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Ultrafast electron diffraction

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Ultrafast electron diffraction (UED), also known as femtosecond electron diffraction (FED), is a pump-probe experimental method based on the combination of optical pump-probe spectroscopy and electron diffraction. UED provides information on the dynamical changes of the structure of materials. It is very similar to time resolved crystallography, but instead of using X-rays as the probe, it uses electrons. In the UED technique, a femtosecond (fs) laser optical pulse excites (pumps) a sample into an excited, usually non-equilibrium, state. The pump pulse may induce chemical, electronic or structural transitions. After a finite time interval, a fs electron pulse is incident upon the sample. The electron pulse undergoes diffraction as a result of interacting with the sample. The diffraction signal is, subsequently, detected by an electron counting instrument such as a CCD camera. Specifically, after the electron pulse diffracts from the sample, the scattered electrons will form a diffraction pattern (image) on a CCD camera. This pattern contains structural information about the sample. By adjusting the time difference between the arrival (at the sample) of the pump and probe beams, one can obtain a series of diffraction patterns as a function of the various time differences. The diffraction data series can be concatenated in order to produce a motion picture of the changes that occurred in the data. UED can provide a wealth of dynamics on charge carriers, atoms, and molecules.

History

The design of early ultrafast electron diffraction instruments was based on x-ray streak cameras, the first reported UED experiment demonstrating an electron pulse length of 100 ps.[1]

Electron Pulse Production

The electron pulses are typically produced by the process of photoemission in which a fs optical pulse is directed toward a photocathode.[2] If the incident laser pulse has an appropriate energy, electrons will be ejected from the photocathode through a process known as photoemission. The electrons are subsequently accelerated to high energies, ranging from tens of kiloelectron-volts[3] to several megaelectron-volts,[4] using an electron gun.

Electron Pulse Compression

Generally, two methods are used in order to compress electron pulses in order to overcome pulsewidth expansion due to Coulomb repulsion. Generating high-flux ultrashort electron beams has been relatively straightforward, but pulse duration below a picosecond proved extremely difficult due to space-charge effects. Space-charge interactions increase in severity with bunch charge and rapidly act to broaden the pulse duration, which has resulted in an apparently unavoidable trade-off between signal (bunch charge) and time-resolution in ultrafast electron diffraction (UED) experiments. Radio-frequency (RF) compression has emerged has an leading method of reducing the pulse expansion in UED experiments, achieving temporal resolution well below 50 femtoseconds.[5] Shorter electron beams below 10 femtoseconds are ultimately required to probe the fastest dynamics in solid state materials and observe gas phase molecular reactions.[6]

Single shot

Schematic of Ultrafast Electron Diffraction showing the pump pulse (red) exciting the sample prior to the arrival of the electron probe pulse (blue)

For studying irreversible process, a diffraction signal is obtained from a single electron bunch containing or more particles.[7]

Stroboscopic

When studying reversible process, especially weak signals caused by, e.g., thermal diffuse scattering, a diffraction pattern is accumulated from many electron bunches, as many as .[8]

Resolution

The resolution of an ultrafast electron diffraction apparatus can be characterized both in space and in time. Spatial resolution comes in two distinct parts: real space and reciprocal space. Real space resolution is determined by the physical size of the electron probe on the sample. A smaller physical probe size can allow experiments on crystals that cannot feasibly be grown in large sizes.[9]

High reciprocal space resolution allows for the detection of Bragg diffraction spots that correspond to long periodicity phenomena. It can be calculated with the following equation:[4]

,

where Δs is the reciprocal space resolution, λe is the Compton wavelength of the electrons, ϵn is the normalized emittance[disambiguation needed] of the electrons, and σx is the size of the probe on the sample.

Temporal resolution is primarily a function of the bunch length of the electrons and the relative timing jitters between the pump and probe.[4]

Detectors

See also

References

  1. ^ Mourou, Gerard; Williamson, Steve (1982). "Picosecond electron diffraction". Applied Physics Letters. 41 (1): 44. Bibcode:1982ApPhL..41...44M. doi:10.1063/1.93316.
  2. ^ Srinivasan, R.; Lobastov, V.; Ruan, C.-Y.; Zewail, A. (2003). "Ultrafast Electron Diffraction (UED)". HCA. 86 (6): 1761–1799. doi:10.1002/hlca.200390147.
  3. ^ Siwick, Bradley J.; Dwyer, Jason R.; Jordan, Robert E.; Miller, R. J. Dwayne (21 Nov 2003). "An Atomic-Level View of Melting Using Femtosecond Electron Diffraction". Science. 302 (5649): 1382–1385. Bibcode:2003Sci...302.1382S. doi:10.1126/science.1090052. PMID 14631036. S2CID 4593938.
  4. ^ a b c Weathersby, S. P. (2015). "Mega-electron-volt ultrafast electron diffraction at SLAC National Accelerator Laboratory". Review of Scientific Instruments. 86 (7): 073702. Bibcode:2015RScI...86g3702W. doi:10.1063/1.4926994. PMID 26233391. S2CID 17652180.
  5. ^ Qi, F. (2020). "Breaking 50 Femtosecond Resolution Barrier in MeV Ultrafast Electron Diffraction with a Double Bend Achromat Compressor". Physical Review Letters. 124 (13): 134803. arXiv:2003.08046. Bibcode:2020PhRvL.124m4803Q. doi:10.1103/PhysRevLett.124.134803. PMID 32302182. S2CID 212747515.
  6. ^ Gliserin, A. (2015). "Sub-phonon-period compression of electron pulses for atomic diffraction". Nat Commun. 6 (8723): 4. Bibcode:2015NatCo...6.8723G. doi:10.1038/ncomms9723. PMC 4640064. PMID 26502750.
  7. ^ Siwick, Bradley J; Dwyer, Jason R; Jordan, Robert E; Miller, RJ Dwayne (2003). "An atomic-level view of melting using femtosecond electron diffraction". Science. 302 (5649): 1382–1385. Bibcode:2003Sci...302.1382S. doi:10.1126/science.1090052. PMID 14631036. S2CID 4593938.
  8. ^ de Cotret, Laurent P Ren{\'e}; Otto, Martin R; P{\"o}hls, Jan-Hendrik; Luo, Zhongzhen; Kanatzidis, Mercouri G; Siwick, Bradley J (2022). "Direct visualization of polaron formation in the thermoelectric SnSe". Proceedings of the National Academy of Sciences. 119 (3). arXiv:2111.10012. Bibcode:2022PNAS..11913967R. doi:10.1073/pnas.2113967119. PMC 8784136. PMID 35012983. S2CID 244463218.
  9. ^ Bie, Ya-Qing; Zong, Alfred; Wang, Xirui; Jarillo-Herrero, Pablo; Gedik, Nuh (2021). "A versatile sample fabrication method for ultrafast electron diffraction". Ultramicroscopy. 230: 113389. doi:10.1016/j.ultramic.2021.113389. PMID 34530284. S2CID 237546671.

Sources

  • Srinivasan, Ramesh; Lobastov, Vladimir A.; Ruan, Chong-Yu; Zewail, Ahmed H. (2003). "Ultrafast Electron Diffraction (UED): A New Development for the 4D Determination of Transient Molecular Structures". Helvetica Chimica Acta. 86 (6): 1761. doi:10.1002/hlca.200390147.