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Advanced X-Ray Imaging Study on the Mechanism of Nanoparticle Formation during Laser Ablation in Liquid

Subject Area Physical Chemistry of Molecules, Liquids and Interfaces, Biophysical Chemistry
Synthesis and Properties of Functional Materials
Term from 2014 to 2020
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 262558940
 
Final Report Year 2021

Final Report Abstract

The goal of the present project has been to resolve the dynamics of pulsed laser ablation in liquids (PLAL) by hierarchical in-situ methods and to correlate the nanoparticle genesis during this process with the macroscopic phenomenology. This requires the development and application of methods, which are sensitive to a millimeter down to a nanometer length scale including high time resolution on the microsecond scale. This has been achieved by correlating spatiotemporally resolved smallangle X-ray scattering (SAXS), UV-visual spectroscopic methods, visual stroboscopy (VISIMG) with fast X-ray imaging (XI) with contrast variation (XHI). In the first part of the project, we have developed contrast variation (as Hartmann imaging) in order to be sensitive to the macroscale (absorption XR and phase-contrast XPC) and nanoscale (dark-field contrast). At the same time, the correlation of bubble dynamics and particle formation in terms of particle size distribution and yield has been explored. In the second part (project prolongation) specifically, the origins of bimodal size distribution have been investigated as well as speciation in post-ablation particle oxidation. XHI has been fully developed to use X-ray lens arrays as an X-ray variant of Shack-Hartmann sensing. Several milestone results have been achieved that drew considerable attention in the scientific community: Particle size distribution, in particular, the usually observed bi- or multimodal distribution have inherent origins in the early stages of the process itself: Large (liquid) particles may be ejected in short-pulse (picosecond) PLAL through the mechanism of liquid film detachment and jet formation, while also a second-stage agglomeration of particles trapped inside the bubble will cause size coarsening. Quenching of particle sizes therefore can already be active in the bubble, if electrolytes are added and prevent agglomeration during bubble collapse. The coupling of energy into the system and thus process efficiency can be monitored by the bubble sizes, both in terms of laser fluence and coupling-related incubation. Oxidation, in particular in the zinc system is characterized by the initial production of metallic zinc particles, which undergo gradual oxidation in water to form ZnO. Time-resolved X-ray absorption spectroscopy was for the first time employed for the study. In long-pulse (nanosecond) ablation a large fraction of the ablated species inside the bubble consists of isolated, active zinc species, which grow into particles within the duration of the first bubble. Method development aiding the resolution of dynamics and detection of formed nanoparticles includes a thorough discussion of size definition through alternative (ex-situ) methods, development of time-resolved X-ray small-angle scattering (SAXS), X-ray imaging (XI), and X-ray spectroscopy (XAS). In particular, XI and SAXS could be merged into a contrast variable imaging technique using a Shack-Hartmann setup with arrays of X-ray microbeams. This technique stimulated further developments at KIT.

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