排序方式: 共有43条查询结果,搜索用时 312 毫秒
11.
We have measured W 4f7/2 core-level photoemission spectra from W(1 1 0) in the presence of Pd overlayers for coverages up to ∼1 pseudomorphic monolayer (ML). At coverages close to 0.05 ML a striking change in the W core-level spectrum is observed, which we interpret as indicating a long-range lateral effect of 2D Pd islands upon the W electronic structure in both the first and second W layers. As the coverage increases the long-range effect weakens and finally vanishes near 0.85 ML. Above this coverage the W spectra are typical for a W-based bimetallic interface, with the first-layer W atoms exhibiting a small interfacial core-level shift (−95 ± 5 meV) compared to the bulk atoms. 相似文献
12.
We have measured W and Pt 4f7/2 core-level photoemission spectra from interfaces formed by ultrathin Pt layers on W(1 1 0), completing our core-level measurements of W(1 1 0)-based bimetallic interfaces involving the group-10 metals Ni, Pd, and Pt. With increasing Pt coverage the sequence of W spectra can be described using three interfacial core-level peaks with binding-energy (BE) shifts (compared to the bulk) of −0.220 ± 0.015, −0.060 ± 0.015, and +0.110 ± 0.010 eV. We assign these features to 1D, 2D pseudomorphic (ps), and 2D closed-packed (cp) Pt phases, respectively. For ∼1 ps ML the Pt 4f7/2 BE is 71.40 ± 0.02 eV, a shift of +0.46 ± 0.09 eV with respect to the BE of bulk Pt metal. The W 4f7/2 core-level shifts induced by all three adsorbates are semiquantitatively described by the Born-Haber-cycle based partial-shift model of Nilsson et al. [39]. As with Ni/W(1 1 0), the difference in W 4f7/2 binding energies between ps and cp Pt phases has a large structural contribution. The Pt 4f lineshape is consistent with a small density of states at the Fermi level, reflective of the Pt monolayer having noble-metal-like electronic structure. 相似文献
13.
14.
Newcomb K. Chaney L. Compagno W. Judson Marsh J. G. Fairchild L. Bertiaux G. W. Morden B. P. Richardson A. K. Balls C. C. McDonell W. H. Ross W. S. Hendrikson Le Roy W. McCay L. M. Dennis B. J. Lemon P. A. von der Meulen Easton O. L. Shinn Ch. A. Peters 《Analytical and bioanalytical chemistry》1917,56(6-7):317-318
15.
Shinn JL Wilson JW Badavi FF Benton EV Csige I Frank AL Benton ER 《Radiation measurements》1994,23(1):57-64
A nonperturbative analytic solution of the high charge and energy (HZE) Green's function is used to implement a computer code for laboratory ion beam transport in multiple-layered materials. The code is established to operate on the Langley nuclear fragmentation model used in space engineering applications. Computational procedures are established to generate linear energy transfer (LET) distributions for a specified ion beam and target for comparison with experimental measurement. Comparison with 56Fe ion with Pb-Al and Pb-(CH2)x targets shows reasonable agreement. 相似文献
16.
Chien‐Hsin Liu Shinn‐Horng Chen Yun Chen 《Journal of polymer science. Part A, Polymer chemistry》2006,44(12):3882-3895
Soluble and well‐defined 9,9‐dihexylfluorene and 9‐dimethylaminopropylcarbazole based copolymers PFCN and 5PFCN have been prepared by Suzuki coupling polymerization. For comparison, alternate copolymer of 9,9‐dihexylfluorene and 9‐hexylcarbazole (PFC) was also prepared with the same method. Furthermore, alternate copolymer of 9,9‐dihexylfluorene and 9‐dimethylethylammoniumpropylcarbazole (PFCNE) was prepared from PFCN by the ethylation of its dimethylaminopropyl groups with bromoethane. These copolymers were soluble in organic solvents and showed high glass‐transition temperatures (75–160 °C). The optimized architecture of PFCN from a simulation was a spiral, which was different from the linear structure of poly(9,9‐dihexylfluorene) (PFO). Thermogravimetric analysis showed that the residual weights of 5PFCN, PFCN, PFC, and PFCNE at 800 °C were all greater then 50%, whereas PFO showed complete thermal decomposition. Both the absorption and photoluminescence emission peaks of these copolymers showed blueshifts after the introduction of the carbazole units because of reduced conjugation. Moreover, the introduction of 9‐hexylcarbazole and 9‐dimethylamionpropylcarbazole moieties into copolymers PFC and PFCN, respectively, effectively prevented the excimer formation of PFO. According to cyclic voltammetry results, PFCNE containing quaternary amino pendant groups exhibited the most stable reduction–oxidation cycles. The turn‐on electric fields of their electroluminescence devices decreased with increasing carbazole content because of the more balanced carrier injection. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3882–3895, 2006 相似文献
17.
Ruei‐Tang Chen Shinn‐Horng Chen Bar‐Yuan Hsieh Yun Chen 《Journal of polymer science. Part A, Polymer chemistry》2009,47(11):2821-2834
A series of fluorene derivatives containing nonsymmetric and bulky aromatic groups at C‐9 position were synthesized and used for the preparation of blue‐light‐emitting copolyfluorenes ( P1 – P4 ) by the Suzuki coupling polycondensation. The copolymers were characterized by molecular weight determination, elemental analysis, differential scanning calorimeter, thermogravimetric analysis, absorption and emission spectroscopy, cyclic voltammetry, and differential pulse voltammetry. Their decomposition temperatures and glass transition temperatures are 423–441 °C and >120 °C, respectively. In film state, the copolyfluorenes exhibit blue photoluminescence at 425–450 nm, which remains almost unchanged after annealing at 200 °C in air for 60 min. Polymer light‐emitting diodes [ITO/PEDOT:PSS/ P1 – P4 /Ca(50 nm)/Al(100 nm)] show stable blue‐light emission under device operation with the CIE co‐ordinates being between (0.16, 0.07) and (0.17, 0.09). The light‐emitting diodes devices from P1 and P3 containing electron‐deficient oxadiazole units display enhanced performance, with the maximum brightness and maximum current efficiency being (4510 cd/m2 and 2.40 cd/A) and (2930 cd/m2, 1.19 cd/A), respectively. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 2821–2834, 2009 相似文献
18.
19.
Analysis of a TE011 mode composite sapphire-rutile dielectric resonator has been carried out to study the temperature variation of resonance
frequency, close to the Cs atomic clock hyperfine frequency of 9.192 GHz. The complementary behavior of dielectric permittivity
with temperature of the composite has been exploited to obtain the desired turning point in the resonant frequency. The frequency
of the composite structure is found to be independent of the shield diameter beyond four times the puck diameter. 相似文献
20.
Chi‐Jung Chang Shinn‐Jen Chang Susan Tsou Shou‐I Chen Feng‐Mei Wu Mei‐Wen Hsu 《Journal of Polymer Science.Polymer Physics》2003,41(16):1909-1920
Good jetting performance and pigment‐dispersing stability are necessary for pigment‐based ink‐jet inks. This study investigates how the chemical structures of the polymeric dispersants affect the pigment‐dispersing stability and jetting performance of ink‐jet inks. A series of polymeric dispersants containing styrene (hydrophobic unit) and acrylic acid (hydrophilic unit) with different ratios have been synthesized and used to disperse different pigments. Because 3000–12,000 ink drops can be expelled from the nozzle of a thermal bubble‐type ink‐jet printer within 1 s, the jetting behavior is related to the rheology variation of a dilute solution under a high shear. An in situ drop formation system has been used to study the high‐shear‐rate rheology (dynamic surface tension and dynamic viscosity) of a solution with a viscosity lower than 3 cps, which no commercial rheometer can measure. Excellent ink‐jet inks can only be produced by the combination of pigments, dispersants, and surfactants with appropriate hydrophilicity. Moreover, the correlation of the pigment surface properties, the chemical structures of the polymeric dispersants, and ink formulation is discussed. The effects of the surfactants and firing conditions on the jetting behavior of the ink‐jet ink are also examined. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 1909–1920, 2003 相似文献