首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Exploring the Structure of Paramagnetic Centers in SBA-15 Supported Vanadia Catalysts with Pulsed One- and Two-Dimensional Electron Paramagnetic Resonance (EPR) and Electron Nuclear Double Resonance (ENDOR)
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Exploring the Structure of Paramagnetic Centers in SBA-15 Supported Vanadia Catalysts with Pulsed One- and Two-Dimensional Electron Paramagnetic Resonance (EPR) and Electron Nuclear Double Resonance (ENDOR)

机译:一维和二维脉冲电子顺磁共振(EPR)和电子核双共振(ENDOR)的SBA-15支撑的Vanadia催化剂中顺磁性中心的结构探索

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摘要

Using pulsed EPR and ENDOR, the full set of g matrix and vanadium hyperfine parameters of the persistent paramagnetic V~(4+) center in "as prepared" and H2 reduced SBA-15 supported VO_x catalysts has been measured. The determination of relative signs of the vanadium hyperfine tensor elements by ENDOR using orientation selection allowed an unambiguous extraction of the isotropic part of this interaction. This allowed for identification of the persistent V~(4+) center as a surface exposed deprotonated vanadium site. The same site topology was found for oxidized and H2 reduced catalysts, thus indicating that the identified sites represent catalytically active centers. Hyperfine interaction with distant protons indicates formation of an oligomeric structure even for samples with vanadium loadings of less than 2 wt %. This conclusion is confirmed by applying 2D EPR for measuring the hyperfine interaction with neighboring vanadium atoms, covalently linked to reduced V~(4+) sites. Hence, application of 2D EPR enabled us to directly identify the previously proposed V— O—V structural motif on Si02 supported VO_x catalysts for the first time.
机译:使用脉冲EPR和ENDOR,已测量了“准备好的”和H2还原的SBA-15负载的VO_x催化剂中永久顺磁性V〜(4+)中心的g矩阵和钒超细参数的完整集合。通过使用方向选择的ENDOR确定钒超细张量元素的相对符号,可以明确提取这种相互作用的各向同性部分。这可以将持久性V〜(4+)中心识别为表面暴露的去质子化钒位点。对于氧化和H 2还原的催化剂,发现相同的位点拓扑,因此表明所确定的位点代表催化活性中心。与远距离质子的超精细相互作用表明,即使对于钒载量小于2 wt%的样品,也会形成低聚结构。这一结论是通过应用二维EPR测量与邻近的钒原子(与还原的V〜(4+)位点共价连接)的超精细相互作用来证实的。因此,二维EPR的应用使我们能够首次直接在SiO2负载的VO_x催化剂上直接识别先前提出的VOV结构。

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