Embodiments of the present invention relate to treatments for atom probe components, including treatments for atom probe components used in atom probe devices (e.g., atom probe microscopes).
An atom probe (e.g., atom probe microscope) is a device which allows specimens to be analyzed on an atomic level. For example, a typical atom probe includes a specimen mount, an electrode, and a detector. During analysis, a specimen is carried by the specimen mount and a positive electrical charge (e.g., a baseline voltage) is applied to the specimen. The detector is spaced apart from the specimen and is negatively charged. The electrode is located between the specimen and the detector, and is either grounded or negatively charged. A positive electrical pulse (above the baseline voltage) and/or a laser pulse (e.g., photonic energy) is intermittently applied to the specimen. Alternately, a negative pulse can be applied to the electrode. With each pulse, one or more atom(s) on the specimen surface is ionized. The ionized atom(s) separate or “evaporate” from the surface, pass though an aperture in the electrode, and impact the surface of the detector. The identity of an ionized atom can be determined by measuring its time of flight between the surface of the specimen and the detector, which varies based on the mass/charge ratio of the ionized atom. The location of the ionized atom on the surface of the specimen can be determined by measuring the location of the atom's impact on the detector. Accordingly, as the specimen is evaporated, a three-dimensional map of the specimen's constituents can be constructed.
Specimens, electrodes, and other related components used in, or that are part of, the atom probe can be degraded or contaminated when various components are transferred from a preparation area (e.g., a focused ion beam (FIB) station or an electrical discharge machining (EDM) workstation) to the atom probe. For example, oxidation, corrosion, or other forms of contamination can occur during this transfer process, which in turn can influence ionization characteristics. In some cases, changes in ionization characteristics can decrease the likelihood of successful atom probe analysis (see e.g., M. K. Miller, Atom Probe Tomography (2000), which is fully incorporated herein by reference).
This problem can be exacerbated by the fact that specimens, electrodes, and related components can be prepared or assembled at one location and shipped great distances prior to being placed in an atom probe at another location. In addition, atom probe components can be stored at times in an uncontrolled environment at a given facility for long periods of time between preparation and use. Storage, shipping and handling typically occur in uncontrolled environments where these components can be contaminated or become oxidized. Oxidation and contamination of these components can degrade the performance of the atom probe. Even solvent and/or ultrasonic cleaning (standard ultra high vacuum (UHV) procedures) are often insufficient to clean these components after they have become contaminated or oxidized.
Historically some atom probe specimens have been heated to remove some contaminants from the surface of the specimens. However, in some cases, heating can degrade the atomic structure of the specimen, which in turn can affect the quality of analysis provided by the atom probe (see e.g., Miller). Ultraviolet lamps have also been used inside of atom probe chambers to desorb water vapor and other gasses (e.g. carbon dioxide) that have adsorbed onto the walls during venting of the instrument. Dry nitrogen purges have also been used to reduce the moisture or oxygen level in an atom probe chamber. In some cases, reaction chambers have been used to purposely oxidize or rapidly age specimens to simulate some real-world process in order to analyze materials that have been aged or used in service. Field-induced ion sputtering has also been used to sharpen atom probe specimens (see e.g., A. P. Janssen et al, The Sharpening of Field Emitter Tips by Ion Sputtering, J. Phys. D: Appl. Phys. 4, 118-123 (1971) and D. J. Larson et al., Sharpening and Positioning of Regions of Interest in Atom Probe Samples Using In-Situ Sputtering, Microscopy Microanal 9 (Suppl. 2) (2003), both of which are fully incorporated herein by reference). However, this process is labor intensive and somewhat problematic because the condition of the specimen must be manually monitored and the voltage used in the sputtering process must be manually adjusted. Accordingly, adjustments are often made too slowly or too inaccurately, potentially resulting in damage to the specimen. Accordingly, there is a need for additional atom probe component treatment processes.
The present invention is directed generally toward treatments for atom probe components. One aspect of the invention is directed toward a method for treating an atom probe component that includes providing an atom probe component having a surface. The method further includes removing material from the surface while the surface is positioned within at least a portion of an atom probe device or within a chamber that is attachable to an atom probe device.
Another aspect of the invention is directed toward a method for treating an atom probe specimen that includes providing an atom probe specimen. The method further includes sensing at least one parameter associated with a shape of the specimen. The method still further includes removing material from the surface of the specimen using an ion sputtering process and using a computing device to automatically control a voltage used in the ion sputtering process based on the at least one parameter.
Still another aspect of the invention is directed toward a method for treating an atom probe component that includes providing an atom probe component having a surface. The method further includes introducing photonic energy proximate to the surface of the atom probe component to at least one of (a) remove material from the surface, (b) make the surface smoother, and (c) alter the microstructure of the surface.
Yet another aspect of the invention is directed toward a method for treating an atom probe component that includes providing an atom probe component having a surface. The method further includes heating at least a portion of the surface to a high temperature. The method still further includes cooling a portion of the surface to anneal the at least a portion of the surface.
Still another aspect of the invention is directed toward a method for treating an atom probe component that includes providing an atom probe component having a surface. The method further includes coating at least a portion of the surface with a material to at least one of (a) increase an effective radius of a protrusion, (b) change the work function associated with the surface, and (c) protect the surface from contamination.
Yet another aspect of the invention includes a method for treating an atom probe component that includes positioning an atom probe component in an atom probe device. The method further includes cooling at least a portion of the atom probe component to at least one of (a) reduce a potential for field emissions, (b) reduce a potential for thermionic emission, and (c) reduce or slow a migration of contaminants within the atom probe device.
This Summary is provided to introduce a selection of concepts in a simplified form that are further described below in the Detailed Description. This Summary is not intended to identify key features or essential features of the claimed subject matter, nor is it intended to be used as an aid in determining the scope of the claimed subject matter.
In the following description, numerous specific details are provided in order to give a thorough understanding of embodiments of the invention. One skilled in the relevant art will recognize, however, that the invention may be practiced without one or more of the specific details, or with other methods, components, materials, etc. In other instances, well known structures, materials, or operations are not shown or described in order to avoid obscuring aspects of the invention.
References throughout the specification to “one embodiment” or “an embodiment” means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment of the present invention. Thus, the appearances of the phrase “in one embodiment” or “in an embodiment” in various places throughout the specification are not necessarily all referring to the same embodiment. Furthermore, the particular features, structures, or characteristics may be combined in any suitable manner in one or more embodiments.
Accordingly, various embodiments of the invention are described below. First, the structure and operation of atom probe devices are discussed. Then, various treatment processes in accordance with embodiments of the invention are described.
In the illustrated embodiment, each chamber 101 is operatively coupled to a fluid control system 105 (e.g., a vacuum pump, turbo molecular pump, and/or an ion pump) that is capable of lowering the pressure in the chambers 101 individually. Additionally, the atom probe device 100 can include sealable passageways 104 (e.g., gate valves) positioned in the walls 106 of the chambers 101 that allow items to be placed in, removed from, and/or transferred between the chambers 101. In the illustrated embodiment, a first passageway 104a is positioned between the interior of the load lock chamber 101a and the exterior of the atom probe device 100, a second passageway 104b is positioned between the interior of the load lock chamber 101a and the interior of the buffer chamber 101b, and a third passageway 104c is positioned between the interior of the buffer chamber 101b and the interior of the analysis chamber 101c. In certain embodiments, a transfer device 194 (e.g., a mechanical arm) can be positioned to move items between the chambers 104 and/or place or remove items on/in the atom probe assembly 110.
In
The fluid control system 105 can then lower the pressure in the buffer chamber 101b (e.g., reduce the pressure to 10−8-10−9 torr). The pressure in the analysis chamber 101c can be set at approximately the same or a lower pressure than the buffer chamber 101b. The third passageway 104c can be opened, the specimen 130 can be transferred to the analysis chamber 101c, and the third passageway 104c can be sealed.
The fluid control system 105 can then reduce the pressure in the analysis chamber 101c (e.g., the pressure can be lowered to 10−10-10−11 torr) prior to analysis of the specimen 130. In the illustrated embodiment, a getter 192 is positioned in the analysis chamber 101c to aid in lowering the pressure. In other embodiments, a getter 192 can be used in other chambers 101 or not used in the atom probe device. In still other embodiments, multiple items can be loaded or positioned in the chambers 101 of the atom probe device 100 using a similar method. For example, multiple specimens 130 and/or electrodes 120 can be positioned in the buffer chamber 101b on one or more carousels 196 (shown in further detail in
In selected embodiments, the carousel 196 can include pucks or holders 197 that carry the specimens 130 and/or electrodes 120 on the carousel. The holders 197 can be removable from the carousel to facilitate movement and installation of individual specimens 130 and/or electrodes 120 in the atom probe assembly 110. In the illustrated embodiment, the carousel carries first holders 197a configured to hold electrodes 120 and second holders 197b configured to hold specimens. In selected embodiments, the carousel 196 and/or holders 197 can include labeling 198. The labeling 198 can be used to identify various portions of the carousel and holders so that various atom probe components can be identified and located by their position on a carousel. For example, the labeling 198 can be used to identify one carousel from another, various carousel, positions, and individual holders.
During analysis of the specimen 130, a positive electrical charge (e.g., a baseline voltage) can be applied to the specimen. The detector can be negatively charged and the electrode can be either grounded or negatively charged. A positive electrical pulse (above the baseline voltage) can be intermittently applied to the specimen 130 or a negative electrical pulse can be applied to the electrode 120. The electric field(s) created by the electrical charges can provide energy to ionize one or more atom(s) on the surface of the specimen 130. These ionized atom(s) can separate or “evaporate” from the surface, pass though an aperture in the electrode 120, and impact the surface of the detector 114. As the specimen 130 is evaporated, a three-dimensional map of the specimen's constituents can be constructed.
In certain embodiments, laser or photonic energy from the emitting device 150 can be used to thermally pulse a portion of the specimen 130 to assist with the evaporation process (e.g., the removal of ionized atoms). Additionally, in certain embodiments a temperature control device 116 can be used to cool the specimen 130 to reduce thermal motion and thermionic emission from the specimen. Thermionic emission includes the flow of one or more electrons from a metal or metal oxide surface, caused by thermal vibrational energy overcoming the electrostatic forces holding electrons to the surface. Thermionic emission from portions of the specimen 130 (or specimens in a multiple array) can reduce the accuracy of the analysis process.
In other embodiments, the atom probe device 100 can have more, fewer, and/or other arrangements of components. For example, in certain embodiments the atom probe device 100 can include more or fewer chambers, or no chambers. In selected embodiments, the atom probe device 100 can include one or more chambers dedicated for carrying out one or more of the atom probe component treatment processes discussed below.
In other embodiments, the atom probe device can include multiple atom probe electrodes 120 and/or electrode(s) 120 having different configurations/placements (e.g., planar electrode(s)). In still other embodiments, the atom probe device 100 includes more, fewer, or different emitting devices 150; more, fewer, or different temperature control systems 116; and/or more, fewer or different electrical sources 112. As used here in, atom probe components 180 can include any component associated with an atom probe device. For example, atom probe components 180 can include specimens, electrodes, the atom probe assembly, specimen holders, electrode holders, carousels, and other atom probe device components (e.g. chamber walls and gate valve surfaces).
Selected embodiments of the invention include treatment processes for various atom probe components. For example, selected embodiments include processes for removing contaminates from various atom probe components. Other embodiments include treatment processes that prevent contamination. Still other embodiments include processes that improve the surface characteristics of various atom probe components. For example, various treatment processes can include ion milling, plasma cleaning/etching, chemical etching, annealing, coating, component cooling, laser or photonic energy application, and automated field induced ion sputtering.
In certain circumstances, some of these embodiments can improve the operation of the atom probe device and/or the analysis process. For example, some of the embodiments can improve viability in atom probe analysis by reducing field electron emission, gaseous vacuum discharge, and/or specimen fracture rate. Additionally, some treatments can improve the overall vacuum level and integrity in the atom probe device by liberating or oxidizing materials adsorbed on the interior of the atom probe chambers. Still other embodiments can decrease non-uniformities (e.g., distortions) in the electric field(s) used during analysis, which can interfere with the operation of the atom probe (e.g., non-uniformities in the electric field(s) can cause interfere with the orderly evaporation of the specimen and/or cause electrode or specimen field emission).
Many or all of the embodiments discussed below can be performed in the atom probe device (e.g., in the load lock chamber, buffer chamber, and/or the analysis chamber). Some of the embodiments discussed below can be performed in a minimally controlled environment (e.g., at room temperatures and ambient pressure) or in clean rooms having controlled environments where various environmental characteristics (e.g., temperature, pressure, and the composition of the surrounding fluid) can be selected and/or controlled. Accordingly, certain process portions can be accomplished under selected environmental conditions (e.g., in a high or low temperature environment and/or in a high or low pressure environment). The atom probe component(s) can then be transferred to the atom probe device (e.g., via a controlled environment chamber). Additionally, many or all of the processes can be performed in an environmentally controlled container or chamber that is couplable to the atom probed device, allowing the atom probe component to be transferred to the atom probe device while remaining in a controlled environment.
In the illustrated embodiment, an atom probe electrode 420 is positioned in the container 490 and coupled to an energy source 412 (e.g., electrical source) and a thermal control device 416. In
For example in certain embodiments, the container 490 does not include a specimen mount 411 and/or an emitting device 450. In other embodiments, a getter is used to control (e.g., lower) the pressure in the container 490 instead of the fluid control system 405. In still other embodiments, the thermal control device 416 has other arrangements. For example, the thermal control device 416 can be configured to cool or heat other atom probe components, a fluid in the container 490, and/or the entire container. In yet other embodiments, the atom probe component is treated in an environmentally controlled or uncontrolled lab and an environmentally controlled container 490 (e.g., a nitrogen dry box) is used to store the atom probe component and/or transport the atom probe component to an atom probe device.
In certain embodiments, removing the material from the surface of the atom probe component can include removing at least a portion of a contaminant carried on the atom probe component. For example, a contaminant can include any unwanted material on or integral with the surface of the atom probe component, including oxidations, oxides, nitrides, solvents, oil, passive layers, hydrocarbons, other environmental contaminants, and the like. In other embodiments, the surface can include an original surface and removing material from the surface of the atom probe component can include removing at least a portion of the original surface to form a new surface, so that (a) the new surface has fewer protrusions than the original surface, (b) an effective radius of one or more protrusions on the new surface is increased over the one or more protrusions on the original surface, or (c) both (a) and (b).
For example,
In selected embodiments, material can be removed from the surface of the atom probe component using an ion milling process. In other embodiments, material can be removed from the surface of the atom probe component using a plasma or plasma based process. In still other embodiments, material can be removed from the surface of the atom probe component using a chemical etching process. In yet other embodiments, material can be removed from the surface of the atom probe component using a laser or photonic energy emitter (e.g., to remove a layer of material from the surface of the atom probe device).
For example, in certain embodiments an ion beam milling process can be used to remove material from a surface of an atom probe component. The process can include impacting material on the surface of the atom probe and removing material from the surface using the ion beam. In a selected embodiment, the process can be performed in the container 490, shown in
In certain embodiments, ion milling treatments can be particularly useful for removing contaminants, surface oxides, or surface nitrides. Additionally, in selected embodiments ion milling can extend the useful life of an atom probe electrode or result in better data quality (due to reduced noise). In still other embodiments, use of ion milling can enable analysis of materials that could not previously be analyzed in an atom probe due to fast forming passivation layers. In selected embodiments, a masking material (e.g., a photoresist material) or physical barrier can be used to block or occlude the ion beam from impacting certain portions of the atom probe component and/or selected atom probe components that are positioned in a chamber where an ion milling process is being used. This feature can allow selective milling of desired areas or components.
In other embodiments, a plasma or plasma process can also be used to remove material from an atom probe component. For example, the process can include introducing a plasma proximate to a surface of an atom probe component and removing material from the surface of the atom probe component using the plasma. For example, in selected embodiments the plasma process can be carried out in the container 490, shown in
In still other embodiments plasma processes can be accomplished in an atom probe device (e.g., in the load lock or buffer chamber). For example, as shown in
In selected embodiments, plasma can be generated from oxygen, nitrogen, argon, nitrogen triflouride, and/or the like. In certain embodiments, plasmas can be used that are particularly well suited to react with certain types of materials. For example, in selected embodiments a plasma can be used that is particularly well suited for removing specific contaminants. In some embodiments, a plasma process can be carried out at high or low temperatures or pressures. For example, in certain embodiments when using a plasma generated from nitrogen triflouride, with or without argon, elevated temperatures can expedite material removal.
In yet other embodiments, a chemical process or chemical etching process can be used to remove material from a surface of an atom probe component. For example, the process can include introducing a chemical agent proximate to the surface of the atom probe component and removing material from the surface of the atom probe component using the chemical agent. Various chemical-based material removal methods (including both wet chemistry and vapor etch) can be used to remove material from an atom probe components. For example, sulfur hexafluoride (SF6) can etch away portions of protrusions on a silicon surface of an atom probe component when the surface is maintained in an environment with a pressure of 0.6-2 mbar.
In selected embodiments, a chemical etching process can be carried out in the container 490 shown in
In still other embodiments, laser or photonic energy can be used to remove material from a surface of an atom probe component. For example, in selected embodiments the emitting device 450 in the container 490, shown in
As shown in
In selected embodiments, the annealing process can cause changes in the microstructure of the material. In certain embodiments the strength and hardness of the surface can be altered, as well as the crystalline structure and electronic properties. For example, the grain size of the material on the surface of an atom probe component can be increased when a surface is heated close to the melting point for a prolonged period of time. In selected embodiments, a larger grain size can reduces a materials susceptibility to absorb water vapor, thereby reducing outgassing in an atom probe analysis chamber. Additionally, in some embodiments a larger grain size can raise the overall field emission threshold of the material, thereby reducing the emission rate of electrons from the material and/or improving the electric field homogeneity. Because it is suspected that electron emission from components within the chamber located proximate to (e.g., within a few hundred microns on a specimen can create spurious emission of atoms from the specimen, an annealing process might be used on these components to reduce these spurious emissions. By reducing these emissions it is expected that the overall noise can be reduced during the analysis process.
In still other embodiments, the annealing process may be useful in preventing certain components form oxidizing, forming other contaminant layers, and/or picking up contaminants. Because the annealing process can alter the microstructure of an atom probe component surface, in selected embodiments annealing the surface may reduce the tendency for the surface to react with certain contaminants or with the environment. Accordingly, in certain embodiments the annealing process might be used on atom probe components that are going to be shipped or stored in an uncontrolled environment.
As illustrated in
For example, in selected embodiments thick film deposition techniques including, but not limited to, electroplating can be used to apply a coating to an atom probe component. In one embodiment the container 490, shown in
In other embodiments, a coating having a high work function material (e.g., platinum or tungsten) can be used. Materials with a high work function include materials which require larger amounts of energy to liberate electrons from their surfaces as compared to materials having low work functions. By adding material having a high work function through a coating process, the effective work function of the component being coated can be increased, thereby reducing electron emission from the surface during atom probe analysis. In embodiments where high work function material is used to coat a specimen, the high work function material can be removed from the tip of the specimen for analysis while the high work function coating is retained on other portions of the specimen.
In other embodiments, it can be desirable to coat an atom probe component with a low work function material. For example, in some embodiments the deposition of a low work function material may inhibit oxidation or corrosion on a component (e.g., on the apex of a specimen). Because the low work function material is more easily field evaporated, the material can be readily removed during the atom probe analysis process.
In other embodiments, thin film coating techniques can be used. These techniques can include Vapor or plasma deposition, chemical vapor deposition, physical vapor deposition, electron beam deposition, molecular beam epitaxy (MBE) and/or the like. Many of these processes can be used with or without an electrical bias or field being applied to the atom probe component and can be accomplished in the container 490, shown in
As illustrated in
In selected embodiments, after the specimen has been cooled the specimen can be analyzed via the atom probe analysis process. In selected embodiments, cooling can continue during the analysis process. For example, in one embodiment, a first portion (e.g., the base) of the specimen can be cooled and laser or photonic energy can be applied to a second portion (e.g., the tip or apex) of the specimen to aid in evaporation. In selected embodiments, this feature can reduce field emissions from the base of the specimen during the analysis process. Although, for illustrative purposes the cooling process was discussed with reference to a specimen, the cooling process can be used on other atom probe components (e.g., electrodes, mounts, and/or the like).
As illustrated in
For example, in
In still other embodiments, photonic energy can be applied to the surface of the atom probe component to heat the surface (e.g., to anneal the surface similar to the annealing process discussed above). In yet other embodiments, laser or photonic energy can be applied to the surface to melt the surface. As the surface cools a smoother surface can be formed, thereby reducing protrusions and/or the potential for field emissions. In selected embodiments, annealing and/or melting the surface can alter the atomic structure of the surface and/or affect the work function associated with the surface. Additionally, as discussed above, photonic energy can also be used to remove material from the surface of the atom probe component. In still other embodiments, the process of applying photonic energy can be carried out on a portion of an atom probe device (e.g., in the load lock, buffer chamber, and/or analysis chamber).
In selected embodiments, coatings can be used in conjunction with photonic energy to obtain a desired effect. For example, in certain embodiments a coating configured to absorb photonic energy can be used to enhance the effectiveness of the photonic energy. For instance, specimens made from certain materials have poor emissivity do not absorb photonic energy effectively. By applying a thin coating that absorbs laser or photonic energy efficiently (e.g., gold or silicon oxy-nitride), the specimen may be thermally pulsed via the photonic energy during the analysis process.
In other embodiments, a coating configured to reflect photonic energy can be used to control the absorption of photonic energy into an atom probe component. For example, a reflective coating can be applied to a specimen below the apex or tip. As the tip of the specimen is exposed to photonic energy, the photonic energy can almost exclusively be absorbed in the tip of the specimen (e.g., at least a portion of the photonic energy can be reflected away from the coated portion of the specimen). The result can be a very controlled absorption of the laser or photonic energy in the tip region, and therefore a very controlled heating of the region of interest. In selected embodiments, this can result in better mass resolution and lower noise during analysis.
As described in Sharpening and Positioning of Regions of Interest in Atom Probe Samples using In-Situ Sputtering, an ion sputtering process is accomplished by applying a negative potential to a field ion sample to induce field emission in the presence of neon gas atoms at a reduced pressure in a chamber of an atom probe device (e.g., in the analysis chamber in which neon gas has been introduced via a fluid control device). Emitted electrons ionize the neon gas atoms and the electric field from the sample accelerates the ions back to the sample, from which they remove material by ion sputtering. This process may be used not only to sharpen samples, but also to position the specimen apex at the region of interest.
Currently, this process is accomplished manually. For example, an operator manually selects a voltage and observes the sputtering process (e.g., by using a scanning electron microscope to examine the specimen and/or observing a field ion image quality). The operator then adjusts the negative potential (e.g., the sputtering current) by some amount and observes the sputtering process. This process is labor intensive and results in significant time delays between sputtering current adjustments.
In selected embodiments of the invention, the computer 115 (shown in
For example, in one embodiment an operator can select a desired amount of material to be removed from the specimen. For instance, in certain embodiments the operator can select a desired sharpness of the specimen tip, a desired shape of the specimen, the amount of material to be removed (e.g., to remove a contaminant, to create a new surface with fewer protrusions, to create a new surface with a protrusion having an increased effective radius, and/or the like). Based on the desired amount of material to be removed, the computer 115 can command the sensor 175 to sense a parameter associated with the shape of the specimen 130. The sensor can sense the parameter and send data corresponding to the parameter to the computer 115. The computer can compute a desired sputtering current and send a command to the electrical source 112 to provide the desired amount of current to the specimen.
Based on changes and/or the rate of changes in the parameter (or lack thereof) the computer can adjust the sputtering current via the same process. Once the parameter indicates that the desired sharpness of the specimen tip, a desired shape of the specimen, and/or the desired amount of material removal has been achieved, the computer can automatically terminate the sputtering process (e.g., set the sputtering current to zero). In selected embodiments, this automated sputtering process can be much less labor intensive and the sputtering current can be adjusted in a more timely manner as compared to the manual process.
In other embodiments, the automated sputtering process can be carried out in other chambers of the atom probe device or in a chamber similar to the container 490, shown in
In selected embodiments, many or all of the treatment strategies or processes discussed above can be automated (e.g., as computer implemented processes) and stored in a database or other computer readable medium. Accordingly, individual processes can be recalled and used at the appropriate time. For example, in one embodiment atom probe chambers that have been exposed to the atmosphere, say during service, may undergo a more rigorous cleaning regimen than atom probe chambers that are being cleaned or treated after use. In other embodiments, certain specimens, electrodes or carousels may require specific and/or different cleaning treatments or treatment intervals. Accordingly, the labeling 198 (shown in
From the foregoing, it will be appreciated that specific embodiments of the invention have been described herein for purposes of illustration, but that various modifications may be made without deviating from the invention. Additionally, aspects of the invention described in the context of particular embodiments may be combined or eliminated in other embodiments. Although advantages associated with certain embodiments of the invention have been described in the context of those embodiments, other embodiments may also exhibit such advantages. Additionally, not all embodiments need necessarily exhibit such advantages to fall within the scope of the invention. Accordingly, the invention is not limited except as by the appended claims.
This application claims the benefit of U.S. Provisional Patent Application No. 60/691,004, filed Jun. 16, 2005, entitled ATOM PROBE COMPONENT TREATMENTS, which is fully incorporated herein by reference.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US06/23532 | 6/16/2006 | WO | 00 | 8/12/2008 |
Number | Date | Country | |
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60691004 | Jun 2005 | US |