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Ganbat Duvjir Seung Mi Lee Otgonbayar Dugerjav Chu Van Chiem Jae M. Seo 《Surface science》2009,603(15):2312-4607
Using scanning tunneling microscopy (STM), it has been found that the reconstruction of Si(1 1 4) is transformed irreversibly from a 2 × 1 structure composed of dimer (D), rebonded atom (R), and tetramer (T) rows (phase A) to a different kind of 2 × 1 structure composed of D, T, and T rows (phase B) by C incorporation. It has been confirmed by high-resolution synchrotron core-level photoemission spectroscopy (PES) that such an irreversible structural transformation is due to stable subsurface C atoms. They induce anisotropic compressive stress on the surface, which results in insertion of Si dimers to an R row to form a T row. 相似文献
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Hidong Kim Otgonbayar Dugerjav Ganbat Duvjir Huiting Li Jae M. Seo 《Surface science》2012,606(7-8):744-748
By combined investigation of STM and synchrotron PES on Ge/Si(5 5 12)-2 × 1 at 530 °C, it has been found that, in addition to the upward-relaxed surface Si atoms, a subsurface Si atom is also readily replaced by an arriving Ge atom at the initial adsorption stage. Such enhanced interdiffusion is due to a unique character of one-dimensional chain structures of the reconstructed substrate, such as π-bonded and honeycomb chains not existing on other low-index Si surfaces such as Si(001)-c(4 × 2) and Si(111)-7 × 7, applying a tensile surface stress to the neighbouring subsurface atoms. Interdiffusion of Ge having lower surface energy induces adsorption of the displaced Si atoms on the surface to form sawtooth-like facets composed of (113)/(335) and (113)/(112) with arriving Ge atoms until the surface is filled with those facets. Such displacive adsorption is the origin of high Si concentration of formed facets. 相似文献
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Hidong Kim Ganbat Duvjir Otgonbayar Dugerjav Huiting Li Moaaed Motlak Amarmunkh Arvisbaatar Jae M. Seo 《Surface science》2012,606(19-20):1512-1519
The atomic structure and interfacial bonding of the ordered-and-isolated CaF nanowires on Si(5 5 12)-2 × 1 have been disclosed by scanning tunneling microscopy and synchrotron photoemission spectroscopy. Initially, CaF molecules dissociated from thermally deposited CaF2 molecules are adsorbed preferentially on the chain structures of Si(5 5 12)-2 × 1 held at 500 °C. With increasing CaF2 deposition amount, one-dimensional (1D) CaF nanowires composed of (113) and (111) facets are formed. The line density of these CaF nanowires increases as a function of deposition amount. Finally, at a submonolayer coverage, the surface is saturated with these 1D nanowires except for the (225) subunit, while the original period of Si(5 5 12)-2 × 1, 5.35 nm, is preserved. It has been deduced by the present studies that, owing to these preferential adsorption of CaF and facet-dependent growth of a CaF layer within a unit periodic length of Si(5 5 12)-2 × 1, such a self-limited growth of the CaF nanowire with a high aspect ratio becomes possible. 相似文献
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This study aimed to improve the performance of the activated carbon-based cathode by increasing the Li content and to analyze the effect of the combination of carbon and oxidizing agent. The crystal structure and chemical structure phase of Li-high surface area activated carbon material (Li-HSAC) was analyzed by X-ray diffraction (XRD) and Raman spectroscopy, the surface state and quantitative element by scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX) and the surface properties with pore-size distribution by Brunauer–Emmett–Teller (BET), Barrett–Joyner–Halenda (BJH) and t-plot methods. The specific surface area of the Li-YP80F is 1063.2 m2/g, micropore volume value is 0.511 cm3/g and mesopore volume is 0.143 cm3/g, and these all values are higher than other LiOH-treated carbon. The surface functional group was analyzed by a Boehm titration, and the higher number of acidic groups compared to the target facilitated the improved electrolyte permeability, reduced the interface resistance and increased the electrochemical properties of the cathode. The oxidizing agent of LiOH treated high surface area of activated carbon was used for the cathode material for EDLC (electric double layer capacitor) to determine its electrochemical properties and the as-prepared electrode retained excellent performance after 10 cycles and 100 cycles. The anodic and cathodic peak current value and peak segregation of Li-YP80F were better than those of the other two samples, due to the micropore-size and physical properties of the sample. The oxidation peak current value appeared at 0.0055 mA/cm2 current density and the reduction peak value at –0.0014 mA/cm2, when the Li-YP80F sample used to the Cu-foil surface. The redox peaks appeared at 0.0025 mA/cm2 and –0.0009 mA/cm2, in the case of using a Nickel foil, after 10 cycling test. The electrochemical stability of cathode materials was tested by 100 recycling tests. After 100 recycling tests, peak current drop decreased the peak profile became stable. The LiOH-treated high surface area of activated carbon had synergistically upgraded electrochemical activity and superior cycling stability that were demonstrated in EDLC. 相似文献
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Otgonbayar Zambaga Yang Sunhye Kim Ick-Jun Oh Won-Chun 《Journal of Solid State Electrochemistry》2022,26(12):2841-2859
Journal of Solid State Electrochemistry - Li-doped high surface area of activated carbon (LHSAC) for Li ion capacitor (LIC) has been prepared by controlling the LiOH amounts for surface... 相似文献
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Hidong Kim Otgonbayar Dugerjav Ganbat Duvjir Huiting Li Seunghun Jang Moonsup Han B.D. Yu Jae M. Seo 《Surface science》2012,606(3-4):312-319
Combined investigation of STM, high-resolution synchrotron photoemission, and density functional theory calculations allowed us to understand the Sb-induced structural-transformation of Si(114)-2 × 1. When 2 ML of Sb is deposited on Si(114)-2 × 1 at room temperature and postannealed at 500 °C, all of the surface Si atoms with dangling bonds are replaced by Sb atoms. Among one-dimensional (1D) structures consisting of Si(114)-2 × 1, such as a dimer with a 6-membered ring (D6) row, a rebonded-atom (R) row, and a tetramer (T) row [D6-R-T], the T row is split into a dimer row with a 7-membered ring (D7) and an R row [D6-R-D7-R]. Since the R-D7-R unit, a building block of Sb/Si(113)2 × 2, is under stress-balance, the Sb/Si(114)-2 × 1 surface is stressed compressively due to the extra D6 unit. As a result, with additional postannealing at 600 °C, two periods of this 2 × 1 [(D6-R-D7-R)-(D6-R-D7-R)] are gradually converted to 2 × 2 [(D6-R-D6-R)-(R-D7-R)], where the D6-R (115) unit is stress-balanced. The corresponding photoemission data obtained from both of the phases show that all of the surface components of the clean surface have disappeared, instead the single Sb–Si interfacial component has appeared, which indicates that the charge transfers from interfacial Si to surface Sb atoms. Finally, the density functional theory calculations have also confirmed that there are two distinct phases determined by the chemical potential of passivating Sb atoms. 相似文献
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