Abstract: Embodiments described herein relate to flat optical devices with a coating layer including monolayers selected from the group consisting of molybdenum disulfide (MoS2), tungsten disulfide (WS2), tungsten diselenide (WSe2), molybdenum diselenide (MoSe2), molybdenum ditelluride (MoTe2), titanium disulfide (TlS2), zirconium disulfide (ZrS2), zirconium diselenide (ZrSe2), hafnium disulfide (HfS2), platinum disulfide (PtS2), tin disulfide (SnS2), or combinations thereof. The coating layer is disposed over a plurality of optical device structures of the optical device. The monolayers may alternate between the materials to form the coating layer or may be a uniform coating layer of a single material. The coating layer is disposed over each optical device structure of the plurality of optical device structures.

Abstract: Disclosed herein are methods of producing metal sulfide materials, including cathode materials. In some embodiments, the metal sulfide material comprises a secondary cluster of metal sulfide nanoparticles surrounded by a carbon layer. The carbon layer may be created by carbonizing one or more polymer layers disposed about the secondary cluster. The carbonized layer may aid in optimizing performance of the cathode material. Also disclosed herein are methods, processes, devices, and systems for removing hydrogen sulfide from a waste stream. In some embodiments, the waste stream containing hydrogen sulfide is a gas. The waste stream can be combined with a solvent containing a metal-catalyst complex, and the reaction of hydrogen sulfide with the metal results in production of a hydrogen gas and a solid comprising metal sulfide.

Abstract: Disclosed herein are methods of producing metal sulfide materials, including cathode materials. In some embodiments, the metal sulfide material comprises a secondary cluster of metal sulfide nanoparticles surrounded by a carbon layer. The carbon layer may be created by carbonizing one or more polymer layers disposed about the secondary cluster. The carbonized layer may aid in optimizing performance of the cathode material. Also disclosed herein are methods, processes, devices, and systems for removing hydrogen sulfide from a waste stream. In some embodiments, the waste stream containing hydrogen sulfide is a gas. The waste stream can be combined with a solvent containing a metal-catalyst complex, and the reaction of hydrogen sulfide with the metal results in production of a hydrogen gas and a solid comprising metal sulfide.

Abstract: A chemical process captures and convert hydrogen sulfide (H2S) gas into elemental sulfur, polysulfide, sulfur dioxide and/or sulfuric acid while regenerating sodium hydroxide capture agent for further use in an initial H2S capture step. Processing may include initial sodium hydroxide scrubbing of gas streams containing H2S, electrochemical regeneration of the sodium hydroxide from sodium hydrosulfide or sodium sulfide, recovery of sulfur and/or sulfur dioxide from the electrochemical processing, and production of sulfuric acid from such sulfur and/or sulfur dioxide.

Abstract: The present disclosure generally relates to lithium ion battery cathode materials, and methods of making and using the same.

Abstract: A chemical process captures and convert hydrogen sulfide (H2S) gas into elemental sulfur, polysulfide, sulfur dioxide and/or sulfuric acid while regenerating sodium hydroxide capture agent for further use in an initial H2S capture step. Processing may include initial sodium hydroxide scrubbing of gas streams containing H2S, electrochemical regeneration of the sodium hydroxide from sodium hydrosulfide or sodium sulfide, recovery of sulfur and/or sulfur dioxide from the electrochemical processing, and production of sulfuric acid from such sulfur and/or sulfur dioxide.

Abstract: The present invention concerns size- and shape-controlled, colloidal superparticles (SPs) and methods for synthesizing the same. Ligand-functionalized nanoparticles such as nonpolar-solvent-dispersible nanoparticles, are used, and the solvophobic interactions can be controlled. Advantageously, supercrystalline SPs having a superlattice structure, such as a face-centered cubic structure, can be produced. Further, the methods of the invention can provide SPs that self-assemble and are monodisperse. The SPs can be doped with organic dyes and further assembled into more complex structures.

Abstract: An embodiment of the invention is a device for photo-stimulated color emission having at least one plurally doped semiconducting nanoparticle comprising at least one semiconducting material and a plurality of at least one dopant coupled with an irradiation source such that the plurally doped semiconducting nanoparticle emit electromagnetic radiation at two or more wavelengths where the intensities of the emissions depend on the intensity of the irradiation. In an embodiment of the invention, the plurally doped semiconducting nanoparticle can be a doped core/shell nanoparticle where the plurality of dopants can reside in exclusively the core, exclusively the shell, or in both the core and shell.

Abstract: The present invention concerns size- and shape-controlled, colloidal superparticles (SPs) and methods for synthesizing the same. Ligand-functionalized nanoparticles such as nonpolar-solvent-dispersible nanoparticles, are used, and the solvophobic interactions can be controlled. Advantageously, supercrystalline SPs having a superlattice structure, such as a face-centered cubic structure, can be produced. Further, the methods of the invention can provide SPs that self-assemble and are monodisperse. The SPs can be doped with organic dyes and further assembled into more complex structures.

Abstract: An embodiment of the invention is a device for photo-stimulated color emission having at least one plurally doped semiconducting nanoparticle comprising at least one semiconducting material and a plurality of at least one dopant coupled with an irradiation source such that the plurally doped semiconducting nanoparticle emit electromagnetic radiation at two or more wavelengths where the intensities of the emissions depend on the intensity of the irradiation. In an embodiment of the invention, the plurally doped semiconducting nanoparticle can be a doped core/shell nanoparticle where the plurality of dopants can reside in exclusively the core, exclusively the shell, or in both the core and shell.