An initial laser pulse will trigger a reaction in the sample that is followed an instant later
by an electron pulse to produce an image of that reaction.
How it works: An initial laser pulse triggers a reaction in a sample that is followed an instant later
by an electron pulse to produce an image.
Not exact matches
In the long term,
electrons accelerated
by high - repetition PW
pulses could slash the cost of particle physicists» dream machine: a 30 - kilometer - long
electron - positron collider that would be a successor to the Large Hadron Collider at CERN, the European particle physics laboratory near Geneva, Switzerland.
For the first time, they managed to control the shape of the laser
pulse to keep an
electron both free and bound to its nucleus, and were at the same time able to regulate the electronic structure of this atom dressed
by the laser.
These feature make ultrashort
electron pulse trains an ideal tool with which to monitor, in real time, the ultrafast processes initiated
by the impact of light oscillations onto matter.
The machine developed
by the Brookhaven team uses a laser
pulse to give
electrons in a sample material a «kick» of energy.
By varying the time delay between the
pulse and the probe, the scientists can capture the subtle shifts in atomic arrangements as the lattice responds to the «kicked - up»
electrons.
The researchers in Erlangen and Jena have now achieved this
by focusing laser
pulses onto a nanometre - sharp metal tip, causing the tip to emit
electrons.
By tuning
electron pulses and recording those
electrons that went through to the other side, the researchers were able to map the energy and momentum of
electrons within the material.
Using tunneling ionization and ultrashort laser
pulses, scientists have been able to observe the structure of a molecule and the changes that take place within billionths of a billionth of a second when it is excited
by an
electron impact.
Electron motions induced
by a strong electric field are mapped in space and time with the help of femtosecond x-ray
pulses.
Depending on their size, so called near - fields (electromagnetic fields close to the particle surface) were induced
by the laser
pulses, resulting in a controlled directional emission of
electrons.
In the experiments,
electrons are set in motion
by a very strong electric field which is provided for the very short time interval of 50 fs (1 fs = 10 - 15 s)
by a strong optical
pulse interacting with the LiH material.
A weak UV
pulse excited an outer
electron to a higher state, followed
by a strong infrared
pulse creating a field in which the
electron escaped from the molecule due to the tunneling effect.
The researchers observed this effect
by using particle detectors to monitor the flight paths of
electrons emitted from the near - fields of the nanospheres within the passage of the laser
pulse.
By adjusting the time delay between the two
pulses, the scientists gained a very precise measurement — within a matter of attoseconds — of how long it takes the
electron to decay.
The
electrons were then carried along
by the laser
pulse and almost instantly smashed back into the neon nuclei.
Researchers use a similar trick to study atomic
electrons —
by pinging atoms with exceedingly short light
pulses, they can watch
electrons» quantum states evolve in unprecedented detail.
The ejected
electron was detected
by the infrared laser
pulse as soon as it left the atom in response to the excitation
by XUV light.
Electrons within a target atom are first excited
by a photon contained within the pump
pulse, which is then followed after a short delay
by a second photon in a probe
pulse.
By using what is known as an ion microscope to detect these ions, the scientists were able, for the first time, to observe the interaction of two photons confined in an attosecond
pulse with
electrons in the inner orbital shells of an atom.
In UEC, a sample of crystalline GeTe is bombarded with a femtosecond laser
pulse, followed
by a
pulse of
electrons.
These accelerators work
by shooting
pulses of intense laser light into plasma to create a wave rippling through the cloud of ionised gas, leaving a wake of
electrons akin to those that form behind a speedboat in water.
By irradiating oriented molecules with powerful laser
pulses, the researchers were able to obtain high - harmonic spectra reflecting the state of a molecule's
electron shell.
«The work shows how magnetization of nanoscale magnets can be steered
by intense ultrashort
electron pulses,» said Alexander Schäffer, a doctoral student at Martin - Luther - Universität Halle - Wittenberg in Halle, Germany, and lead author of the paper.
Those
electron bunches are actually initiated
by rapid - fire laser
pulses produced
by an
electron «gun.»
Varga's research focuses on the interaction of lasers and matter at the atomic scale and is part of the new field of attosecond science — an attosecond is a billion billionths of a second — that is allowing scientists to study extremely short - lived phenomena such as the making and breaking of chemical bonds and tracking the real - time motion of
electrons within semiconductors
by probing them with attosecond
pulses of laser light.
The Nitrogen - Vacancy defect (NV centre) in diamonds and diamond nanocrystals (nanodiamonds) provides a unique alternative for DNP as the NV centre
electron spin can be optically polarized to over 90 % polarization at room temperature
by short laser
pulses.
These opportunities include the use of short -
pulsed X-ray sources for extracting time - dependent structural information from proteins; and the revolutionary new possibilities created
by X-ray Free
Electron Lasers, which combine ultrafast X-ray
pulses with high brilliance focussing capabilities to create an entirely new regime of pre-damage time - resolved serial femtosecond crystallography on unprecedented time - scales.