A compound strontium fluoroborate, nonlinear optical crystal of strontium fluoroborate, preparation method thereof; the chemical formula of the compound is SrB5O7F3, its molecular weight is 310.67, and it is prepared by solid-state reaction; the chemical formula of the crystal is SrB5O7F3, its molecular weight is 310.67, the crystal is of the orthorhombic series, the space group is Ccm21, and the crystal cell parameters are=10.016(6) Å, b=8.654(6)(4) Å, c=8.103(5) Å, Z=4, and V=702.4(8) Å3. A SrB5O7F3 nonlinear optical crystal has uses in the preparation of a harmonic light output when doubling, tripling, quadrupling, quintupling, or sextupling the frequency of a 1064-nm fundamental-frequency light outputted by a Nd:YAG laser, or the generation of a deep-ultraviolet frequency doubling light output lower than 200 nm, or in the preparation of a frequency multiplier, upper or lower frequency converter, or an optical parametric oscillator.

New formulation for pyrite scale removal from oil and gas wells and a method of pyrite scale removal are disclosed. The chemical formulation is composed of K.sub.2B.sub.4O.sub.7-4H.sub.2O, in a concentration of about 9-20 wt. % of the composition, preferably about 14 wt. % of the composition. The new formulation has the ability to dissolve pyrite without generation of the toxic H.sub.2S. Furthermore, the new formulation is cheaper and has very low corrosion rate compare to 15 wt. % HCl with corrosion inhibitor. The disclose method uses the disclosed new formulation to dissolve iron sulphide scale, performed at about 100-150° C. and about 500-2000 psi.

According to the present invention, there are provided a composite body that enables the formation of a lithium ion conductor that exhibits good lithium ion conductivity by a pressurization treatment without sintering at a high temperature (about 1,000° C.) while using a lithium-containing oxide having excellent safety and stability, as well as a lithium ion conductor, an all-solid state lithium ion secondary battery, an electrode sheet for an all-solid state lithium ion secondary battery, and lithium tetraborate. The composite body according to the embodiment of the present invention contains a lithium compound having a lithium ion conductivity of 1.0×10.sup.−6 S/cm or more at 25° C. and lithium tetraborate that satisfies the following requirement 1.

The requirement 1: In a reduced two-body distribution function G(r) obtained from an X-ray total scattering measurement of the lithium tetraborate, a first peak in which a peak top is located in a range where r is 1.43±0.2 Å and a second peak in which a peak top is located in a range where r is 2.40±0.2 Å are present, G(r) of the peak top of the first peak and G(r) of the peak top of the second peak indicate more than 1.0, and an absolute value of G(r) is less than 1.0 in a range where r is more than 5 Å and 10 Å or less.

The present exemplary embodiments relate to a cathode active material, a manufacturing method thereof, and a lithium secondary battery including the same. A cathode active material according to an exemplary embodiment is a lithium metal oxide particle in the form of a secondary particle including a primary particle, a coating layer including a boron compound is positioned on at least a portion of a surface of the primary particle, and the boron compound includes an amorphous structure.

A lead-based alloy containing alloying additions of bismuth, antimony, arsenic, and tin is used for the production of doped leady oxides, lead-acid battery active materials, lead-acid battery electrodes, and lead-acid batteries.

A fluid composition suitable for chemical mechanical polishing a substrate can in include a multi-valent metal borate, at least one oxidizer, and a solvent. The fluid composition can be essentially free of abrasive particles and may achieve a high material removal rate and excellent surface finish.

A composition suitable for chemical mechanical polishing a substrate can comprise abrasive particles, a multi-valent metal borate, at least one oxidizer and a solvent. The composition can polish a substrate with a high material removal rate and a very smooth surface finish.

A positive electrode active material includes a lithium transition metal oxide represented by Formula 1, and a lithium-containing inorganic compound layer formed on a surface of the lithium transition metal oxide,
Li.sub.1+a(Ni.sub.bCo.sub.cX.sub.dM.sup.1.sub.eM.sup.2.sub.f).sub.1−aO.sub.2  [Formula 1] in Formula 1, X is at least one selected from the group consisting of manganese (Mn) and aluminum (Al), M.sup.1 is at least one selected from the group consisting of sulfur (S), fluorine (F), phosphorus (P), and nitrogen (N), M.sup.2 is at least one selected from the group consisting of zirconium (Zr), boron (B), cobalt (Co), tungsten (W), magnesium (Mg), cerium (Ce), tantalum (Ta), titanium (Ti), strontium (Sr), barium (Ba), hafnium (Hf), F, P, S, lanthanum (La), and yttrium (Y), 0≤a≤0.1, 0.6≤b≤0.99, 0≤c≤0.2, 0≤d≤0.2, 0<e≤0.1, and 0<f≤0.1. A method of preparing the positive electrode active material, a positive electrode and a lithium secondary battery are also provided.

The present invention relates to a positive active material for lithium secondary battery, its manufacturing method, and lithium secondary battery including the same, and it provides that a positive active material for lithium secondary battery, comprising: a core and a coating layer, wherein, the core is lithium metal oxide, the coating layer comprises boron, the boron compound in the coating layer comprises a lithium boron oxide and a boron oxide, the lithium boron oxide is included 70 wt % or more and 99 wt % in the entire coating layer, the lithium boron oxide comprises Li.sub.2B.sub.4O.sub.7, with respect to the lithium boron oxide 100 wt %, the content of Li.sub.2B.sub.4O.sub.7 is 55 wt % or more and 99 wt % or less.

Novel three-dimensional molecular clusters and methods of their synthesis are provided. The three-dimensional molecular clusters may be perfunctionalized polyhedral boranes and carboranes. The three-dimensional clusters may be configured to manipulate the photophysical properties of other materials, including, for example, for use as photooxidants or as components in organic light-emitting diode materials. Methods are also provided for synthesizing and perfunctionalizing such three-dimensional clusters. The three-dimensional clusters may also be configured for use as organomimetic materials.