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141.
Harald Gabasch Konrad Hayek Evgueni Kleimenov Spiros Zafeiratos Axel Knop-Gericke Jinyi Han Balazs Aszalos-Kiss Dmitry Zemlyanov 《Surface science》2006,600(15):2980-2989
The oxidation of the Pd(1 1 1) surface was studied by in situ XPS during heating and cooling in 0.4 mbar O2. The in situ XPS data were complemented by ex situ TPD results. A number of oxygen species and oxidation states of palladium were observed in situ and ex situ. At 430 K, the Pd(1 1 1) surface was covered by a 2D oxide and by a supersaturated Oads layer. The supersaturated Oads layer transforms into the Pd5O4 phase upon heating and disappears completely at approximately 470 K. Simultaneously, small clusters of PdO, PdO seeds, are formed. Above 655 K, the bulk PdO phase appears and this phase decomposes completely at 815 K. Decomposition of the bulk oxide is followed by oxygen dissolution in the near-surface region and in the bulk. The oxygen species dissolved in the bulk is more favoured at high temperatures because oxygen cannot accumulate in the near-surface region and diffusion shifts the equilibrium towards the bulk species. The saturation of the bulk “reservoir” with oxygen leads to increasing the uptake of the near-surface region species. Surprisingly, the bulk PdO phase does not form during cooling in 0.4 mbar O2, but the Pd5O4 phase appears below 745 K. This is proposed to be due to a kinetic limitation of PdO formation because at high temperature the rate of PdO seed formation is compatible with the rate of decomposition. 相似文献
142.
Thenahandi Prasanthi Deepthika De Silva Sang Gil Youm Frank R. Fronczek Girija Sahasrabudhe Evgueni E. Nesterov Isiah M. Warner 《Molecules (Basel, Switzerland)》2021,26(21)
Three novel small organic heterocyclic compounds: 2-(1,2-diphenyl)-1H-benzimidazole-7-tert-butylpyrene (compound A), 1,3-di(1,2-diphenyl)-1H-benzimidazole-7-tert-butylpyrene (compound B), and 1,3,6,8-tetra(1,2-diphenyl)-1H-benzimidazolepyrene (compound C) were synthesized and characterized for possible applications as blue OLED emitters. The specific molecular design targeted decreasing intermolecular aggregation and disrupting crystallinity in the solid-state, in order to reduce dye aggregation, and thus obtain efficient pure blue photo- and electroluminescence. Accordingly, the new compounds displayed reasonably high spectral purity in both solution- and solid-states with average CIE coordinates of (0.160 ± 0.005, 0.029 ± 0.009) in solution and (0.152 ± 0.007, 0.126 ± 0.005) in solid-state. These compounds showed a systematic decrease in degree of crystallinity and intermolecular aggregation due to increasing steric hindrance, as revealed using powder X-ray diffraction analysis and spectroscopic studies. An organic light-emitting diode (OLED) prototype fabricated using compound B as the non-doped emissive layer displayed an external quantum efficiency (EQE) of 0.35 (±0.04)% and luminance 100 (±6) cd m−2 at 5.5 V with an essentially pure blue electroluminescence corresponding to CIE coordinates of (0.1482, 0.1300). The highest EQE observed from this OLED prototype was 4.3 (±0.3)% at 3.5 V, and the highest luminance of 290 (±10) cd m−2 at 7.5 V. These values were found comparable to characteristics of the best pure blue OLED devices based on simple fluorescent small-molecule organic chromophores. 相似文献
143.
Andrei A. Levchenko Evgueni M. Antipov Nikolaj A. Plate' Manfred Stamm 《Macromolecular Symposia》1999,146(1):145-151
In the present investigation X-ray diffraction techniques, DSC and dynamic mechanical relaxation (DMR) methods have been employed to compare the structure and thermal behaviour of Kevlar (“DuPont”, USA) and Armos (Russia) fibers. Our recent studies have indicated that the non-crystalline phase of copolyesters always contains LC smectic structure in addition to some part of the nematic LC mesophase. It turned out that the copolyamides also possess this interesting feature. Moreover, on heating of a semicrystalline copolyester always the second order phase transition from the crystalline state to condis mesophase has been observed, whereas in the case of copolyamides such a transition has the «virtual» character. As was established by other authors both polymers under study reveal the moisture content. The changes in wide angle X-ray scattering of copolyamides under heat treatment were interpreted in terms of desorption of bound water and structural rearrangement in the plane perpendicular to the chain axis involving of the hydrogen bonding between neighboring macromolecules. 相似文献