Investigation of the self-discharge behaviors of the LiMn2O4 cathode at elevated temperatures: in situ X-ray diffraction analysis and a co-doping mitigation strategy

2019 ◽  
Vol 7 (21) ◽  
pp. 13364-13371 ◽  
Author(s):  
Xiaoyu Tang ◽  
Jie Zhou ◽  
Miao Bai ◽  
Weiwei Wu ◽  
Shaowen Li ◽  
...  
Keyword(s):  
Diffraction Analysis ◽  
Elevated Temperatures ◽  
Lithium Ion ◽  
Mitigation Strategy ◽  
The Self ◽  
X Ray Diffraction ◽  
X Ray ◽  
Co Doping ◽  
Limn2o4 Cathode

The lithium ion re-intercalated into the LiMn2O4 lattice during self-discharge.

Study of Structural Changes in LiNi0.8Co0.1Mn0.1O2 Cathode Material for Lithium-Ion Batteries by X-Ray Diffraction Analysis in the In Situ Mode

2019 ◽  
Vol 92 (7) ◽  
pp. 1013-1019 ◽  
Author(s):  
P. A. Novikov ◽  
A. E. Kim ◽  
K. A. Pushnitsa ◽  
Wang Quingsheng ◽  
M. Yu. Maksimov ◽  
...  
Keyword(s):  
Cathode Material ◽  
Diffraction Analysis ◽  
Lithium Ion Batteries ◽  
Structural Changes ◽  
Lithium Ion ◽  
X Ray Diffraction ◽  
X Ray

Advances in High-Throughput in-Situ X-Ray Diffraction Analysis of Lithium Ion Batteries

2020 ◽  
Vol MA2020-01 (2) ◽  
pp. 328-328
Author(s):  
Scott A Speakman ◽  
Marco Sommariva ◽  
Milen Gateshki ◽  
Fabio Masiello ◽  
Thomas Degen
Keyword(s):  
Diffraction Analysis ◽  
Lithium Ion Batteries ◽  
High Throughput ◽  
Lithium Ion ◽  
X Ray Diffraction ◽  
X Ray

In-Situ X-Ray Diffraction Studies On Lithium- Ion Battery Cathodes

1999 ◽  
Vol 575 ◽  
Author(s):  
Mark A. Rodriguez ◽  
David Ingersoll ◽  
Daniel H. Doughty
Keyword(s):  
Phase Transformation ◽  
Monoclinic Phase ◽  
Hexagonal Lattice ◽  
Lithium Ion ◽  
Hexagonal Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Co Doping ◽  
In Situ Xrd

ABSTRACTLiNi0.8Co0.2O2 and LiNiO2 have been characterized in-situ XRD. LiNi0.8Co0.2O2 does not undergo a monoclinic phase transformation but remains a hexagonal lattice throughout the entire charging cycle. It is hypothesized that Co-doping may help stabilize the hexagonal structure.

A furnace forin situX-ray diffraction studies of insertion processes in electrode materials at elevated temperatures

2001 ◽  
Vol 34 (5) ◽  
pp. 654-657 ◽  
Author(s):  
T. Eriksson ◽  
A. M. Andersson ◽  
Ö. Bergström ◽  
K. Edström ◽  
T. Gustafsson ◽  
...  
Keyword(s):  
Structural Changes ◽  
Electrode Materials ◽  
Elevated Temperatures ◽  
Lithium Ion ◽  
X Ray Diffraction ◽  
X Ray ◽  
Electrochemical Cycling ◽  
Flat Cell ◽  
And Storage

A furnace is described forin situX-ray diffraction studies, in transmission mode, of structural changes in electrode materials for Li-ion (polymer) batteries in the ambient to 300°C temperature range. The method exploits the thin flat-cell geometry of the lithium-polymer battery concept. The flat sample is able to oscillate about a horizontal axis in its own plane in the X-ray beam, to provide better averaging during the diffraction experiment. The use of the device is demonstrated in a study of lithium intercalation in graphite (a commonly used anode material in lithium-ion batteries) during electrochemical cycling and storage at 70°C.

scholarly journals Insertion of Phosphenium Ions into a Bicyclo[1.1.0]Tetraphosphabutane Iron Complex

Molecules ◽  
2021 ◽  
Vol 26 (13) ◽  
pp. 3920
Author(s):  
Martin Weber ◽  
Gábor Balázs ◽  
Alexander V. Virovets ◽  
Eugenia Peresypkina ◽  
Manfred Scheer
Keyword(s):  
Diffraction Analysis ◽  
Room Temperature ◽  
31P Nmr ◽  
Spectroscopic Studies ◽  
Iron Complex ◽  
The Novel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Phosphenium Ions

By reacting [{Cp‴Fe(CO)2}2(µ,η1:1-P4)] (1) with in situ generated phosphenium ions [Ph2P][A] ([A]− = [OTf]− = [O3SCF3]−, [PF6]−), a mixture of two main products of the composition [{Cp‴Fe(CO)2}2(µ,η1:1-P5(C6H5)2)][PF6] (2a and 3a) could be identified by extensive 31P NMR spectroscopic studies at 193 K. Compound 3a was also characterized by X-ray diffraction analysis, showing the rarely observed bicyclo[2.1.0]pentaphosphapentane unit. At room temperature, the novel compound [{Cp‴Fe}(µ,η4:1-P5Ph2){Cp‴(CO)2Fe}][PF6] (4) is formed by decarbonylation. Reacting 1 with in situ generated diphenyl arsenium ions gives short-lived intermediates at 193 K which disproportionate at room temperature into tetraphenyldiarsine and [{Cp‴Fe(CO)2}4(µ4,η1:1:1:1-P8)][OTf]2 (5) containing a tetracyclo[3.3.0.02,7.03,6]octaphosphaoctane ligand.

Synthesis and Luminescence Properties of Chalcopyrite-Type CuAlS2

2006 ◽  
Vol 301 ◽  
pp. 177-180 ◽  
Author(s):  
Yuichiro Kuroki ◽  
Tomoichiro Okamoto ◽  
Masasuke Takata
Keyword(s):  
Diffraction Analysis ◽  
Room Temperature ◽  
Single Phase ◽  
Elevated Temperatures ◽  
Emission Peak ◽  
Maximum Intensity ◽  
X Ray Diffraction ◽  
Ultraviolet Emission ◽  
X Ray ◽  
Copper Aluminum

Copper aluminum disulfide (CuAlS2) powders were synthesized in an evacuated ampoule at elevated temperatures. X-ray diffraction analysis revealed that the powders heated at temperatures higher than 800oC were single-phase CuAlS2. In the cathodoluminescence (CL) spectra measured at room temperature, the powders heated at temperatures higher than 600oC exhibited a visible emission peak at approximately 1.8 eV and a distinct ultraviolet emission peak at 3.45 eV. The powder heated at 700oC showed the maximum intensity of ultraviolet emission which is considered to be associated with excitons.

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