SummaryPulsed-laser atom-probe tomography is used to compare the field-evaporation mass spectrum and spatial distribution of molecular fragments from various poly(3-alkylthiophene) films deposited on sharpened aluminium specimen carriers using two different deposition methods. Films deposited via a modified solution-cast methodology yield small fragments with a uniform structural morphology whereas films deposited via an electrospray ionization methodology yield a wide range of fragments with a very non-uniform structural morphology. The main field-evaporated chemical species identified for both deposition types were, in order of typical relative abundance, C 2 H 5 + , CH 3 + , C 2 H 4 + , followed by C 3 H 7,8 + /SC + and SCH + . Thick electrospray depositions allowed investigation of the influence of laser-pulse energy on the analysis. Evidence is presented supporting the presence of a critical laser-pulse energy whereby changes in film morphology are signalled by the appearance of a new mass fragment at 190 Da.
Our group has reported atom probe tomography (APT) results for poly(3-alkylthiophene)s deposited on metal carrier tips previously [1,2]. The tip topology and mass fragment distributions were found to be dependent on both incident laser energy density and the deposition method. Mass peaks clearly identifiable as sulfur-containing were difficult to assign, but the alkane signature peaks were abundant and very easy to identify. Because sulfur has two isotopes of reasonable abundance (95% S 32 , 4.2% S 34 ) the potential for sulfur-containing fragments can be assessed by looking for pairs of peaks with an appropriate intensity ratio. In order to broaden our understanding of the pulsed-laser APT affects on the analysis of sulfur-alkane-containing organic systems, we prepared and analyzed metal carrier tips with deposits of octadecanethiol (C18) (SH-(CH 2 ) 17 -CH 3 ). This molecule is commonly used to form self-assembled-monolayers on a number of different metal surfaces [3] and as such, has been studied by APT [4,5]. By heating C18 above its melting point to 50 o C and dipping sharp metal carrier tips into the liquid for a period of hours, we were able to prepare bulk material specimens to see how analysis of an oligomer compares to that of related polymer specimens. Greater than 6.7 million ion fragments were collected in laser-and voltage-pulsing modes for a variety of laser energy densities all from a single specimen. Fig. 1 shows a 900k-ion mass spectrum collected during APT analysis of C18. Integer mass peaks dominate the spectrum while some weak ½-integer peaks (i.e. 35.5, 42.5, and 49.5 Dalton) are observed indicating the presence of doubly-ionized evaporation events. Surprisingly, no peaks identifiable as atomic carbon or sulfur can be identified, but the series of peaks labeled n=1-18 in black are identifiable as singly charged alkane fragments, C n H~2 n . The peaks labeled 2.5-4.5 in brown are potential doubly-charged alkane fragments; although no peaks corresponding to doublycharged ions for the first 3 alkane fragments are observed. Fig. 2 shows the low-mass region of the same data in linear scale. The insets in Fig. 2 help assess sulfur-containing ion peaks. The peak at 35 Dalton is likely C 5 H 10 ++ because of the lack of a peak at 37, while the peaks at 49 and 63 Dalton are likely SOH + and SOH(CH 2 ) + because of the corresponding peaks at 51 and 65.Fig 3 shows 500k ions acquired at 20% pulse fraction under voltage-pulsing conditions. A significant increase in background due to between-pulse evaporation events is observed as well as degradation in mass peak resolution, perhaps contributing to the lack of any peaks beyond 60 Dalton. Nevertheless, many of the primary low-mass fragments in Fig. 2 are also observed here. New peaks are observed at 31, 32.5, 37, and 45 Dalton. Here, limited resolution and intensity do not allow for sulfur peak assessment based on S 34 , but it is also difficult to assign these as singly-or doubly-charged alkane fragments as well. Assuming these peaks are either sulfur-c...
The recent development of laser-pulsed Local Electrode Atom Probe (LEAP ®) has provided an avenue to move beyond the analysis of metals and expand into many new areas of materials research. The successful analysis of semiconductor devices, high-k dielectric materials, ceramics, and data storage materials have all been recently reported [1]. In this paper we report on advances in specimen preparation techniques that have enabled the analysis of organic and biological materials. We will limit our discussion to the analysis of self-assembled monolayers (SAMs) and the analysis of buckminsterfullerene (C60) embedded within a compatible polymer matrix of poly(3dodecylthiophene) (P3DDT). These simple examples serve to support general techniques that will enable more sophisticated specimen preparation of nanoparticles and biomaterials/molecules of interest.
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