TY - JOUR
T1 - Imaging elliptically polarized infrared near-fields on nanoparticles by strong-field dissociation of functional surface groups
AU - Rosenberger, Philipp
AU - Dagar, Ritika
AU - Zhang, Wenbin
AU - Sousa-Castillo, Ana
AU - Neuhaus, Marcel
AU - Cortes, Emiliano
AU - Maier, Stefan A.
AU - Costa-Vera, Cesar
AU - Kling, Matthias F.
AU - Bergues, Boris
N1 - Publisher Copyright:
© 2022, The Author(s).
PY - 2022/6
Y1 - 2022/6
N2 - Abstract: We investigate the strong-field ion emission from the surface of isolated silica nanoparticles aerosolized from an alcoholic solution, and demonstrate the applicability of the recently reported near-field imaging at 720 nm [Rupp et al., Nat. Comm., 10(1):4655, 2019] to longer wavelength (2 μm) and polarizations with arbitrary ellipticity. Based on the experimental observations, we discuss the validity of a previously introduced semi-classical model, which is based on near-field driven charge generation by a Monte-Carlo approach and classical propagation. We furthermore clarify the role of the solvent in the surface composition of the nanoparticles in the interaction region. We find that upon injection of the nanoparticles into the vacuum, the alcoholic solvent evaporates on millisecond time scales, and that the generated ions originate predominantly from covalent bonds with the silica surface rather than from physisorbed solvent molecules. These findings have important implications for the development of future theoretical models of the strong-field ion emission from silica nanoparticles, and the application of near-field imaging and reaction dynamics of functional groups on isolated nanoparticles. Graphical abstract: [Figure not available: see fulltext.].
AB - Abstract: We investigate the strong-field ion emission from the surface of isolated silica nanoparticles aerosolized from an alcoholic solution, and demonstrate the applicability of the recently reported near-field imaging at 720 nm [Rupp et al., Nat. Comm., 10(1):4655, 2019] to longer wavelength (2 μm) and polarizations with arbitrary ellipticity. Based on the experimental observations, we discuss the validity of a previously introduced semi-classical model, which is based on near-field driven charge generation by a Monte-Carlo approach and classical propagation. We furthermore clarify the role of the solvent in the surface composition of the nanoparticles in the interaction region. We find that upon injection of the nanoparticles into the vacuum, the alcoholic solvent evaporates on millisecond time scales, and that the generated ions originate predominantly from covalent bonds with the silica surface rather than from physisorbed solvent molecules. These findings have important implications for the development of future theoretical models of the strong-field ion emission from silica nanoparticles, and the application of near-field imaging and reaction dynamics of functional groups on isolated nanoparticles. Graphical abstract: [Figure not available: see fulltext.].
UR - https://www.scopus.com/pages/publications/85132991310
U2 - 10.1140/epjd/s10053-022-00430-6
DO - 10.1140/epjd/s10053-022-00430-6
M3 - 文章
AN - SCOPUS:85132991310
SN - 1434-6060
VL - 76
JO - European Physical Journal D
JF - European Physical Journal D
IS - 6
M1 - 109
ER -