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Attosecond-controlled photoemission from metal nanowire tips in the few-electron regime
Author(s) -
Byungnam Ahn,
Johannes Schötz,
Mijeong Kang,
W. A. Okell,
Sambit Mitra,
Benjamin Förg,
Sergey Zherebtsov,
Frederik Süßmann,
C. P. Burger,
M. Kübel,
C. Liu,
A. Wirth,
Enzo Di Fabrizio,
Hirofumi Yanagisawa,
Dong Eon Kim,
Geonu Kim,
Matthias F. Kling
Publication year - 2017
Publication title -
apl photonics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.094
H-Index - 34
ISSN - 2378-0967
DOI - 10.1063/1.4974529
Subject(s) - attosecond , electron , photoelectric effect , nanowire , atomic physics , femtosecond , inverse photoemission spectroscopy , plasmon , laser , physics , quantum tunnelling , materials science , angle resolved photoemission spectroscopy , optoelectronics , optics , ultrashort pulse , condensed matter physics , electronic structure , quantum mechanics
Metal nanotip photoemitters have proven to be versatile in fundamental nanoplasmonics research and applications, including, e.g., the generation of ultrafast electron pulses, the adiabatic focusing of plasmons, and as light-triggered electron sources for microscopy. Here, we report the generation of high energy photoelectrons (up to 160 eV) in photoemission from single-crystalline nanowire tips in few-cycle, 750-nm laser fields at peak intensities of (2-7.3) × 1012 W/cm2. Recording the carrier-envelope phase (CEP)-dependent photoemission from the nanowire tips allows us to identify rescattering contributions and also permits us to determine the high-energy cutoff of the electron spectra as a function of laser intensity. So far these types of experiments from metal nanotips have been limited to an emission regime with less than one electron per pulse. We detect up to 13 e/shot and given the limited detection efficiency, we expect up to a few ten times more electrons being emitted from the nanowire. Within ...

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