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Atom probe

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or a voltage pulse (typically 1-2 kV) with pulse repetition rates in the hundreds of kilohertz range is applied to a counter electrode. The application of the pulse to the sample allows for individual atoms at the sample surface to be ejected as an ion from the sample surface at a known time. Typically the pulse amplitude and the high voltage on the specimen are computer controlled to encourage only one atom to ionize at a time, but multiple ionizations are possible. The delay between application of the pulse and detection of the ion(s) at the detector allow for the computation of a mass-to-charge ratio.
210:. It incorporated the features of the 10-cm Atom-Probe yet “... departs completely from atom probe philosophy. Rather than attempt to determine the identity of a surface species producing a preselected ion-image spot, we wish to determine the complete crystallographic distribution of a surface species of preselected mass-to-charge ratio. Now suppose that instead of operating the continuously, it is turned on for a short time coincidentally with the arrival of a preselected species of interest by applying a 31: 66:, in that the magnification effect comes from the magnification provided by a highly curved electric field, rather than by the manipulation of radiation paths. The method is destructive in nature removing ions from a sample surface in order to image and identify them, generating magnifications sufficient to observe individual atoms as they are removed from the sample surface. Through coupling of this magnification method with 94:. Furthermore, in normal operation (as opposed to a field ionization modes) the atom probe does not utilize a secondary source to probe the sample. Rather, the sample is evaporated in a controlled manner (field evaporation) and the evaporated ions are impacted onto a detector, which is typically 10 to 100 cm away. 1126:
Ion overlap in some samples (e.g. between oxygen and sulfur) resulted in ambiguous analysed species. This may be mitigated by selection of experiment temperature or laser input energy to influence the ionisation number (+, ++, 3+ etc.) of the ionised groups. Data analysis can be used in some cases to
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The data obtained from the evaporative process is however not without artefacts that form the physical evaporation or ionisation process. A key feature of the evaporation or field ion images is that the data density is highly inhomogeneous, due to the corrugation of the specimen surface at the atomic
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Typically the sweep takes the simple form of advancement of the surface, such that the surface is expanded in a symmetric manner about its advancement axis, with the advancement rate set by a volume attributed to each ion detected and identified. This causes the final reconstructed volume to assume a
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The computational conversion of the ion sequence data, as obtained from a position-sensitive detector to a three-dimensional visualisation of atomic types, is termed "reconstruction". Reconstruction algorithms are typically geometrically based and have several literature formulations. Most models for
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Thus for an ion which traverses a 1 m flight path, across a time of 2000 ns, given an initial accelerating voltage of 5000 V (V in Si units is kg.m^2.s^-3.A^-1) and noting that one amu is 1Ă—10 kg, the mass-to-charge ratio (more correctly the mass-to-ionisation value ratio) becomes
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ion under the sample conditions would have acquired roughly 1.4x10^6/1.41 ms. If a detector was placed at a distance of 1 m, the ion flight times would be 1/1.4x10^6 and 1.41/1.4x10^6 s. Thus, the time of the ion arrival can be used to infer the ion type itself, if the evaporation time
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to some nominal ground potential, the speed at which the ion is travelling can be estimated by the energy transferred into the ion during (or near) ionisation. Therefore, the ion speed can be computed with the following equation, which relates kinetic energy to energy gain due to the electric field,
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patent, was developed by Mike Miller starting in 1983 and culminated with the first prototype in 1986. Various refinements were made to the instrument, including the use of a so-called position-sensitive (PoS) detector by Alfred Cerezo, Terence Godfrey, and George D. W. Smith at Oxford University in
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was a “new and simple atom probe which permits rapid, in depth species identification or the more usual atom-by atom analysis provided by its predecessors ... in an instrument having a volume of less than two liters in which tip movement is unnecessary and the problems of evaporation pulse stability
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methods. Since 2006, commercial systems with laser pulsing have become available and this has expanded applications from metallic only specimens into semiconducting, insulating such as ceramics, and even geological materials. Preparation is done, often by hand, to manufacture a tip radius sufficient
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These poles and zone-lines, whilst inducing fluctuations in data density in the reconstructed datasets, which can prove problematic during post-analysis, are critical for determining information such as angular magnification, as the crystallographic relationships between features are typically well
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chamber. After introduction into the vacuum system, the sample is reduced to cryogenic temperatures (typically 20-100 K) and manipulated such that the needle's point is aimed towards an ion detector. A high voltage is applied to the specimen, and either a laser pulse is applied to the specimen
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Specimen geometry during the analysis is uncontrolled, yet controls projection behaviour, hence there is little control over the magnification. This induces distortions into the computer generated 3D dataset. Features of interest might evaporate in a physically different manner to the bulk sample,
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Collectable ion volumes were previously limited to several thousand, or tens of thousands of ionic events. Subsequent electronics and instrumentation development has increased the rate of data accumulation, with datasets of hundreds of million atoms (dataset volumes of 10 nm). Data collection
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The first few decades of work with APT focused on metals. However, with the introduction of the laser pulsed atom probe systems applications have expanded to semiconductors, ceramic and geologic materials, with some work on biomaterials. The most advanced study of biological material to date using
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When reconstructing the data, owing to the evaporation of successive layers of material from the sample, the lateral and in-depth reconstruction values are highly anisotropic. Determination of the exact resolution of the instrument is of limited use, as the resolution of the device is set by the
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to convert detector positions back to a 2D surface embedded in 3D space, R. By sweeping this surface through R as a function of the ion sequence input data, such as via ion-ordering, a volume is generated onto which positions the 2D detector positions can be computed and placed three-dimensional
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a time T after the evaporation pulse has reached the specimen. If the duration of the gate pulse is shorter than the travel time between adjacent species, only that surface species having the unique travel time T will be detected and its complete crystallographic distribution displayed.” It was
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Through successive evaporation of material, layers of atoms are removed from a specimen, allowing for probing not only of the surface, but also through the material itself. Computer methods are used to rebuild a three-dimensional view of the sample, prior to it being evaporated, providing atomic
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Atom probe has typically been employed in the chemical analysis of alloy systems at the atomic level. This has arisen as a result of voltage pulsed atom probes providing good chemical and sufficient spatial information in these materials. Metal samples from large grained alloys may be simple to
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The resultant deflection means that in these regions of high curvature, atomic terraces are belied by a strong anisotropy in the detection density. Where this occurs due to a few atoms on a surface is usually referred to as a "pole", as these are coincident with the crystallographic axes of the
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This form of data manipulation allows for rapid computer visualisation and analysis, with data presented as point cloud data with additional information, such as each ion's mass to charge (as computed from the velocity equation above), voltage or other auxiliary measured quantity or computation
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respectively. Since then, there have been many refinements to increase the field of view, mass and position resolution, and data acquisition rate of the instrument. The Local Electrode Atom Probe was first introduced in 2003 by Imago Scientific Instruments. In 2005, the commercialization of the
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The magnification in an atom is due to the projection of ions radially away from the small, sharp tip. Subsequently, in the far-field, the ions will be greatly magnified. This magnification is sufficient to observe field variations due to individual atoms, thus allowing in field ion and field
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Field evaporation is an effect that can occur when an atom bonded at the surface of a material is in the presence of a sufficiently high and appropriately directed electric field, where the electric field is the differential of electric potential (voltage) with respect to distance. Once this
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Whilst the uncertainty in the atomic mass computed by time-of-flight methods in atom probe is sufficiently small to allow for detection of individual isotopes within a material this uncertainty may still, in some cases, confound definitive identification of atomic species. Effects such as
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The canonical feature of atom probe data, is its high spatial resolution in the direction through the material, which has been attributed to an ordered evaporation sequence. This data can therefore image near atomically sharp buried interfaces with the associated chemical information.
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Optionally, an atom probe may also include laser-optical systems for laser beam targeting and pulsing, if using laser-evaporation methods. In-situ reaction systems, heaters, or plasma treatment may also be employed for some studies as well as a pure noble gas introduction for FIM.
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Semi-conductor materials are often analysable in atom probe, however sample preparation may be more difficult, and interpretation of results may be more complex, particularly if the semi-conductor contains phases which evaporate at differing electric field strengths.
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with a proximity focussed, dual channel plate detector, an 11.8 cm drift region and a 38° field of view. An FIM image or a desorption image of the atoms removed from the apex of a field emitter tip could be obtained. The 10-cm Atom Probe has been called the
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Results may be contingent on the parameters used to convert the 2D detected data into 3D. In more problematic materials, correct reconstruction may not be done, due to limited knowledge of the true magnification; particularly if zone or pole regions cannot be
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with a mass spectrometer having a single particle detection capability and, for the first time, an instrument could “... determine the nature of one single atom seen on a metal surface and selected from neighboring atoms at the discretion of the observer”.
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superposition of differing ions with multiple electrons removed, or through the presence of complex species formation during evaporation may cause two or more species to have sufficiently close time-of-flights to make definitive identification impossible.
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Such data is critical in determining the effect of alloy constituents in a bulk material, identification of solid-state reaction features, such as solid phase precipitates. Such information may not be amenable to analysis by other means (e.g.
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1988. The Tomographic Atom Probe (TAP), developed by researchers at the University of Rouen in France in 1993, introduced a multichannel timing system and multianode array. Both instruments (PoSAP and TAP) were commercialized by
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scale. This corrugation gives rise to strong electric field gradients in the near-tip zone (on the order of an atomic radii or less from the tip), which during ionisation deflects ions away from the electric field normal.
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Applications such as ion implantation may be used to identify the distribution of dopants inside a semi-conducting material, which is increasingly critical in the correct design of modern nanometre scale electronics.
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Many designs have been constructed since the method's inception. Initial field ion microscopes, precursors to modern atom probes, were usually glass blown devices developed by individual research laboratories.
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Whilst the magnification of both the field ion and atom probe microscopes is extremely high, the exact magnification is dependent upon conditions specific to the examined specimen, so unlike for conventional
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Whether evaporated from the material itself, or ionised from the gas, the ions that are evaporated are accelerated by electrostatic force, acquiring most of their energy within a few tip-radii of the sample.
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condition is met, it is sufficient that local bonding at the specimen surface is capable of being overcome by the field, allowing for evaporation of an atom from the surface to which it is otherwise bonded.
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A counter electrode that can be a simple disk shape (like earlier generation atom probes), or a cone-shaped Local Electrode. The voltage pulse (negative) is typically applied to the counter electrode.
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and produce a projected image of protruding atoms at the tip apex. The image resolution is determined primarily by the temperature of the tip but even at 78 Kelvin atomic resolution is achieved.
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Valley, John W.; Reinhard, David A.; Cavosie, Aaron J.; Ushikubo, Takayuki; Lawrence, Daniel F.; Larson, David J.; Kelly, Thomas F.; Snoeyenbos, David R.; Strickland, Ariel (2015-07-01).
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pulsed laser atom probe (PLAP) expanded the avenues of research from highly conductive materials (metals) to poor conductors (semiconductors like silicon) and even insulating materials.
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scale information on the structure of a sample, as well as providing the type atomic species information. The instrument allows the three-dimensional reconstruction of up to billions of
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Assuming that the ion is accelerated during a very short interval, the ion can be assumed to be travelling at constant velocity. As the ion will travel from the tip at voltage V
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Modern day atom probe tomography uses a position sensitive detector aka a FIM in a box to deduce the lateral location of atoms. The idea of the APT, inspired by J. A. Panitz's
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Atom probe samples are shaped to implicitly provide a highly curved electric potential to induce the resultant magnification, as opposed to direct use of lensing, such as via
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the tip radius. A practical tip to screen distances may range from several centimeters to several meters, with increased detector area required at larger to subtend the same
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times vary considerably depending upon the experimental conditions and the number of ions collected. Experiments take from a few minutes, to many hours to complete.
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cathode when subjected to a sufficiently high electric field (~3-6 V/nm). The needle is oriented towards a phosphor screen to create a projected image of the
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data with attributed experimentally measured values, such as ion time of flight or experimentally derived quantities, e.g. time of flight or detector data.
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at the tip apex. The image resolution is limited to (2-2.5 nm), due to quantum mechanical effects and lateral variations in the electron velocity.
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Practically speaking, the usable magnification will be limited by several effects, such as lateral vibration of the atoms prior to evaporation.
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MyScope Atom Probe Tomography - An online learning environment for those who want to learn about atom probe provided by Microscopy Australia
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Relativistic effects in the ion flight are usually ignored, as realisable ion speeds are only a very small fraction of the speed of light.
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altering projection geometry and the magnification of the reconstructed volume. This yields strong spatial distortions in the final image.
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MĂĽller, Erwin W.; Bahadur, Kanwar (1956). "Field Ionization of gases at a metal surface and the resolution of the field ion microscope".
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Visualisation of data obtained from an atom probe, each point represents a reconstructed atom position from detected evaporated ions.
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Gordon, L. M.; Joester, D. (2011). "Nanoscale chemical tomography of buried organic–inorganic interfaces in the chiton tooth".
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A cooling system to reduce atomic motion, such as a helium refrigeration circuit - providing sample temperatures as low as 15K.
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A vacuum system for maintaining the low pressures (~10 to 10 Pa) required, typically a classic 3 chambered UHV design.
1857:"Atom Probe Tomography of Human Tooth Enamel and the Accurate Identification of Magnesium and Carbon in the Mass Spectrum" 1004:) etc. Where the edges of an atomic terrace causes deflection, a low density line is formed and is termed a "zone line". 250: 851: 565: 97:
The samples are required to have a needle geometry and are produced by similar techniques as TEM sample preparation
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Gordon, L.M.; Tran, L.; Joester, D. (2012). "Atom Probe Tomography of Apatites and Bone-Type Mineralized Tissues".
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Subsequently, atom probe has been used in the analysis of the chemical composition of a wide range of alloys.
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The standard projection model for the atom probe is an emitter geometry that is based upon a revolution of a
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Subsequently, the accelerative force on any given ion is controlled by the electrostatic equation, where
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www.atomprobe.com - A CAMECA provided community resource with contact information and an interactive FAQ
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fabricate, particularly from wire samples, with hand-electropolishing techniques giving good results.
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and alignment common to previous designs have been eliminated.” This was accomplished by combining a
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Atom probe field Ion Microscopy: Field Ion emission and Surfaces and interfaces at atomic resolution
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A high voltage system to raise the sample standing voltage near the threshold for field evaporation.
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Seidman, David N. (2007). "Three-Dimensional Atom-Probe Tomography: Advances and Applications".
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In field ion microscopy, the tip is cooled by a cryogen and its polarity is reversed. When an
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A system for the manipulation of samples inside the vacuum, including sample viewing systems.
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A detection system for single energetic ions that includes XY position and TOF information.
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reconstruction assume that the tip is a spherical object, and use empirical corrections to
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To conduct an atom probe experiment a very sharp needle shaped specimen is placed in an
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David J. Larson, Ty J. Prosa, Robert M. Ulfig, Brian P. Geiser, Thomas F. Kelly (2013)
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Monographs on the Physics and Chemistry of Materials, Oxford: Oxford University Press.
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Waugh, A. J. (1978). "An imaging atom probe using a single time-gated channel plate".
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where a stream of tunneling electrons is emitted from the apex of a sharp needle-like
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Volume selectability can be limited. Site specific preparation methods, e.g. using
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and thus one can substitute these values to obtain the mass-to-charge for the ion.
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Bunton, J.; Lenz, D; Olson, J; Thompson, K; Ulfig, R; Larson, D; Kelly, T (2006).
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MĂĽller, E. W. (1970). "The Atom-Probe Field Ion Microscope". Naturwissenschaften.
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preparation, although more time-consuming, may be used to bypass such limitations.
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Michael K. Miller, George D.W. Smith, Alfred Cerezo, Mark G. Hetherington (1996)
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ion acquires a resulting velocity of 1.4x10^6 ms at 10~kV. A singly charged
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the negative arising from the loss of electrons forming a net positive charge.
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from a sharp tip (corresponding to specimen volumes of 10,000-10,000,000 
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At a minimum, an atom probe will consist of several key pieces of equipment.
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Baptiste Gault, Michael P. Moody, Julie M. Cairney, SImon P. Ringer (2012)
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Atom Probe Microanalysis: Principles and Applications to Materials Problems
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A high voltage pulsing system, use to create timed field evaporation events
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given a known flight distance. F, for the ion, and a known flight time, t,
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Qi, Jiayuwen; Marquis, Emmanuelle A.; Windl, Wolfgang (24 July 2024).
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Let's say that for at a certain ionization voltage, a singly charged
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to induce a high electric field, with radii on the order of 100 
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Kelly, T. F.; Larson, D. J. (2012). "Atom Probe Tomography 2012".
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Video demonstrating Field Ion images, and pulsed ion evaporation
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is the radius of the detection screen from the tip centre, and r
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APT involved analyzing the chemical structure of teeth of the
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in the chiton teeth, fibers which were often co-located with
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Jet Propulsion Laboratory California Institute of Technology
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From the above equation, it can be re-arranged to show that
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Materials implicitly control achievable spatial resolution.
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of later atom probes including the commercial instruments.
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Local Electrode Atom Probe Tomography - A User's Guide
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Field ion microscope coupled with a mass spectrometer
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Atom Probe Tomography: Analysis at the Atomic Level.
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Fontaine, Alexandre La; Cairney, Julie (July 2017).
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physical properties of the material under analysis.
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Atom Probe Tomography: Analysis at the Atomic Level
830:evaporation modes for the imaging of single atoms. 911: 809: 729: 690: 607: 540: 445: 403: 358: 1579:Panitz, John A. "Field Desorption Spectrometer". 1632:(1978). "Imaging Atom-Probe Mass Spectroscopy". 1461:Panitz, John A. (1973). "The 10 cm Atom Probe". 912:{\displaystyle M={\frac {r_{screen}}{r_{tip}}}.} 1174:(1968). "The Atom-Probe Field Ion Microscope". 1142:samples have been used to overcome limitations. 608:{\displaystyle U={\sqrt {\frac {2neV_{1}}{m}}}} 62:Atom probes are unlike conventional optical or 1762: 1760: 963:rounded-conical shape, similar to a badminton 369:This can be equated with the mass of the ion, 8: 446:{\displaystyle a={\frac {q}{m}}\nabla \phi } 141:Field ion microscopy is a modification of 1880: 1722: 1720: 1700: 1334: 892: 867: 861: 853: 801: 787: 776: 750: 748: 717: 709: 680: 669: 656: 640: 638: 592: 575: 567: 532: 510: 498: 497: 480: 472: 427: 419: 381: 336: 1538:Journal of Vacuum Science and Technology 1276: 1274: 324:is the ionisation state of the ion, and 1520:10.1146/annurev.matsci.37.052506.084200 1155: 1235: 1224: 183:time of flight (TOF) mass spectrometer 1285:. Kluwer Academic/Plenum Publishers. 44:14th Field Emission Symposium in 1967 7: 1751:10.1146/annurev-matsci-070511-155007 967:. The detected events thus become a 328:is the fundamental electric charge. 1730:Annual Review of Materials Research 1499:Annual Review of Materials Research 1375:Field emission and field ionization 559:, the following relation is found: 282:. This has been furthered to study 505: 502: 499: 437: 395: 350: 25: 555:is the ion velocity. Solving for 1976:Atom Probe Field Ion Microscopy 1916:(1) – via Oxford Academic. 1463:Review of Scientific Instruments 1362:from the original on 2022-10-09. 1176:Review of Scientific Instruments 730:{\displaystyle U={\frac {f}{t}}} 404:{\displaystyle ma=q\nabla \phi } 359:{\displaystyle F=ne\nabla \phi } 68:time of flight mass spectrometry 1127:statistically recover overlaps. 1405:. Cambridge University Press. 1257:. Materials Research Society. 1: 1253:Miller, M; Smith, G. (1989). 229:Field Desorption Spectrometer 217:Field Desorption Spectrometer 1910:Microscopy and Microanalysis 1861:Microscopy and Microanalysis 1681:Microscopy and Microanalysis 1654:10.1016/0079-6816(78)90002-3 1377:. Harvard University Press. 1130:Low molecular weight gases ( 251:Imago Scientific Instruments 206:) was introduced in 1974 by 1993:New York: Kluwer Academic. 1634:Progress in Surface Science 373:, via Newton's law (F=ma): 223:Atom Probe Tomography (APT) 2090: 1616:10.1088/0022-3735/11/1/012 134: 1989:Michael K. Miller (2000) 1882:10.1017/S1431927617004044 1702:10.1017/S1431927606065809 143:field emission microscopy 1596:J. Phys. E: Sci. Instrum 956:stereographic projection 215:patented in 1975 as the 1448:10.1103/PhysRev.102.624 1234:Cite journal requires 913: 811: 731: 692: 609: 542: 447: 405: 360: 267:Chaetopleura apiculata 176:, invented in 1973 by 42:was introduced at the 35: 2064:Scientific techniques 2005:Atom Probe Microscopy 1932:www.sciencedirect.com 1581:U.S. Patent 3,868,507 1315:American Mineralogist 914: 812: 732: 693: 610: 543: 448: 406: 361: 33: 18:Atom-probe tomography 1336:10.2138/am-2015-5134 943:electron microscopes 852: 837:, such as a sphere, 747: 708: 637: 566: 471: 418: 380: 335: 137:Field ion microscopy 131:Field ion microscopy 64:electron microscopes 56:field ion microscope 48:Erwin Wilhelm MĂĽller 1873:2017MiMic..23S.676L 1828:(12): 10667–10675. 1791:10.1038/nature09686 1783:2011Natur.469..194G 1743:2012AnRMS..42....1K 1693:2006MiMic..12.1730B 1646:1978PrSS....8..219P 1608:1978JPhE...11...49W 1550:1974JVST...11..206P 1512:2007AnRMS..37..127S 1475:1973RScI...44.1034P 1440:1956PhRv..102..624M 1327:2015AmMin.100.1355V 1281:Miller, M. (2000). 1188:1968RScI...39...83M 515: 909: 807: 727: 688: 605: 538: 493: 443: 401: 356: 234:Oxford Nanoscience 200:Imaging Atom-Probe 194:Imaging Atom Probe 36: 2027:978-1-4614-8721-0 2013:978-1-4614-3436-8 1834:10.1021/nn3049957 1777:(7329): 194–197. 1558:10.1116/1.1318570 1483:10.1063/1.1686295 1412:978-0-521-36379-2 1384:978-1-56396-124-3 1373:Gomer, R (1961). 1292:978-0-306-46415-7 1264:978-0-931837-99-9 1196:10.1063/1.1683116 1172:McLane, S. Brooks 1121:Focussed ion beam 904: 795: 758: 725: 686: 648: 603: 602: 488: 435: 303:Field evaporation 115:ultra high vacuum 16:(Redirected from 2081: 1963: 1962: 1956: 1948: 1942: 1941: 1939: 1938: 1924: 1918: 1917: 1901: 1895: 1894: 1884: 1852: 1846: 1845: 1817: 1811: 1810: 1764: 1755: 1754: 1724: 1715: 1714: 1704: 1687:(2): 1730–1731. 1672: 1666: 1665: 1626: 1620: 1619: 1591: 1585: 1584: 1576: 1570: 1569: 1530: 1524: 1523: 1493: 1487: 1486: 1469:(8): 1034–1038. 1458: 1452: 1451: 1423: 1417: 1416: 1395: 1389: 1388: 1370: 1364: 1363: 1361: 1338: 1321:(7): 1355–1377. 1312: 1303: 1297: 1296: 1278: 1269: 1268: 1250: 1244: 1243: 1237: 1232: 1230: 1222: 1214: 1208: 1207: 1164:MĂĽller, Erwin W. 1160: 918: 916: 915: 910: 905: 903: 902: 887: 886: 862: 816: 814: 813: 808: 806: 805: 800: 796: 788: 781: 780: 759: 751: 736: 734: 733: 728: 726: 718: 697: 695: 694: 689: 687: 685: 684: 675: 674: 673: 657: 649: 641: 614: 612: 611: 606: 604: 598: 597: 596: 577: 576: 547: 545: 544: 539: 537: 536: 514: 509: 508: 489: 481: 452: 450: 449: 444: 436: 428: 410: 408: 407: 402: 365: 363: 362: 357: 174:10-cm Atom Probe 168:10-cm Atom Probe 103:focused ion beam 99:electropolishing 54:. It combined a 21: 2089: 2088: 2084: 2083: 2082: 2080: 2079: 2078: 2054: 2053: 2035: 1971: 1969:Further reading 1966: 1954: 1950: 1949: 1945: 1936: 1934: 1926: 1925: 1921: 1903: 1902: 1898: 1867:(S1): 676–677. 1854: 1853: 1849: 1819: 1818: 1814: 1766: 1765: 1758: 1726: 1725: 1718: 1674: 1673: 1669: 1630:Panitz, John A. 1628: 1627: 1623: 1593: 1592: 1588: 1578: 1577: 1573: 1534:Panitz, John A. 1532: 1531: 1527: 1495: 1494: 1490: 1460: 1459: 1455: 1425: 1424: 1420: 1413: 1397: 1396: 1392: 1385: 1372: 1371: 1367: 1359: 1310: 1305: 1304: 1300: 1293: 1280: 1279: 1272: 1265: 1252: 1251: 1247: 1233: 1223: 1216: 1215: 1211: 1168:Panitz, John A. 1162: 1161: 1157: 1153: 1109: 1096: 1076: 1071: 1062: 1027: 1018: 981: 951: 929: 925: 888: 863: 850: 849: 827: 783: 782: 772: 745: 744: 706: 705: 676: 665: 658: 635: 634: 588: 578: 564: 563: 528: 469: 468: 462: 416: 415: 378: 377: 333: 332: 314: 305: 300: 225: 196: 170: 139: 133: 128: 92:magnetic lenses 88: 28: 23: 22: 15: 12: 11: 5: 2087: 2085: 2077: 2076: 2074:Nanotechnology 2071: 2066: 2056: 2055: 2052: 2051: 2046: 2041: 2034: 2033:External links 2031: 2030: 2029: 2015: 2001: 1987: 1970: 1967: 1965: 1964: 1943: 1919: 1896: 1847: 1812: 1756: 1716: 1667: 1640:(6): 219–263. 1621: 1586: 1571: 1544:(1): 207–210. 1525: 1488: 1453: 1434:(1): 624–631. 1418: 1411: 1390: 1383: 1365: 1298: 1291: 1270: 1263: 1245: 1236:|journal= 1209: 1154: 1152: 1149: 1148: 1147: 1143: 1128: 1124: 1117: 1113: 1108: 1105: 1095: 1094:Semiconductors 1092: 1075: 1072: 1070: 1067: 1061: 1058: 1053: 1052: 1049: 1046: 1043: 1040: 1037: 1034: 1026: 1023: 1017: 1014: 980: 977: 950: 949:Reconstruction 947: 927: 923: 920: 919: 908: 901: 898: 895: 891: 885: 882: 879: 876: 873: 870: 866: 860: 857: 826: 823: 818: 817: 804: 799: 794: 791: 786: 779: 775: 771: 768: 765: 762: 757: 754: 738: 737: 724: 721: 716: 713: 699: 698: 683: 679: 672: 668: 664: 661: 655: 652: 647: 644: 616: 615: 601: 595: 591: 587: 584: 581: 574: 571: 549: 548: 535: 531: 527: 524: 521: 518: 513: 507: 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Panitz 39: 37: 2069:Microscopes 1506:: 127–158. 1107:Limitations 1060:Performance 975:therefrom. 969:point cloud 965:shuttlecock 839:hyperboloid 158:imaging gas 2058:Categories 1999:0306464152 1937:2022-10-13 1221:: 222–230. 1151:References 1140:deuterated 1074:Metallurgy 992:specimen ( 843:paraboloid 627:is known. 312:Ion flight 290:and human 212:gate pulse 188:progenitor 40:atom probe 1891:1431-9276 1711:1431-9276 1662:0079-6816 1566:0022-5355 1428:Phys. Rev 1345:0003-004X 1204:0034-6748 1146:observed. 764:− 654:− 624:deuterium 520:− 441:ϕ 438:∇ 399:ϕ 396:∇ 354:ϕ 351:∇ 280:magnesium 272:magnetite 245:acquired 1842:23176319 1822:ACS Nano 1799:21228873 1737:: 1–31. 1401:(1990). 1399:Tsong, T 1357:Archived 1353:51933115 1132:Hydrogen 620:hydrogen 86:Overview 1869:Bibcode 1807:4430261 1779:Bibcode 1739:Bibcode 1689:Bibcode 1642:Bibcode 1604:Bibcode 1546:Bibcode 1508:Bibcode 1471:Bibcode 1436:Bibcode 1323:Bibcode 1184:Bibcode 1016:Systems 1008:known. 959:space. 922:Where r 126:History 2025:  2011:  1997:  1982:  1889:  1840:  1805:  1797:  1770:Nature 1709:  1660:  1564:  1409:  1381:  1351:  1343:  1289:  1261:  1202:  1136:Helium 1134:& 924:screen 551:Where 298:Theory 292:enamel 288:dentin 276:sodium 263:chiton 259:radula 247:CAMECA 243:AMETEK 238:CAMECA 1955:(PDF) 1803:S2CID 1360:(PDF) 1349:S2CID 1311:(PDF) 101:, or 76:atoms 2023:ISBN 2009:ISBN 1995:ISBN 1980:ISBN 1887:ISSN 1838:PMID 1795:PMID 1707:ISSN 1658:ISSN 1562:ISSN 1407:ISBN 1379:ISBN 1341:ISSN 1287:ISBN 1259:ISBN 1240:help 1200:ISSN 236:and 198:The 172:The 50:and 38:The 1877:doi 1830:doi 1787:doi 1775:469 1747:doi 1697:doi 1650:doi 1612:doi 1554:doi 1516:doi 1479:doi 1444:doi 1432:102 1331:doi 1319:100 1192:doi 1088:TEM 1002:HCP 998:BCC 994:FCC 928:tip 841:or 278:or 261:of 204:IAP 147:tip 82:). 46:by 2060:: 1957:. 1930:. 1914:30 1912:. 1908:. 1885:. 1875:. 1865:23 1863:. 1859:. 1836:. 1824:. 1801:. 1793:. 1785:. 1773:. 1759:^ 1745:. 1735:42 1733:. 1719:^ 1705:. 1695:. 1685:12 1683:. 1679:. 1656:. 1648:. 1636:. 1610:. 1600:11 1598:. 1560:. 1552:. 1542:11 1540:. 1514:. 1504:37 1502:. 1477:. 1467:44 1465:. 1442:. 1430:. 1355:. 1347:. 1339:. 1329:. 1317:. 1313:. 1273:^ 1231:: 1229:}} 1225:{{ 1198:. 1190:. 1180:39 1178:. 1170:; 1166:; 1000:, 996:, 934:. 294:. 286:, 110:. 108:nm 80:nm 1986:. 1961:. 1940:. 1893:. 1879:: 1871:: 1844:. 1832:: 1826:6 1809:. 1789:: 1781:: 1753:. 1749:: 1741:: 1713:. 1699:: 1691:: 1664:. 1652:: 1644:: 1638:8 1618:. 1614:: 1606:: 1583:. 1568:. 1556:: 1548:: 1522:. 1518:: 1510:: 1485:. 1481:: 1473:: 1450:. 1446:: 1438:: 1415:. 1387:. 1333:: 1325:: 1295:. 1267:. 1242:) 1238:( 1219:5 1206:. 1194:: 1186:: 907:. 900:p 897:i 894:t 890:r 884:n 881:e 878:e 875:r 872:c 869:s 865:r 859:= 856:M 803:2 798:) 793:f 790:t 785:( 778:1 774:V 770:e 767:2 761:= 756:n 753:m 723:t 720:f 715:= 712:U 682:2 678:U 671:1 667:V 663:e 660:2 651:= 646:n 643:m 600:m 594:1 590:V 586:e 583:n 580:2 573:= 570:U 557:U 553:U 534:1 530:V 526:e 523:n 517:= 512:2 506:n 503:o 500:i 495:U 491:m 486:2 483:1 478:= 475:E 461:1 433:m 430:q 425:= 422:a 393:q 390:= 387:a 384:m 371:m 348:e 345:n 342:= 339:F 326:e 322:n 202:( 20:)

Index

Atom-probe tomography

14th Field Emission Symposium in 1967
Erwin Wilhelm MĂĽller
J. A. Panitz
field ion microscope
electron microscopes
time of flight mass spectrometry
atoms
nm
magnetic lenses
electropolishing
focused ion beam
nm
ultra high vacuum
Field ion microscopy
field emission microscopy
work function
J. A. Panitz
time of flight (TOF) mass spectrometer
J. A. Panitz
Oxford Nanoscience
CAMECA
AMETEK
CAMECA
Imago Scientific Instruments
radula
chiton
Chaetopleura apiculata
magnetite

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