A discharge energy recovery and formation capacity grading apparatus for a soft-package power battery comprises a rack, a condition-variable charge and discharge power box arranged on the rack, a battery formation capacity-grading clamping movement mechanism for clamping positive and negative electrode lugs of the soft-package power battery, a battery tray for, a movement mechanism control assembly for controlling the movement of the battery formation and capacity grading clamping movement mechanism, a safety protection sensor assembly, and a battery formation capacity-grading control mechanism. The charge and discharge power box, the battery formation capacity-grading clamping movement mechanism, the battery tray, the movement mechanism control assembly, and the safety protection sensor assembly are all in signal connection with the battery formation capacity-grading control mechanism. The power transmission end of the charge and discharge power box is electrically connected with the power transmission end of the battery formation capacity-grading clamping movement mechanism.

A separator for a lithium-sulfur battery and a lithium-sulfur battery including the same are provided. More particularly, a separator for a lithium-sulfur battery including a porous substrate; and a coating layer present on at least one surface of the porous substrate, wherein the coating layer includes a polymer including a main chain, with a functional group having a non-covalent electron pair present in the main chain and a side chain with an aromatic hydrocarbon group present in the side chain.

A separator for a lithium-sulfur battery and a lithium-sulfur battery including the same are provided. More particularly, a separator for a lithium-sulfur battery including a porous substrate; and a coating layer present on at least one surface of the porous substrate, wherein the coating layer includes a polymer including a main chain, with a functional group having a non-covalent electron pair present in the main chain and a side chain with an aromatic hydrocarbon group present in the side chain.

A battery comprising an acidified metal oxide (“AMO”) material, preferably in monodisperse nanoparticulate form 20 nm or less in size, having a pH <7 when suspended in a 5 wt % aqueous solution and a Hammett function H.sub.0 >−12, at least on its surface.

A battery comprising an acidified metal oxide (“AMO”) material, preferably in monodisperse nanoparticulate form 20 nm or less in size, having a pH <7 when suspended in a 5 wt % aqueous solution and a Hammett function H.sub.0 >−12, at least on its surface.

Disclosed are a transition metal precursor for preparation of a lithium transition metal oxide, in which a ratio of tap density of the precursor to average particle diameter D50 of the precursor satisfies the condition represented by Equation 1 below, and a lithium transition metal oxide prepared using the same. $\begin{array}{cc}0<\frac{\mathrm{Tap}\mathrm{density}}{\begin{array}{c}\mathrm{Average}\mathrm{particle}\mathrm{diameter}D50\\ \mathrm{of}\mathrm{transition}\mathrm{of}\mathrm{metal}\mathrm{precursor}\end{array}}<3500\left(g/\mathrm{cc}.Math.\mathrm{cm}\right)& \left(1\right)\end{array}$

Disclosed are a transition metal precursor for preparation of a lithium transition metal oxide, in which a ratio of tap density of the precursor to average particle diameter D50 of the precursor satisfies the condition represented by Equation 1 below, and a lithium transition metal oxide prepared using the same. $\begin{array}{cc}0<\frac{\mathrm{Tap}\mathrm{density}}{\begin{array}{c}\mathrm{Average}\mathrm{particle}\mathrm{diameter}D50\\ \mathrm{of}\mathrm{transition}\mathrm{of}\mathrm{metal}\mathrm{precursor}\end{array}}<3500\left(g/\mathrm{cc}.Math.\mathrm{cm}\right)& \left(1\right)\end{array}$

Provided is a post-treatment method of a lithium secondary battery including: an activation step of charging a heated lithium secondary battery to an activation voltage and maintaining the battery at the voltage, in a state in which the lithium secondary battery including a positive electrode including a nickel-rich (Ni-rich) lithium-transition metal composite oxide having a layered structure containing 0.8 moles or more of Ni based on a total of 1 mole of transition metals as a positive electrode active material; a negative electrode; a separator interposed between the positive electrode and the negative electrode; and an electrolyte solution, which are built in a battery case, is heated, the activation voltage being equal to or higher than a voltage generating phase transition of the lithium-transition metal composite oxide.

Provided is a post-treatment method of a lithium secondary battery including: an activation step of charging a heated lithium secondary battery to an activation voltage and maintaining the battery at the voltage, in a state in which the lithium secondary battery including a positive electrode including a nickel-rich (Ni-rich) lithium-transition metal composite oxide having a layered structure containing 0.8 moles or more of Ni based on a total of 1 mole of transition metals as a positive electrode active material; a negative electrode; a separator interposed between the positive electrode and the negative electrode; and an electrolyte solution, which are built in a battery case, is heated, the activation voltage being equal to or higher than a voltage generating phase transition of the lithium-transition metal composite oxide.

A miniature electrochemical cell having a volume of less than 0.5 cc is described. The cell has a casing of first and second ceramic substrates that are hermetically secured to each other to provide an internal space housing an electrode assembly. First and second conductive pathways extend through the ceramic substrates. The pathways have respective inner surfaces that are conductively connected to the respective anode and cathode current collectors and respective outer surfaces that provide for connection to a load. An electrolyte in the internal space of the housing activates the electrode assembly.