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Probing the Effects of Popular Substrates on Laser Desorption of Ions and Neutrals

机译:探讨流行基材对离子和中育型激光解吸的影响

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For SALDI, very similar spectra were obtained using porous Si and graphite despite the differences in the substrate electronic structure and surface chemistry. Interestingly SALDI does not occur initially using single crystal Si(100) substrates, however, adsorption of water at 130 K produces a spectrum similar to that observed from porous Si and graphite. SALDI spectra produced protonated molecular ion peaks. The absence of molecular ions indicates that analyte molecules were not directly ionized by photons in the gas phase. An increase in sample solution acidity resulted in an increase in ion yield for all amino acids, indicating important roles of surface/interface layer acidity and proton affinity of desorbing amino acid. Multiphoton induced ionization of interfacial water and terminal-OH derived surface states may be important in SALDI. Surface morphologies which lead to the adsorption of water matrices with dispersed analytes are most effective since they enhance and maximize protonated complex formation and escape. This data collectively indicates that SALDI depends more on the presence of water and the intrinsic proton or hydronium ion content than the substrate bulk electronic structure.
机译:对于SALDI,尽管基板电子结构和表面化学差异,但是使用多孔Si和石墨获得非常相似的光谱。有趣的是,最初使用单晶Si(100)衬底不会发生SALDI,然而,在130 k下对水的吸附产生类似于从多孔Si和石墨观察到的光谱。 SALDI光谱产生质子化分子离子峰。没有分子离子表明分析物分子不通过气相中的光子直接电离。样品溶液酸度的增加导致所有氨基酸的离子产量增加,表明表面/界面层酸度和解吸氨基酸的质子亲和力的重要作用。界面水和末端-OH衍生表面状态的多光子诱导电离可能在Saldi中重要。导致水基质吸附具有分散分析物的表面形态最有效,因为它们增强和最大化质子化复杂的形成和逃逸。该数据集体表明SALDI在存在水和内在质子或纳温子含量的情况下更加依赖于基板散装电子结构。

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