Patent classifications
H01M4/38
ELECTRODE FOR LITHIUM SECONDARY BATTERY, METHOD FOR PREPARING SAME, ELECTRODE ASSEMBLY FOR LITHIUM SECONDARY BATTERY COMPRISING SAME, AND LITHIUM SECONDARY BATTERY COMPRISING SAME
The present invention relates to an electrode for a lithium secondary battery, a method for preparing the same, an electrode assembly for a lithium secondary battery comprising the same, and a lithium secondary battery comprising the same, wherein the electrode comprises an electrode active material, an aqueous binder, a compound represented by Formula 1, and a compound represented by Formula 2. Formula 1 and Formula 2 are the same as set forth in the specification. The electrode for a lithium secondary battery improves the physical properties of the aqueous binder in a manner whereby a cross-linking reaction material is combined with the aqueous binder, so that the electrode can improve initial charge/discharge efficiency and the life span of a lithium secondary battery, preferably a lithium sulfur battery, and improve the area capacity of the electrode.
Powder, Electrode and Battery Comprising Such a Powder
Powder comprising particles comprising a matrix material and silicon-based domains dispersed in this matrix material, whereby the matrix material is carbon or a material that can be thermally decomposed to carbon, whereby either part of the silicon-based domains are present in the form of agglomerates of silicon-based domains whereby at least 98% of these agglomerates have a maximum size of 3 μm or less, or the silicon-based domains are not at all agglomerated into agglomerates.
COMPOSITE MATERIALS
A permeable composite material for making an electrode for an electrochemical cell, the composite material comprising: a support defining pores; and alkali metal deposited on the support within a plurality of said pores. An electrode comprising the composite material is also described, as are methods of making the material and cells and assemblies comprising the electrode.
Negative Electrode Active Material for Electric Device and Electric Device Using the Same
A negative electrode active material including a silicon-containing alloy having a predetermined composition is used in an electric device. A ratio value (B/A) of a diffraction peak intensity B of a (001) plane of Sn to a diffraction peak intensity A of a (111) plane of Si is 0.3 or more and 3.7 or less in an X-ray diffraction measurement of the silicon-containing alloy using a CuKα1 ray. Here, the diffraction peak of the (111) plane of Si is present in a range of 2θ=24 to 33° and the diffraction peak of the (001) plane of Sn is present in a range of 2θ=26 to 35°.
Negative Electrode Active Material for Electric Device and Electric Device Using the Same
A negative electrode active material includes a silicon-containing alloy having a composition represented by: Si.sub.xSn.sub.yM.sub.zA.sub.a (A is unavoidable impurities, M is one or more transition metal elements, x, y, z, and a represent values of percent by mass, and 0<x<100, 0<y<100, 0<z<100, and 0≦a <0.5 and x+y+z+a=100). The silicon-containing alloy has a lattice image subjected to Fourier transform processing to obtain a diffraction pattern and a size determined as an average value of maximum five major axis diameters of regions having a periodic array from a Fourier image obtained by subjecting a diffraction ring portion present in a width of from 0.7 to 1.0 when a distance between Si regular tetrahedrons is 1.0 in this diffraction pattern to inverse Fourier transform is 10 nm or less.
SO.SUB.2.-based electrolyte for a rechargeable battery cell, and rechargeable battery cells
This disclosure relates to an SO.sub.2-based electrolyte for a rechargeable battery cell containing at least one conducting salt of the Formula (I) ##STR00001##
wherein M is a metal selected from the group consisting of alkali metals, alkaline earth metals, metals of group 12 of the periodic table of the elements and aluminum; x is an integer from 1 to 3; the substituents R, R.sup.2, R.sup.3 and R.sup.4 are each independently selected from the group consisting of C.sub.1-C.sub.10 alkyl, C.sub.2-C.sub.1 alkenyl, C.sub.2-C.sub.1 alkynyl, C.sub.3-C.sub.10 cycloalkyl, C.sub.6-C.sub.14 aryl, and C.sub.5-C.sub.14 heteroaryl; and Z is aluminum or boron.
ANODE ACTIVE MATERIAL, LITHIUM SECONDARY BATTERY COMPRISING SAME, AND METHOD FOR PREPARING ANODE ACTIVE MATERIAL
The present invention provides an anode active material and a method for preparing the same, wherein the anode active material has a core-shell structure having formula (MOx-Liy)-C (here, M is a metal (or metalloid), x is greater than 0 and less than 1.5, and y is greater than 0 and less than 4) and including a core part containing an alloy of a metal (or metalloid) oxide-Li (MOx-Liy) and a shell part containing a carbon material coated on a surface of the core part, wherein the shell part contains lithium in an amount less than 5 atm % in the surface and the inner portion thereof. The anode active material can provide high capacity, excellent cycle characteristics, excellent volume expansion control capability, and high initial efficiency.
LITHIUM ATTACHED ELECTRODES AND METHOD OF MAKING SAME
A method for fabricating an electrode includes: determining a thickness of an active layer; selecting lithium (Li) foil having a specified thickness; determining widths of one or more Li strips based on an active layer to Li layer weight ratio or volume ratio; laminating the active layer onto a conductive substrate; forming one or more grooves in the active layer exposing a bare surface of the conductive substrate; and pressing the one or more Li strips into the one or more grooves, wherein widths of the one or more grooves are slightly larger than the widths of the Li strips.
Electrolytes for improved performance of cells with high-capacity anodes based on micron-scale moderate volume-changing particles
A metal-ion battery cell is provided that comprises anode and cathode electrodes, a separator, and an electrolyte. The anode electrode may, for example, have a capacity loading in the range of about 2 mAh/cm2 to about 10 mAh/cm2 and comprise anode particles that (i) have an average particle size in the range of about 0.2 microns to about 40 microns, (ii) exhibit a volume expansion in the range of about 8 vol. % to about 180 vol. % during one or more charge-discharge cycles of the battery cell, and (iii) exhibit a specific capacity in the range of about 600 mAh/g to about 2600 mAh/g. The electrolyte may comprise, for example, (i) one or more metal-ion salts and (ii) a solvent composition that comprises one or more low-melting point solvents that each have a melting point below about −70° C. and a boiling point above about +70° C.
Method and system for water based phenolic binders for silicon-dominant anodes
Systems and methods for water based phenolic binders for silicon-dominant anodes may include an electrode coating layer on a current collector, where the electrode coating layer is formed from silicon and a pyrolyzed water-based phenolic binder. The water-based phenolic binder may include phenolic/resol type polymers crosslinked with poly(methyl vinyl ether-alt-maleic anhydride), poly(methyl vinyl ether-alt-maleic acid), and/or Poly(acrylamide-co-diallyldimethylammonium chloride) (PDADAM). The electrode coating layer may further include conductive additives. The current collector may comprise one or more of a copper, tungsten, stainless steel, and nickel foil in electrical contact with the electrode coating layer. The electrode coating layer may include more than 70% silicon. The electrode may be in electrical and physical contact with an electrolyte, where the electrolyte includes a liquid, solid, or gel. The battery electrode may be in a lithium ion battery.