| Patent application number | Description | Published |
|---|
| 20100102265 | GEL ELECTROLYTE OF DYE SENSITIZED SOLAR CELL AND METHOD FOR MANUFACTURING THE SAME - Disclosed is a gel electrolyte for a photosensitive dye and method for manufacturing the same. First, bismaleimide and barbituric acid are dissolved in Brönsted base solution to form a gelling additive. Subsequently, the gelling additive is added into an ionic liquid electrolyte. The liquid electrolyte is then gelled at room temperature to form a gel electrolyte for the photosensitive dye utilized in dye sensitized solar cells. In addition, barbituric acid is further added into the gelling additive to enhance the gelling rate of the ionic liquid electrolyte. | 04-29-2010 |
| 20100130625 | PROTON EXCHANGE MEMBRANE AND METHOD FOR MANUFACTURING THE SAME - A proton exchange membrane and method for formation the same is disclosed. When forming the proton exchange membrane, first, a bismaleimide and barbituric acid are copolymerized to form a hyper-branched polymer. Next, the solvent of the sulfonated tetrafluorethylene copolymer (Nafion) aqueous solution is replaced with dimethyl acetamide (DMAc). 10 to 15 parts by weight of the hyper-branched polymer is added to 90 to 85 parts by weight of the Nafion in the DMAc solution, stood and heated to 50° C. for inter-penetration of the hyper-branched polymer and the Nafion. The heated solution is coated on a substrate, baked, and pre-treated to remove residue solvent to complete formation of the proton exchange membrane. | 05-27-2010 |
| 20100167101 | PROTON EXCHANGE MEMBRANE COMPOSITION - Proton exchange membrane compositions having high proton conductivity are provided. The proton exchange membrane composition includes a hyper-branched polymer, wherein the hyper-branched polymer has a DB (degree of branching) of more than 0.5. A polymer with high ion conductivity is distributed uniformly over the hyper-branched polymer, wherein the hyper-branched polymer has a weight ratio equal to or more than 5 wt %, based on the solid content of the proton exchange membrane composition. | 07-01-2010 |
| 20100167102 | INTER-PENETRATED PROTON EXCHANGE MEMBRANE, METHOD FOR MANUFACTURING THE SAME, AND PROTON EXCHANGE MEMBRANE FUEL CELL UTILIZING THE SAME - The disclosed forms a proton exchange membrane. First, multi-maleimide and barbituric acid are copolymerized to form a hyper-branched polymer. Next, the solvent of the sulfonated tetrafluorethylene copolymer (Nafion) aqueous solution is replaced from water with dimethyl acetamide (DMAc). 10 to 20 parts by weight of the hyper-branched polymer is added to the 90 to 80 parts by weight of the Nafion in a DMAc solution, stood and heated to 50° C. to inter-penetrate the hyper-branched polymer and the Nafion. The heated solution is coated on a substrate, baked, and pre-treated to remove residue solvent for completing an inter-penetrated proton exchange membrane. | 07-01-2010 |
| 20120171573 | HYBRID MATERIALS USING IONIC PARTICLES - A separator substrate include a substrate having a bulk portion and a surface portion, the surface portion having at least one porous area with a net charge; and ionic particles coupling to at least a part of the at least one porous area. The ionic particles have a net charge of an opposite sign to the net charge of the at least one porous area. The coupling between the part of the at least one porous area and the ionic particles may result in at least one of a good electrochemical performance, chemical stability, thermal stability, wettability, and mechanical strength of the separator substrate. | 07-05-2012 |
| 20120171576 | NON-AQUEOUS ELECTROLYTE AND LITHIUM SECONDARY BATTERY INCLUDING THE SAME - A non-aqueous electrolyte including a lithium salt, an organic solvent, and an electrolyte additive is provided. The electrolyte additive is a meta-stable state nitrogen-containing polymer formed by reacting Compound (A) and Compound (B). Compound (A) is a monomer having a reactive terminal functional group. Compound (B) is a heterocyclic amino aromatic derivative as an initiator. A molar ratio of Compound (A) to Compound (B) is from 10:1 to 1:10. A lithium secondary battery containing the non-aqueous electrolyte is further provided. The non-aqueous electrolyte of this disclosure has a higher decomposition voltage than a conventional non-aqueous electrolyte, such that the safety of the battery during overcharge or at high temperature caused by short-circuit current is improved. | 07-05-2012 |
| 20120171579 | NON-AQUEOUS ELECTROLYTE AND LITHIUM SECONDARY BATTERY INCLUDING THE SAME - A non-aqueous electrolyte including a lithium salt, an organic solvent, and an electrolyte additive is provided. The electrolyte additive is a meta-stable state nitrogen-containing polymer formed by reacting Compound (A) and Compound (B). Compound (A) is a monomer having a reactive terminal functional group. Compound (B) is a heterocyclic amino aromatic derivative as an initiator. A molar ratio of Compound (A) to Compound (B) is from 10:1 to 1:10. A lithium secondary battery containing the non-aqueous electrolyte is further provided. The non-aqueous electrolyte of this disclosure has a higher decomposition voltage than a conventional non-aqueous electrolyte, such that the safety of the battery during overcharge or at high temperature caused by short-circuit current is improved. | 07-05-2012 |
| 20120172558 | META-STABLE STATE NITROGEN-CONTAINING POLYMER - A meta-stable state nitrogen-containing polymer formed by reacting Compound (A) and Compound (B) is described. Compound (A) is a monomer having a reactive terminal functional group. Compound (B) is a heterocyclic amino aromatic derivative as an initiator. The molar ratio of Compound (A) to Compound (B) is from 10:1 to 1:10. The meta-stable state nitrogen-containing polymer has a variance less than 2% in its narrow molecular weight distribution after being retained at 55° C. for one month. | 07-05-2012 |
| 20120172593 | META-STABLE STATE NITROGEN-CONTAINING POLYMER - A meta-stable state nitrogen-containing polymer formed by reacting Compound (A) and Compound (B) is described. Compound (A) is a monomer having a reactive terminal functional group. Compound (B) is a heterocyclic amino aromatic derivative as an initiator. The molar ratio of Compound (A) to Compound (B) is from 10:1 to 1:10. The meta-stable state nitrogen-containing polymer has a variance less than 2% in its narrow molecular weight distribution after being retained at 55° C. for one month. | 07-05-2012 |
