X-RAY ABSORPTION SPECTROSCOPY IN NaCo2O4, LaCoO3andSrCoO3

2002 ◽  
Vol 09 (02) ◽  
pp. 1327-1331 ◽  
Author(s):  
TOMOHIRA MATSUSHITA ◽  
MASAICHIRO MIZUMAKI ◽  
NAOSHI IKEDA ◽  
MAKOTO NAKAZAWA ◽  
AKANE AGUI ◽  
...  

We have performed Co 2p X-ray absorption spectroscopy (XAS) on a mixed valence hexagonal layered system NaCo 2 O 4, which shows large thermopower and metallic conductivity. We also measured XAS for SrCoO 3 and LaCoO 3 as examples of typical Co ionic states. The Co ions of the last two materials are octahedrally surrounded by oxygen atoms. A Co atom in NaCo 2 O 4 also has octahedral coordination with oxygen atoms but it is distorted slightly. The Co ions in SrCoO 3 and LaCoO 3 are in the d5 and d6 configuration respectively. The spectrum of NaCo 2 O 4 resembles that of LaCoO 3 rather than that of SrCoO 3; the Co ions in NaCo 2 O 4 can be regarded as the d6 configuration. Also, we have tried to calculate the XAS spectra by using the charge-transfer multiplet model (CT-M). Although we could not find out the best-fitting parameters, the results suggested the itinerancy of the Co 3d states.

2019 ◽  
Vol 683 ◽  
pp. 53-56 ◽  
Author(s):  
Munetaka Taguchi ◽  
Fumihiko Matsui ◽  
Naoyuki Maejima ◽  
Hirosuke Matsui ◽  
Hiroshi Daimon

2017 ◽  
Vol 19 (8) ◽  
pp. 5715-5720 ◽  
Author(s):  
Alessandro Minguzzi ◽  
Alberto Naldoni ◽  
Ottavio Lugaresi ◽  
Elisabetta Achilli ◽  
Francesco D'Acapito ◽  
...  

1990 ◽  
Vol 210 ◽  
Author(s):  
C. Lévy-Clèment ◽  
C. Mondoloni ◽  
C. Godart ◽  
R. Cortès

AbstractThis paper presents applications of in situ X-ray diffraction and absorption techniques to the study of H+/MnO2 alkaline batteries. The two complementary in situ techniques are described. Investigation of the electrochemical insertion and deinsertion of H+ has been made through its influence on the evolution of the crystallographic structure of γ-MnO2, while investigation of the transfer of e has been undertaken through the variation of the oxidation state of the manganese during the discharging and charging process of a battery. New insights in the understanding of the mechanisms of proton insertion and charge transfer into γ-MnO2 are discussed.


1997 ◽  
Vol 251 (1-2) ◽  
pp. 103-106 ◽  
Author(s):  
C.J. Hatterer ◽  
B. Eustache ◽  
L. Collin ◽  
A. Michalowicz ◽  
J. Moscovici ◽  
...  

2008 ◽  
Vol 10 (38) ◽  
pp. 5882 ◽  
Author(s):  
Sébastien Bonhommeau ◽  
Niko Pontius ◽  
Saioa Cobo ◽  
Lionel Salmon ◽  
Frank M. F. de Groot ◽  
...  

2016 ◽  
Vol 683 ◽  
pp. 012020 ◽  
Author(s):  
Akira Yamada ◽  
Ryuji Higashinaka ◽  
Kengo Fushiya ◽  
Takuya Asano ◽  
Tatsuma D. Matsuda ◽  
...  

2020 ◽  
Author(s):  
Teresa Zahoransky ◽  
Christian Mikutta

<p>Being one of Earth´s most redox-active elements, manganese participates in a great variety of environmental processes and is recognized as a key player controlling carbon turnover and oxidative transformation of organic and inorganic pollutants in soils. Moreover, Mn(III), Mn(IV) or mixed-valence Mn(III/IV) oxides and (oxy)hydroxides are highly effective sorbents for metal pollutants and nutrients in soils. Chemical reactivity, mobility, and bioavailability of Mn depend crucially on its speciation (chemical form). Yet, speciation studies on soil Mn are scarce. Therefore, we employed Mn K-edge (6,539 eV) X-ray absorption spectroscopy (XAS) to determine the oxidation states and local coordination environment (<5 Å) of Mn in oxic bulk soils (Cambisols, Luvisols, Stagnosol) from various field sites in Germany. Our XAS analyses cover 23 soil L, O, A, B, and C horizons exhibiting total Mn concentrations of between 200 and 2,300 mg/kg. For comparison, we also analyze a suite of 31 Mn reference compounds, including Mn carbonate, phosphate, oxides and (oxy)hydroxides, silicates, organic Mn compounds as well as clay and hydroxide minerals with adsorbed Mn(II). X-ray absorption near-edge structure (XANES) spectra are evaluated for the oxidation states of soil Mn using linear combination fit (LCF) analysis. In addition, the average local coordination environment of Mn in the soil samples is assessed by shell-fitting of extended X-ray absorption fine structure (EXAFS) spectra. Based on our XAS results, we will test the following hypotheses: (1) Soil L/O horizons comprise predominantly organically complexed Mn(II) and Mn(III), dominated by the former Mn species; (2) soil A horizons are dominated by Mn(III/IV) in Mn(III/IV)-oxide structures owing to high microbial activity, release of Mn(II) from primary silicates and/or plant residues, and its subsequent (a)biotic oxidation and precipitation as Mn(III/IV) oxides; (3) soil B horizons of different genesis differ in their bulk Mn speciation; Bt horizons of Luvisols are dominated by Mn(II) associated with phyllosilicates, whereas the Stagnosol Bg horizon is dominated by layer-type Mn(III/IV) oxides. In summary, our study will provide first comprehensive data on bulk Mn speciation in three major European soil types. This knowledge is a prerequisite for a better understanding of the biogeochemical Mn cycle in soils.</p>


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