32 research outputs found

    Termination of Graphene Edges Created by Hydrogen and Deuterium Plasmas

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    Edge engineering is important for both fundamental research and applications as the device size decreases to nanometer scale. This is especially the case for graphene because a graphene edge shows totally different electronic properties depending on the atomic structure and the termination. It has recently been shown that an atomically precise zigzag edge can be obtained by etching graphene and graphite using hydrogen (H) plasma. However, edge termination had not been studied directly. In this study, termination of edges created by H-plasma is studied by high-resolution electron energy loss spectroscopy (HREELS) to show that the edge is sp2\mathrm{sp}^{2} bonded and the edge carbon atom is terminated by only one H atom. This suggests that an ideal zigzag edge, which is not only atomically precise but also sp2\mathrm{sp}^{2} bonding, can be obtained by H-plasma etching. Etching of the graphite surface with plasma of a different isotope, deuterium (D), is also studied by scanning tunneling microscopy (STM) to show that D-plasma anisotropically etches graphite less efficiently, although it can make defects more efficiently, than H-plasma.Comment: 8 pages, 5 figure

    Efficacy of soft palatal augmentation prosthesis for oral functional rehabilitation in patients with dysarthria and dysphagia: a protocol for a randomised controlled trial

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    Introduction Palatal augmentation prosthesis (PAP) is used in patients with articulation and swallowing disorders caused by postoperative loss of tongue tissue due to tongue cancer, cerebrovascular disease sequelae and age-related hypofunction. We have previously reported a newly designed soft PAP fabricated using an thermoplastic material that is particularly appropriate for early intervention. However, the effect of soft PAP on oral function improvement remains to be elucidated. The aim of this study is to investigate whether soft PAP can improve dysarthria and dysphagia occurring as cerebrovascular disease sequelae. Methods and analysis This prospective, randomised, controlled trial will compare the immediate and training effects of rehabilitation using soft PAP with those of rehabilitation without using it. Primary outcomes are the single-word intelligibility test score and pharyngeal transit time (PTT). Secondary outcomes are tongue function (evaluated based on maximum tongue pressure, repetitions of tongue pressure and endurance of tongue pressure), articulation function (evaluated based on speech intelligibility, oral diadochokinesis, Voice-Related Quality of Life (V-RQOL)) and swallowing function (evaluated using Eating Assessment Tool-10). The study results will help determine the efficacy of Soft PAP in improving functional outcomes of word intelligibility and PTT. We hypothesised that early rehabilitation using Soft PAP would more effectively improve articulation and swallowing function compared with conventional rehabilitation without using soft PAP. Ethics and dissemination Ethical approval was obtained from the Okayama University Certified Review Board. The study findings will be published in an open access, peer-reviewed journal and presented at relevant conferences and research meetings

    Possible interpretations of the joint observations of UHECR arrival directions using data recorded at the Telescope Array and the Pierre Auger Observatory

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    Spectroscopic Characterization and Transport Properties of Aromatic Monolayers Covalently Attached to Si(111) Surfaces

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    We fabricated self-assembled monolayers (SAMs) composed of aromatic molecules with different anchor groups on Si(111) surfaces by wet chemical reactions. We investigated the bonding structures and transport properties by spectroscopic and electrical measurements, respectively. By using simple aromatic molecules (phenol, styrene, and phenylacetylene) as initial precursors, we successfully fabricated aromatic SAMs covalently bonded to Si(111) surfaces through different anchor structures (Si–O–, Si–CH<sub>2</sub>–CH<sub>2</sub>–, and Si–CHCH−). Transmission infrared spectroscopy clarify that the phenyl rings in the SAMs are oriented almost perpendicular to the Si surfaces. High-resolution X-ray photoelectron spectroscopy reveals that the aromatic molecules attach to the Si surface with the surface coverage of ∼0.5. The experimental results of these spectroscopies lead to a conclusion that the aromatic SAMs form densely packed monolayers on Si(111). Current density–voltage measurements of Hg/aromatic SAM–Si(111) sandwiched structures revealed that the “Si­(111)–O–Ph” (SAM from phenol) show higher conductivity compared with the long-chain alkyl SAM on Si(111)

    Mechanism of Olefin Hydrogenation Catalysis Driven by Palladium-Dissolved Hydrogen

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    The Pd-catalyzed hydrogenation of CC double bonds is one of the most important synthetic routes in organic chemistry. This catalytic surface reaction is known to require hydrogen in the interior of the Pd catalyst, but the mechanistic role of the Pd-dissolved H has remained elusive. To shed new light into this fundamental problem, we visualized the H distribution near a Pd single crystal surface charged with absorbed hydrogen during a typical catalytic conversion of butene (C<sub>4</sub>H<sub>8</sub>) to butane (C<sub>4</sub>H<sub>10</sub>), using H depth profiling via nuclear reaction analysis. This has revealed that the catalytic butene hydrogenation (1) occurs between 160 and 250 K on a H-saturated Pd surface, (2) is triggered by the emergence of Pd bulk-dissolved hydrogen onto this surface, but (3) does not necessarily require large stationary H concentrations in subsurface sites. Even deeply bulk-absorbed hydrogen proves to be reactive, suggesting that Pd-dissolved hydrogen chiefly acts by directly providing reactive H species to the surface after bulk diffusion rather than by indirectly activating surface H through modifying the surface electronic structure. The chemisorbed surface hydrogen is found to promote hydrogenation reactivity by weakening the butene-Pd interaction and by significantly reducing the decomposition of the olefin
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