http://utw10193.utweb.utexas.edu/Archive/RuoffsPDFs/160.pdf

Synthesis of graphene-based nanosheets via chemical reduction of exfoliated graphite oxide

https://www.surfacesciencewestern.com/wp-content/uploads/2012/01/ass11_biesinger.pdf

Resolving surface chemical states in XPS analysis of first row transition metals, oxides and hydroxides: Sc, Ti, V, Cu and Zn

Analysis of XPS spectra of Fe2+ and Fe3+ ions in oxide materials

The reduction of graphene oxide

Graphene nanoribbons, narrow straight-edged strips of the single-atom-thick sheet form of carbon, are predicted to exhibit remarkable properties, making them suitable for future electronic applications. Before this potential can be realized, more chemically precise methods of production will be required. Cai et al. report a step towards that goal with the development of a bottom-up fabrication method that produces atomically precise graphene nanoribbons of different topologies and widths. The process involves the deposition of precursor monomers with structures that 'encode' the topology and width of the desired ribbon end-product onto a metal surface. Surface-assisted coupling of the precursors into linear polyphenylenes is then followed by cyclodehydrogenation. Given the method's versatility and precision, it could even provide a route to more unusual graphene nanoribbon structures with tuned chemical and electronic properties. Graphene nanoribbons (GNRs) have structure-dependent electronic properties that make them attractive for the fabrication of nanoscale electronic devices, but exploiting this potential has been hindered by the lack of precise production methods. Here the authors demonstrate how to reliably produce different GNRs, using precursor monomers that encode the structure of the targeted nanoribbon and are converted into GNRs by means of surface-assisted coupling. Graphene nanoribbons—narrow and straight-edged stripes of graphene, or single-layer graphite—are predicted to exhibit electronic properties that make them attractive for the fabrication of nanoscale electronic devices1,2,3. In particular, although the two-dimensional parent material graphene4,5 exhibits semimetallic behaviour, quantum confinement and edge effects2,6 should render all graphene nanoribbons with widths smaller than 10 nm semiconducting. But exploring the potential of graphene nanoribbons is hampered by their limited availability: although they have been made using chemical7,8,9, sonochemical10 and lithographic11,12 methods as well as through the unzipping of carbon nanotubes13,14,15,16, the reliable production of graphene nanoribbons smaller than 10 nm with chemical precision remains a significant challenge. Here we report a simple method for the production of atomically precise graphene nanoribbons of different topologies and widths, which uses surface-assisted coupling17,18 of molecular precursors into linear polyphenylenes and their subsequent cyclodehydrogenation19,20. The topology, width and edge periphery of the graphene nanoribbon products are defined by the structure of the precursor monomers, which can be designed to give access to a wide range of different graphene nanoribbons. We expect that our bottom-up approach to the atomically precise fabrication of graphene nanoribbons will finally enable detailed experimental investigations of the properties of this exciting class of materials. It should even provide a route to graphene nanoribbon structures with engineered chemical and electronic properties, including the theoretically predicted intraribbon quantum dots21, superlattice structures22 and magnetic devices based on specific graphene nanoribbon edge states3.

Atomically precise bottom-up fabrication of graphene nanoribbons

Practical surface analysis: By auger and x-ray photoelectron spectroscopy

Analysis of XPS spectra of Fe2 and Fe3 ions in oxide April 15th, 2019 Carbon is ubiquitous and is present on all surfaces for XPS analysis It is common practice to use the carbon C 1s peak at 285 eV as a reference for charge correction In routine XPS analyses of samples prepared outside the high vacuum chamber relatively thick carbon layers are formed on the surfaces and the corrected XPS peak positions are independent of the apparent or experimentally

Practical Surface Analysis

Description of the spectrometer x-ray source monochromator electron lens hemispherical analyser multichannel detector sample analysis chamber charge compensation performance on conducting samples performance on insulating samples performance on testing of the spectrometer experimental protocol sample mounting data acquisition correction of binding energy scale for sample charging curve fitting lineshapes shake-up structure valence bands impurities x-ray degradation organization of the database list of polymers and acronyms the database appendix 1 - primary C 1s shifts appendix 2 - secondary C 1s shifts appendix 3.1 - 0 1s binding energies in CHO polymers appendix 3.2 - 0 1s binding energies in other polymers appendix 4 - N 1s binding energies appendix 5 - F 1s binding energies appendix 6 - binding energies and spin-orbit constants for core-line doublets apendix 7 - binding energies of peaks appearing in the valence band region.

David Briggs

Papers

Practical surface analysis: By auger and x-ray photoelectron spectroscopy

Practical Surface Analysis

High Resolution XPS of Organic Polymers: The Scienta ESCA300 Database

High resolution XPS of organic polymers

Surface Analysis by Auger and X-Ray Photoelectron Spectroscopy