REVIEW 2 cited by
Attomicroscopy imaging and control of electron motion in graphene
Not yet reviewed by Pith; the record is open.
This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.
SPECIMEN: schema-true, not a live event
T0 review · schema-true
One-sentence machine reading of the paper's core claim.
pith:XXXXXXXX · record.json · timestamp
read the original abstract
Attosecond science has leveraged the highly nonlinear interactions between intense few-cycle laser pulses and matter, allowing for unprecedented observation and control of electron motion with remarkable temporal resolution. However, most existing experiments focusing on laser-controlled attosecond dynamics have dealt with quasi-bound electrons released in the ionization continua of atoms, molecules, or conduction bands in solid-state systems. Here, we employed the recently developed attomicroscopy imaging tool to investigate, visualize, and manipulate the motion of bound electrons in graphene. By adjusting the carrier-envelope phase and the field strength of the driving electric field, we were able to control both the amplitude and direction of the field-induced electron current between carbon atoms in graphene. This research opens new avenues for understanding and controlling dynamic, on-demand electron motion processes, including chemical reactions, molecular bonding, and the electronic properties of materials.
Forward citations
Cited by 2 Pith papers
-
Comment on 'Attosecond electron microscopy and diffraction'
A critical comment showing that Hui et al.'s attosecond electron microscopy and diffraction experiment cannot produce properly gated electrons and that the reported signals are statistically incompatible with attoseco...
-
Comment on "Comment on Attosecond electron microscopy and diffraction"
A team defends its 2024 attosecond electron microscopy result, using control scans to argue the observed graphene dynamics are not optical interference artifacts.
Discussion (0). Continue with ORCID to comment.