Abstract: A paper medium skew correcting device includes: a support including a pair of fixed stop plates arranged in parallel; a skew correcting tapered roller assembly including a tapered roller, a reference plate located at a large end face of the tapered roller and a transmission shaft a tapered cover plate covering on the tapered roller with a skew correcting passage formed between an inner wall of the tapered cover plate and an outer wall of the tapered roller, an auxiliary pressure roller mechanism is mounted on an outer wall of the tapered cover plate and is configured to press a paper medium against the outer wall of the tapered roller tightly, the tapered cover plate is provided with an opening; and a driving transmission assembly. The device fully uses combined action of centrifugal force and friction force to realize skew correction and conveying of the paper medium.

Abstract: Improved V2O5 materials are disclosed herein in the form of 2D leaf-like nanosheets. Methods of forming the V2O5 nanosheets and batteries (e.g., lithium-ion) incorporating the V2O5 nanosheets are also provided.

Abstract: A deflection correcting device includes a banknote running passage defined by a first passage plate and a second passage plate. Deflection correcting wheels are arranged in the banknote running passage and a deflection correcting direction of the deflection correcting wheels is deflected from a reference side of the banknote running passage. A lateral guiding mechanism is provided at the reference side, and configured to drive a banknote that reaches the reference side to move in the transmission direction of the banknote running passage; and a deflection correcting adjusting wheel is provided at a tail end in a deflection direction of the plurality of the deflection correcting wheels, and a deflection correcting direction of the deflection correcting adjusting wheel is deflected from the reference side. The banknote is prevented from jamming at the reference side and the passage.

Abstract: Methods are provided for forming films of orthorhombic V2O5. Additionally provided are the orthorhombic V2O5 films themselves, as well as batteries incorporating the films as cathode materials. The methods use electrodeposition from a precursor solution to form a V2O5 sol gel on a substrate. The V2O5 gel can be annealed to provide an orthorhombic V2O5 film on the substrate. The V2O5 film can be freestanding such that it can be removed from the substrate and integrated without binders or conductive filler into a battery as a cathode element. Due to the improved intercalation properties of the orthorhombic V2O5 films, batteries formed using the V2O5 films have extraordinarily high energy density, power density, and capacity.

Abstract: A sheet-type medium deviation correction device comprises an upper holding plate, a lower holding plate, a front guide wheel set, a front end position detecting element, a lateral border position detecting unit, a deviation correction assembly, and a delivery assembly. The deviation correction assembly comprises a belt and a pair of belt pulleys. The delivery direction of the belt is perpendicular to the lateral border of the upper holding plate or the lower holding plate. The delivery assembly comprises a pair of delivery wheels. The delivery direction of the delivery wheels is perpendicular to that of the belt. The belt is used for delivering a sheet-type medium to the border of the belt to be aligned with the lateral border of the holding plate, thereby achieving the deviation correction purpose.

Abstract: A structure is provided having a substrate and a direct write deposited lead zirconate titanate (PZT) nanoparticle ink based piezoelectric sensor assembly deposited on the substrate. The PZT nanoparticle ink based piezoelectric sensor assembly has a PZT nanoparticle ink based piezoelectric sensor with a PZT nanoparticle ink deposited onto the substrate via an ink deposition direct write printing process. The PZT nanoparticle ink does not require a high temperature sintering/crystallization process once deposited. The PZT nanoparticle ink based piezoelectric sensor assembly further has a power and communication wire assembly coupled to the PZT nanoparticle ink based piezoelectric sensor. The power and communication wire assembly has a conductive ink deposited onto the substrate via the ink deposition direct write printing process.

Abstract: Phosphors formed using silicon nanoparticles are provided. The phosphors exhibit bright fluorescence and high quantum yield, making them ideal for lighting applications. Methods for making the silicon phosphors are also provided, along with lighting devices that incorporate the silicon phosphors.

Abstract: Phosphors formed using silicon nanoparticles are provided. The phosphors exhibit bright fluorescence and high quantum yield, making them ideal for lighting applications. Methods for making the silicon phosphors are also provided, along with lighting devices that incorporate the silicon phosphors.

Abstract: Phosphors formed using silicon nanoparticles are provided. The phosphors exhibit bright fluorescence and high quantum yield, making them ideal for lighting applications. Methods for making the silicon phosphors are also provided, along with lighting devices that incorporate the silicon phosphors.

Abstract: A structure is provided having a substrate and a direct write deposited lead zirconate titanate (PZT) nanoparticle ink based piezoelectric sensor assembly deposited on the substrate. The PZT nanoparticle ink based piezoelectric sensor assembly has a PZT nanoparticle ink based piezoelectric sensor with a PZT nanoparticle ink deposited onto the substrate via an ink deposition direct write printing process. The PZT nanoparticle ink does not require a high temperature sintering/crystallization process once deposited. The PZT nanoparticle ink based piezoelectric sensor assembly further has a power and communication wire assembly coupled to the PZT nanoparticle ink based piezoelectric sensor. The power and communication wire assembly has a conductive ink deposited onto the substrate via the ink deposition direct write printing process.

Abstract: Improved V2O5 materials are disclosed herein in the form of 2D leaf-like nanosheets. Methods of forming the V2O5 nanosheets and batteries (e.g., lithium-ion) incorporating the V2O5 nanosheets are also provided.

Abstract: A substrate for surface enhanced Raman spectroscopy analysis (SERS) comprises a ferroelectric single crystal having polarization-inverted patterns of spontaneous polarizations including polarization-inverted portions and non-inverted polarization portions, and metallic dots positioned at only either one polarized surfaces of the polarization-inverted portions and the non-inverted polarization portions. The provided SERS substrate produces a high enhancement effect. A microfluidic device incorporating the SERS substrate is also provided.

Abstract: Methods for forming lead zirconate titanate (PZT) nanoparticles are provided. The PZT nanoparticles are formed from a precursor solution, comprising a source of lead, a source of titanium, a source of zirconium, and a mineralizer, that undergoes a hydro thermal process. The size and morphology of the PZT nanoparticles are controlled, in part, by the heating schedule used during the hydro thermal process.

Abstract: Methods for forming lead zirconate titanate (PZT) nanoparticles are provided. The PZT nanoparticles are formed from a precursor solution, comprising a source of lead, a source of titanium, a source of zirconium, and a mineralizer, that undergoes a hydrothermal process. The size and morphology of the PZT nanoparticles are controlled, in part, by the heating schedule used during the hydrothermal process.

Abstract: The present application is directed to electric double layer capacitance (EDLC) devices. In one aspect, the present application is directed to an electrode comprising an activated carbon cryogel having a tunable pore structure wherein: the surface area is at least 1500 m2/g as determined by nitrogen sorption at 77K and BET analysis; and the pore structure comprises a pore volume ranging from about 0.01 cc/g to about 0.25 cc/g for pores having a pore diameter of 0.6 to 1.0 nm. In another aspect, the present application is directed to an Electric Double Layer Capacitor (EDLC) device comprising an activated cryogel.

Abstract: Methods for forming lead zirconate titanate (PZT) nanoparticles are provided. The PZT nanoparticles are formed from a precursor solution, comprising a source of lead, a source of titanium, a source of zirconium, and a mineraliser, that undergoes a hydro thermal process. The size and morphology of the PZT nanoparticles are controlled, in part, by the heating schedule used during the hydro thermal process.

Abstract: Phosphors formed using silicon nanoparticles are provided. The phosphors exhibit bright fluorescence and high quantum yield, making them ideal for lighting applications. Methods for making the silicon phosphors are also provided, along with lighting devices that incorporate the silicon phosphors.

Abstract: The present application is directed to electric double layer capacitance (EDLC) devices. In one aspect, the present application is directed to an electrode comprising an activated carbon cryogel having a tunable pore structure wherein: the surface area is at least 1500 m2/g as determined by nitrogen sorption at 77K and BET analysis; and the pore structure comprises a pore volume ranging from about 0.01 cc/g to about 0.25 cc/g for pores having a pore diameter of 0.6 to 1.0 nm. In another aspect, the present application is directed to an Electric Double Layer Capacitor (EDLC) device comprising an activated cryogel.

Abstract: Carbon cryogels, methods for making the carbon cryogels, methods for storing a gas using the carbon cryogels, and devices for storing and delivering a gas using the carbon cryogels.

Abstract: The invention provides devices, systems, and methods for detecting an analyte vapor. Particularly, electronegative analyte vapors, such as those vapors evolving from explosive compounds, are typical analytes detected the devices. The devices operate using a resistivity change mechanism wherein a nanostructured chemiresistive material undergoes a resistivity change in the presence of an analyte vapor. A resistivity change indicates the presence of an analyte.