AVS 61st International Symposium & Exhibition
    Applied Surface Science Monday Sessions
       Session AS+BI+MC+SS-MoA

Invited Paper AS+BI+MC+SS-MoA6
Organic Depth Profiling Alchemy: Can We Transmute Data into Meaning?

Monday, November 10, 2014, 3:40 pm, Room 316

Session: The Liquid Interface & Depth Profiling and Sputtering with Cluster Ion Beams
Presenter: Alexander Shard, National Physical Laboratory, UK
Correspondent: Click to Email

Argon cluster sources suitable for depth profiling organic materials have developed rapidly and are now widely available and routinely used to analyse materials ranging from organic electronic devices to biological samples. This fantastic progress allows detailed insight into the chemistry and structure of organic materials with depth resolutions below 10 nm over many micrometres. When combined with 2D surface chemical imaging, detailed 3D reconstructions can be obtained allowing the label-free visualisation of chemical distributions which were previously impossible to obtain. However, because detailed understanding of the processes involved is still developing, it is necessary to view such data with scepticism when a quantitative answer is required. Conversely, the ability to perform nearly damage-free profiles of organic materials allows us to answer fundamental questions about surface analytical methods provided that the sample analysed has a known structure and composition.

The recurring questions in organic depth profiling and 3D imaging relate to the depth scale and the translation of a signal into a concentration, or amount of material. At NPL, we have developed reference materials which are designed to address these questions and in this talk an overview of developments in quantitative organic depth profiling will be provided. The use of XPS is shown to provide accurate compositions, as expected. However, there are some practical issues to be understood involving X-ray and electron damage and sample heating. Additionally, XPS suffers from low sensitivity, specificity and lateral resolution compared to SIMS. Whilst SIMS is fast, specific, sensitive and has high lateral resolution it suffers from the lack of an adequate means of converting data into compositions. Here, reference materials have been constructed which enable the most important effects of the sample on SIMS data to be described. These effects are outlined and include an apparent depth of origin difference for secondary ions, surface transient behaviour and the matrix effect. It is also shown how it is possible to use the matrix effect to assess the nanoscale phase separation of materials.