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排序方式: 共有1327条查询结果,搜索用时 187 毫秒
81.
B. Ittermann M. Füllgrabe M. Heemeier F. Kroll F. Mai K. Marbach P. Meier D. Peters G. Welker W. Geithner S. Kappertz S. Wilbert R. Neugart P. Lievens U. Georg M. Keim 《Hyperfine Interactions》2000,129(1-4):423-441
β-active probe nuclei are implanted in nominally undoped ZnSe crystals. β-radiation detected nuclear magnetic resonance (β-NMR)
studies are described for two different probe nuclei, 8Li and 12B. This way, the implantation behavior of two “opposite”dopants, one acceptor (Li) and one donor (B) can be characterized
by the same microscopic technique. Such characterizations are attempted in terms of the structure of intermediate or final
lattice sites, defect charge states, or the kinetics of defect reactions and site changes.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
82.
Acid‐treated g‐C3N4‐Cu2O composite catalyst with enhanced photocatalytic activity under visible‐light irradiation 下载免费PDF全文
Shiyu Zuo Haiming Xu Wei Liao Lei Sun Donghui Han Jie Zan Binyang Zhang Dongya Li Dongsheng Xia 《应用有机金属化学》2018,32(9)
Acid‐treated g‐C3N4‐Cu2O was prepared by hydrothermal reduction followed by high temperature calcination and acid exfoliation. The structures and properties of as‐synthesized samples were characterized using a range of techniques, such as X‐ray photoelectron spectroscopy, scanning electron microscopy, Photoluminescence Spectroscopy and the Brunauer–Emmett–Teller (BET) theory. The photocatalytic activity was evaluated by measuring the photodegradation of methyl orange under visible‐light irradiation. Based on the results of TEM, XPS, EPR and other techniques, it was verified that a heterojunction was formed. The acid treatment process can increase the specific surface area to form abundant heterojunction interfaces as channels for photo‐generated carrier separation, thereby enhancing its light utilization and quantum efficiency. Results indicate that acid‐treated g‐C3N4‐Cu2O possesses a large specific surface area, which provides plentiful activated sites for heterojunctions to form; in addition, it showed a high visible light effect and the minimum charge‐transfer resistance. Furthermore, the g‐C3N4‐Cu2O material exhibits high levels of effectiveness and stability. Electron paramagnetic resonance and a series of radical trapping experiments demonstrate that the holes and ?O2? could be the main active species in methyl orange photodegradation. This work could provide new insights into the fabrication of composite materials as high‐performance photocatalysts, and facilitate their application in addressing environmental protection issues. 相似文献
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A. Gautier C. Mai G. Lockemann H. B. Bishop und Zoltan de Vamossy 《Fresenius' Journal of Analytical Chemistry》1906,45(12):767-768
Ohne Zusammenfassung 相似文献
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Viktor Csokai Diem Lan Ha Mai Olívia Varga Klára Tóth Miklós Kubinyi Alajos Grün 《Tetrahedron》2008,64(6):1058-1063
Novel fluorogenic 1,3-alt thiacalix[4](N-phenylazacrown-5)ether ionophore has been synthesized by conjugation of the N-phenyl group with borondipyrromethene (BODIPY) fluorophore moiety. The ionophore exhibits pronounced off-on type fluorescent responses to some transition metal ions, in particular to Cu2+. In a PVC membrane electrode, distinct Ag+ selectivity was observed in potentiometric transduction. 相似文献
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This article is concerned with the use of integrated radial‐basis‐function networks (IRBFNs) and nonoverlapping domain decompositions (DDs) for numerically solving one‐ and two‐dimensional elliptic problems. A substructuring technique is adopted, where subproblems are discretized by means of one‐dimensional IRBFNs. A distinguishing feature of the present DD technique is that the continuity of the RBF solution across the interfaces is enforced with one order higher than with conventional DD techniques. Several test problems governed by second‐ and fourth‐order differential equations are considered to investigate the accuracy of the proposed technique. © 2008 Wiley Periodicals, Inc. Numer Methods Partial Differential Eq 2008 相似文献
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