Oxidized metal complexes are formed using methods which adjust the pH of solutions to obtain oxidized metal complexes having particular physicochemical properties. A method for preparing an oxidized metal complex includes providing a first solution comprising a highly oxidized metal and having a pH between 0 to 7; providing a second solution comprising one or more ligands or a ligand precursor and having a pH between 7 to 13 or greater; and combining the first solution and the second solution to form a third solution comprising the first oxidized metal complex. A method for preparing an oxidized metal complex includes providing a species solution comprising a first oxidized metal complex and having a pH of at least pH 11; and adjusting the pH of the species solution to form a second oxidized metal complex. Compositions and methods for preparing and using same are provided.

A reflective granular composition including a reflective pigment material including a majority of kaolin clay and a hardening additive including a sodium salt or another salt. A method for making a reflective granular composition includes the steps of mixing together a reflective pigment material including a majority of kaolin clay and a hardening additive including a sodium salt or another salt to form a particulate mixture, forming a slurry from the particulate mixture by adding to the particulate mixture water and a binder material, granulating the slurry, drying the granulated slurry, and kilning the dried, granulated slurry to form the reflective granular composition. Methods of analyzing the strength of a reflective granular composition are also disclosed.

The present invention discloses a process for the preparation of metal sulphide quantum dots by using a very low cost sulphur precursor as a sulphur source. The metal sulphide quantum dots finds application in optical devices selected from photovoltaic cells, photodetectors and light-emission devices.

A method for separating a metallofullerene M@C.sub.82, comprises steps of: a) adding a Lewis acid to an extract containing the metallofullerene M@C.sub.82 to react therewith, producing a complex precipitate; b) washing the precipitate, followed by dissolving and filtering to obtain a purified metallofullerene M@C.sub.82 extract, wherein M is one or more selected from the group consisting of lanthanide metals Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb, and Lu; and the Lewis acid is one or more selected from the group consisting of zinc chloride, nickel chloride, copper chloride, zinc bromide, nickel bromide, and copper bromide.

The present disclosure relates to novel multifunctionalized silicon nanoparticles, to processes for their preparation and to compositions comprising the novel multifunctionalized silicon nanoparticles. The disclosure also relates to the use of the novel multifunctionalized silicon nanoparticles in electrochemiluminescence based detection methods and in the in vitro detection of an analyte. In particular, the disclosure relates to methods for measuring an analyte by in vitro methods employing the novel multifunctionalized silicon nanoparticles.

The present disclosure provides functionalized powder particles and methods of forming functionalized powder particles. The functionalization is acquired through the formation of primary and/or secondary structures on a powder particle. Functionalization can be controlled to bring about changes in a broad range of physical and/or chemical properties.

The present disclosure relates to a strategy to synthesize antimony- and zinc-doped tin oxide particles with tunable band gap characteristics. The methods yield stable and monodispersed particles with great control on uniformity of shape and size. The methods produce undoped and antimony and zinc-doped tin oxide stand-alone and core-shell particles, both nanoparticles and microparticles, as well as antimony and zinc-doped tin oxide shells for coating particles, including plasmonic core particles.

A method for preparing carbon-functionalized praseodymium oxide includes the following steps: dissolving Pr(NO.sub.3).sub.3.6H.sub.2O in an acid dye solution and stirring to form a mixed solution; adding NH.sub.3H.sub.2O dropwise in the mixed solution while stirring to adjust a pH value of the mixed solution, thereby forming a suspension, and then aging the suspension for 2 to 4 hours; filtering, washing with water, washing with alcohol, and drying the aged suspension to obtain a carbon-functionalized Pr.sub.6O.sub.11 precursor; and placing the carbon-functional zed Pr.sub.6O.sub.11 precursor in a tube furnace under a protection of nitrogen, heating the carbon-functionalized Pr.sub.6O.sub.11 precursor to a sintering temperature at a heating rate of 4 to 6 degrees Celsius/min, keeping at the sintering temperature for 3 to 4 hours, and then cooling to room temperature, thereby obtaining the carbon-functionalized. Pr.sub.6O.sub.11.

Organic-inorganic halide perovskite (OIHP) materials through their promising material properties, simple solution processability, low material cost, high photon absorption, carrier mobilities, and tunable band gap are suitable for large area coatings in the fabrication of optical displays, LEDs, photovoltaic cells and photodetectors. However, OIHP stability and shelf life have been limited to date as exposed perovskite films do not survive long in ambient air causing further issues for large scale OIHP based device production and deployment. Accordingly, the inventors have established three-cation material system variants using an innovative single solution thiocyanate (SCN) doped three cation material system allowing tailoring of perovskite grain size and microstructure to minimize degradation from exposure to atmospheric conditions. Further, solvent engineering techniques using the innovative single solution SCN doped three cation material system established by the inventors allow for large area processing, compact OIHP films with large crystal grains (>4 μm), and passivated grain boundaries.

A particle is provided that includes a first material and a second material, arranged to provide a Fano resonance effect, for example in the visible portion of electromagnetic spectrum. The first and second materials may be substantially clear in the visible portion of the electromagnetic spectrum. The first material may include an inorganic material, such as SiO.sub.2, TiO.sub.2, HfO.sub.2, ZrO.sub.2, diamond, or a combination thereof. The second material may include a polymer. The first material has a first refractive index and the second material has a second refractive index, where the first refractive index and second refractive index have a difference of 0.5 or greater, and 1.0 or less. The first material may form a core and the second material may form a shell surrounding the core. Alternatively, the first and second materials may form a Janus particle, an asymmetric dimer, or an aggregate.