Ion trap

An ion trap, used for precision measurements of radium ions, inside a vacuum chamber. View ports surrounding the chamber allow laser light to be directed into the trap.

An ion trap is a combination of electric and/or magnetic fields used to capture charged particles — known as ions — often in a system isolated from an external environment. Atomic and molecular ion traps have a number of applications in physics and chemistry such as precision mass spectrometry, improved atomic frequency standards, and quantum computing.[1] In comparison to neutral atom traps, ion traps have deeper trapping potentials (up to several electronvolts) that do not depend on the internal electronic structure of a trapped ion. This makes ion traps more suitable for the study of light interactions with single atomic systems. The two most popular types of ion traps are the Penning trap, which forms a potential via a combination of static electric and magnetic fields, and the Paul trap which forms a potential via a combination of static and oscillating electric fields.[2]

Penning traps can be used for precise magnetic measurements in spectroscopy. Studies of quantum state manipulation most often use the Paul trap. This may lead to a trapped ion quantum computer[3] and has already been used to create the world's most accurate atomic clocks.[4][5] Electron guns (a device emitting high-speed electrons, used in CRTs) can use an ion trap to prevent degradation of the cathode by positive ions.

  1. ^ H. Häffner; C. F. Roos; R. Blatt (2008). "Quantum computing with trapped ions". Physics Reports. 469 (4): 155–203. arXiv:0809.4368. Bibcode:2008PhR...469..155H. doi:10.1016/j.physrep.2008.09.003. S2CID 15918021.
  2. ^ D. Leibfried; R. Blatt; C. Monroe; D. Wineland (2003). "Quantum dynamics of single trapped ions". Reviews of Modern Physics. 75 (1): 281–324. Bibcode:2003RvMP...75..281L. doi:10.1103/RevModPhys.75.281.
  3. ^ R. Blatt; D. J. Wineland (2008). "Entangled states of trapped atomic ions" (PDF). Nature. 453 (7198): 1008–1014. Bibcode:2008Natur.453.1008B. doi:10.1038/nature07125. PMID 18563151. S2CID 316118.
  4. ^ T. Rosenband; D. B. Hume; P. O. Schmidt; C. W. Chou; A. Brusch; L. Lorini; W. H. Oskay; R. E. Drullinger; T. M. Fortier; J. E. Stalnaker; S. A. Diddams; W. C. Swann; N. R. Newbury; W. M. Itano; D. J. Wineland; J. C. Bergquist (2008). "Frequency Ratio of Al+ and Hg+ Single-Ion Optical Clocks; Metrology at the 17th Decimal Place" (PDF). Science. 319 (5871): 1808–1812. Bibcode:2008Sci...319.1808R. doi:10.1126/science.1154622. PMID 18323415. S2CID 206511320.
  5. ^ S. M. Brewer; J.-S. Chen; A. M. Hankin; E. R. Clements; C. W. Chou; D. J. Wineland; D. B. Hume; D. R. Leibrandt (2019). "Al+ Quantum-Logic Clock with a Systematic Uncertainty below 10^-18". Phys. Rev. Lett. 123 (3): 033201. arXiv:1902.07694. Bibcode:2019PhRvL.123c3201B. doi:10.1103/PhysRevLett.123.033201. PMID 31386450. S2CID 119075546.

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