Hybrid electrodes for batteries are disclosed having a protective electrochemically active layer on a metal layer. Other hybrid electrodes include a silicon salt on a metal electrode. The protective layer can be formed directly from the reaction between the metal electrode and a metal salt in a pre-treatment solution and/or from a reaction of the metal salt added in an electrolyte so that the protective layer can be formed in situ during battery formation cycles.

An electrochemical battery cell comprising an anode having a primary anode active material, a cathode, and an ion-conducting electrolyte, wherein the cell has an initial output voltage, Vi, measured at 10% depth of discharge (DoD), selected from a range from 0.3 volts to 0.8 volts, and a final output voltage Vf measured at a DoD no greater than 90%, wherein a voltage variation, (Vi−Vf)/Vi, is no greater than ±10% and the specific capacity between Vi and Vf is no less than 100 mAh/g or 200 mAh/cm.sup.3 based on the cathode active material weight or volume, and wherein the primary anode active material is selected from lithium (Li), sodium (Na), potassium (K), magnesium (Mg), aluminum (Al), zinc (Zn), titanium (Ti), manganese (Mn), iron (Fe), vanadium (V), cobalt (Co), nickel (Ni), a mixture thereof, an alloy thereof, or a combination thereof.

A solid-state battery includes: a first current collector layer having a first current collector tab protruding from one side of a quadrilateral; a first active material layer laminated on the first current collector layer; a second current collector layer having a second current collector tab protruding from one side of a quadrilateral; a second active material layer laminated on the second current collector layer; and a solid electrolyte layer arranged between the first active material layer and the second active material layer and including a polymer electrolyte, wherein, in three sides other than the one side where the first current collector tab is arranged, the solid electrolyte layer is arranged so as to cover end surfaces of the first current collector layer and the first active material layer.

A high-capacity and long-life negative electrode hydrogen storage material of La—Mg—Ni type for secondary rechargeable nickel-metal hydride battery and a method for preparing the same are provided in the present invention. A chemical formula of the negative electrode hydrogen storage material of La—Mg—Ni type is La.sub.1-x-yRe.sub.xMg.sub.y(Ni.sub.1-a-bAl.sub.aM.sub.b).sub.z, wherein Re is at least one of Ce, Pr, Nd, Sm, Y, and M is at least one of Ti, Cr, Mo, Nb, Ga, V, Si, Zn, Sn; 0≤x≤0.10, 0.3≤y≤0.5, 0<a≤0.05, 0≤b≤0.02, 2.3≤z<3.0. The negative electrode hydrogen storage material of La—Mg—Ni type in the present invention has excellent charge-discharge capacity and cycle life. The negative electrode hydrogen storage material of La—Mg—Ni type can be applied in both common secondary rechargeable nickel-metal hydride battery and secondary rechargeable nickel-metal hydride battery with ultra-low self-discharge and long-term storage performance.

A positive electrode active material for lithium secondary batteries includes a lithium composite metal compound containing secondary particles that are aggregates of primary particles which are capable of being doped or dedoped with lithium ions and satisfies all of specific requirements (1) to (4).

There is provided an air battery including a first housings accommodating a base cell including a negative electrode, a positive electrode, and a separator disposed between the negative electrode and the positive electrode, and a second housing containing an electrolyte solution or water, in which the first housing and the negative electrode each have a hole leading to the separator, the second housing has a hole that is capable of being sealed, and the first housing and the second housing are disposed to face the hole of the first housing and the hole of the second housing each other.

Methods and systems for the electrochemical conversion of halogenated compounds are provided. In some embodiments, a method comprises converting a halogenated compound (e.g., fluorinated gas) to relatively non-hazardous products via one or more electrochemical reactions. The electrochemical reaction(s) may occur under relatively mild conditions (e.g., low temperature) and/or without the aid of a catalyst. In some embodiments, the electrochemical reaction may produce a relatively large amount of energy. In some such cases, systems, described herein, may be designed to facilitate the conversion of the halogenated compound (e.g., SF6, NF3) while harnessing (e.g., storing, converting) the energy associated with the electrochemical reaction. System and methods described herein may be used in a wide variety of applications, including waste management (e.g., environmental remediation, greenhouse gas mitigation), energy recovery (e.g., industrial energy recovery), and primary batteries (e.g., metal-gas batteries).

A hydrogen absorbing alloy negative electrode is provided. The hydrogen absorbing alloy negative electrode has a hydrogen absorbing alloy, and an additive including yttrium fluoride. A mass of the yttrium fluoride is 0.1 parts by mass or more and 0.2 parts by mass or less based on a hydrogen absorbing alloy powder of 100 parts by mass.

Various embodiments may relate to an electrode. The electrode may include an electrode core including an electrode active material. The electrode may also include one or more monolayer amorphous films. Each of the one or more monolayer amorphous films may be a continuous layer surrounding the electrode core.

An aluminum foil comprising an aluminum foil substrate that has a porous region, wherein the porous region is formed throughout the entirety of the aluminum foil substrate in the thickness direction thereof.