(electronics) A device in which gas ions are produced, focused, accelerated, and emitted as a narrow beam. Also known as ion gun; ionization source.
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(electronics) A device in which gas ions are produced, focused, accelerated, and emitted as a narrow beam. Also known as ion gun; ionization source.
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Devices which produce positive or negative electrically charged atoms or molecules. See also Ion.
In general, ion sources fall into three major categories: those designed for positive-ion generation, those for negative-ion generation, and a highly specialized type of source designed to produce a polarized ion beam. The positive-ion source category may further be subdivided into sources specifically designed to generate singly charged ions and those designed to produce very highly charged ions.
Ion sources have acquired a wide variety of applications. They are used in a variety of different types of accelerators for nuclear research; have application in the field of fusion research; and are used for ion implantation, in isotope separators, in ion microprobes, as a means of rocket propulsion, in mass spectrometers, and for ion milling. See also Ion implantation; Ion propulsion; Mass spectroscope;
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An ion source is an electro-magnetic device that is used to create charged particles. These are used primarily within mass spectrometers, particle accelerators, ion implanters and ion engines.
In mass spectrometry, an ion source is a piece of equipment used to ionize analyte molecules and, if necessary, free them from the solid or liquid phase. Once the analyte ions are free to move electric fields will direct them into the mass analyzer.
Electron ionization is widely used in mass spectrometry, particularly for organic molecules. The gas phase reaction producing electron ionization is

where M is the atom of molecule being ionized, e − is the electron, and
is the resulting ion.
Spark ionization is used to produce gas phase ions from a solid sample. When incorporated with a mass spectrometer the complete instrument is referred to as a spark ionization mass spectrometer or as a spark source mass spectrometer (SSMS).[1]
Chemical ionization is a lower energy process than electron ionization.[2] The lower energy yields less fragmentation, and usually a simpler spectrum. A typical CI spectrum has an easily identifiable molecular ion.[3]
In a CI experiment, ions are produced through the collision of the analyte with ions of a reagent gas in the ion source. Some common reagent gases include: methane, ammonia, and isobutane. Inside the ion source, the reagent gas is present in large excess compared to the analyte. Electrons entering the source will preferentially ionize the reagent gas. The resultant collisions with other reagent gas molecules will create an ionization plasma. Positive and negative ions of the analyte are formed by reactions with this plasma. For example, protonation occurs by
(primary ion formation),
(reagent ion formation),
(product ion formation, e.g. protonation).Ion-attachment ionization is similar to chemical ionization in which a cation is attached to the analyte molecule in a reactive collision:

Where M is the analyte molecule, X+ is the cation and A is a non-reacting collision partner.[4]
In fast atom bombardment the analytes is mixed with a non-volatile chemical protection environment called a matrix and is bombarded under vacuum with a high energy (4000 to 10,000 electron volts) beam of atoms.[5] The atoms are typically from an inert gas such as argon or xenon. Common matrices include glycerol, thioglycerol, 3-nitrobenzyl alcohol (3-NBA), 18-Crown-6 ether, 2-nitrophenyloctyl ether, sulfolane, diethanolamine, and triethanolamine. This technique is similar to secondary ion mass spectrometry and plasma desorption mass spectrometry.
Field desorption refers to an ion source in which a high-potential electric field is applied to an emitter with a sharp surface, such as a razor blade, or more commonly, a filament from which tiny "whiskers" have formed.[6] This results in a very high electric field which can result in ionization of gaseous molecules of the analyte. Mass spectra produced by FI have little or no fragmentation. They are dominated by molecular radical cations M+. and less often, protonated molecules [M + H] + .
MALDI is a soft ionization technique allowing the analysis of biomolecules (biopolymers such as proteins, peptides and sugars) and large organic molecules (such as polymers, dendrimers and other macromolecules), which tend to be fragile and fragment when ionized by more conventional ionization methods. It is most similar in character to electrospray ionization both in relative softness and the ions produced (although it causes many fewer multiply charged ions). The ionization is triggered by a laser beam (normally a nitrogen laser). A matrix is used to protect the biomolecule from being destroyed by direct laser beam and to facilitate vaporization and ionization.
Atmospheric pressure chemical ionization is a form of chemical ionization which takes place at atmospheric pressure.[7] A spray of solvent is heated to relatively high temperatures (above 400 degrees Celsius), sprayed with high flow rates of nitrogen and the entire aerosol cloud is subjected to a corona discharge that creates ions. APCI is not as "soft" an ionization technique as ESI.[8]
Atmospheric pressure photoionization uses a source of photons, usually a UV lamp, to ionize the elute in place of the corona pin used in APCI. A spray of solvent is heated to relatively high temperatures (above 400 degrees Celsius), sprayed with high flow rates of nitrogen for desolvation and the entire aerosol cloud is subjected to UV radiation to create ions.
In electrospray ionization, a liquid is pushed through a very small, charged and usually metal, capillary.[9] This liquid contains the substance to be studied, the analyte, dissolved in a large amount of solvent, which is usually much more volatile than the analyte. Volatile acids, bases or buffers are often added to this solution too. The analyte exists as an ion in solution either in its anion or cation form. Because like charges repel, the liquid pushes itself out of the capillary and forms an aerosol, a mist of small droplets about 10 μm across. The aerosol is at least partially produced by a process involving the formation of a Taylor cone and a jet from the tip of this cone. An uncharged carrier gas such as nitrogen is sometimes used to help nebulize the liquid and to help evaporate the neutral solvent in the droplets. As the solvent evaporates, the analyte molecules are forced closer together, repel each other and break up the droplets. This process is called Coulombic fission because it is driven by repulsive Coulombic forces between charged molecules. The process repeats until the analyte is free of solvent and is a bare ion. The ions observed are created by the addition of a proton (a hydrogen ion) and denoted [M + H] + , or of another cation such as sodium ion, [M + Na] + , or the removal of a proton, [M − H] − . Multiply-charged ions such as [M + 2H]2 + are often observed. For large macromolecules, there can be many charge states, occurring with different frequencies; the charge can be as great as [M + 25H]25 + , for example.
Desorption electrospray ionization uses an electrospray source to create charged droplets that are directed at a solid sample a few millimeters to a few centimeters away. The charged droplets pick up the sample through interaction with the surface and then form highly charged ions that can be sampled into a mass spectrometer.[10]
Ions can be created in an electric glow discharge.
Ions can be created in an inductively coupled plasma, which is a plasma source in which the energy is supplied by electrical currents which are produced by electromagnetic induction, that is, by time-varying magnetic fields.[11]
Microwaves are capable of exciting electrodeless gas discharges to create ions.
Thermospray is a form of atmospheric pressure ionization in mass spectrometry. It transfers ions from the liquid phase to the gas phase for analysis. It is particularly useful in liquid chromatography-mass spectrometry. [12]
A Direct analysis in real time source operates by exposing the sample to a dry gas stream (typically helium or nitrogen) that contains long-lived electronically or vibronically excited neutral atoms or molecules (or "metastables"). Excited states are typically formed in the DART source by creating a glow discharge in a chamber through which the gas flows.
Sonic spray ionization is method for creating ions from a liquid solution, for example, a mixture of methanol and water.[13] A pneumatic nebulizer is used to turn the solution into a supersonic spray of small droplets. Ions are formed when the solvent evaporates and the statistically unbalanced charge distribution on the droplets leads to a net charge and complete desolvation results in the formation of ions.
Matrix-assisted laser desorption electrospray ionization (MALDESI)[14] is an atmospheric pressure ionization source for generation of multiply-charged ions. An ultraviolet or infrared laser is directed onto a solid or liquid sample containing the analyte of interest and matrix (UV = organic acid, IR = sacrificial analyte or water of hydration) desorbing neutral analyte molecules which are postionized by interaction with electrosprayed solvent droplets generating multiply charged ions.
In Aerosol time-of-flight mass spectrometry, micrometer sized solid aerosol particles extracted from the atmosphere are simultaneously desorbed and ionized by a precisely timed laser pulse as they pass through the center of a time-of-flight ion extractor.[15][16]
In particle accelerators an ion source creates a particle beam at the beginning of the machine, the Source. The technology to create ion sources for particle accelerators depends strongly on the type of particle that needs to be generated: electrons, protons, H- ion or a heavy ion.
Electrons are generated with an electron gun, and there are many varieties of these.
Protons are generated with a plasma-based device, like a duoplasmatron or a magnetron.
H- ions are generated with a magnetron or a Penning source. A magnetron consists of a central cylindrical cathode surrounded by an anode. The discharge voltage is typically greater than 150 V and the current drain is around 40 A. A magnetic field of about 0.2 tesla is parallel to the cathode axis. Hydrogen gas is introduced by a pulsed gas valve. Caesium is often used to lower the work function of the cathode, enhancing the amount of ions that are produced.
For a Penning source, a strong magnetic field parallel to the electric field of the sheath guides electrons and ions on cyclotron spirals from cathode to cathode. Fast H-minus ions are generated at the cathodes as in the magnetron. They are slowed down due to the charge exchange reaction as they migrate to the plasma aperture. This makes for a beam of ions that is colder than the ions obtained from a magnetron.
Heavy ions are generated with an electron cyclotron resonance ion source. The use of electron cyclotron resonance (ECR) ion sources for the production of intense beams of highly charged ions has immensely grown over the last decade. ECR ion sources are used as injectors into linear accelerators, Van-de-Graaff generators or cyclotrons in nuclear and elementary particle physics. In atomic and surface physics ECR ion sources deliver intense beams of highly charged ions for collision experiments or for the investigation of surfaces. For the highest charge states, however, Electron beam ion sources (EBIS) are needed. They can generate even bare ions of mid-heavy elements. The Electron beam ion trap (EBIT), based on the same principle, can produce up to bare uranium ions and can be used as an ion source as well.
Gas flows through the ion source between the anode and the cathode. A positive voltage is applied to the anode. This voltage, combined with the high magnetic field between the tips of the internal and external cathodes allow a plasma to start. Ions from the plasma are repelled by the anode electric field. This creates an ion beam.[17]
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