A method for preparing an ultrathin Li complex includes the steps of preparing an organic transition layer on a substrate in advance, and contacting the substrate having transition layer with molten Li in argon atmosphere with H.sub.2O≤0.1 ppm and O.sub.2≤0.1 ppm. The molten Li spreads rapidly on the surface of the substrate to form a lithium thin layer. The ultrathin Li layer stores lithium on the current collector beforehand. It can be used as a safe lithium anode to inhibit dendrites.

Development of a flexible battery based on periodate/iodate-zinc system is disclosed. H.sub.3PO.sub.4—KCl dual quasi-solid electrolytes separated by an anion-exchange-membrane maintain the desired pH in electrodes and block unwanted ion movements. Poly(acrylic acid) fortifies the electrodes, enhances electrode flexibility, and avoids the free-flow of liquids. The NaMnIO.sub.6 shows a specific capacity of 650 mAg.sup.−1, approximately 81% of its theoretical capacity even when cells are bent. The overall technology is scalable by printing methods.

Multi-phase electrochemical cells and related systems and methods are generally described.

A lithium-sulfur battery includes a casing, a top lid circumferentially welded to the casing, a negative contact surface positioned opposite the top lid, a positive terminal disposed within the casing, welded to the top lid, and configured as a mandrel, a glass insulator circumferentially wound around the mandrel, and a jelly roll including at least an anode and a cathode wound around the mandrel. The jelly roll may also include a top surface not in contact with the top lid, a bottom surface partially in contact with the negative contact surface, and partially in contact with a plurality of non-hollow carbonaceous spherical particles disposed between the bottom surface of the jelly roll and the negative contact surface. At least some of the non-hollow carbonaceous spherical particles may provide one or more electrically-conductive pathways between the bottom surface and the negative contact surface.

The present invention relates to a current collector for a negative electrode, coated with at least one electronically conducting and ionically insulating layer, to the method for producing such a collector, and to batteries containing same.

The present invention relates to a covalent organic framework and a covalent organic framework derived Na-ion battery electrode. The present invention further relates to a method of tuning the electronic energy level of covalent organic framework for crafting high-rate Na-ion battery anode and an inclusion of functional modules capable of enhancing the electron accumulation on Covalent Organic Frameworks (COFs) based anodes.

Battery systems, methods of in-situ grid-scale battery construction, and in-situ battery regeneration methods are disclosed. The battery system features controllable capacity regeneration for grid-scale energy storage. The battery system includes a battery comprising a plurality of cells. Each cell includes a cathode comprising cathode electrode materials disposed on a first current collector, an anode comprising anode electrode materials disposed on a second current collector, a separator or spacer disposed between the cathode and the anode an electrolyte to fill the battery in the spaces between electrodes. The battery system includes a battery system controller, wherein the battery system controller is configured to selectively charge and discharge the battery at a normal cutoff voltage and wherein the battery system controller is further configured to selectively charge and discharge the battery at a capacity regeneration voltage as part of a healing reaction to generate active electrode materials.

3D bundle-shaped multi-walled carbon nanotubes and preparation method, includes the following steps: uniformly mixing bi-component alloy catalyst and transition metal in an inert gas environment in order to obtain a three-component nano-intermetallic alloy catalyst; disposing the intermetallic catalyst on the substrate; allowing hydrogen to flow through the substrate, and heating the substrate to a first temperature, and using the hydrogen to undergo a reduction of the intermetallic catalyst at the first temperature; applying a protective gas and a carbon source gas, heating the substrate to a second temperature, undergoing a reaction at the second temperature to generate the 3D bundle-shaped multi-walled carbon nanotubes, and collecting the 3D bundle-shaped multi-walled carbon nanotubes after annealing; wherein the second temperature is greater than or equal to the first temperature; a working electrode includes conductive drain material, a conductive bonding gent and a plurality of 3D bundle-shaped multi-walled carbon nanotubes.

Disclosed is a method of manufacturing a lithium metal unit cell for sulfide-based all-solid-state batteries and a unit cell manufactured using the same, and more particularly to a method of manufacturing a lithium metal unit cell for sulfide-based all-solid-state batteries wherein pressing is performed using cold isostatic pressing at higher than 100 MPa to lower than 470 MPa irrespective of time or pressing is performed at 470 MPa for 1 minute in order to reduce interface resistance of a sulfide-based all-solid-state battery using a lithium metal as a negative electrode and a unit cell manufactured using the same.

A negative electrode plate includes a three-dimensional framework structure. The three-dimensional framework structure includes fibers and rigid particles. Mohs hardness of the rigid particles is greater than or equal to 2, and an elastic modulus of the rigid particles is greater than or equal to 40 Gpa. The three-dimensional framework structure can mitigate volume expansion of the negative active material during cycling. On the other hand, the rigid particles help to stabilize the three-dimensional framework structure and can serve as a lithium wetting material to induce lithium to deposit inside the three-dimensional framework, thereby reducing the generation of lithium dendrites and improving safety performance and cycle performance of the formed electrochemical device.