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On the use of guanidine hydrochloride soft template in the synthesis of Na2/3Ni1/3Mn2/3O2 cathodes for sodium-ion batteries
Several P2-Na2/3Ni1/3Mn2/3O2 layered oxides have been prepared by a modified synthesis procedure using guanidine hydrochloride as a soft template. X-ray diffraction patterns will reveal a decrease of both crystallite size and strain for guanidine hydrochloride treated samples, favoring sodium access...
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Published in: | Journal of alloys and compounds 2019-06, Vol.789, p.1035-1045 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Several P2-Na2/3Ni1/3Mn2/3O2 layered oxides have been prepared by a modified synthesis procedure using guanidine hydrochloride as a soft template. X-ray diffraction patterns will reveal a decrease of both crystallite size and strain for guanidine hydrochloride treated samples, favoring sodium accessibility at the electrode/electrolyte interface. Also, guanidine hydrochloride promotes anisotropic particles for intermediate amounts. This specific morphology may contribute to a partial suppression of the P2-O2 phase transition. Galvanostatic tests at different rates and potential windows will evidence better capacity retention and low charge-discharge hysteresis for NaNMO-2% in close relationship with the low internal resistance values at the electrode-electrolyte interphase and apparent diffusion coefficients determined by impedance spectroscopy. A performing full sodium-ion cell will demonstrate the reliability of this material as an electrode for Na-ion cells.
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•P2-Na2/3Ni1/3Mn2/3O2 was prepared using guanidine hydrochloride as a soft template.•Samples with intermediate guanidine content feature better capacity retention.•Their kinetic improvement is due to low impedances and high diffusion coefficient.•A full cell delivered an energy density of 210 W h kg−1 after discharging at C/20. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2019.03.093 |