Patent classifications
C01B32/152
LASER-INDUCED CARBON NANOSTRUCTURES
A method of manufacturing a carbon nanostructure, such as a carbon foam material, is disclosed. The method comprises the steps of: (a) using a first laser beam to irradiate an encapsulated or sub-surface region of a carbon pre-cursor material below a surface of the material, to create carbon foam in that sub-surface region, and a disorganised, amorphous non-graphene material above the carbon foam, and then (b) using a second laser beam to remove or ablate the disorganised, amorphous non-graphene material sitting above the carbon foam, to expose at least some of the carbon foam. The resultant carbon foam material shows a significant D peak; the 2D peak is significantly less than the G peak; and the peak D: peak G ratio is significantly above zero. In appearance and Raman signature, it appears similar to a carbon nano-onion material. It can be used in biosensors, supercapacitors and pseudo-capacitors.
LASER-INDUCED CARBON NANOSTRUCTURES
A method of manufacturing a carbon nanostructure, such as a carbon foam material, is disclosed. The method comprises the steps of: (a) using a first laser beam to irradiate an encapsulated or sub-surface region of a carbon pre-cursor material below a surface of the material, to create carbon foam in that sub-surface region, and a disorganised, amorphous non-graphene material above the carbon foam, and then (b) using a second laser beam to remove or ablate the disorganised, amorphous non-graphene material sitting above the carbon foam, to expose at least some of the carbon foam. The resultant carbon foam material shows a significant D peak; the 2D peak is significantly less than the G peak; and the peak D: peak G ratio is significantly above zero. In appearance and Raman signature, it appears similar to a carbon nano-onion material. It can be used in biosensors, supercapacitors and pseudo-capacitors.
LASER-INDUCED CARBON NANOSTRUCTURES
A method of manufacturing a carbon nanostructure, such as a carbon foam material, is disclosed. The method comprises the steps of: (a) using a first laser beam to irradiate an encapsulated or sub-surface region of a carbon pre-cursor material below a surface of the material, to create carbon foam in that sub-surface region, and a disorganised, amorphous non-graphene material above the carbon foam, and then (b) using a second laser beam to remove or ablate the disorganised, amorphous non-graphene material sitting above the carbon foam, to expose at least some of the carbon foam. The resultant carbon foam material shows a significant D peak; the 2D peak is significantly less than the G peak; and the peak D: peak G ratio is significantly above zero. In appearance and Raman signature, it appears similar to a carbon nano-onion material. It can be used in biosensors, supercapacitors and pseudo-capacitors.
LASER-INDUCED CARBON NANOSTRUCTURES
A method of manufacturing a carbon nanostructure, such as a carbon foam material, is disclosed. The method comprises the steps of: (a) using a first laser beam to irradiate an encapsulated or sub-surface region of a carbon pre-cursor material below a surface of the material, to create carbon foam in that sub-surface region, and a disorganised, amorphous non-graphene material above the carbon foam, and then (b) using a second laser beam to remove or ablate the disorganised, amorphous non-graphene material sitting above the carbon foam, to expose at least some of the carbon foam. The resultant carbon foam material shows a significant D peak; the 2D peak is significantly less than the G peak; and the peak D: peak G ratio is significantly above zero. In appearance and Raman signature, it appears similar to a carbon nano-onion material. It can be used in biosensors, supercapacitors and pseudo-capacitors.
LASER-INDUCED CARBON NANOSTRUCTURES
A method of manufacturing a carbon nanostructure, such as a carbon foam material, is disclosed. The method comprises the steps of: (a) using a first laser beam to irradiate an encapsulated or sub-surface region of a carbon pre-cursor material below a surface of the material, to create carbon foam in that sub-surface region, and a disorganised, amorphous non-graphene material above the carbon foam, and then (b) using a second laser beam to remove or ablate the disorganised, amorphous non-graphene material sitting above the carbon foam, to expose at least some of the carbon foam. The resultant carbon foam material shows a significant D peak; the 2D peak is significantly less than the G peak; and the peak D: peak G ratio is significantly above zero. In appearance and Raman signature, it appears similar to a carbon nano-onion material. It can be used in biosensors, supercapacitors and pseudo-capacitors.
Carbon nanostructure preblends and their applications
A method for preparing a preblend of nano-structured carbon, such as nanotubes, fullerenes, or graphene, and a particulate solid, such as carbon black, graphitic particles or glassy carbon involving wet-mixing and followed by optional drying to remove the liquid medium. The preblend may be in the form of a core-shell powder material with the nano-structured carbon as the shell on the particulate solid core. The preblend may provide particularly improved dispersion of single-wall nanotubes in ethylene--olefin elastomer compositions, resulting in improved reinforcement from the nanotubes. The improved elastomer compositions may show simultaneous improvement in both modulus and in elongation at break. The elastomer compositions may be formed into useful rubber articles.
Laser-induced carbon nanostructures
A method of manufacturing a carbon nanostructure, such as a carbon foam material, is disclosed. The method comprises the steps of: (a) using a first laser beam to irradiate an encapsulated or sub-surface region of a carbon pre-cursor material below a surface of the material, to create carbon foam in that sub-surface region, and a disorganised, amorphous non-graphene material above the carbon foam, and then (b) using a second laser beam to remove or ablate the disorganised, amorphous non-graphene material sitting above the carbon foam, to expose at least some of the carbon foam. The resultant carbon foam material shows a significant D peak; the 2D peak is significantly less than the G peak; and the peak D:peak G ratio is significantly above zero. In appearance and Raman signature, it appears similar to a carbon nano-onion material. It can be used in biosensors, supercapacitors and pseudo-capacitors.
STRUCTURE, SLIDING MATERIAL, AND MANUFACTURING METHOD THEREOF
A step is included in which an iron oxide is immersed in a benzotriazole solution containing a fullerene. The immersion is performed until a fullerene concentration in the benzotriazole solution decreases compared with that before the immersion, and a structure is obtained having the fullerene on the surface of the iron oxide. A sliding body is used in which the surface of the iron oxide having the fullerene of the structure is arranged on a sliding surface.
Ternary blend organic solar cells based on one donor polymer and two acceptors
An organic solar cell comprises a photoactive layer that comprises at least one donor polymer and two non-fullerene molecular acceptors. Further, an organic solar cell comprises a photoactive layer that comprises one donor polymer, one fullerene acceptor, and one non-fullerene molecular acceptor. The donor polymer may exhibit temperature dependent aggregation (TDA) properties in solution, wherein the absorption onset of the polymer solution exhibits a red shift of at least 80 nm when the solution is cooled from 100 C. to room temperature or the absorption onset of the polymer solution exhibits a red shift of at least 40 nm when the solution is cooled from 100 C. to 0 C.
Ternary blend organic solar cells based on one donor polymer and two acceptors
An organic solar cell comprises a photoactive layer that comprises at least one donor polymer and two non-fullerene molecular acceptors. Further, an organic solar cell comprises a photoactive layer that comprises one donor polymer, one fullerene acceptor, and one non-fullerene molecular acceptor. The donor polymer may exhibit temperature dependent aggregation (TDA) properties in solution, wherein the absorption onset of the polymer solution exhibits a red shift of at least 80 nm when the solution is cooled from 100 C. to room temperature or the absorption onset of the polymer solution exhibits a red shift of at least 40 nm when the solution is cooled from 100 C. to 0 C.