A faujasite-type zeolite has an IR spectrum in which the IR spectrum has an absorption band 1 including surface silanol groups and having a local maximum in a range from 3730 cm.sup.−1 to 3760 cm.sup.−1, and an absorption band 2 including acidic hydroxyl groups and having a local maximum in a range from 3550 cm.sup.−1 to 3700 cm.sup.−1, a ratio (h1/h2) of a peak height (h1) of the absorption band 1 to a peak height (h2) of the absorption band 2 being less than 1.2.

A sulfide solid electrolyte to be used in a lithium-ion secondary battery, including: a crystal phase; and an anion existing in a crystal structure of the crystal phase, in which the crystal phase includes an argyrodite crystal containing Li, P, S, and Ha; Ha is at least one element selected from the group consisting of F, Cl, Br, and I; the anion includes an oxide anion having a Q0 structure having an M-O bond that is a bond of M and O; and M is at least one element selected from the group consisting of metal elements and semimetal elements belonging to Groups 2 to 14 of a periodic table.

Disclosed herein are modified zeolites and methods for making modified zeolites. In one or more embodiments disclosed herein, a modified zeolite may include a microporous framework comprising a plurality of micropores having diameters of less than or equal to 2 nm. The microporous framework may include at least silicon atoms and oxygen atoms. The modified zeolite may further include organometallic moieties each bonded to bridging oxygen atoms. The organometallic moieties may include a titanium atom. The titanium atom may be bonded to a bridging oxygen atom, and the bridging oxygen atom may bridge the titanium atom of the organometallic moiety and a silicon atom of the microporous framework.

The embodiments of the present disclosure relate to a method and apparatus for producing a carbon nanomaterial product (CNM) product that may comprise carbon nanotubes and various other allotropes of nanocarbon. The method and apparatus employ a consumable carbon dioxide (CO.sub.2) and a renewable carbonate electrolyte as reactants in an electrolysis reaction in order to make CNTs. In some embodiments of the present disclosure, operational conditions of the electrolysis reaction may be varied in order to produce the CNM product with a greater incidence of a desired allotrope of nanocarbon or a desired combination of two or more allotropes.

A nitrogen-containing carbon material includes carbon atoms, nitrogen atoms, and halogen atoms. The nitrogen-containing carbon material has a ratio of a number of moles of pyridinic nitrogen atoms to a total number of moles of the nitrogen atoms that is higher than 59% and a total content ratio of the nitrogen atoms with respect to the nitrogen-containing carbon material that is 7 at % or higher. The nitrogen-containing carbon material includes a fused polycyclic aromatic moiety formed by condensation of three or more aromatic rings, and the fused polycyclic aromatic moiety includes a partial structure for two pyridinic nitrogen atoms to be linked to each other through two carbon atoms.

Provided is a negative electrode material for a secondary battery, which is in a particle form including: a matrix including a silicon oxide, a composite oxide of silicon and one or more doping elements selected from the group consisting of alkali metals, alkaline earth metals, and post transition metals, or a mixture thereof; and silicon nanoparticles dispersed and embedded in the matrix, wherein a compressive strength (St) of the particles is 100 MPa or more, and a ratio (A.sub.1/A.sub.2) between an area of a first peak (A.sub.1) and an area of a second peak (A.sub.2) satisfies 0.8 to 6, a diffraction angle 2θ being positioned in a range of 10° to 27.4° in the first peak and being positioned in a range of 28±0.5° in the second peak, in an X-ray diffraction pattern using a CuKα ray.

This disclosure relates to the manufacture an alkali metal quaternary crystalline nanomaterial. an alkali metal quaternary crystalline nanomaterial having general Formula A (I.sub.2-II-IV-VI.sub.4); and wherein I is sodium (Na) or lithium (Li), II and IV are Zn or Sn, and VI is a chalcogens selected from the group comprising: sulphur (S), selenium (Se) or tellurium (Te). The crystal phase of the alkali metal quaternary crystalline nanomaterial may be a primitive mixed Cu—Au like structure (PMCA) and may have a space group: P42m. The nanomaterials may be adapted to provide a solar cell. Methods of manufacture are also provided.

A lithium iron complex oxide is represented by Li.sub.5FeO.sub.4, two peaks with different quadrupole splitting values (QS) analyzed using .sup.57Fe Mössbauer spectroscopy are shown, one of the two peaks, a peak A, satisfies QS>0, and the other one of the two peaks, a peak B, satisfies QS=0.

A method of making a titanium dioxide nanowire array includes contacting a substrate with a solvent comprising a titanium (III) precursor, an acid, and an oxidant while microwave heating the solvent, thereby forming a hydrogen titanate H2Ti2O5.H2O nanowire array. The hydrogen titanate nanowire array is annealed to form a titanium dioxide nanowire array. The substrate is seeded with titanium dioxide before starting the hydrothermal synthesis of the hydrogen titanate nanowire array. The titanium dioxide nanowire array is loaded with a platinum group metal to form an exhaust gas catalyst. The titanium dioxide nanowire array can be used to catalyze oxidation of combustion exhaust.

An electrochromic device comprising a substrate, a set of electrodes disposed on or within the substrate, and a layer comprising ε-WO.sub.3 disposed in electrical communication with the set of electrodes, wherein the layer of ε-WO.sub.3 exhibits polarization switching are described. Methods of making and using the electrochromic devices are also described. The electrochromic devices are used for detecting acetone in a fluid. The observed change in color of the ε-WO.sub.3 layer can be correlated with a subject's medical condition, such as diabetes.