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Understanding the role of Na-doping on Ni-rich layered oxide LiNi0.5Co0.2Mn0.3O2
- Source :
- Journal of Alloys and Compounds. 689:318-325
- Publication Year :
- 2016
- Publisher :
- Elsevier BV, 2016.
-
Abstract
- Na-doped Ni-rich layered oxide LiNi 0.5 Co 0.2 Mn 0.3 O 2 cathode materials are synthesized via co-precipitation method in this work. The crystal structure, thermal stability as well as electrochemical performance are studied. Results show that when the Na-doping amount is less than and equal to 2%, the samples can exhibit better electrochemical performance than the parent compound. One reason is that the Na doping can reduce the cationic mixing in the compound, as confirmed by X-Ray powder diffraction (XRD). Beside, results from X-ray photoelectron spectroscopy (XPS) and galvanostatic intermittent titration technique (GITT) show that the introduced sodium can also impact the chemical environment of lithium, making the latter become more easily de-intercalated from the bulk material. However, as the Na-doping amount increases, the electrochemical properties of the samples were deteriorated. Furthermore, results from differential scanning calorimetry (DSC) measurement indicate that the added Na + is also beneficial for improving the thermal stability of the layered oxide.
- Subjects :
- Materials science
Mechanical Engineering
Inorganic chemistry
Doping
technology, industry, and agriculture
Metals and Alloys
Oxide
chemistry.chemical_element
02 engineering and technology
010402 general chemistry
021001 nanoscience & nanotechnology
Electrochemistry
01 natural sciences
0104 chemical sciences
chemistry.chemical_compound
Differential scanning calorimetry
chemistry
X-ray photoelectron spectroscopy
Mechanics of Materials
Materials Chemistry
Lithium
Thermal stability
0210 nano-technology
Powder diffraction
Subjects
Details
- ISSN :
- 09258388
- Volume :
- 689
- Database :
- OpenAIRE
- Journal :
- Journal of Alloys and Compounds
- Accession number :
- edsair.doi...........f2b14971be2cc947aa94b69d5b6607c0
- Full Text :
- https://doi.org/10.1016/j.jallcom.2016.07.230