A positive electrode active material precursor for a secondary battery is in the form of a secondary particle in which a plurality of primary particles are aggregated, wherein major axes of the primary particles are arranged in a direction from a center of the secondary particle toward a surface thereof, wherein the primary particle includes crystallines in which a (001) plane is arranged in a direction having an angle of 20° to 160° with respect to a major axis direction of the primary particle. A method of preparing the positive electrode active material precursor is also provided.

The present invention relates to a ceramic, to a process for preparing the ceramic and to the use of the ceramic as a dielectric in a capacitor.

A method for preparing a γ-Ga.sub.2O.sub.3 nanomaterial, comprising a step of treating a mixture comprising a gallium element, water, and an organic solvent with ultrasound. The preparation process and equipment requirements are simple, the cost of materials is low, there are fewer experimental parameters, and experimental conditions are mild, with no additional heat source and/or pressure being applied. The γ-Ga.sub.2O.sub.3 nanomaterial can be prepared, in kilograms or above, quickly at an ambient temperature and pressure.

A prussian blue analog having a core-shell structure, which has a core and a cladding layer that dads the core, wherein

the chemical formula of the core is the following Formula 1,

Na.sub.xP[R(CN).sub.6].sub.δ.zH.sub.2O and the chemical formula of the cladding layer is the following Formula 2, A.sub.yL[M(CN).sub.6].sub.α.wH.sub.2O is described. The prussian blue analog has good storage stability, and thus can greatly reduce the manufacturing cost at the subsequent battery cell level. A method for preparing the prussian blue analog having a core-shell structure, as well as a sodium-ion secondary battery, a battery module, a battery pack and a powered device comprising the same are described.

A platform for sequestering carbon dioxide using a body of water is described. The platform has a vessel for holding solid metal hydroxide and for exposing the solid metal hydroxide to a flow of water to create a solution of a metal hydroxide having a pH level. The solution containing metal hydroxide is released into the body of water, causing a reaction with the carbon dioxide present in the body of water, thereby producing metal carbonate/bicarbonate, thus sequestering the carbon dioxide. A choice of the metal in the metal hydroxide, a rate of the releasing the solution containing the metal hydroxide into the body of water, and a flow rate of the flow of water so that to substantially maintain the solution containing the metal hydroxide at the pH level that is defined as environmentally safe and not changing chemistry of seawater. A corresponding method is also provided.

A novel material and a transistor including the novel material are provided. One embodiment of the present invention is a composite oxide including at least two regions. One of the regions includes In, Zn and an element M1 (the element M1 is one or more of Al, Ga, Si, B, Y, Ti, Fe, Ni, Ge, Zr, Mo, La, Ce, Nd, Hf, Ta, W, Mg, V, Be, and Cu) and the other of the regions includes In, Zn, and an element M2 (the element M2 is one or more of Al, Ga, Si, B, Y, Ti, Fe, Ni, Ge, Zr, Mo, La, Ce, Nd, Hf, Ta, W, Mg, V, Be, and Cu). In an analysis of the composite oxide by energy dispersive X-ray spectroscopy, the detected concentration of the element M1 in a first region is less than the detected concentration of the element M2 in a second region, and a surrounding portion of the first region is unclear in an observed mapping image of the energy dispersive X-ray spectroscopy.

Provided is a method of manufacturing MoS.sub.2 having a 1T crystal structure. The method includes performing phase transition from a 2H crystal structure of MoS.sub.2 to the 1T crystal structure by reacting MoS.sub.2 having the 2H crystal structure with CO gas. The phase transition includes annealing the MoS.sub.2 having the 2H crystal structure in an atmosphere including CO gas.

A sparsely pillared organic-inorganic hybrid compound is provided. The sparsely pillared organic-inorganic hybrid compound includes: two inorganic material layers, each extending in one direction and facing each other; and an organic material layer disposed between the two inorganic material layers, wherein each of the inorganic material layers has a gibbsite structure in which a divalent metal cation is doped to an octahedral site, and the organic material layer includes a plurality of pillar portions, each of which is chemically bound to each of the two inorganic material layers such that the two inorganic material layers are connected to each other.

The present disclosure provides a cobalt-free cathode material of a lithium ion battery, a method for preparing the cobalt-free cathode material, and the lithium ion battery. A general formula of the cobalt-free cathode material is Li.sub.xNi.sub.aMn.sub.bR.sub.cO.sub.2, wherein, 1≤x≤1.15, 0.5≤a≤0.95, 0.02≤b≤0.48, 0<c≤0.05, and R is aluminum or tungsten. Therefore, as the cobalt-free cathode material is free of metal cobalt, the cost of the cathode material can be lowered effectively. Aluminum or tungsten in the cobalt-free cathode material can stabilize a crystal structure of the cathode material better, such that the lithium ion battery has excellent rate capability and cycle performance, and furthermore, good cycling stability of the lithium ion battery can be still maintained under a high-temperature and high-pressure testing condition.

The present invention comprises: an overlithiated layered oxide represented by chemical formula 1 below; and an ion-conductive coating layer on the overlithiated layered oxide represented by chemical formula 1: [chemical formula 1] .sub.rLi.sub.2MnO.sub.3.Math.(1-r)Li.sub.aNi.sub.xCo.sub.yMn.sub.zM1.sub.1−(x+y+z)O.sub.2 (in chemical formula 1, 0<r≤0.6, 0<a≤1, 0≤x≤1, 0≤y<1, 0≤z<1, and 0<x+y+z<1, and M1 is at least one selected from among Na, K, Mg, Al, Fe, Cr, Y, Sn, Ti, B, P, Zr, Ru, Nb, W, Ba, Sr, La, Ga, Mg, Gd, Sm, Ca, Ce, Fe, Al, Ta, Mo, Sc, V, Zn, Cu, In, S, B, Ge, Si, and Bi).