Ultrahigh-mobility organic field-effect transistors (OFETs) based on a CDT-BTZ donor-acceptor copolymer are realized by reaching high molecular order and pronounced alignment in single fibers within a short OFET channel via solution processing. The macromolecules directionally self-assemble in a quasi crystal-like order in the fibers providing in this way an unhindered charge carrier pathway with mobilities as high as 5.5 cm(2) V(-1) s(-1).

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A wide range of analytical techniques were used to investigate rock varnish from different locations (Negev, Israel; Knersvlakte, South Africa; Death Valley and Mojave Desert, California): a 200 nm-femtosecond laser ablation-inductively coupled plasma-mass spectrometer (LA-ICP-MS), an electron probe microanalyzer (EPMA), focused ion beam (FIB) slicing, and scanning transmission X-ray microscopy-near edge X-ray absorption fine structure spectroscopy (STXM-NEXAFS). This combination enables comprehensive high-spatial-resolution analysis of rock varnish. Femtosecond LA-ICP-MS and EPMA were used for quantitative determination of element concentrations. In-situ measurements were conducted on thick and thin sections with a resolution of 10-40 mu m and 2 mu m, respectively. The results demonstrate that some elements, such as Mn, Co, Pb, Ni, and Cu, are highly enriched in varnish relative to the upper continental crust (up to a factor of 100). The varnish composition is not influenced by the composition of the underlying rock, which is witnessed by plots of MnO2 vs. SiO2 contents. Furthermore, the Mn-free end members fall in the range of average dust compositions. The varnishes from the various locations show distinct differences in some elemental ratios, in particular Mn/Fe (0.3-25.1), Mn/Ba (4-170), Ni/Co (0.03-1.8) and Pb/Ni (0.4-23). The rare earth element (REE) patterns vary with La-N/Yb-N = 3.5-12 and different degrees of Ce anomalies (Ce/Ce* = 1.5-5.3). To study the internal structure of the varnish, 100-200 nm thick FIB slices were prepared and mappings of Fe, Mn, N, CO32-, Ca, C, and Si at the nm scale performed. Banded internal structures of Mn, Fe and organic C were observed in the Israeli and Californian samples, however, no Fe-rich layers are present in the South African rock varnish samples. Furthermore, cavities were found that are partly filled by C, Fe, and Mn rich material. Internal structures are different for varnish from different locations, which might reflect different types of genesis. The results of the combined microanalytical techniques give important detailed insights towards unraveling the genesis of rock varnish. (C) 2015 Elsevier B.V. All rights reserved

Abstract. The spatial distribution of transition metal valence states is of broad interest in the microanalysis of geological and environmental samples. An example is rock varnish, a natural manganese (Mn)-rich rock coating, whose genesis mechanism remains a subject of scientific debate. We conducted scanning transmission X-ray microscopy with near-edge X-ray absorption fine-structure spectroscopy (STXM-NEXAFS) measurements of the abundance and spatial distribution of different Mn oxidation states within the nano- to micrometer thick varnish crusts. Such microanalytical measurements of thin and hard rock crusts require sample preparation with minimal contamination risk. Focused ion beam (FIB) slicing was used to obtain ∼100–1000 nm thin wedge-shaped slices of the samples for STXM, using standard parameters. However, while this preparation is suitable for investigating element distributions and structures in rock samples, we observed artifactual modifications of the Mn oxidation states at the surfaces of the FIB slices. Our results suggest that the preparation causes a reduction of Mn4+ to Mn2+. We draw attention to this issue, since FIB slicing, scanning electron microscopy (SEM) imaging, and other preparation and visualization techniques operating in the kilo-electron-volt range are well-established in geosciences, but researchers are often unaware of the potential for the reduction of Mn and possibly other elements in the samples.