The invention relates in general to devices and methods of using an ambient environment as a propulsion fluid, more particularly although not exclusively, the invention relates to a high pressure field emitter and field device used to generate plasma and provide propulsion in an ambient environment, photoionization, and plasma initiation methods.
Patent application (US 2004/0070340, U.S. application Ser. No. 10/44,638) discusses the background and foundation for the use of an ambient environment as the propulsive medium, where ambient environment refers to the medium in an ionization region, which may or may not surround a vehicle.
Conventional motorized atmospheric vehicles utilize engines that have moving parts to compress, combust and expel ambient atmosphere to provide propulsive thrust to the attached vehicle. The moving parts have lifetimes associated with the imposed stress, both pressure and thermal, and are limited in the energies imparted to the combusted air.
Strong thin films of micron and submicron size, able to withstand pressure differences between a vacuum on one side of the film and atmospheric pressure on the opposite side, while still allowing an energetic electrons to pass through has been discussed in Neukermans (U.S. Pat. No. 4,486,282), incorporated by reference herein it entirety, for use in cathode ray tubes. The thin films can be made of SiC, BN, B4C, Si3N4, Al4C3, and other similar strength materials as known by one of ordinary skill in the relevant arts that have similar electron penetration characteristics, low stress, and pinhole free.
In addition to electron ionization of neutrals into plasma. photoionization can be used to generate plasmas at relatively high pressures. Lasers have been used to preionize organic gas Tetrakis (dimethylamine) ethylene to initiate a plasma at 80 Torr, then use roughly 2.8 kW of RF power to form a stable plasma density (“Radiofrequency Initiation and Radiofrequency Sustainment of Laser Intiate Seeded High Pressure Plasma”, Eric S. Paller, et Al., Radio Power in Plasma: 14th Topical Conf., Edited by T. K. Mau and J. deGrassie, 2001 American Institute of Physics 0-7354-0038-5, herein referred to as the Paller reference).
Another method of photo ionization is to tailor the laser to the ionization energy of the medium in the plasma generation chamber. One method of generating a powerful yet low power consumption laser is to utilize pumped cavity photonic crystals (see U.S. Pat. No. 6,711,420, filed 23 Mar. 2004). A background in photonic crystals is discussed in “Photonic Crystals: The Road from Theory to Practice”, Steven G. Johnson et al., ISBN 0-7923-7609-9, 2002, and “Photonic Crystals: Molding the Flow of Light”, John D. Joannopoulos et al., ISBN 0-691-03744-2, 1995 both of which are incorporated by reference in their entirety. Several methods of photonic crystal fabrication are known for example U.S. patent application Ser. No. 11/265,041 discusses the formation of three dimensional photonic crystals using aphrons.
At least one exemplary embodiment is directed to an engine, using high pressure field emitters as an ionizing electron source to produce a plasma, which is E×B drifted to produce propulsion.
At least one exemplary embodiment is directed to an engine, using electromagnetic heating to produce a plasma, which is E×B drifted to produce propulsion.
At least one exemplary embodiment is directed to a vehicle surface, using high pressure field emitters as an ionizing electron source to produce a plasma, which is E×B drifted to produce propulsion.
At least one exemplary embodiment is directed to a vehicle surface, using electromagnetic heating to produce a plasma, which is E×B drifted to produce propulsion.
At least one exemplary embodiment is directed to a field emitter that can operate at atmospheric pressures.
At least one exemplary embodiment is directed to a charged fluid seeding system providing the initial ionization charged particles for plasma initialization and sustainment.
At least one exemplary embodiment is directed to an electric and magnetic field device that can provide E×B field to accelerate a plasma.
Further areas of applicability of embodiments of the present invention will become apparent from the detailed description provided hereinafter. It should be understood that the detailed description and specific examples, while indicating exemplary embodiments of the invention, are intended for purposes of illustration only and are not intended to limited the scope of the invention.
Exemplary embodiments of the present invention bill become apparent from the following detailed description, taken in conjunction with the drawings in which:
The following description of exemplary embodiment(s) is merely illustrative in nature and is in no way intended to limit the invention, its application, or uses.
Processes, methods, materials and devices known by one of ordinary skill in the relevant arts may not be discussed in detail but are intended to be part of the enabling discussion where appropriate (e.g., the processes and materials in “Principles of Plasma Discharges and Materials Processing”, Michael A. Lieberman, et al., ISBN 0-471-00577-0, 1994). For example although air is used as an example of an ambient environment used in the illustrative examples the ambient environment can be include any gas or fluid that can be charged, (e.g. by either electron addition/removal or ion addition/removal/creation), and accelerated in a E×B drift mode (for example charged micro droplets of water, Nitrogen Gas, CO2, and any other material that can be charged and E×B drifted as known by one of ordinary skill in the relevant art and equivalents). Additionally, examples of electric and magnetic field generation device(s) are discussed, however exemplary embodiments are not limited to any particular device for generating electric and magnetic fields.
Note that in non-limiting examples an engine with a plasma generation chamber is discussed. However at least one exemplary embodiment can be used to form the skin of a vehicle, the skin now being used to propel the vehicle.
Exemplary embodiments are provided for illustrative non-limiting purposes only.
The first exemplary embodiment is directed to an engine or a vehicle surface, using high pressure field emitters as an ionizing electron source to produce a plasma, which is E×B drifted to produce propulsion. In the example, a planar configuration of ionizing plates including micro high pressure field emitter electron sources is illustrated in combination with an an electric/magnetic field device.
The second exemplary embodiment is directed to an engine or a vehicle surface, using an electromagnetic ionizing source to produce a plasma, which is E×B drifted to propulsion. In the non-limiting example provided, a planar configuration of ionizing plates including ionizing photon emitters is illustrated in combination with an electric/magnetic field device.
In a third exemplary embodiment, a charged fluid is injected into a chamber; the charged fluid droplets evaporating naturally or aided by laser heating; the resultant free electron are oscillated by an electromagnetic field producing plasma in the chamber, and an E×B field is created to drive the plasma in a direction.
1. First Exemplary Embodiment
1.A. High Pressure Field Emitter
Field emitters typically operate in very high vacuums (often better than 10−8 Torr for Spindt types and nanowires, and 10−7 Torr for nanotubes. This is because the gate voltages required to generate field emitted currents are also sufficient to produce arc discharge between the gate layer 330 and emitter tip 340 at higher pressure levels consistent with other low vacuum electronic products. The vacuum requirements limit the number of field emitter (FE) applications to those employing expensive high vacuum systems. The FEs must also the handled with care because a single dust particle can short out a FE. Thus conventional FEs are prone to arcing at elevated pressure (> about 10−7 Torr) and shorting due to contaminants (e.g., oil or dust, particle).
The substrate layer 310 can be formatted of an suitable material such as a semiconductor material, silicon, germanium, III-V semiconductor materials (e.g., GaAs), insulating materials (e.g., glass, plastic), with a semi conductive layer forms on the insulating material, other materials as known by one of ordinary skill in the relevant arts and equivalents. The substrate layer 310 can also be doped so that a potential difference between the gate layer 330 and the field emitter tip 340 will allow current to flow to the emitter tip 340.
The first insulating layer 320 can be made of various insulating materials (e.g., silicon dioxide, silicon nitride, Si, other insulating materials as known by one of ordinary skill in the relevant arts and equivalents). The first insulating layer can have various thicknesses (e.g., 0.25 micrometer to 10 micrometer) and should be large enough to support the gate layer voltage.
The gate layer 330 can be any type of conductive material (e.g., a refractory metal, molybdenum, niobium chromium, hafnium, combinations of metals and their carbides, other conductive materials as known by one of ordinary skill in the relevant art and equivalents). The conducting gate layer can vary in thickness (e.g., 0.01 micrometer to 10 micrometer), and should be thick enough to allow conduction of a gate current.
The field emitter tip 340 can be formed from a refractory metal (e.g., molybdenum, niobium, hafnium, and a combination of such materials), a nanotube, a nanowire (e.g., ZnO, a refractory metal, a refractory metal carbides, or diamond), or other types of emitter tips as known by one of ordinary skill in the relevant art and equivalents. A tip an be formed by various processes, for example U.S. Pat. No. 5,731,597 to Lee et al. illustrates a method, which is incorporated by reference herein in its entirety. Nanotubes can be formed by electric discharge, pulsed laser ablation, chemical deposition, and other methods as known by one of ordinary skill in the relevant arts and equivalents. Nanowires can be grown by several methods, for example electro-deposition. Field emitter arrays (FEA) can include array of the field emitters, for example millions, sometimes with various pitches (distance between array element (individual field emitter)), for example on the order of a micrometer.
A conventional field emitter emits electrons forming a beam current. Several references discuss the characteristics of a beam current and methods of control, for example U.S. Published Application US2004/0183456 incorporated by reference herein in its entirety. Note that the beam current can be unstable due to contaminants on the field emitter tip, which changes the electric field characteristics near the tip. The voltage difference between the gate layer 330 and the field emitter tips 340 (gate to tip voltage) can be on the order of volts (e.g., 1 to 10000V), with beam currents on the order of micro to nano amps, depending upon the environment in the emitter chamber (B) (
At least one exemplary embodiment can use a high pressure field emitter (
For example the barrier layer can be chosen to be made of platinum, or carbon, where the thickness is chosen so that less than 1% of the ambient thermal (e.g., 1.2 eV) constituents (e.g., N2) can tunnel through the barrier layer in a given time, while over 50% of the field emitted electrons at a chosen, reference voltage (e.g., 102 eV) can tunnel through in the same time. Note also that the barrier layer (e.g., 360b) can also be the gate layer.
Thus, the ambient environment (A) can effectively be separated from the emitter chamber (B). Additionally if it is suspected that the emitter camber's pressure has risen to a level that it is desirable to reduce, for example over 10−7 Torr, then the field emission electron energies can be chosen to ionize constituents in the emitter chamber (B), then with a reversed gate to tip voltage those ionized constituents can be accelerated out of the chamber through the barrier layer (e.g., also 360a).
Thus with an oscillating voltage (oscillating electrons at a chosen ionizing energy) ionization of emitter chamber contaminants can occur, and then with a reversed voltage the positive ions removed from the emitter chamber (B) to facilitate the reduction of the emitter chamber (B) pressure to a more desirable level. Thus, a high pressure field emitter in accordance with at least one exemplary embodiment can pump ambient constituents and other contaminants that happen to accumulate in the emitter chamber (B) out of the emitter chamber (B). Several non-limiting example field emitters will be discussed below, and then at least one non-limiting method of fabrication. A discussion of the materials will not be made in detailed below since such discussion has already been made above with respect to similar parts. The barrier layer 360a can be either conductive (
To calculate the minimum design thickness of the barrier layer (e.g., 360a) one can approximate the electron penetration depth, for example by:
Where E0 is the accelerating voltage in keV (e.g., the gate to tip voltage). ? is the density of the barrier layer 360a (g/cm3). For example a gate to tip voltage of 15 keV, using a silicate material for the barrier layer 360a, 2.5 g/cm3 gives a thickness of 2.3 μm. Note that for a 1.2 eV thermal ambient energy particle (e.g., electron, ion, neutral atom or molecule) the thickness is on the order of 10−6 μm. Note also that neutrals can have cross sections thousands of times less than a charged particle, so to accurately determine the penetration of neutrals compared to charged particles the relative cross sections can be used, where the cross sections have been cited in numerous literature.
Suppose one wishes to have field emission electrons with 100 eV when they pass into the ambient environment (A). Then if we assume that half the energy is lost going through the barrier layer then we start with a gate to tip voltage of 200 Volts (200 eV with the electrons). Then we calculate the thickness required to stop 100 eV electrons (i.e., the thickness needed to bleed off ½ the energy). The calculated design thickness of the barrier layer is approximately 0.001 micrometer.
Small thicknesses can be difficult to deposit precisely, thus for a second computational example, lets assume that we wish to use a 10 micrometer thickness film, using silicate material (2.5 g/cm3). Such a barrier layer will approximately stop a 39.5 eV electron. Thus one can design the gate to tip voltage to be 140 Volts to provide about 100 eV electrons into the ambient environment. Note also that as the electrons pass through the barrier layer beam spreading can occur, which can actually be of use when trying to form a plasma in the ambient environment. When a more directed beam is needed (e.g., for display systems) a higher gate to tip gate voltage will tend to reduce the relative beam spread.
For the non-limiting example discussed above approximately 40 eV per electron is deposited in the barrier layer, heating the barrier layer. If the barrier layer is conductive the heat can be conducted away. The heat can also be transferred to the ambient environment (via convection, conduction or radiation). In the non-limiting example discussed, if we assume that 40 eV is deposited in the barrier layer 360a per electron, then the total amount of energy deposited will be a function of the beam current. For illustrative purposes lets assume that 1 microamp current is being produced by the field emitted electrons. Then the total power deposited can be calculated as:
which, for a microamp current is equivalent to 6.25×1012 electrons/sec being deposited. To cool the barrier film heat conduction, radiation, and/or convection should be equal to or greater than 4×10−5 W for the given example values. For example suppose we would like radiative transfer to cool the thin film. Then one starts with the 4×10−5 W and works backwards to arrive at a desired emissivity. If radiative transfer alone can't provide the full cooling then convection and/or conduction can be added to arrive at an equilibrium condition (energy radiated, conducted, and convected=total power deposited). Continuing with the example lets assume that the radiative area is only one side of the thin film the side facing the ambient environment (A). Lets also assume the emitter chamber (B) has a horizontal barrier layer 360a extend of 1 micrometer diameter for a surface area of π(D/2)2=7.85×10−13 m3. The radiative power can be expressed as:
Wr=eσAT4=e(5.67×10−8 W/m2K4)(7.85×10−13 m2)T4=4×10−5 Watt (3)
If we assume a value of the emissivity of 1.0 then the equilibrium temperature for radiation cooling only is 5475 K. Thus conduction and convection might be needed and the material of the barrier film made of a high melting temperature in this particular example. Additionally the surface area can be increased by the addition of fins.
Often the operating temperature is determinative, so one can start there and work backwards. Thus, one can work backwards from a design temperature and desired current and obtain the energy per electron deposited, then calculate the thickness of the barrier layer needed. Then the thickness can be check with the operating pressure difference between the emitter chamber (B) pressure and the ambient environment (A) pressure to see if structurally the film can resist the pressure difference without rupture, the needed stress can narrow the selection of materials. For this example lets assume that we don't want the temperature to be greater than 300K. Lets assume the emissivity is 0.5, and the desired current is 1×10−8 Amp. Using equation (3) with the radiative between standard temperature of 273K we get:
Wr=eσAT4=(0.5)(5.67×10−8 W/m2K2)(7.85×10−33m2)(300A−273A)=5.66×10×Watt (4)
Now one can use equation (2) to obtain the eV deposited, which for this non-limiting example can be expressed as:
Solving the ?eV one gets about 0.00566 eV. Such calculations can continue until a reasonable temperature and electron deposition is acquired.
Note however that electron energy deposition in the film will not mean that neutrals and ions in the ambient environment greater than that energy can pass through the film.
The barrier film thickness for the example where the deposited electron energy is 0.00566 eV can be calculated from equation (1), with an assumption of a gate to tip voltage, which we will choose at 100 eV, which can be expressed as:
The discussions above are meant to illuminate the cyclic calculations that can follow the determination of materials to be used, gate to tip voltages to use, and barrier thicknesses to use. For example an assumption can be made and the temperature calculated, if the temperature is too high, a new assumption on the temperature can be made and the calculations worked backwards to obtain the energy deposited.
To this point the calculations have centered around the emitted electrons, however we could start calculations with the ambient thermal temperature of the constituent neutrals and ions and work forwards and calculate the minimum energy that electrons will need to penetrate the barrier. The ambient environment is typically made of neutral atoms and molecules of an appreciable amount of electrons to start with (Thermal temperatures are approximately 0.025 eV).
The following formulas can be used to approximate the penetration depth or stopping power of various neutrals, ions, and electrons. The following formulas are non-limiting examples that can be used to calculate the stopping distances of various energies and constituents.
The following harmonic equation for the stopping power has been used to examine the stopping power (keV/μm) of protons and antiprotons (Direct measurements of the stopping power for antiprotons of light and heavy targets, S. P Moller et al., Physical Review A, Vol. 56, No. 4, October 1977) incorporated herein by reference in it's entirety:
Where, N is the target density, Z2 is the target atomic number, Z1 is the projectile charge, ν is the projectile velocity, and L is the Bethe stopping function. In general the Bethe stopping function can be expressed as:
L=L0+Z1L1+Z12L2+ (8)
Where L0, L1, and L2 are various functions of the Bohr velocity
mean ionization, and other projectile and target properties, L1 however is the distant collision Barkas effect and is related to the polarization of the medium induced by the projectile, thus negatively charge projectiles will have a lower stopping power, for example a proton uses L0+L1+L2 to calculate the stopping power, while an antiproton uses L0−L1+L2. Thus for example if both have a kinetic energy of 20 keV, then the proton has a stopping power of 200 keV/μm while an antiproton has a stopping power of 50 keV/μm.
The Bethe-Bloch formula has been used to calculate the stopping power for energetic projectiles with variations for lower energies. Additionally the continuously slowing down approximation (CDSA) has been calculated for the stopping range. For example a 100 eV electron will have a stopping range of about 50 angstroms in gold.
The next issue is that any barrier layer will have to be strong enough to support the pressure difference. As discussed in Neukermans (U.S. Pat. No. 4,468,282) incorporated herein in it's entirety, there are several materials that can be used that can withstand the pressure difference between a vacuum and atmospheric pressure (approximately 14.7 pounds per square inch). Thus although not discussed in detail the pressure stress considerations with respect to the film material chosen would be known by one of ordinary skill in the arts.
Although the examples of exemplary embodiments utilize modifications of a “Spindt type” field emitter, the concepts of exemplary embodiments can be used in other types of field emitters.
Other variations are possible within the scope of exemplary embodiments where a barrier layer is deposited to isolate the chamber region (B) from the ambient environment (A).
To develop a thin enough barrier layer, the barrier layer 470 can be deposited on a separate stop layer 480, which itself can be deposited on a base layer 490 forming a multilayer structure. The barrier layer 470 can be deposited to the desired thickness. The multilayer structure can be flipped and attached to the structure formed in
In at least one exemplary embodiment a portion 480 (e.g., a circular ring etch) around the barrier film 470 can be etched (
Each field emitter (FE) as illustrated in
where μ is the permeability (e.g., in a vacuum of 4π×10−7 (N/Amp2)). I is the current (in Amps) around the loop, where N is the number of loops, “a” is the radius of a coil loop, and “z” is the distance from the end of the coil (e.g., along the field line direction “Ba”). Generally μ in a vacuum can be used and then a separate magnetic field added due to the magnetic field added by a ferromagnetic core material, which in totality can be equated to equation (7) using μ, or the magnetic permeability of the core material. To increase the number of loops, concentric shells of coils can be set within each other. For example
In the example illustrated, three concentric coils (e.g., 610, 611, and 613) are illustrated, providing N1, N2, and N3 turns respectively. Each coil surrounds a ferromagnetic shell (e.g., 601 and 603) or a ferromagnetic core 605, providing increased magnetic field output. Each shell can be separated by a μ metal sheath (e.g., 602, 604) to avoid an inner coil from creating an opposing field to an outer coil, thus each shell or coil produces a component magnetic field, for example B3 for the innermost coil 613, B2 for the middle coil 611, and B1 for the outermost coil.
Each coil can be driven individually, in parallel, or in series. An example of a serially driven coil array circuit is illustrated in
An E×B engine according to at least one exemplary embodiment is illustrated in
Other methods of ionization and plasma generation can be used, and further examples using ionizing light, and charged fluid evaporation, will be discussed later. In the present example an electric field E0 is created by the two voltage plates having a voltage difference, and the magnetic field B0 is created by the magnetic field device 530. The direction of the fields (E0 and B0) can be varied, for example by reversing the current in the coils of the magnetic device 530 and varying the voltage difference between plates V1 and V2. Any plasma in the field regions will be E×B drifted imparting an impulse in the devices generating the fields as discussed in Ser. No. 10/441,638 filed 20 May 2003. While E×B drifting a portion of the plasma will recombine becoming neutral at which point that portion will no longer be subject to the electric and magnetic fields. Some of the plasma may not have recombined before leaving the field region and thus will be collected by the excess charge plates (e.g., 560 and 570).
As discussed above if high pressure field emitters are used to create the plasma then the field emitter arrays 500 can heat up. Coolant tubes can be used to cool the field emitter arrays.
The engine illustrated in
II. Second Exemplary Embodiment
II.A. Electromagnetic Plasma Formation Source
Ionization of an atom can be generally expressed as:
Where e is the charge of an electron 1.6×10−19 C, m is the mass of an electron 9.11×10−31 Kg, k=¼ε0=9.00×109 Nm2/C2, h=6.63×10−34 Js, Z is the charge on the nucleus, and ‘n’ is the quantum condition where n=1 is the ground state. For example the ionization of Hydrogen in the ground state is 13.6 eV, He is 54.4 eV, and for N (Z=7, outer electron on n=2 orbital) the ionization of an outer electron is about 14.53 eV. For air constituents, it takes about 15.58 eV to ionize an outer electron from N2, and about 12.07 eV to ionize an outer electron from O2. Generally photon energy from 5 eV to 20 eV will be sufficient to ionize both atoms and molecules. The equivalent photon energy can be calculated as:
E=hf=hc/? (11)
Where “f” is the frequency of the light, ‘c’ is the speed of light c=3.0×108 m/s, and ? is the photons wavelength. For example photons with energies from 1 eV to 1000 eV have wavelengths from 1 μm to 1 nm respectively, from the near infrared to UV to soft X-ray. Where for the main range for ionization of air constituents photons range from 5 eV to 20 eV have wavelengths of about 500 nm and 90 nm respectively. Thus, for O2 and N2 typically about a 95 nm wavelength photon is needed for ionization, which corresponds to the UV. For comparison, visible light ranges from about 400 nm to 700 nm or violet to red respectively, corresponding to about 6 eV to 3 eV respectively. Thus, if a medium is composed of O2 and N2 then a photon generator can be used to ionize a portion of the medium. How far an ionizing photon penetrates into a medium depends on the medium's density. For example the mean free path in air for 1 atmosphere (number density of about 2.5×1025/m3) is about 6×10−8 m. For other similar values see the Handbook of Chemistry and Physics, 75th Ed., ISBN 0-8493-0475.
Calculating the photon flux needed will depend on the recombination rate, the medium density, and the desired portion of ionization. U.S. patent application Ser. No. 10/441,638, incorporated herein by reference in it's entirety, describes the recombination rate, and penetration depth when using electron ionization.
Table 1 lists several atoms and molecules and the associated ground state ionization energy needed and the associated wavelength in angstroms:
One method of ionization is using a laser or light source with a photon frequency needed to ionize the ambient medium and/or medium in the plasma generation chamber. One such laser/light source in accordance with at least one exemplary embodiment is a photonic crystal laser using a cavity (e.g., of the appropriate size, see table 1) field with a gain material.
II.B. Illustrative Example of the Second Exemplary Embodiment (Photonic UV Source)
Many methods can be used to move the moveable photonic crystal in and out of the top section 1100c, for example a groove 1175 and gear system 1170 is illustrated in
The middle section 1100b includes two electrodes 1120, fed via leads 1130. The middle section 1100b also includes a gain region 1140, where the gain region 1140 creates stimulated radiation of a wavelength related to the size of the gain region 1140, the size and spacing of each of the photonic crystal dielectric pattern (e.g., periodic dielectric (e.g., liquid, solid or gas filled) spheres placed within the substrate). The voltages across the two electrodes 1120 are varied to drive the stimulated emission of radiation from the gain region 1140. However the spacing and size of the periodic structure is designed so that the stimulated radiation produced from the gain region 1140 is within the photonic crystal band gap. Thus the stimulated region can not escape the photonic crystal. If the cavity 1157 however is placed close the gain region 1140 then the stimulated radiation can escape through the cavity 1157. Appropriate gain material from the gain region 1140 are known but several examples are InGaAs, InGaP, InGaAsP, an excited dimer material, cerium-doped fluorides and lithium strontium such as lithium calcium aluminum fluoride, or Ce3+:LiCalF6 (Ce:LiCAF); a lithium strontium aluminum fluoride, or Ce3+:LiSrAlF6 (e.g., which produce tunable output directly in the 280- to 330-nm spectral region), Nd—YAG, ArF (193 nm), KrF (248 nm), XeCl (308 nm) and other gain material as known by one of ordinary skill in the relevant arts and equivalents.
In at least one exemplary embodiment the laser power of each photonic crystal laser can be approximately 500 micro Watt, so that the plate roughly has 3.1 kW/cm2.
Thus at least one exemplary embodiment is directed to a laser photonic crystal comprising: a first photonic crystal layer; a second photonic crystal layer where the second photonic crystal layer includes at least a first cavity, and at least two electrodes a first electrode and a second electrode, where the first cavity is at least partially filled with a gain material, where a potential difference between the electrodes can excite the gain material into stimulated emission of radiation, where the radiation stimulated has a wavelength in the band gap of the second photonic crystal layer; and a third photonic crystal layer, where the third photonic crystal layer includes a first portion that can be adjusted to move a second cavity to a position so that a second portion of the stimulated radiation passes through the third photonic crystal layer. In at least one exemplary embodiment the stimulated radiation can be reflected between the electrodes through the first cavity.
At least one exemplary embodiment further includes a vertical comb drive that is operatively connected to a fourth photonic crystal section, where the fourth photonic crystal section includes the second cavity, where the vertical comb drive is moved to move the fourth photonic crystal in and out of the third photonic crystal layer so as to move the second cavity above the first cavity. While the second cavity is not positioned above the first cavity a continuation of the photonic crystal results in a band gap within which the stimulated radiation's wavelength lies. When the second cavity is positioned above the first cavity an allowed waveband, within which the wavelength of the stimulated radiation lies, is created within the band gap allowing the stimulated radiation to pass through the second cavity and through the third photonic crystal layer.
At least one further exemplary embodiment includes a cover layer, wherein the cover layer covers the third photonic crystal layer and is substantially transparent to the wavelength of the stimulated radiation.
III. Third Exemplary Embodiment
III.A. Charged Fluid Evaporation System
Instead of using an injected electron or photon from a surface to ionize an ambient medium, a charged droplet (e.g., one with net negative charge (i.e., electrons)) can be injected into a chamber, in which the droplet is evaporated (e.g.. via heat, microwaves, or other appropriate method as known by one of ordinary skill in the relevant arts depending upon the material that the droplet is made of). When the droplet is evaporated the excess charge is now available in the ambient medium to be used in ionizing the ambient environment (e.g., via oscillation of the free electrons using ionizing frequency driven electromagnetic waves, or other electron oscillation and/or acceleration methods known by one of ordinary skill in the relevant arts to utilize the free electrons and/or ions and/or charged droplets to ionize at least a portion of the ambient environment. Charged droplets and aphrons and their formation is discussed in U.S. patent application Ser. No. 11/265,041, filed Nov. 2, 2005, incorporated by reference in it's entirety.
In summary of when a charged droplet, for example one with excess electrons is created, the droplet can break into smaller droplets (if the net charge is high enough e.g., the Coulomb force is greater than the surface tension). The charged drop also can start to evaporate until the size is such that net charge will break it into smaller droplets. Even if the droplet did not break into smaller droplets eventually the evaporation will turn the liquid base into a gas carrying net free charges. The net free charges can be acted upon by electric and/or magnetic fields to oscillate at a certain frequencies (e.g., see table 1) and used to ionize the ambient medium. Alternatively the free charges can be accelerated (e.g., using E×B drift) to the ionization energies of the ambient medium (e.g., see table 1 for energies) and impacted with a neutral ambient ionizing it in the process, triggering ambient medium plasma initiation. For example if using E×B drift via an E and B field generation system, the free charges + and − will be accelerated into the same direction. Once the energy equivalent to the ionization energy is reached then the collisions the free charges have with ambient neutrals can result in ionizations of the neutrals. The ions and electrons formed from the neutrals can result in ionizations feel the effect of an E×B drift, also colliding with neutrals and ionizing them. Thus the initial free charges can be used to initiate a larger plasma, which is E×B drifted (e.g., before they recombine back into neutrals, see patent application Ser. No. 10/441,638 for detailed discussion) to provide thrust.
The engine 1200 can include a ram cone 1210 (not drawn to scale); and an inlet 1220 where ambient or stored fluid flow 1205 (e.g., air, gas, water, and other fluids as known by one of ordinary skill in the relevant arts). The entered fluid flow then enters the plasma generation chamber where a portion 1217 is ionized. The ionization can be initiated by free electrons and/or ions in the plasma generation chamber inserted via charged fluid injection via a charged fluid injection system 1215. The free electrons and/or ions can be oscillated in the plasma generation chamber either via an injected electromagnetic wave at the correct frequency (e.g., see table 1, or plasma frequency) or by varying an electrostatic voltage differences across plates bordering either side of plasma generation chamber. The oscillated free electrons and/or ions can ionize a portion 1217 of the fluid in the plasma generation chamber. The plasma can be accelerated via an E×B magnetic-electric field generator. Any remaining free charges 1260 can be accumulated by accumulation plates 1250.
Thus, at least one exemplary embodiment is directed to a propulsion device comprising: at least a first charged fluid injector, where the first charged fluid injector is configured to inject a charged fluid into a plasma generation chamber including a medium, where the charged fluid provides free charges, where the free charges are energized, and where the energized free charges ionize at least a first portion of the medium; and a field generation device, where the field generation device is configured to generate an electric and magnetic field, and where the electric and magnetic fields have a E×B component, wherein the E×B component accelerates a second portion of the first portion producing a thrust.
At least one exemplary embodiment is directed to a propulsion device also including a heating unit, wherein the heating unit changes the phase of the charged fluid into a gas including the free charges. For example if the charged fluid is water the heating unit can be a microwave source to evaporate the charged fluid and/or droplets along their path so that a substantial portion is converted into a gaseous phase including free charges.
In at least one exemplary embodiment the propulsion device further includes a free charge energizing device including an oscillating electromagnetic field generator, where the oscillation frequency is selected to ionize the first portion. For example if the kinetic energy of the free charges is such that it is equal to or greater than the average ionization energy of the medium in eth plasma generation chamber then oscillating free charges will ionize a portion of the medium. The frequency needed to oscillate the free charges can be determined by calculating the average velocity of the free charges during oscillation and using the average mass of one free charge and calculating an average energy. The average energy of a free charge is set to be equal to or greater than the average ionization energy. Thus the velocity needed can be calculated and the oscillation frequency calculated. The oscillation field can be generated by oscillating voltage plates on either side of the plasma generation chamber or region. For example the oscillation frequency can be set to the plasma frequency associated with the free charges in the mediums, thus heating the free charges.
Alternatively in at least one exemplary embodiment the free charges can be accelerated via a potential difference along an axial direction of the plasma generation chamber energizing the translation energy of the free charges to an energy at least the minimum ionization energy of the medium. For example rings around the plasma generation chamber spaced along the axial directed can have various voltages resulting in a potential difference accelerating the free charges.
While the present invention has been described with reference to exemplary embodiments, it is to be understood that the invention is not limited to the disclosed exemplary embodiments. The scope of the following claims is to be accorded the broadest interpretation so as to encompass all such modifications and equivalent structures and functions.
This application claims the priority benefit of and is a continuation in part, under 35 U.S.C. § 120, of U.S. patent application Ser. No. 10/441,638 filed on 20 May 2003, incorporated herein by reference in it's entirety.
Number | Date | Country | |
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Parent | 10441638 | May 2003 | US |
Child | 11383847 | May 2006 | US |