Measuring biological samples by atom probe tomography (APT) in their natural environment, i.e. aqueous solution, would take this analytical method, which is currently well established for metals, semi-conductive materials and non-metals, to a new level. It would give information about the 3D chemical structure of biological systems, which could enable unprecedented insights into biological systems and processes, such as virus protein interactions. For this future aim, we present as a first essential step the APT analysis of pure water (Milli-Q) which is the main component of biological systems. After Cryo-preparation, nanometric water tips are field evaporated with assistance by short laser pulses. The obtained data sets of several tens of millions of atoms reveal a complex evaporation behavior. Understanding the field evaporation process of water is fundamental for the measurement of more complex biological systems. For the identification of the individual signals in the mass spectrum, DFT calculations were performed to prove the stability of the detected molecules.

Atom probe tomography (APT) has been established in the microscopic chemical and spatial analysis of metallic or semiconductors nanostructures. In recent years, and especially with the development of a transfer shuttle system and adapted preparation protocols, the field of frozen liquids has been opened up. Still, very limited knowledge is available about the evaporation and fragmentation behavior of frozen liquids in APT. In this work, efforts were made to extend the method toward organic and biological soft matter, which are mostly built from hydrocarbon chains, the evaporation and fragmentation behavior of simple alkane chains (n-tetradecanes). Tetradecane shows a very complex evaporation behavior whereby peaks of C1–C15 can be observed. Based on multihit events and the representation of these in correlation plots, more detailed information about the evaporation behavior and the decay of molecules into smaller fragments in the region near the tip can be studied. A variety of different dissociation tracks of larger molecules in their excited state and their subsequent decay in low-field regions, on the way to the detector, could be observed and the dissociation zone in the low-field region was calculated.

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