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Ion implantation

Use of ions to cause chemical changes

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General principle

Ion implantation equipment typically consists of an ion source, where ions of the desired element are produced, an accelerator, where the ions are electrostatically accelerated to a high energy or using radiofrequency, and a target chamber, where the ions impinge on a target, which is the material to be implanted. Thus ion implantation is a special case of particle radiation. Each ion is typically a single atom or molecule, and thus the actual amount of material implanted in the target is the integral over time of the ion current. This amount is called the dose. The currents supplied by implants are typically small (micro-amperes), and thus the dose which can be implanted in a reasonable amount of time is small. Therefore, ion implantation finds application in cases where the amount of chemical change required is small.

Typical ion energies are in the range of 10 to 500 keV (1,600 to 80,000 aJ). Energies in the range 1 to 10 keV (160 to 1,600 aJ) can be used, but result in a penetration of only a few nanometers or less. Energies lower than this result in very little damage to the target, and fall under the designation ion beam deposition. Higher energies can also be used: accelerators capable of 5 MeV (800,000 aJ) are common. However, there is often great structural damage to the target, and because the depth distribution is broad (Bragg peak), the net composition change at any point in the target will be small.

The energy of the ions, as well as the ion species and the composition of the target determine the depth of penetration of the ions in the solid: A monoenergetic ion beam will generally have a broad depth distribution. The average penetration depth is called the range of the ions. Under typical circumstances ion ranges will be between 10 nanometers and 1 micrometer. Thus, ion implantation is especially useful in cases where the chemical or structural change is desired to be near the surface of the target. Ions gradually lose their energy as they travel through the solid, both from occasional collisions with target atoms (which cause abrupt energy transfers) and from a mild drag from overlap of electron orbitals, which is a continuous process. The loss of ion energy in the target is called stopping and can be simulated with the binary collision approximation method.

Accelerator systems for ion implantation are generally classified into medium current (ion beam currents between 10 μA and ~2 mA), high current (ion beam currents up to ~30 mA), high energy (ion energies above 200 keV and up to 10 MeV), and very high dose (efficient implant of dose greater than 1016 ions/cm2).

Ion source

All varieties of ion implantation beamline designs contain general groups of functional components (see image). The first major segment of an ion beamline includes an ion source used to generate the ion species. The source is closely coupled to biased electrodes for extraction of the ions into the beamline and most often to some means of selecting a particular ion species for transport into the main accelerator section.

The ion source is often made of materials with a high melting point such as tungsten, tungsten doped with lanthanum oxide (lanthanated tungsten), molybdenum and tantalum. Lanthanum oxide helps extend the life of the ion source. Often, inside the ion source a plasma is created between two tungsten electrodes, called reflectors, using a gas often based on fluorine or hydrogen containing the ion to be implanted whether it is germanium, boron, or silicon, such as boron trifluoride, boron difluoride, germanium tetrafluoride or silicon tetrafluoride. Arsine gas or phosphine gas can be used in the ion source to provide arsenic or phosphorus respectively for implantation. The ion source also has an indirectly heated cathode. Alternatively this heated cathode can be used as one of the reflectors, eliminating the need for a dedicated one, or a directly heated cathode is used.

Oxygen-based gases (oxides) can be used to provide ions for implantation such as carbon dioxide for implanting carbon. Hydrogen or hydrogen with xenon, krypton or argon may be added to the plasma to delay the degradation of tungsten components due to the halogen cycle. The hydrogen can come from a high pressure cylinder or from a hydrogen generator that uses electrolysis. Repellers at each end of the ion source continually move the atoms from one end of the ion source to the other, resembling two mirrors pointed at each other constantly reflecting light.

The ions are extracted from the source by an extraction electrode outside the ion source through a slit shaped aperture in the source, then the ion beam then passes through an analysis magnet to select the ions that will be implanted and then passes through one or two linear accelerators (linacs) that accelerate the ions before they reach the wafer in a process chamber. In medium current ion implanters there is also a neutral ion trap before the process chamber to remove neutral ions from the ion beam.

Some dopants such as aluminum, are often not provided to the ion source as a gas but as a solid compound based on Chlorine or Iodine that is vaporized in a nearby crucible such as Aluminium iodide or Aluminium chloride or as a solid sputtering target inside the ion source made of Aluminium oxide or Aluminium nitride. Implanting antimony often requires the use of a vaporizer attached to the ion source, in which antimony trifluoride, antimony trioxide, or solid antimony are vaporized in a crucible and a carrier gas is used to route the vapors to an adjacent ion source, although it can also be implanted from a gas containing fluorine such as antimony hexafluoride or vaporized from liquid antimony pentafluoride. Gallium, Selenium and Indium are often implanted from solid sources such as selenium dioxide for selenium although it can also be implanted from hydrogen selenide. Crucibles often last 60–100 hours and prevent ion implanters from changing recipes or process parameters in less than 20–30 minutes. Ion sources can often last 300 hours.

The "mass" selection (just like in mass spectrometer) is often accompanied by passage of the extracted ion beam through a magnetic field region with an exit path restricted by blocking apertures, or "slits", that allow only ions with a specific value of the product of mass and velocity/charge to continue down the beamline. If the target surface is larger than the ion beam diameter and a uniform distribution of implanted dose is desired over the target surface, then some combination of beam scanning and wafer motion is used. Finally, the implanted surface is coupled with some method for collecting the accumulated charge of the implanted ions so that the delivered dose can be measured in a continuous fashion and the implant process stopped at the desired dose level.

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