Manufacturing method of positive active material precursor for sodium rechargeable batteries, positive active material precursor for sodium rechargeable batteries made by the same, and manufacturing method of positive active material for sodium rechargeable batteries, positive active material for sodium rechargeable batteries made by the same
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examples 1 to 4
[0045]In a reactor, 4 L of distilled water filled and stirred at 1000 rpm while adding ammonia as the first pH adjusting agent so as to maintain the pH in the reactor at 7 and the internal temperature at 50° C. Into the reactor, a 4 M NaOH solution as the second pH adjusting agent was introduced and the pH in the reactor was adjusted to 10.2 and maintained for 30 minutes.
[0046]As an aqueous solution of transition metal compounds, NiSO4.6H2O, FeSO4.7H2O, and MnSO4.5H2O were mixed together in an equivalent ratio and introduced into the reactor together with NH4OH as the complexing agent, thereby producing a precursor represented by Ni0.25Fe0.25Mn0.5(OH)2 as presented in the following Table 1.
[0047]The precursors of Examples 2 to 4 respectively represented by Ni0.25Fe0.35Mn0.4(OH)2, Ni0.25Fe0.5Mn0.25(OH)2 and Ni0.15Fe0.35Mn0.5(OH)2 were produced in the same manner as in Example 1 except that the mixing ratio of the aqueous solution of transition metal compounds was adjusted in Example ...
experimental example 1
Taking of SEM Image
[0048]The SEM images of the precursors produced in Examples 1 to 4 were taken and the images taken are illustrated in FIGS. 1 to 4.
experimental example 2
Measurement of particle size distribution
[0049]The particle size distribution of the precursors produced in Examples 1 to 4 was measured and the results are illustrated in FIGS. 5 to 8.
[0050]It can be seen that the particle size distribution of the precursor particles produced in Examples of the embodiments of the inventive concept is a monodisperse type from FIGS. 5 to 8.
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