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Henri Lezec

Publications and source records attributed to Henri Lezec.

3 recordsLinked to original sources

Pulsed Laser Template Engineering- PLATEN

Thin films of functional inorganic materials, particularly oxides, play a vital role in optoelectronics, enabling applications that range from active optical components to MEMS-based architectures. Achieving high aspect ratio patterning of these functional materials remains a significant challenge, as many of their constituent elements do not readily form volatile compounds required for conventional reactive ion etch processes. We introduce a novel approach, Pulsed Laser Template ENgineering (PLATEN), which offers a more accessible route for patterning materials that are typically difficult to etch. This technique involves depositing functional films using the Pulsed Laser Deposition (PLD) process onto silicon substrates that have been pre-patterned using reactive ion etching to create high aspect ratio features. Due to the highly forward-directed nature of the PLD process, the deposited films replicate closely the topography of the patterned silicon, without coatings the sidewalls. This process remains effective even at feature sizes down to approximately 50 nm. The oxide films replicate the underlying silicon pattern to a thickness of 80 nm. For thickness beyond 80 nm the patterns develop a waist at the midpoint which scales with film thickness and is not dependent on the feature size. In this paper, we present a detailed analysis of the PLATEN process, including deviations from ideal pattern replication in sub-micron features as a function of film thickness, and demonstrate near single crystalline growth of oxides on the patterned silicon substrate, demonstrating the potential of PLATEN technique for active opto-electronic materials.

cond-mat.mtrl-sci

A Space-Time Knife-Edge In Epsilon-Near-Zero Films for Ultrafast Pulse Characterization

Epsilon-near-zero (ENZ) materials have shown strong refractive nonlinearities that can be fast in an absolute sense. While continuing to advance fundamental science, such as time varying interactions, the community is still searching for an application that can effectively make use of the strong index modulation offered. Here we combine the effect of strong space-time index modulation in ENZ materials with the beam deflection technique to introduce a new approach to optical pulse characterization that we term a space-time knife edge. We show that in this approach, we are able to extract temporal and spatial information of a Gaussian beam with only two time resolved measurements. The approach achieves this without phase-matching requirements (<1 micron thick film) and can achieve a high signal to noise ratio by combining the system with lock-in detection, facilitating the measurement of weak refractive index changes (delta_n ~ 10^-5) for low intensity beams. Thus, the space-time knife edge can offer a new avenue for ultrafast light measurement and demonstrates a use cases of ENZ materials. In support of this, we outline temporal dynamics for refractive index changes in non-colinear experiments opening avenues for better theoretical understanding of both the spatial and temporal dynamics of emerging ENZ films.

physics.optics

Probing gas adsorption on individual facets of a metal nanoparticle

Metal nanoparticle surfaces comprise of multiple planes with various atomic arrangements that interact with gases differently1,2. Identification of gas adsorption properties on all facets is an essential prerequisite for rational design of metal nanoparticles for catalysis, energy storage and gas sensing. Adsorbed gas molecules alter the electron density at metal surfaces3, changing the energy of the surface plasmon resonance4,5. All-optical methods using light as the excitation source can identify, in situ, gas-metal interactions in an ensemble of metal nanoparticles by measuring energy shifts of either stationary surface plasmon resonances over an entire particle, or delocalized symmetric modes on multiple regions in a particle6-8. Such methods preclude the characterization of facet-dependent gas adsorption for individual nanoparticles. Here, by using in situ electron-energy-loss spectroscopy in an environmental scanning-transmission electron microscope, we show that localized, stationary surface plasmons on individual facets of triangular crystalline Au nanoparticles in vacuum and in gaseous environments can be excited using a nanometer size electron probe. We then show that, by exploiting this localized spatial resolution, selective gas adsorption on specific sets of facets can be characterized. We anticipate that this method can be extended to quantify the concentration of adsorbed molecules, derive the binding energy for specific facets for certain gas species, and design facet-controlled nanoparticles to achieve specific gas adsorption properties.

cond-mat.mtrl-sci