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Martin J Iedema

Publications and source records attributed to Martin J Iedema.

2 recordsLinked to original sources

Nanometer-resolved interfacial fluidity.

Confined liquids can have properties that are poorly predicted from bulk parameters. We resolve with 0.5 nm resolution the nanoscale perturbations that interfaces cause on fluidity, in thin 3-methylpentane (3MP) films. The films of glassy 3MP are much less viscous at the vacuum-liquid interface and much more viscous at the 3MP-metal interface, compared to the bulk of the film. We find that the viscosity at the interfaces continuously returns to the bulk value over about a 3 nm distance. The amorphous 3MP films are constructed using molecular beam epitaxy on a Pt(111) substrate at low temperatures (<30 K). Ions are gently inserted at specific distances from the substrate with a 1 eV hydronium (D(3)O(+)) or Cs(+) ion beam. The voltage across the film, which is directly proportional to the position of the ions within the film, is monitored electrostatically as the film is heated at a rate of 0.2 K/s. Above the bulk glass transition temperature (T(g)) of 3MP (77 K), the ions are expected to begin to move down through the film. However, ion movement is observed at temperatures as low as 50 K near the vacuum interface, well below the bulk T(g). The fitted kinetics predict that at 85 K, the glass is about 6 orders of magnitude less viscous near the free interface compared to that of the bulk.

Journal Article↗

Quantitative time-resolved monitoring of nitrate formation in sea salt particles using a CCSEM/EDX single particle analysis.

Progress of the nitrate formation in individual sea salt particles was detected as a function of time using aerosol samples collected during the TexAQS 2080 experiment We demonstrate that the time-resolved collection approach coupled with the automated EDX single particle analysis made it possible to follow in detail the time evolution of sea salt particles within a diverse aerosol mixture. Using a custom built Time-Resolved Aerosol Collector (TRAC), particulate samples were taken sequentially on grid-supported 50 nm carbon films with a time resolution of 10 min between two consecutive samples. The samples were analyzed in the laboratory using Computer Controlled Scanning Electron Microscopy with Energy-Dispersed analysis of X-rays (CCSEM/EDX). Between midnight of 08/16/00 and the early morning of 08/17/00, a steady, particularly sea salt rich aerosol was observed at the measurement site, which later showed the effects of atmospheric processing. During the night of 08/17/00 the sea salt particles were almost unprocessed, having elemental composition close to that of seawater. By 12 noon, the evolving atmosphere was able to completely convert them, predominantly to sodium nitrate particles. During the next night this process had nearly stopped and fairly virgin sea salt particles appeared again.

Aerosols↗