Format

Send to

Choose Destination
ACS Nano. 2014 Sep 23;8(9):8810-8. doi: 10.1021/nn503199v. Epub 2014 Aug 13.

Mapping nanoscale absorption of femtosecond laser pulses using plasma explosion imaging.

Author information

1
JILA and Department of Physics, University of Colorado , Boulder, Colorado 80309, United States.

Abstract

We make direct observations of localized light absorption in a single nanostructure irradiated by a strong femtosecond laser field, by developing and applying a technique that we refer to as plasma explosion imaging. By imaging the photoion momentum distribution resulting from plasma formation in a laser-irradiated nanostructure, we map the spatial location of the highly localized plasma and thereby image the nanoscale light absorption. Our method probes individual, isolated nanoparticles in vacuum, which allows us to observe how small variations in the composition, shape, and orientation of the nanostructures lead to vastly different light absorption. Here, we study four different nanoparticle samples with overall dimensions of ∼100 nm and find that each sample exhibits distinct light absorption mechanisms despite their similar size. Specifically, we observe subwavelength focusing in single NaCl crystals, symmetric absorption in TiO2 aggregates, surface enhancement in dielectric particles containing a single gold nanoparticle, and interparticle hot spots in dielectric particles containing multiple smaller gold nanoparticles. These observations demonstrate how plasma explosion imaging directly reveals the diverse ways in which nanoparticles respond to strong laser fields, a process that is notoriously challenging to model because of the rapid evolution of materials properties that takes place on the femtosecond time scale as a solid nanostructure is transformed into a dense plasma.

KEYWORDS:

femtosecond lasers; finite-difference time-domain; local field enhancement; photoion spectroscopy; plasmonics

PMID:
25100104
DOI:
10.1021/nn503199v

Supplemental Content

Full text links

Icon for American Chemical Society
Loading ...
Support Center