Positive electrode active material and preparation method thereof, positive electrode plate, secondary battery, battery module, battery pack, and electric apparatus
US-2024429384-A1 · Dec 26, 2024 · US
US9748563B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9748563-B2 |
| Application number | US-201314374032-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 22, 2013 |
| Priority date | Jan 31, 2012 |
| Publication date | Aug 29, 2017 |
| Grant date | Aug 29, 2017 |
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An electrode material of the present invention includes surface-coated Li x A y D z PO 4 particles obtained by coating surfaces of Li x A y D z PO 4 (in which, A represents one or more selected from the group consisting of Co, Mn, Ni, Fe, Cu and Cr, D represents one or more selected from the group consisting of Mg, Ca, Sr, Ba, Ti, Zn, B, Al, Ga, In, Si, Ge, Sc, Y and rare earth elements, 0<x≦2, 0<y≦1, and 0≦z≦1.5) particles with a carbonaceous coat, and an elution amount of Li is in a range of 200 ppm to 700 ppm and an elution amount of P is in a range of 500 ppm to 2000 ppm when the surface-coated Li x A y D z PO 4 particles are immersed in a sulfuric acid solution having a hydrogen-ion exponent of 4 for 24 hours.
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We claim: 1. A manufacturing method for an electrode material, wherein any one of surface-coated Li x A y D z PO 4 particles obtained by coating surfaces of Li x A y D z PO 4 particles with a carbonaceous coat, wherein A represents one or more selected from the group consisting of Co, Mn, Ni, Fe, Cu and Cr, D represents one or more selected from the group consisting of Mg, Ca, Sr, Ba, Ti, Zn, B, Al, Ga, In, Si, Ge, Sc, Y and rare earth elements, 0<x≦2, 0<y≦1, and 0≦z≦1.5, and agglomerated particles obtained by agglomerating a plurality of the surface-coated Li x A y D z PO 4 particles are thermally treated in a non-oxidizing atmosphere at a temperature in a range of 40° C. to 500° C. over 0.1 hours to 1000 hours, wherein an elution amount of Li is in a range of 200 ppm to 700 ppm and an elution amount of P is in a range of 500 ppm to 2000 ppm when the surface-coated Li x A y D z PO 4 particles are immersed in a sulfuric acid solution having a hydrogen-ion exponent of 4 for 24 hours. 2. A manufacturing method for an electrode plate, wherein a positive electrode material layer containing any one of surface-coated Li x A y D z PO 4 particles obtained by coating surfaces of Li x A y D z PO 4 particles with a carbonaceous coat wherein A represents one or more selected from the group consisting of Co, Mn, Ni, Fe, Cu and Cr, D represents one or more selected from the group consisting of Mg, Ca, Sr, Ba, Ti, Zn, B, Al, Ga, In, Si, Ge, Sc, Y and rare earth elements, 0<x≦2, 0<y≦1, and 0≦z≦1.5, and agglomerated particles obtained by agglomerating a plurality of the surface-coated Li x A y D z PO 4 particles is formed on a collector, and then an electrode plate having the positive electrode material layer formed on the collector is thermally treated in a non-oxidizing atmosphere at a temperature in a range of 40° C. to 500° C. over 0.1 hours to 1000 hours, wherein an elution amount of Li is in a range of 200 ppm to 700 ppm and an elution amount of P is in a range of 500 ppm to 2000 ppm when the surface-coated Li x A y D z PO 4 particles are immersed in a sulfuric acid solution having a hydrogen-ion exponent of 4 for 24 hours. 3. A manufacturing method for an electrode material comprising: stirring surface-coated Li x A y D z PO 4 particles, wherein A represents one or more selected from the group consisting of Co, Mn, Ni, Fe, Cu and Cr, D represents one or more selected from the group consisting of Mg, Ca, Sr, Ba, Ti, Zn, B, Al, Ga, In, Si, Ge, Sc, Y and rare earth elements, 0<x≦2, 0<y≦1, and 0≦z≦1.5, with a carbonaceous coat in a sulfuric acid solution having a mass that is 10 times the mass of the particles and a pH of 4 at 25° C.; immersing the surface-coated Li x A y D z PO 4 particles at 25° C. for 24 hours; and measuring the elution amount of Li and the elution amount of P eluted from the surface-coated Li x A y D z PO 4 particles into the sulfuric acid solution by inductively coupled plasma spectrometry after the 24 hours.
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