An all-solid-state battery, wherein on a first side surface of an all-solid-state battery laminate, a first electrode current collector layer includes a first electrode current collector protruding part, which protrudes in a surface direction, and a second electrode current collector layer includes a second electrode current collector protruding part, which protrudes in a surface direction, a surface direction area of a second electrode-solid electrolyte laminate is larger than a surface direction area of a first electrode laminate, the first electrode laminate is laminated on the inside of the second electrode-solid electrolyte laminate when viewed from the lamination direction, and on the first side surface, an edge of the second electrode-solid electrolyte laminate in the surface direction is at least partially covered with a resin layer so that the first electrode current collector protruding part does not directly contact the edge in the surface direction of the second electrode-solid electrolyte laminate.

An electropositive metal electrode coated by an ion-selective conformable polymer provides the negative electrode and the solid-state electrolyte for a rechargeable bi-electrolyte displacement battery that further includes a molten salt electrolyte having a melting temperature below 140° C. interposed between the conformable polymer coating and a positive electrode. Suitable electropositive metals include lithium, sodium, magnesium, and aluminum and the molten salt incorporates a soluble salt of the metal of the negative electrode. Positive electrodes may incorporate metals including Fe, Ni, Bi, Pb, Zn, Sn, and Cu, and thanks to the ion-selective conformable solid-state electrolyte the molten salt is able to incorporate a soluble salt of the metal of the positive electrode. The conformable polymer-coated electropositive metal electrode may be manufactured by a process involving electroplating electropositive metal through a conformable polymer-coated conductive substrate. The conformable polymer-coated conductive substrate may be prepared by coating the conductive substrate in a conformable polymer solution followed by evaporating the solvent. Alternatively, an electropositive metal electrode may be coated directly with the conformable polymer.

A lithium (Li) secondary battery having a Li buffer layer compressed between a Li metal anode and an electrolyte of the battery cell and a porous structure positioned between the Li metal anode and a current collector of the battery cell. The Li buffer layer is effective in preventing uncontrollable dendrite growth. The porous structure layer is effective in guiding the location of the Li deposition, thereby reducing the volume changes of the Li anode during the charge and discharge cycles of the lithium secondary battery.

Improved electrolytes for lithium-based cells can include a dual salt combination of lithium hexafluorophosphate and lithium bis(fluorosulfonyl)imide or lithium bis(trifluoro-methanesulfonyl)imide, and a solvent that includes dimethyl carbonate, ethylmethyl carbonate and 5 to 25 volume percent of fluoroethylene carbonate. The improved electrolytes can include additives triethyl phosphate, ethoxy(pentafluoro)cyclotriphosphazene, 1,3-propane sultone, or mixtures thereof, and have small limited amounts of additional cosolvents and/or lithium-free organic additives. The improved electrolytes can be used to prepare lithium-based cells with silicon-based active materials as negative electrodes and nickel rich lithium metal oxides as positive electrodes. The lithium-based cells can achieve high energy, high power, fast charge and long cycle life along with good thermal stability.

Improved electrolytes for lithium-based cells can include a dual salt combination of lithium hexafluorophosphate and lithium bis(fluorosulfonyl)imide or lithium bis(trifluoro-methanesulfonyl)imide, and a solvent that includes dimethyl carbonate, ethylmethyl carbonate and 5 to 25 volume percent of fluoroethylene carbonate. The improved electrolytes can include additives triethyl phosphate, ethoxy(pentafluoro)cyclotriphosphazene, 1,3-propane sultone, or mixtures thereof, and have small limited amounts of additional cosolvents and/or lithium-free organic additives. The improved electrolytes can be used to prepare lithium-based cells with silicon-based active materials as negative electrodes and nickel rich lithium metal oxides as positive electrodes. The lithium-based cells can achieve high energy, high power, fast charge and long cycle life along with good thermal stability.

A method of making anode active material including silicon, elemental sulfur and a polymer material for an electrochemical energy storage device, includes mixing together silicon particles, elemental sulfur, and at least one polymer to form a mixture; coating the mixture onto a copper current collector to form a coated copper current collector; and subjecting the coated copper current collector to a temperature treatment. An electrochemical energy storage device includes the anode active material, cathode and electrolyte.

A method of making anode active material including silicon, elemental sulfur and a polymer material for an electrochemical energy storage device, includes mixing together silicon particles, elemental sulfur, and at least one polymer to form a mixture; coating the mixture onto a copper current collector to form a coated copper current collector; and subjecting the coated copper current collector to a temperature treatment. An electrochemical energy storage device includes the anode active material, cathode and electrolyte.

A lithium ion conductive solid electrolyte contains a lithium ion conductive powder having a garnet-type crystal structure including at least Li, La, Zr, and O, and a lithium ion conductive polymer. The lithium ion conductive solid electrolyte can maintain its shape without use of an additional polymer different from the lithium ion conductive polymer. The lithium ion conductive solid electrolyte exhibits an activation energy of 30 kJ/mol or less at 20° C. to 80° C.

Covalent organic frameworks (COFs) usually crystallize as insoluble powders and their processing for suitable devices has been thought to be limited. Here, it is demonstrated that COFs can be mechanically pressed into shaped objects having anisotropic ordering with preferred orientation between the hk0 and 00/ crystallographic planes. Pellets prepared from bulk COF powders impregnated with LiClO.sub.4 displayed room temperature conductivity up to 0.26 mS cm.sup.−1 and stability up to 10.0 V (vs. Li.sup.+/Li.sup.0). This outcome portends use of COFs as solid-state electrolytes in batteries.

Covalent organic frameworks (COFs) usually crystallize as insoluble powders and their processing for suitable devices has been thought to be limited. Here, it is demonstrated that COFs can be mechanically pressed into shaped objects having anisotropic ordering with preferred orientation between the hk0 and 00/ crystallographic planes. Pellets prepared from bulk COF powders impregnated with LiClO.sub.4 displayed room temperature conductivity up to 0.26 mS cm.sup.−1 and stability up to 10.0 V (vs. Li.sup.+/Li.sup.0). This outcome portends use of COFs as solid-state electrolytes in batteries.