < 1/3) was prepared using coprecipitation–calcination method. X-ray Rietveld analyses showed that most Fe and Mn ions were on both 4 g and 2 b sites and small amount of them occupy on 2 c and 4 h sites in monoclinic Li2 MnO3 -type structure. Neutron Rietveld analysis revealed that Mn ion was mainly on the 4 g site, whereas Fe ion was on both 4 g and 2 b sites. Temperature dependence of magnetization detected a cusp at 30 K for the sample, originating from its antiferromagnetic nature. The 57 Fe Mössbauer spectrum at 300 K consisted of two symmetric doublets with different isomer shifts. From the isomer shifts, Fe ion existed as 3+ δ and 4+ δ states (0 < δ < 1). Below 200 K, the Fe 4+δ component split to two doublets having two isomer shift values assigned as 4+ and 5+ states. At 3 K, the spectrum consisted of magnetically ordered 3+, 4+, and 5+ irons and paramagnetic 4+ state iron. The magnetically ordered pentavalent and tetravalent Fe ions can be stabilized at a highly distorted octahedral 4 g site, whereas magnetically ordered trivalent and paramagnetic tetravalent Fe ions exist mainly on the less distorted octahedral 2 b site. Highlights: 20% Fe-substituted Li2 MnO3 synthesized by coprecipitation – calcination method. The sample is antiferromagnet below 30 K. Above 250 K, 57 Fe Mössbauer spectrum showed that Fe 3+δ and Fe 4+δ components (0 < δ < 1) were coexisted. Below 200 K, 57 FeAbstract: 20% Fe substituted Li2 MnO3 (Li1+ x (Fe0.2 Mn0.8 )1- x O2, 0 < x < 1/3) was prepared using coprecipitation–calcination method. X-ray Rietveld analyses showed that most Fe and Mn ions were on both 4 g and 2 b sites and small amount of them occupy on 2 c and 4 h sites in monoclinic Li2 MnO3 -type structure. Neutron Rietveld analysis revealed that Mn ion was mainly on the 4 g site, whereas Fe ion was on both 4 g and 2 b sites. Temperature dependence of magnetization detected a cusp at 30 K for the sample, originating from its antiferromagnetic nature. The 57 Fe Mössbauer spectrum at 300 K consisted of two symmetric doublets with different isomer shifts. From the isomer shifts, Fe ion existed as 3+ δ and 4+ δ states (0 < δ < 1). Below 200 K, the Fe 4+δ component split to two doublets having two isomer shift values assigned as 4+ and 5+ states. At 3 K, the spectrum consisted of magnetically ordered 3+, 4+, and 5+ irons and paramagnetic 4+ state iron. The magnetically ordered pentavalent and tetravalent Fe ions can be stabilized at a highly distorted octahedral 4 g site, whereas magnetically ordered trivalent and paramagnetic tetravalent Fe ions exist mainly on the less distorted octahedral 2 b site. Highlights: 20% Fe-substituted Li2 MnO3 synthesized by coprecipitation – calcination method. The sample is antiferromagnet below 30 K. Above 250 K, 57 Fe Mössbauer spectrum showed that Fe 3+δ and Fe 4+δ components (0 < δ < 1) were coexisted. Below 200 K, 57 Fe Mössbauer spectrum represented that the Fe 4+δ component split to Fe 4+ and Fe 5+ components. … (more)
- Is Part Of:
- Journal of physics and chemistry of solids. Volume 150(2021)
- Journal:
- Journal of physics and chemistry of solids
- Issue:
- Volume 150(2021)
- Issue Display:
- Volume 150, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 150
- Issue:
- 2021
- Issue Sort Value:
- 2021-0150-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-03
- Subjects:
- Oxides -- Chemical synthesis -- Mössbauer spectroscopy -- Neutron scattering -- Magnetic properties
Solids -- Periodicals
Solides -- Périodiques
Solids
Periodicals
530.41 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00223697 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jpcs.2020.109862 ↗
- Languages:
- English
- ISSNs:
- 0022-3697
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5036.500000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 15411.xml