There are provided an aqueous electrolyte solution having an extended potential window, in particular, an aqueous electrolyte solution whose potential window is further wider than those exhibited by conventional concentrated aqueous electrolyte solutions, and an aqueous electrolyte solution in which the cycle characteristics can be improved. A non-aqueous electrolyte solution capable of achieving a higher energy density is provided, the non-aqueous electrolyte solution containing easily available and inexpensive materials and having further improved characteristics. One aqueous electrolyte solution of the present embodiment contains a salt of at least one selected from the group consisting of sodium, magnesium, potassium and lithium, and a chaotropic additive. One other non-aqueous electrolyte solution of the present embodiment contains a salt of at least one selected from the group consisting of sodium, magnesium, potassium and lithium, and a chaotropic additive.

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.

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.

A composition includes a first portion including Ni-rich LiNi.sub.xCo.sub.γMn.sub.zO.sub.2, where 0.5<x<1, 0<y<1, 0<z<1; a second portion including Li.sub.αZr.sub.βO.sub.γ, where 0<α<9, 0<β<3, and 1<γ<10 such that the second portion is coated on the first portion, and the first portion is doped with an elemental metal selected from at least one of Zr, Si, Sn, Nb, Ta, Al, and Fe. A method of forming a composition includes mixing a metal precursor with nickel-cobalt-manganese (NCM) precursor to form a first mixture; adding a lithium-based compound to the first mixture to form a second mixture; and calcining the second mixture at a predetermined temperature for a predetermined time to form the composition.

A composition includes a first portion including Ni-rich LiNi.sub.xCo.sub.γMn.sub.zO.sub.2, where 0.5<x<1, 0<y<1, 0<z<1; a second portion including Li.sub.αZr.sub.βO.sub.γ, where 0<α<9, 0<β<3, and 1<γ<10 such that the second portion is coated on the first portion, and the first portion is doped with an elemental metal selected from at least one of Zr, Si, Sn, Nb, Ta, Al, and Fe. A method of forming a composition includes mixing a metal precursor with nickel-cobalt-manganese (NCM) precursor to form a first mixture; adding a lithium-based compound to the first mixture to form a second mixture; and calcining the second mixture at a predetermined temperature for a predetermined time to form the composition.

An electrolytic copper foil includes a raw foil layer having a first surface and a second surface opposite to the first surface. In the X-ray diffraction spectrum of the first surface, a ratio of the diffraction peak intensity I(200) of the (200) crystal face of the first surface relative to the diffraction peak intensity I(111) of the (111) crystal face of the first surface is between 0.5 and 2.0. In the X-ray diffraction spectrum of the second surface, a ratio of the diffraction peak intensity I(200) of the (200) crystal face of the second surface relative to the diffraction peak intensity I(111) of the (111) crystal face of the second surface is also between 0.5 and 2.0. A method for producing the electrolytic copper foil, and a lithium ion secondary battery is also provided.

The present invention relates to a lithium secondary battery including a pre-lithiated carbon-based negative electrode, a positive electrode, a separator, and an inorganic electrolyte represented by the following Formula 1 and a method of preparing the same.

LiMX_n(SO.sub.2)  [Formula 1]

In Formula 1, M is at least one metal selected from an alkali metal, a transition metal, and a post-transition metal, X is a halogen element, and n is an integer of 1 to 4.

The present invention relates to a lithium secondary battery including a pre-lithiated carbon-based negative electrode, a positive electrode, a separator, and an inorganic electrolyte represented by the following Formula 1 and a method of preparing the same.

LiMX_n(SO.sub.2)  [Formula 1]

In Formula 1, M is at least one metal selected from an alkali metal, a transition metal, and a post-transition metal, X is a halogen element, and n is an integer of 1 to 4.

According to one embodiment, a secondary battery (100) including a positive electrode (5), a negative electrode (3), a first electrolyte (9), and a second electrolyte (8). The negative electrode (3) includes a lithium titanium oxide having a degree of proton substitution of 0.01 to 0.2. The first electrolyte (9) includes water and in contact with the positive electrode (5). The second electrolyte (8) includes water and in contact with the negative electrode (3).

According to one embodiment, a secondary battery (100) including a positive electrode (5), a negative electrode (3), a first electrolyte (9), and a second electrolyte (8). The negative electrode (3) includes a lithium titanium oxide having a degree of proton substitution of 0.01 to 0.2. The first electrolyte (9) includes water and in contact with the positive electrode (5). The second electrolyte (8) includes water and in contact with the negative electrode (3).