Title of Invention

PRE-EQUILIBRIUM CHEMICAL REACTION ENERGY CONVERTER

Abstract

The use of newly discovered chemical reaction products, created when reactants combine to form products on the surface of a catalyst, to generate electricity, beams of radiation or mechanical motion. The invention also provides methods to convert the products into electricity or motion. The electric generator consists of a catalyst nanocluster, nanolayer or quantum well placed on a substrate consisting of a semiconductor diode, and a semiconductor diode on the surface of the substrate near the catalyst. The device to generate mechanical motion consists of a catalyst nanocluster, nanolayer or quantum well placed on a substrate, and a hydraulic fluid in contact with the non-reaction side of the substrate, with the surfaces of both the catalyst and substrate mechanically formed to enhance the unidirectional forces on the fluid. Both devices use a fuel-oxidizer mixture brought in contact with the catalyst. The apparatus converts a substantial fraction of the reaction product energy into useful work during the brief interval before such products equilibrate with their surroundings.

Full Text

PRE-EQUILIBRIUM CHEMICAL REACTION ENERGY CONVERTER Field Of The Invention The present invention relates to the extraction of electrical or mechanical energy or coherent radiation from chemical reactions occurring on the surface of a catalyst before thermal equilibrium has been reached by the forms of the released energy. Background Information Recent experimental observations have revealed clues to various catalytic processes occurring: 1) during the 0.01 pico-second time interval during which chemical reactants form bonds with the surface of a catalyst, causing the emission of charge carriers, such as electrons and holes; 2) during the picosecond time interval during which reactants adsorb and lose energy in quantum steps after becoming trapped at a potential well between an adsorbate and a catalyst surface, producing electronic friction, charge carrier currents and phonon emission; and 3) during the nanosecond and longer time intervals during which reaction intermediates and products radiate electromagnetic energy,, either while trapped on a catalyst surface or immediately after escaping it. These processes entail three energy releasing processes, namely: l) charge carrier emission (electrons and holes), 2) phonon emission and 3) photon emission. The discovery of these pre-equilibrium emissions provides new pathways to convert the high grade chemical energy available during pre-equilibrium phases into useful work. The term "pre-equilibrium" refers to the period, however brief, during which the products of reactions have not yet come to thermal equilibrium. These products include energy emissions, such as charge carriers; high frequency phonons normally associated with the optical branch lattice vibrations and with acoustic branch vibrations of similar wavelength and energy; and excited state chemical product species. Prior to the discovery of these rapid energy emission pathways, the energies resulting from a catalytic process, such as the heat of adsorption and the heat of formation, were considered to be heat associated with an equilibrium condition. Indeed, after tens of femtoseconds, emitted charge carriers have thermalized and after a few to hundreds of picoseconds, emitted phonons have thermalized. Summary Of The Invention In an exemplary embodiment of the present invention, the emissions of charge carriers, such as electron-hole pairs, generated by chemical activity and reactions on or within catalyst surfaces, clusters or nanoclusters, are converted into electric potential. In an exemplary embodiment, semiconductor diodes such as p-n junctions and Schottky diodes formed between the catalyst and the semiconductors are used to carry out the conversion. The diodes are designed to collect ballistic charge carriers and can be Schottky diodes, pn junction diodes or diodes formed by various combinations of metal-semiconductor-oxide structures. The interlayer oxide thickness is preferably Less than the particular ballistic mean free path associated with the energy loss of the appropriate charge carrier (e.g., hole or electron). The diodes are placed in contact with or near the catalyst nanolayer or nanocluster within a distance whose order of magnitude is less than approximately the mean free path of the appropriate ballistic charge carrier originating in the catalyst. In one embodiment, the diode is located adjacent to the catalyst cluster, while in a further embodiment, the diode is located under the catalyst, as a substrate. The charge carriers travel ballistically over distances that can exceed the width of appropriately fabricated semiconductor junctions, similar to a thermionic effect. However, unlike the thermionic effect, the charge carriers in the case of the present Invention need not have energy greater than the work function of the material involved. The charge carrier motion is trapped as a difference in fermi level, or chemical potential, between either side of the junction. The resulting voltage difference is indistinguishable from that of a photovoltaic collector. However, the charge carrier forces itself into the valence or conduction band and the circuit provides a counterpart hole or electron. The present invention also provides devices and methods for converting the energy generated by catalytic reactions to mechanical motion before the energy thermalizes. In an exemplary embodiment, the converted motion is used to move a hydraulic fluid against a resisting pressure. Recent advances in -he art of quantum wells, atomically smooth superlattices and nanometer scale fabrication permit a degree of tailoring of the physical parameters to favor a particular reaction pathway (charge carrier, phonon, photon) or to enhance the efficiency of the energy collector. The temperature of operation of a device in accordance with the present invention can be as low as hundreds of degrees Kelvin, which is much lower than the typical operational temperatures of conventional thermophotovoltaics and thermionic systems (1500 to 2500 Kelvin). Moreover, the power per mass and power per volume ultimately achievable using pre-equilibrium emissions in accordance with the present invention exceeds that of fuel cells, conventional thermo- photovoltaics, and conventional thermionic systems. Furthermore, in comparison to fuel cells which require complex ducting, the devices of the present invention allow mixing of fuel and air in the same duct, thereby simplifying ducting requirements. The combination of high volume and mass power density, simplicity, and lower temperature operation makes the methods and devices of the present invention competitive and uniquely useful. Brief Description Of The_Drawing FIG 1. shows a cross-section of an exemplary embodiment of a device for generating electricity in accordance with the present invention. FIG. 2 shows a cross-section of an exemplary embodiment of a device for converting the energy released by a catalytic reaction into mechanical work. FIG. 3 shows a cross-section of an exemplary embodiment of a device for generating electricity piezoelectrically. FIG. 4 shows an exemplary embodiment of an arrangement for generating electricity or radiation beams in accordance with the present invention. Detailed Description FIG. 1 shows a cross-sectional view of an exemplary embodiment of a device in accordance with the present invention. The device cf FIG. 1, includes a catalyst 105 which is arranged on a top surface of the device to come into contact with oxidizer molecules 103 and fuel molecules 102. In the exemplary embodiment of FIG. 1, the catalyst 105 can be comprised of platinum or palladium, the oxidizer 103 can be comprised of air and the fuel 102 can be comprised of hydrogen or a reactant hydrocarbon such as methanol or ethanol. Exhaust molecules 104 result from the catalyzed reaction. The exemplary device: of FIG. 1 comprises a pair of Schottky diodes which act as charge carrier collectors, with one diode 113 being arranged on the top surface of the device, adjacent to the catalyst 105 (the "adjacent surface diode") and the other diode 109 being arranged in the substrate 108, below the catalyst (the "substrate diode"). An insulating layer 111 is arranged between the adjacent surface diode 113 and the substrate 108, as shown. The diodes 109 and 113 preferably comprise a bipolar semiconductor material such as InGaAsSb with a composition chosen to optimize the chosen operating conditions. For example, the second harmonic of a CO stretch vibration on a catalyst surface at 2340 per cm energies gives a photon energy of 0.58 eV. (This matches the 0.53 eV band gap of a recently developed InGaAsSb diode described in G.W. Charache et al., "InGaAsSb thermophotovoltaic diode: Physics evaluation," Journal of Applied Physics, Vol. 8E , No. 4, Feb. 1999). The diodes 109 and 113 preferably have relatively low barrier heights, such as 0.05 to 0.4 volts. The substrate diode 109 should be forward biased sufficiently (e.g., up to 3 volts) to raise its conduction and valence bands above the fermi level of the catalyst 105 so as to match the energy levels of the adsorbed reactants on the catalyst surface, such at; oxygen or hydrocarbon free radicals. This induces resonant tunneling of energy into the substrate diode 109 by photons. The dimension of the oxide barrier or the depletion region should be kept to less than the ballistic transport dimension, which is on the order of 10 nanometers. A metal such as Mg, Sb, Al,, Ag, Sn Cu or Ni may be used to form an interlayer 106 between the catalyst 105 and the semiconductor of the substrate diode 109. The interlayer 106 serves to provide a lattice parameter match between the catalyst material and the substrate, which in turn provides a smooth and planar interface surface with which to construct a quantum well structure consisting of the catalyst, the vacuum above and the interlayer below. A quantum well structure with smooth interfaces alters the density of electron states in the directions toward the substrate and toward the vacuum, so as to enhance the number of electrons with the desired energy. The thickness of the catalyst and the interlayer should be small enough to permit ballistic transport of charge carriers. This dimension is typically less than 20 nanometers. Quantum well structures with thickness less than 0.5 nanometer are possible in the present state of the art. The quantum well structure may be constructed as an island, like a pancake on a surface (also referred to as a "quantum dot"). The device of FIG. 1 may also include a non-conducting layer 107 arranged between the substrate diode 109 and the catalyst 105. The layer 107, which can be comprised of an oxide, permits forward-biasing of the diode 109 without a significant increase in the forward current. The layer 107 provides a barrier against such forward current. An optional oxide 114 barrier may also be arranged on the surface of the device between the catalyst 105 and the surface diode 113. Electrical contacts 101, 110 and 112 are arranged as shown in FIG. 1. Contacts 101 and 110 serve as electrical output leads for the substrate diode. Contacts 101 and 112 are the electrical output leads for the surface diode. In the device of FIG. 1, the catalyst layer 105 may comprise a quantum well structure (including quantum dots) having a thickness typically less than 20 ran and being sufficiently small so as to alter the density of electron states in the -catalyst to favor the production of substantially monoenergetic holes or electrons. The substrate diode 109 and the catalyst 105 may be separated by an interlayer 106 of metal, that permits matching the lattice parameters of the catalyst to this interlayer. The catalyst 105 and interlayer 106 comprise the quantum well . The interlayer 106 must be sufficiently thin so as to permit non- energy changing electron transport into the diode. The thickness of the interlayer 106 should be preferably less than 20 nanometers. In an exemplary embodiment of a device in accordance with the present invention, the substrate diode 109 comprises an n- type direct band gap semiconductor with a band gap chosen to favor the emission of energetic electrons. In a further exemplary embodiment, the thickness or cluster size (if arranged in clusters) of the catalyst layer 105 is sufficiently small so as to permit the appearance of band gaps, discrete electron states and catalyst properties unlike the same material in bulk. In this case, the catalyst 105 can be comprised, preferably, of gold, silver, copper, or nickel and be arranged as3 monolayer, 200 atom clusters. FIG. 2 shows an exetnplary embodiment of a device in accordance with the present invention in which the emissions of phonons generated by adsorbing and bonding reactions on or within catalyst surfaces clusters or nano-structures are converted into hydraulic fluid pressure. In accordance with the present invention, pressures generated by phonons directed - into a catalyst body on a first side of the catalyst body form a phonon wave which can be guided by the geometry of the catalyst (or. substrate upon which the catalyst may be situated) so that the phonons travel to the other side of the substrate and impart a pressure onto a fluid. The thickness of this travel should be less than the mean distance over which the direction of the phonon remains substantially unperturbed. The phonons arrive at an angle (a "grazing" angle) such that the directional and asymmetric pressure of the arriving phonons appears as wave motion on the other side of the catalyst body which pushes against a fluid such as a liquid metal or sacrificial interface, causing it to move in a direction parallel to the bottom surface. An apparent negative coefficient of friction between the wall and the fluid is exhibited due to the wave motion or directed impulses along the surface of the bottom of the device. The exemplary device comprises a substrate 202 with top and bottom surfaces having a saw-tooth pattern, as shown in the cross-sectional view of FIG. 2. The bottom surface is in contact with a hydraulic fluid 204. As shown in FIG. 2, the substrate can be thought of as comprising a plurality of sub- structures 200 having rectangular cross-sections and arranged adjacent to each other at an angle with respect to the hydraulic fluid 204. At the top surface of the substrate, each sub-structure 200 includes a layer 2C1 comprising a catalyst. On an exposed side surface between adjacent sub-structures, each sub- structure 200 includes a layer 202 of material which is inert with respect to the catalyst and the reactants. The body of each sub-structure is conprised of a substrate 203, which also acts as a phonon waveguide. Platinum can be used for the catalyst layer 201 and for the substrate 203 with air as the oxidizer, ethanol or methanol as the hydrocarbon reactant fuel and water or mercury as the hydraulic fluid 204. The hydraulic fluid can also serve as a coolant for the device, thereby permitting high power density operation. The catalyst 201 and substrate 203 may be comprised of the same material, e.g., platinum. Other substrate materials may be used based on structural considerations, manufacturability and/or impedance matching so as to maximize the propagation of the phonon motion into the hydraulic fluid. The thickness of the platinum catalyst layer 201 and substrate 203 should be less than the energy-changing mean free path of optical branch phonons or high frequency acoustic branch phonons, which is at least of order 10 nanometers and can be as large as one micron. Nanofabrication methods can be used to form the sawtooth patterns on the surfaces of the substrate 202, with the dimension of as unit of such pattern being as large as 1 micron. By depositing the inert layers 202 as shown, e.g., on the right-facing facets of the saw-tooth pattern of the top surface, a preferential direction is thereby established for reactions and thus for phonon propagation, as indicated by the arrow in FIG. 2. Acoustic, ultrasonic or gigahertz acoustic Rayleigh waves on the catalyst side can be used to stimulate the reaction rate and synchronize the emission of phonons. The waves increase the magnitude of. the phonon emission and cause coherent emission, greatly enhancing both the peak and average power. In a further embodiment, a thin layer or layers of material are arranged between the substrate and the fluid. These layers are comprised of materials having acoustic impedances between that cf the substrate 202 and the hydraulic fluid 204, so as to maxirrize the transmission of momentum into the hydraulic fluid and minimize reflections back into the substrate 2 04. The material should be selected so that the bulk modulus and phonon propagation properties of the material cause the phonons emerging from the substrate to be transmittied substantially into the fluid with minimal reflection and energy loss. In a further embodiment of a device in accordance with the present invention, the emissions of phonons generated by catalytic reactions are converted into electrical current by piezo-electric effects within materials as the phonons impact the materials. An exempLary embodiment of such a device is shown in FIG. 3. The exemplary device of FIG. 3 comprises a catalyst layer 301 arranged on a piezo-electric element 303, which is in turn arranged on a supporting substrate 304. The catalyst layer 301 can be implemented as a nanocluster, nanolayer or quantum well. Electrical leads 3 02 are provided at opposite ends of the piezo-electric element 303 across which a potential is developed, in accordance with the present invention. In the exemplary embodiment of FIG. 3, the catalyst layer 301 comprises platinum, with air as the oxidizer and ethanol or methanol as the hydrocarbon reactant fuel. The piezo-electric element 303 can comprise any piezomaterial, including semiconductors that are not normally piezoelectric, such as InGaAsSb. The lattice mismatch between the semiconductor and the platinum produces a strain, commonly called a deformation potential which induces piezoelectric properties in semiconductors, or ferroelectric or piezoelectric materials with a high nonlinearity such as (Ba, Sr)TiO3 thin films, AlxGa1-xAs/GaAs and strained layer InGaAs/GaAs (lll)B quantum well p-i-n structures. Where the- piezoelectric element 3 03 is comprised of a semiconductor, the semiconductor becomes a diode element that converts photons into electricity, collects electrons as electricity, and converts phonons into electricity. In the exemplary embodiment of FIG. 3, as the reactants interact with the catalytic layer 301, phonons generated by the reactions are conducted into the piezoelectric material 303. As a result, a potential is induced in the piezoelectric material 303 at the electrical contacts 302. The geometry of the substrate 303 is preferably such as to focus phonons so as to enhance the nonlinearity of the piezoelectric element 303. This results in self-rectification of the high frequency phonons. In an exemplary embodiment, the piezoelectric element 303 is preferably curved and shaped like a lens or concentrating reflector so as to focus the phonons generated by the catalyst on to the piezoelectric material. The focusing of the phonons causes large amplitude atomic motions at the focus. The atomic motions induced by this focusing cause the piezoelectric material to become nonlinear, causing non-linear responses such as the generation of electricity in the material at the focus. This in turn results in the piezo-material becoming a rectifier of the phonon-induced high frequency current. Acoustic, ultrasonic or gigahertz acoustic Rayleigh waves can be used on the catalyst side of the exemplary device of FIG. 3 to stimulate the reaction rate and synchronize the emission of phonons, to enhance the magnitude of the phonon emission and to cause coherent emission, greatly enhancing both the peak and average power delivered to the piezoelectric material 303. Acoustic Rayleigh waves accelerate oxidation reactions on platinum catalyst surfaces. Surface acoustic waves can be generated on the surface of the catalyst 3 01 using a generator (not shown) . Such waves may have acoustic, ultrasonic or gigahertz frequencies. The Rayleigh waves induce reactions so as to synchronize the reactions, which in turn synchronizes the emission of phonons. The result is a pulsing bunching of the reactions, which enhances the power delivered to the piezoelectric material 303. The frequency of operation of the device of FIG. 3 is preferably in the GHz range and lower so that rectification of the alternating currents produced by the piezoelectric material 303 can be achieved with conventional means, such as with semiconductor diodes. In a further exemplary embodiment of the present invention, electromagnetic radiation, such as infrared photons emitted by excited state products such as highly vibrationally excited radicals and final product molecules, is converted into electricity photovoltaically. Stimulated emission of radiation is used to extract the energy from the excited state products, such as highly vibrationally excited radical and reaction product molecules both on the catalyst surface and desorbing from it. The extracted energy appears in the form of a coherent beam or a super-radiant beam of infra-red or optical energy. The frequencies of the radiation correspond to fundamental (vibration quantum number change of 1) or overtones (vibration quantum number change 2 or greater) of the normal mode vibration frequencies of the reactants. Several different frequencies may be extracted simultaneously in this invention. While; the resulting coherent beam is useful in its own right, this high intensity beam can also be photovoltaically converted into electricity. In accordance with the present invention, such emissions are created by reactions on catalyst surfaces, and are accelerated by the use of optical cavities. FIG. 4 shows an exemplary embodiment of an electric generator for performing such a conversion. The device of FIG. 4 comprises one or more substrates 401 upon which a catalyst 402 is arranged in a plurality of islands, nanoclusters, quantum well clusters or quantum dots. The catalyst clusters are sufficiently spaced apart (e.g., tens of nanometers or more) and the substrate is made sufficiently thin (e.g., Less than a centimeter total optical thickness), so that IR absorbtion is mitigated at the frequencies of specie emission. The assembly of catalyst clusters on the substrates 401 is substantially transparent to the reaction radiations. The catalyst 402 is preferably platinum or palladium. The device preferably comprises a plurality of substrates 401 stacked so as to permit a volume of reactions. The catalyst-substrate stack 401/402 is enclosed in an optical cavity having a highly reflective element 403 and a less reflective element 404 arranged as shown in FIG. 4. The optical cavity and the catalyst-substrate stack 401/402 are preferably resonant to the reaction radiations or their overtones. The optical cavity can be used to stimulate overtone radiation, i.e., multipole radiation where the change in quantum number is 2 or more, to increase the energy of the radiation. The optical cavity preferably has multiple frequencies, as in a Fabrey-Perot cavity, that are tuned to overtones of the specie frequencies. A fuel 407, such as hydrogen, ethanol or methanol and an oxidizer 408, such as air, are introduced into the optical cavity where they interact with the catalyst-substrate stack 401/402. Lean mixtures of fuel can be used so as to minimize resonant transfer, exchange or decay of excited state vibrational energy to other specie of the same chemical makeup in the exhaust stream, during the time these species are in the optical cavity and the photovoltaic converter 405 collects the radiation and converts it into electricity. A stimulated emission initiator and synchronizer device 412 is used to initiate and synchronize the emissions in the optical cavity. The device 412 can be a commonly available The chemical reactants on the catalyst surface permit overtone transitions because they are part of a "ladder" of transitions and strongly polarized on the catalyst surface, which permits all the transitions to have non-zero dipole radiation transition matrix elements. Also, the reactants have no rotational smearing associated with free molecules in a gas because they are attached to the surface and can not rotate. These features permit a near monochromatic overtone light amplification by stimulated emission of radiation. The electromagnetic energy radiated by the stimulation of species, as in the embodiment of FIG. 4, can be formed into high brightness, quasi-monochromatic, poly-chromatic radiations or coherent beams. In each of the above described embodiments which include photovoltaic semiconductors, the catalyst is preferably operated at a high surface power density, e.g., in excess of 10 watts per square centimeter or with a peak surface power density of at least one watt per square centimeter, to enhance the efficiency of the photovoltaic semiconductors. What is claimed is: 1. A method of moving an object, comprising: providing a catalyst on a substrate; placing reactants in contact with the catalyst, the reactants interacting with the catalyst and generating phonons, wherein the phonons propagate into the substrate away from the catalyst; and directing the phonons towards the object. 2. The method of claim 1, wherein the catalyst is arranged in a plurality of clusters. 3. The method of claim 1, wherein the object is a fluid in contact with a surface of the substrate. 4. A method of generating electricity comprising: forming species in highly excited states on a catalyst thereby radiating electromagnetic energy; and converting the electromagnetic energy into electricity with a photovoltaic collector. 5. The method of claim 4, wherein the species includes at least one of an excited state radical and an exhaust product. 6. The method of claim 4, comprising stimulating and accelerating a reaction emission rate using an optical cavity. 7. The method of claim 4, comprising stimulating an overtone radiation using an optical cavity. 8. The method of claim 7, wherein the overtone radiation includes multipole rad:.ation with a change in quantum number of two or more. 9. The method of claim 4, wherein the catalyst operates at a peak surface power density greater than one watt per square centimeter. 10. A method of generating electromagnetic energy comprising: forming species :.n highly excited states on a catalyst; and stimulating the species to emit electromagnetic radiation. 11. A device for generating electricity, comprising: a catalyst, and a substrate, wherein the catalyst is arranged on the substrate and the substrate includes a substrate diode to receive charge carriers from the catalyst, wherein upon introducing a fuel and an oxidizer in contact with the catalyst, charge carriers are emitted by the catalyst and an electrical potential is developed across the substrate diode. 12. The device of claim 11 comprising a non-conducting layer arranged between the substrate diode and the catalyst, wherein the non-conducting layer permits control over a forward-bias and forward current characteristic of the substrate diode. 13. The device of claim 11 comprising a surface diode, the surface diode being arranged on a reactant side of the catalyst to receive and capture electrons. 14. The device of claim 11, wherein the substrate diode is forward biased so as to raise its conduction and valence bands above a fermi level of the catalyst so as to match energy levels of the adsorbed species. 15. The device of claim 11, wherein the substrate diode comprises an InGaAsSb semiconductor. 16. The device of claim 13, wherein the surface diode comprises an InGaAsSb semiconductor. 17. The device of claim 11, wherein the fuel includes at least one of ethanol, methanol and hydrogen. 18. The device of claim 11, wherein the substrate diode is a Schottky diode having a band gap larger than an energy of reactions on a surface of the catalyst. 19. The device of claim 13, wherein the surface diode is a Schottky diode having a band gap larger than a bond energy or a reaction energy. 20. The device of claim 11, wherein the substrate diode is a Schottky diode having a barrier height in a range of 0.05 to 0.4 volts. 21. The device of claim 13, wherein the surface diode is a Schottky diode having a barrier height in a range of 0.05 to 0.4 volts. 22. The device of claim 11,, wherein the catalyst includes at least one of platinum and palladium. 23. The device of claim 11, wherein the catalyst includes at least one of a quantum well and a quantum dot having a thickness sufficiently small so as to alter a density of electron states in the catalyst to favor the production of substantially monoenergetic holes or electrons. 24. The device of claim 11, comprising a layer of metal arranged between the substrate diode and the catalyst, wherein the layer of metal matches a catalyst lattice parameter and allows the metal and catalyst layers to be formed as a quantum well. 25. The device of claim 12, wherein the catalyst has a thickness of one nanometer or less. 26. The device of claim 11, wherein the substrate diode includes an n-type direct band gap semiconductor having a band gap which favors emission of energetic electrons. 27. The device of claim 11, wherein a dimension of the catalyst is sufficiently small so as to have properties unlike the same material in bulk. 28. The device of claim 11, wherein the catalyst includes at least one of gold, silver, copper, and nickel. 29. The device of claim 11 comprising a coolant on a bottom surface of the device. 30. The device of claim 11, wherein the catalyst operates at a peak surface power density greater than one watt per square centimeter. 31. A device for moving a fluid comprising: a catalyst, wherein reactants impinging on a surface of the catalyst cause phonons to be generated; a substrate, wherein the catalyst is arranged on a top side of the substrate; and a hydraulic fluid, wherein the hydraulic fluid is in contact with a bottom side of the substrate, wherein the substrate acts as an acoustic waveguide for the phonons, conveying the phonons to the bottom side of the substrate so as to move the hydraulic fluid in a preferred direction. 32. The device of claim 31, wherein the top side of the substrate has a cross section with a sawtooth pattern. 33. The device of claim 31, wherein the catalyst and an inert material are arranged on portions of the top side of the substrate so as to control the generation of phonons. 34. The device of claim 32, wherein the catalyst and an inert material are arranged on alternating facets of the sawtooth pattern. 35. The device of claim 31, wherein the bottom side of the substrate has a cross section with a sawtooth pattern. 36. The device of claim 31, wherein a wave including at least one of an acoustic, ultrasonic: and a gigahertz acoustic Rayleigh wave is applied to the catalyst to stimulate a reaction rate and synchronize the phonon emission, thereby enhancing a magnitude of the phonon emission and causing coherent emission. 37. The device of claim 31, comprising a layer of material arranged between the substrate and the fluid, wherein the material causes the phonons to be transmitted from the substrate substantially into the fluid. 38. A device for generating electricity comprising: a catalyst; and a substrate, wherein the catalyst is arranged on a surface of the substrate and the substrate includes a piezoelectric element, wherein phonons generated upon interaction of the catalyst with reactants travel through the piezoelectric element which develops an electrical potential as a result. 39. The device of claim 38, wherein the catalyst includes at least one of a nanocluster, nanolayer and a quantum well. 40. The device of claim 38, wherein the piezoelectric element includes a semiconductor having piezoelectric properties caused by a lattice mismatch between the semiconductor and the catalyst. 41. The device of claim 38, wherein the substrate focuses phonons so as to enhance a non-linear responses. 42. The device of claim 38, wherein a wave including at least one of an acoustic, ultrasonic and a gigahertz acoustic Rayleigh wave is applied to the catalyst to stimulate a reaction rate and synchronize the phonon emission, thereby enhancing a magnitude of the phonon emission and causing coherent emission. 43. A device for generating electricity comprising: a catalyst; a substrate, wherein the catalyst is arranged on the substrate; and a a photovoltaic converter, the photovoltaic converter being located anywhere visible to radiation emitted by reactions involving the catalyst. 44. The device of claim 43, wherein the catalyst includes at least one of a nanocluster, a nanolayer and a quantum well. 45. The device of claim 43 comprising an optical cavity, wherein the catalyst is, located in the optical cavity and wherein the optical cavity is tuned to a frequency of an excited state species within the cavity. 46. The device of claim 43, wherein the optical cavity has multiple frequencies that are tuned to overtones of the specie frequencies and wherein the optical cavity stimulates overtone transitions. 47. The device of claim 46, wherein the optical cavity is a Fabrey-Perot cavity. 48. The device of claim 45 comprising an optical oscillator for stimulating emissions in the optical cavity. 49. The device of claim 43, wherein the catalyst includes at least one of an island, nanocluster, quantum well cluster and a quantum dot and the substrate includes a plurality of substrates arranged in a stack, thereby forming a catalyst- substrate stack, wherein the catalyst-substrate stack is tuned to at least one of a frequency or overtone thereof of the radiation. 50. The device of claim 43, comprising cooling means for cooling the photovoltaic converter. 51. The method of claim 4 comprising storing the electrical energy in at least one of a capacitor, a super-capacitor and a battery. 52. The device of claim 11 comprising an electrical storage device, the electrical storage device being coupled to the substrate diode, wherein the electrical storage device includes at least one of a capacitor, a super-capacitor and a battery. 53. The device of claim 38 comprising: electrical contacts, the electrical contacts being arranged on the piezoelectric element, wherein the electrical potential appears at the electrical contacts; and an electrical storage device, the electrical storage device being coupled to the electrical contacts, wherein the electrical storage device includes at least one of a capacitor, a super-capacitor and a battery. 54. The device of claim 43 comprising an electrical storage device, the electrical storage device being coupled to the photovoltaic converter, wherein the electrical storage device includes at least one of a capacitor, a super-capacitor and a battery. The use of newly discovered chemical reaction products, created when reactants combine to form products on the surface of a catalyst, to generate electricity, beams of radiation or mechanical motion. The invention also provides methods to convert the products into electricity or motion. The electric generator consists of a catalyst nanocluster, nanolayer or quantum well placed on a substrate consisting of a semiconductor diode, and a semiconductor diode on the surface of the substrate near the catalyst. The device to generate mechanical motion consists of a catalyst nanocluster, nanolayer or quantum well placed on a substrate, and a hydraulic fluid in contact with the non-reaction side of the substrate, with the surfaces of both the catalyst and substrate mechanically formed to enhance the unidirectional forces on the fluid. Both devices use a fuel-oxidizer mixture brought in contact with the catalyst. The apparatus converts a substantial fraction of the reaction product energy into useful work during the brief interval before such products equilibrate with their surroundings.

Documents:

IN-PCT-2001-1162-KOL-CORRESPONDENCE.pdf

IN-PCT-2001-1162-KOL-FORM 27.pdf

in-pct-2001-1162-kol-granted-abstract.pdf

in-pct-2001-1162-kol-granted-assignment.pdf

in-pct-2001-1162-kol-granted-claims.pdf

in-pct-2001-1162-kol-granted-correspondence.pdf

in-pct-2001-1162-kol-granted-description (complete).pdf

in-pct-2001-1162-kol-granted-drawings.pdf

in-pct-2001-1162-kol-granted-examination report.pdf

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in-pct-2001-1162-kol-granted-form 13.pdf

in-pct-2001-1162-kol-granted-form 18.pdf

in-pct-2001-1162-kol-granted-form 2.pdf

in-pct-2001-1162-kol-granted-form 3.pdf

in-pct-2001-1162-kol-granted-form 5.pdf

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in-pct-2001-1162-kol-granted-reply to examination report.pdf

in-pct-2001-1162-kol-granted-specification.pdf

in-pct-2001-1162-kol-granted-translated copy of priority document.pdf