Abstract:
Suspended nanotubes are used to capture and ionize neutral chemical units, such as individual atoms, molecules, and condensates, with excellent efficiency and sensitivity. Applying a voltage to the nanotube(s) (with respect to a grounding surface) creates an attractive potential between a polarizable neutral chemical unit and the nanotube that varies as 1/r2, where r is the unit's distance from the nanotube. An atom approaching the nanotube with a sub-threshold angular momentum is captured by the potential and eventually spirals towards the nanotube. The atom ionizes as in comes into close proximity with a sidewall of the nanotube, creating an ion whose polarity matches the polarity of the electric potential of the nanotube. Repulsive forces eject the ion, which can be detected more easily than a neutral chemical unit. Suspended nanotubes can be used to detect small numbers of neutral chemical units (e.g., single atoms) for applications in sensing and interferometry.
Abstract:
A field emission electron source (10) includes a conductive base (12), a carbon nanotube (14), and a film of metal (16). The conductive base includes a top (122). One end (142) of the carbon nanotube is electrically connected with the top of the conductive base. The other end (144) of the carbon nanotube extends outwardly away from the top of the conductive base. The film of metal is formed on the nearly entire surface of the carbon nanotube and at least on the portion of the top of the conductive base proximate the carbon nanotube. A method for manufacturing the described field emission electron source is also provided.
Abstract:
An ion source for use in a mass spectrometer includes an electron emitter assembly (30) configured to emit electron beams, wherein the electron emitter assembly comprises carbon nanotube bundles fixed to a substrate for emitting the electron beams, a first control grid configured to control emission of the electron beams, and a second control grid configured to control energies of the electron beams; an ionization chamber (34) having an electron-beam inlet (38) to allow the electron beams to enter the ionization chamber, a sample inlet for sample introduction, and an ion-beam outlet (29) to provide an exit for ionized sample molecules; an electron lens (31) disposed between the electron emitter assembly and the ionization chamber to focus the electron beams; and at least one electrode (37) disposed proximate the ion-beam outlet to focus the ionized sample molecules exiting the ionization chamber.
Abstract:
A boron nitride nanotube paste composition, an electron emission source including the same, an electron emission device including the same and a backlight unit and an electron emission display device including the same are provided. The boron nitride nanotube paste composition includes about 100 parts by weight boron nitride nanotubes, from about 250 to about 1000 parts by weight glass frit, from about 500 to about 1000 parts by weight filler, from about 1000 to about 2000 parts by weight organic solvent, and from about 2000 to about 3000 parts by weight polymer binder. Electron emission devices including the boron nitride nanotube electron emission sources have longer lifespan and improved uniformity among pixels.
Abstract:
Photon Enhanced Thermionic Emission (PETE) is exploited to provide improved efficiency for radiant energy conversion. A hot (greater than 200 0C) semiconductor cathode is illuminated such that it emits electrons. Because the cathode is hot, significantly more electrons are emitted than would be emitted from a room temperature (or colder) cathode under the same illumination conditions. As a result of this increased electron emission, the energy conversion efficiency can be significantly increased relative to a conventional photovoltaic device. In PETE, the cathode electrons can be (and typically are) thermalized with respect to the cathode. As a result, PETE does not rely on emission of non-thermalized electrons, and is significantly easier to implement than hot-carrier emission approaches.
Abstract:
The present invention relates to a method for manufacturing a field emitter electrode, in which nanowires are aligned horizontally, perpendicularly or at any angle between horizontal and perpendicular according to the direction of a generated electromagnetic field. More particularly, the present invention relates to a method for manufacturing a field emitter electrode having nanowires aligned horizontally, perpendicularly or at any angle between horizontal and perpendicular according to the direction of a generated electromagnetic field, the method comprising the steps of diluting nanowires in a solvent, dispersing the resulting solution on a substrate fixed to the upper part of an electromagnetic field generator, and fixing the nanowires aligned in the direction of an electromagnetic field generated from the electromagnetic field generator. According to the present invention, a high capacity field emitter electrode having high density nanowires aligned according to the direction of a generated electromagnetic field can be fabricated by a simple process and nanowires can be used as positive electrode materials for field emission displays (FEDs), sensors, electrodes, backlights and the like.
Abstract:
An ion source for use in a mass spectrometer includes an electron emitter assembly (30) configured to emit electron beams, wherein the electron emitter assembly comprises carbon nanotube bundles fixed to a substrate for emitting the electron beams, a first control grid configured to control emission of the electron beams, and a second control grid configured to control energies of the electron beams; an ionization chamber (34) having an electron-beam inlet (38) to allow the electron beams to enter the ionization chamber, a sample inlet for sample introduction, and an ion-beam outlet (29) to provide an exit for ionized sample molecules; an electron lens (31) disposed between the electron emitter assembly and the ionization chamber to focus the electron beams; and at least one electrode (37) disposed proximate the ion-beam outlet to focus the ionized sample molecules exiting the ionization chamber.
Abstract:
An electron emission device and a method of manufacturing the same are provided. The electron emission device includes i) a hydrophilic resin substrate and ii) carbon nano tubes that are positioned on the resin substrate. Surface roughness Ra of the resin substrate is 7.3 μm to 9.75 μm.
Abstract:
Photon Enhanced Thermionic Emission (PETE) is exploited to provide improved efficiency for radiant energy conversion. A hot (greater than 200° C.) semiconductor cathode is illuminated such that it emits electrons. Because the cathode is hot, significantly more electrons are emitted than would be emitted from a room temperature (or colder) cathode under the same illumination conditions. As a result of this increased electron emission, the energy conversion efficiency can be significantly increased relative to a conventional photovoltaic device. In PETE, the cathode electrons can be (and typically are) thermalized with respect to the cathode. As a result, PETE does not rely on emission of non-thermalized electrons, and is significantly easier to implement than hot-carrier emission approaches.