Defect chemical studies on oxygen release from the Li-rich cathode material Li1.2Mn0.6Ni0.2O2−δ

2019 ◽  
Vol 7 (9) ◽  
pp. 5009-5019 ◽  
Author(s):  
Takashi Nakamura ◽  
Hongze Gao ◽  
Kento Ohta ◽  
Yuta Kimura ◽  
Yusuke Tamenori ◽  
...  

Oxygen release from a Li-rich cathode material was quantitatively evaluated and discussed based on defect chemistry and thermodynamics.

RSC Advances ◽  
2016 ◽  
Vol 6 (28) ◽  
pp. 23677-23685 ◽  
Author(s):  
Wuwei Yan ◽  
Yongning Liu ◽  
Shaokun Chong ◽  
Yi-Fang Wu

The initial stepwise charging suppresses oxygen release and restrains the layered to spinel phase transformation.


2013 ◽  
Vol 1 (13) ◽  
pp. 4207 ◽  
Author(s):  
Craig A. J. Fisher ◽  
Navaratnarajah Kuganathan ◽  
M. Saiful Islam

2020 ◽  
Vol 8 (28) ◽  
pp. 13987-13995 ◽  
Author(s):  
Rajesh Dutta ◽  
Avishek Maity ◽  
Anna Marsicano ◽  
Monica Ceretti ◽  
Dmitry Chernyshov ◽  
...  

Complex oxygen ordering evidenced for the oxygen membrane cathode material Pr2NiO4.25 at room temperature with translational periodicities attaining almost 100 Å by single-crystal synchrotron diffraction studies.


Materials ◽  
2019 ◽  
Vol 12 (8) ◽  
pp. 1348 ◽  
Author(s):  
Navaratnarajah Kuganathan ◽  
Alexander Chroneos

In this work, we employ computational modeling techniques to study the defect chemistry, Na ion diffusion paths, and dopant properties in sodium iron phosphate [Na3Fe2(PO4)3] cathode material. The lowest intrinsic defect energy process (0.45 eV/defect) is calculated to be the Na Frenkel, which ensures the formation of Na vacancies required for the vacancy-assisted Na ion diffusion. A small percentage of Na-Fe anti-site defects would be expected in Na3Fe2(PO4)3 at high temperatures. Long-range diffusion of Na is found to be low and its activation energy is calculated to be 0.45 eV. Isovalent dopants Sc, La, Gd, and Y on the Fe site are exoergic, meaning that they can be substituted experimentally and should be examined further. The formation of Na vacancies and Na interstitials in this material can be facilitated by doping with Zr on the Fe site and Si on the P site, respectively.


Author(s):  
J.R. Mcintosh

The mitotic apparatus is a structure of obvious biological and medical interest, but it has proved to be a difficult cellular machine to understand. The chemical composition of the spindle is only slightly elucidated, largely because of the difficulties in preparing useful isolates of the structure. Chemical studies of the mitotic spindle have been reviewed elsewhere (Mcintosh, 1977), and will not be discussed further here. One would think that structural studies on the mitotic apparatus (MA) in situ would be straightforward, but even with this approach there is some disagreement in the results obtained with various methods and by different investigators. In this paper I will review briefly the approaches which have been used in structural studies of the MA, pointing out the strengths and problems of each approach. I will summarize the principal findings of the different methods, and identify what seem to be fruitful avenues for further work.


Author(s):  
K.A. Carson ◽  
C.B. Nemeroff ◽  
M.S. Rone ◽  
J.S. Kizer ◽  
J.S. Hanker

Biochemical, physiological, pharmacological, and more recently enzyme histo- chemical data have indicated that cholinergic circuits exist in the hypothalamus. Ultrastructural correlates of these pathways such as acetylcholinesterase (AchE) positive neurons in the arcuate nucleus (ARC) and stained terminals in the median eminence (ME) have yet to be described. Initial studies in our laboratories utilizing chemical lesioning and microdissection techniques coupled with microchemical and light microscopic enzyme histo- chemical studies suggested the existence of cholinergic neurons in the ARC which project to the ME (1). Furthermore, in adult male rats with Halasz deafferentations (hypothalamic islands composed primarily of the isolated ARC and the ME) choline acetyltransferase (ChAc) activity, a good marker for cholinergic neurons, was not significantly reduced in the ME and was only somewhat reduced in the ARC (2). Treatment of neonatal rats with high doses of monosodium 1-glutamate (MSG) results in a lesion largely restricted to the neurons of the ARC.


Author(s):  
D. J. Barber ◽  
R. G. Evans

Manganese (II) oxide, MnO, in common with CoO, NiO and FeO, possesses the NaCl structure and shows antiferromagnetism below its Neel point, Tn∼ 122 K. However, the defect chemistry of the four oxides is different and the magnetic structures are not identical. The non-stoichiometry in MnO2 small (∼2%) and below the Tn the spins lie in (111) planes. Previous work reported observations of magnetic features in CoO and NiO. The aim of our work was to find explanations for certain resonance results on antiferromagnetic MnO.Foils of single crystal MnO were prepared from shaped discs by dissolution in a mixture of HCl and HNO3. Optical microscopy revealed that the etch-pitted foils contained cruciform-shaped precipitates, often thick and proud of the surface but red-colored when optically transparent (MnO is green). Electron diffraction and probe microanalysis indicated that the precipitates were Mn2O3, in contrast with recent findings of Co3O4 in CoO.


Author(s):  
K.S. Kosik ◽  
L.K. Duffy ◽  
S. Bakalis ◽  
C. Abraham ◽  
D.J. Selkoe

The major structural lesions of the human brain during aging and in Alzheimer disease (AD) are the neurofibrillary tangles (NFT) and the senile (neuritic) plaque. Although these fibrous alterations have been recognized by light microscopists for almost a century, detailed biochemical and morphological analysis of the lesions has been undertaken only recently. Because the intraneuronal deposits in the NFT and the plaque neurites and the extraneuronal amyloid cores of the plaques have a filamentous ultrastructure, the neuronal cytoskeleton has played a prominent role in most pathogenetic hypotheses.The approach of our laboratory toward elucidating the origin of plaques and tangles in AD has been two-fold: the use of analytical protein chemistry to purify and then characterize the pathological fibers comprising the tangles and plaques, and the use of certain monoclonal antibodies to neuronal cytoskeletal proteins that, despite high specificity, cross-react with NFT and thus implicate epitopes of these proteins as constituents of the tangles.


2007 ◽  
Vol 2007 (suppl_26) ◽  
pp. 483-488
Author(s):  
P. S. Whitfield ◽  
I. J. Davidson ◽  
P. W. Stephens ◽  
L. M. D. Cranswick ◽  
I. P. Swainson

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