Abstract: A method and system for photopolymerization 3D printing is provided. The system includes a processing device, a micro light emitting diode (microLED) array including one or more individually addressable microLED emitters, and a printing component. The processing device is configured to determine one or more printing layers of an object. The microLED array is configured to generate light for each of the one or more printing layers. The printing component is configured to print the one or more printing layers. To generate the light for each of the one or more printing layers, the processing device is further configured to dynamically determine one or more microLED regions in the microLED array, determine one or more region printing parameters for each of the one or more microLED regions; and determine one or more control signals for the one or more individually addressable microLED emitters included in each of the one or more microLED regions based on the one or more region printing parameters.

Abstract: A coated textured glass article is described herein that comprises: a glass body comprising a first surface; a plurality of polyhedral surface features extending from the first surface; and a coating disposed on the first surface of the body and the plurality of polyhedral surface features. Each of the plurality of polyhedral surface features comprises a base on the first surface and a plurality of facets extending from the base and converging toward one another. The coating comprises a multilayer interference stack.

Abstract: A textured article is described herein that may include a glass-based substrate comprising a first major surface and a second major surface. The first major surface may be opposite the second major surface. At least a portion of the first major surface may be textured. The portion of the first major surface that is textured may have a roughness Ra of greater than or equal to 400 nm and an average pitch. A ratio of roughness Ra to average pitch may be from about 0.01 to about 0.04. At least a portion of the textured article may have an opacity of greater than about 70% or may have a coefficient of friction of from about 0.25 to about 0.4. The coefficient of friction may be measured as the kinetic coefficient of friction using a 500 g load on a foam rubber according to ASTM D1984.

Abstract: Disclosed herein are dual-textured glass articles. The glass articles may include a glass substrate comprising a first major surface and a second major surface. The first major surface may be opposite the second major surface. At least a portion of the first major surface comprises a dual-texture. The dual-texture may comprise a plurality of first features and a plurality of second features. The plurality of first features comprise protrusions from the first major surface and the plurality of second features comprise indentations in the first major surface and indentations in the plurality of first features.

Abstract: A method of forming a textured glass article comprises: submerging an aluminosilicate glass article in an etchant to an upper submerging depth from a surface of the etchant and at a tilting angle, wherein the aluminosilicate glass article comprises a first major surface and a second major surface opposite the first surface, wherein the tilting angle is a smallest angle between a normal to the first major surface and a vertical; holding the aluminosilicate glass article in the etchant for a holding time; and after the holding time, cycling the aluminosilicate glass article in the etchant between the upper submerging depth and a lower submerging depth deeper than the upper submerging depth for a cycling time.

Abstract: An etchant comprises: greater than or equal to 20 wt % and less than or equal to 45 wt % ammonium bifluoride; greater than or equal to 0.25 wt % and less than or equal to 10 wt % of a silicon compound; greater than or equal to 5 wt % and less than or equal to 30 wt % hydrochloric acid; greater than or equal to 25 wt % and less than or equal to 60 wt % water; and greater than or equal to 0.5 wt % and less than or equal to 20 wt % of polyhydric alcohol. The silicon compound comprises silica, silica gel, ammonium hexafluorosilicate, potassium hexafluorosilicate, sodium hexafluorosilicate, magnesium hexafluorosilicate, or a combination thereof.

Abstract: The present invention relates to a protonic ceramic fuel cell and a method of making the same. More specifically, the method relates to a cost-effective route which utilizes a single moderate-temperature (less than or equal to about 1400° C.) sintering step to achieve the sandwich structure of a PCFC single cell (dense electrolyte, porous anode, and porous cathode bone). The PCFC layers are stably connected together by the intergrowth of proton conducting ceramic phases. The resulted PCFC single cell exhibits excellent performance (about 450 mW/cm2 at about 500° C.) and stability (greater than about 50 days) at intermediate temperatures (less than or equal to about 600° C.). The present invention also relates to a two step method for forming a PCFC, and the resulting PCFC.

Abstract: The present invention relates to a solid oxide (or protonic ceramic) fuel cell, a cathode for a solid oxide (or protonic ceramic) fuel cell, and a method of making the same. More specifically, the cathode for a solid oxide (or protonic ceramic) fuel cell utilizes a phase-pure perovskite structure of the compound BaCo0.4Fe0.4Zr0.2?xYxO3??, where x is between about 0 and about 0.2. The cathode material may then be utilized in a SOFT or a PCFC as either a thin film porous cathode or as nanoparticles infiltrated into a cathode bone having a different structure.

Abstract: The present invention relates to a protonic ceramic fuel cell, a cathode for a protonic ceramic fuel cell, and a method of making the same. More specifically, the cathode for a protonic ceramic fuel cell utilizes a phase-pure perovskite structure of the compound BaCo0.4Fe0.4Zr0.2-xYxO3-?, where x is between about 0 and about 0.2. The cathode material may then be utilized in a PCFC as either a thin film porous cathode or as nanoparticles infiltrated into a cathode bone having a different structure.

Abstract: The present invention relates to a solid oxide (or protonic ceramic) fuel cell, a cathode for a solid oxide (or protonic ceramic) fuel cell, and a method of making the same. More specifically, the cathode for a solid oxide (or protonic ceramic) fuel cell utilizes a phase-pure perovskite structure of the compound BaCo0.4Fe0.4Zr0.2-xYxO3-6, where x is between about 0 and about 0.2. The cathode material may then be utilized in a SOFT or a PCFC as either a thin film porous cathode or as nanoparticles infiltrated into a cathode bone having a different structure.

Abstract: The present invention relates to a protonic ceramic fuel cell, a cathode for a protonic ceramic fuel cell, and a method of making the same. More specifically, the cathode for a protonic ceramic fuel cell utilizes a phase-pure perovskite structure of the compound BaCo0.4Fe0.4Zr0.2-xYxO3-?, where x is between about 0 and about 0.2. The cathode material may then be utilized in a PCFC as either a thin film porous cathode or as nanoparticles infiltrated into a cathode bone having a different structure.

Abstract: The present invention relates to a protonic ceramic fuel cell and a method of making the same. More specifically, the method relates to a cost-effective route which utilizes a single moderate-temperature (less than or equal to about 1400° C.) sintering step to achieve the sandwich structure of a PCFC single cell (dense electrolyte, porous anode, and porous cathode bone). The PCFC layers are stably connected together by the intergrowth of proton conducting ceramic phases. The resulted PCFC single cell exhibits excellent performance (about 450 mW/cm2 at about 500° C.) and stability (greater than about 50 days) at intermediate temperatures (less than or equal to about 600° C.). The present invention also relates to a two step method for forming a PCFC, and the resulting PCFC.