Electropositive metal containing layers for semiconductor applications
US-2015243508-A1 · Aug 27, 2015 · US
US10637058B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10637058-B2 |
| Application number | US-201615735970-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 21, 2016 |
| Priority date | Oct 21, 2015 |
| Publication date | Apr 28, 2020 |
| Grant date | Apr 28, 2020 |
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The present disclosure relates to a novel process for preparing isotropic carbonaceous composite particles with favorable crystallographic, morphological & mechanical properties, wherein relatively fine carbonaceous primary particles are coated with a carbonaceous binder precursor material, agglomerated and finally heat-treated at temperatures of between about 1850 and 3500° C. to convert the binder precursor material to non-graphitic or graphitic carbon, thereby resulting in stable highly isotropic carbonaceous composite materials wherein the primary particles of the aggregate are held together by the carbonized/graphitized binder. The present disclosure also relates to the isotropic carbonaceous composite particles obtainable by the process described herein. The disclosure further relates to uses of said isotropic carbonaceous composite material in various applications, including as active material in negative electrodes in lithium-ion batteries, and in secondary products containing said isotropic carbonaceous composite material.
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The invention claimed is: 1. Carbonaceous composite particles, characterized in that said particles are comprised of a multiplicity of aggregated primary particles, wherein 22% or more of the primary particles have a sphericity of at least 0.8, as determined by dynamic imaging; further wherein said primary particles are held together by a carbonaceous binder material attached to the surface of the primary particles; and the composite particles are graphitic composite particles characterized by an interlayer distance c/2 of 0.337 nm or less. 2. The carbonaceous composite particles according to claim 1 , wherein said composite particles are further characterized by a pressure stability wherein the BET specific surface area (SSA) does not increase by more than 3.5 m2/g, and/or by more than 80% after pressing the composite particles at 15 kN/cm2 for 10 s, compared to the BET SSA before pressing. 3. The carbonaceous composite particles according to claim 1 , wherein said composite particles are further characterized by a mass loss of non-graphitic carbon according to thermogravimetric analysis of less than 5%. 4. The carbonaceous composite particles according to claim 1 , wherein said composite particles are further characterized by having a crystalline surface with a surface crystallinity expressed by an La of >4 nm, as determined by measuring the ID/IG band amplitude ratio via Raman spectroscopy. 5. The carbonaceous composite particles according to claim 1 , characterized by a near-random or random orientation of the primary particles in the aggregated composite particle. 6. The carbonaceous composite particles according to claim 1 , being isotropic in their electrical, mechanical, and/or heat-conductive properties. 7. The carbonaceous composite particles according to claim 1 , wherein the carbonaceous composite particles are further characterized by a ratio of peak areas of [004] and [110] reflections of lower than 10. 8. The carbonaceous composite particles according to claim 1 , wherein the carbonaceous composite particles are further characterized by i) a BET specific surface area (BET SSA) of between 0.3 and 20 m 2 /g; ii) a crystallite size Lc of less than 300 nm; iii) by a xylene density of at least 2.00, or at least 2.10, or at least 2.20 g/cm 3 ; iv) an Lc/La ratio of at least 1, or at least 2 or at least 3; and/or v) a spring-back of between 10 and 90%; and/or vi) the carbonaceous binder material connecting said primary particles being graphitic, or non-graphitic carbon, or both. 9. The carbonaceous composite particles according to claim 1 , wherein the primary particles are selected from carbonaceous materials. 10. The carbonaceous composite particles according to claim 1 , wherein the primary particles are selected from a single material. 11. The carbonaceous composite particles according to claim 1 , wherein the carbonaceous binder material is of only one type for all primary particles in the composite particle. 12. The carbonaceous composite particles according to claim 1 , wherein the carbonaceous binder material attached to the surface of said primary particles is graphitic carbon. 13. The carbonaceous composite particles according to claim 1 , wherein the carbonaceous binder material attached to the surface of said primary particles is non-graphitic carbon. 14. The carbonaceous composite particles according to claim 1 , wherein an average length of a major axis of the primary particles as observed by scanning electron microscopy (SEM) is between 1 and 15 μm. 15. The carbonaceous composite particles according to claim 1 , wherein the carbonaceous binder material is of multiple types for at least a portion of the primary particles in the composite particle. 16. The carbonaceous composite particles according to claim 15 , wherein the multiple carbonaceous binder materials are obtained by different coating methods and/or by employing different carbon precursors. 17. The carbonaceous composite particles according to claim 1 , further characterized by having one or more of: a particle size distribution (PSD) of the composite particles having a D90 value ranging from 5 to 70 μm, and/or a D50 value ranging from 2 to 30 μm, and/or a D10 value ranging from 0.5 to 20 μm; a polycyclic aromatic hydrocarbon (PAH) concentration of less than 200 mg/kg; and a rate capability 2 C/0.2 C of at least 97% when present as an active material in a negative electrode of a Lithium-ion battery. 18. The carbonaceous composite particles according to claim 1 , further comprising an additive selected from the group consisting of carbon black, colloidal graphite, graphene, graphene nanoplatelets, graphene or carbon fibers, fullerenes, nanographite, char, carbon nanotubes (CNT), including single-walled nanotubes (SWNT), multiwalled nanotubes (MWNT), or mixtures of any of the foregoing, metals/metalloids. 19. Carbonaceous composite particles, characterized in that said particles are comprised of a multiplicity of aggregated primary particles, wherein 22% or more of the primary particles have a sphericity of at least 0.8, as determined by dynamic imaging; further wherein said primary particles are held together by a carbonaceous binder material attached to the surface of the primary particles; and the composite particles are non-graphitic composite particles characterized by an interlayer distance c/2 of at least 0.338 nm. 20. Carbonaceous composite particles, characterized in that said particles are comprised of a multiplicity of aggregated primary particles, wherein 22% or more of the primary particles have a sphericity of at least 0.8, as determined by dynamic imaging; further wherein said primary particles are held together by a carbonaceous binder material attached to the surface of the primary particles; and the carbonaceous composite particles are further characterized by a non-graphitic carbon coating on the surface of the composite particles.
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