A method of making CuAg.sub.3PO.sub.4 nanoparticles is provided. The method includes forming a mixture of at least one silver salt, at least one phosphate salt, and at least one copper (II) salt. The method further includes dissolving the mixture in water. The method further includes sonicating the mixture. The method further includes precipitating the CuAg.sub.3PO.sub.4 nanoparticles or nanoparticles. The copper is present in the nanoparticles in an amount of 2 to 23 weight percent (wt. %) based on the total weight of the CuAg.sub.3PO.sub.4. The nanoparticles of the present disclosure find application in treating cervical cancer, and colorectal cancer. The nanoparticles may also be used in photodegrading environmental pollutants.

The present disclosure relates to oxidized carbon nanoparticles, and a method for producing same. The oxidized carbon nanoparticles are nano-sized spherical particles of oxidized carbon have a C/O atomic ratio from X-ray photoelectron spectroscopy (XPS) of 1 to 9, and the largest fraction of oxygen thereof from XPS is observed in a C—O(OH) bind. The oxidized carbon nanoparticles have better physical properties than typical carbon materials such as graphite or carbon black, and the producing process thereof is economical and environmentally-friendly. Further, the oxidized carbon nanoparticles may be applied as a filling material of an organic/inorganic composite, and when applied as such, is environmentally-friendly, economical, exhibits excellent dispersion properties, and may be immediately used without post-processing, such as functionalization.

This disclosure provides a unique approach for the synthesis of non-stoichiometric, mesoporous metal oxides with nano-sized crystalline wall. The as-synthesized mesoporous metal oxide is very active and stable (durability>11 h) electocatalyst in both acidic and alkaline conditions. The intrinsic mesoporous metal oxide serves as an electrocatalyst without the assistant of carbon materials, noble metals, or other materials, which are widely used in previously developed systems. The as-synthesized mesoporous metal oxide has large accessible pores (2-50 nm), which are able to facilitate mass transport and charge transfer. The as-synthesized mesoporous metal oxide requires a low overpotential and is oxygen deficient. Oxygen vacancies and mesoporosity served as key factors for excellent performance.

Cerium oxide nanoparticles (CNPs) have been proven to exhibit antioxidant properties attributed to its surface oxidation states (Ce4+ to Ce3+ and vice versa) mediated at the oxygen vacancies on the surface of CNPs. Different anions in precursor cerium salts were used to prepare CNPs resulting in disclosed CNPs with varying physicochemical properties such as dispersion stability, hydrodynamic size, and the signature surface chemistry. The antioxidant catalytic activity and oxidation potentials of different CNPs have been significantly altered with the change of anions in the precursor salts. For one, CNPs prepared using precursor salts containing NO.sub.3.sup.− and Cl.sup.− ions exhibited increased antioxidant activity than previously thought possible. The change in oxidation potentials of CNPs with the change in concentration of the nitrate and chloride ions indicates the disclosed CNP's have different surface chemistry and antioxidant properties. These compositions and methods of their synthesis are disclosed.

The present invention relates to a method of reducing a metal oxide comprising the steps of preparing a mixture by mixing a metal oxide and a metal hydride (step 1) and reducing the mixture by heat treatment (step 2) and a method of producing a photocatalyst using the same, and The method of reducing a metal oxide of the present invention can easily reduce such metal oxides as TiO.sub.2, ZrO.sub.2, V.sub.2O.sub.3, and Fe.sub.2O.sub.3.

A ferroelectric perovskite composition, comprising a perovskite oxide ABO.sub.3, and a doping agent selected from perovskites of Ba(Ni,Nb)O.sub.3 and Ba(Ni,Nb)O.sub.3-δ. The ferroelectric perovskite composition may be represented by the formula: xBa(Ni,Nb)O.sub.3.(1-x)ABO.sub.3 or xBa(Ni,Nb)O.sub.3-δ.(1-x)ABO.sub.3. A method of producing the ferroelectric perovskite composition in thin film form is also provided.

A device comprising a nonlinear optical (NLO) material according to the formula XLi.sub.2Al.sub.4B.sub.6O.sub.20F. A device comprising a nonlinear optical material (NLO) according to the formula KSrCO.sub.3F, wherein the NLO comprises at least one single crystal. A nonlinear optical material selected from the group consisting of KSrCO.sub.3F Rb.sub.3Ba.sub.3Li.sub.2Al.sub.4B.sub.6O.sub.20F and K.sub.3Sr.sub.3Li.sub.2Al.sub.4B.sub.6O.sub.20F.

Phosphors include a CaAlSiN.sub.3 family crystal phase, wherein the CaAlSiN.sub.3 family crystal phase comprises at least one element selected from the group consisting of Mn, Ce, Pr, Nd, Sm, Eu, Tb, Dy, Ho, Er, Tm, and Yb.

Nontoxic Near infra-red Reflecting (NIR) inorganic pigments, characteristically blue and well suited for the coloration of a wide variety of substrates, for example, plastics and concrete building roofing material, etc., comprise mixed metal silicate having the general formula: La.sub.xSr.sub.1-xCu.sub.1-yLi.sub.ySi.sub.4O.sub.10, where x is equal to 0 to 0.5 and y is equal to 0 to 0.5. These silicates with tetragonal crystal structure are prepared by calcination method in air atmosphere.

The present invention relates to a quantum dot and a preparation method therefor, and more specifically, to a novel quantum dot composite having high surface stability, and a preparation method therefor. The quantum dot composite according to the present invention constitutes a layered-structure ceramic composite in which the layered-structure ceramic comprises a polymer-quantum dot composite between the layers thereof.