Thermal stability of charged LiNi0.5Co0.2Mn0.3O2 cathode for Li-ion batteries investigated by synchrotron based in situ X-ray diffraction

2013 ◽  
Vol 562 ◽  
pp. 219-223 ◽  
Author(s):  
Yong-Hun Cho ◽  
Donghyuk Jang ◽  
Jeongbae Yoon ◽  
Hyunchul Kim ◽  
Tae Kyu Ahn ◽  
...  
Author(s):  
Partha P. Paul ◽  
Chuntian Cao ◽  
Vivek Thampy ◽  
Hans-Georg Steinrück ◽  
Tanvir R. Tanim ◽  
...  

ChemSusChem ◽  
2019 ◽  
Vol 12 (10) ◽  
pp. 2240-2250 ◽  
Author(s):  
Lea de Biasi ◽  
Alexander Schiele ◽  
Maria Roca‐Ayats ◽  
Grecia Garcia ◽  
Torsten Brezesinski ◽  
...  

2010 ◽  
Vol 25 (8) ◽  
pp. 1601-1616 ◽  
Author(s):  
Jordi Cabana ◽  
Christopher S. Johnson ◽  
Xiao-Qing Yang ◽  
Kyung-Yoon Chung ◽  
Won-Sub Yoon ◽  
...  

The complexity of layered-spinel yLi2MnO3·(1 – y)Li1+xMn2–xO4 (Li:Mn = 1.2:1; 0 ≤ x ≤ 0.33; y ≥ 0.45) composites synthesized at different temperatures has been investigated by a combination of x-ray diffraction (XRD), x-ray absorption spectroscopy (XAS), and nuclear magnetic resonance (NMR). While the layered component does not change substantially between samples, an evolution of the spinel component from a high to a low lithium excess phase has been traced with temperature by comparing with data for pure Li1+xMn2–xO4. The changes that occur to the structure of the spinel component and to the average oxidation state of the manganese ions within the composite structure as lithium is electrochemically removed in a battery have been monitored using these techniques, in some cases in situ. Our 6Li NMR results constitute the first direct observation of lithium removal from Li2MnO3 and the formation of LiMnO2 upon lithium reinsertion.


2008 ◽  
Vol 53 (21) ◽  
pp. 6064-6069 ◽  
Author(s):  
F.U. Renner ◽  
H. Kageyama ◽  
Z. Siroma ◽  
M. Shikano ◽  
S. Schöder ◽  
...  

2016 ◽  
Vol 72 (a1) ◽  
pp. s418-s418 ◽  
Author(s):  
Claudia Cancellieri ◽  
Frank Moszner ◽  
Mirco Chiodi ◽  
Songhak Yoon ◽  
Daniel Ariosa ◽  
...  

2014 ◽  
Vol 904 ◽  
pp. 7-9
Author(s):  
Xiao Hua Gu ◽  
Xi Wei Zhang ◽  
Bao Yun Xu ◽  
Peng Zeng

In this paper, the diphenyl methane diisocyanate (MDI) was used to modify montmorillonoid (MMT) and got the organic montmorillonite (OMMT), which was used with the monomers of PET by in situ polymerization method to prepare PET/MMT nanocomposition. The OMMT was analyzed by the X ray diffraction (XRD) to test the change of the spacing layer. Dispersion of MMT in the PET/MMT nanocomposites were studied with XRD and SEM and by means of thermogravimetric analyzer (TGA) on the thermal stability of PET/MMT nanocomposites. The results showed that, MDI modified MMT successfully, and the compatibility of MMT and PET was increased .


2014 ◽  
Vol 915-916 ◽  
pp. 780-783
Author(s):  
Hong Wang ◽  
Ming Tian Li ◽  
Yue Lu ◽  
Di Liu

Pyrrole and m-toluidine copolymer (P(PY/MT)) / montmorillonite (MMT) Composites were prepared by in situ chemical polymerization of pyrrole with m-toluidine monomer in the presence of montmorillonite. The structural, morphological and thermal properties of these composites were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and differential scanning calorimetry (DSC). X-ray diffraction result for P(PY/MT)-MMT illuminated the intercalation of P(PY/MT) copolymer between the clay layers. The FT-IR result showed the successful incorporation of montmorillonite clay in the prepared P(PY/MT)/MMT composite. The higher thermal stability of high MMT content rate might be attributed to its higher chain compactness due to the interfacial interaction between the P(PY/MT) and the clay.


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