首页> 外文期刊>The Journal of Chemical Physics >Carbon monoxide adsorption at forsterite surfaces as models of interstellar dust grains: An unexpected bathochromic (red) shift of the CO stretching frequency
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Carbon monoxide adsorption at forsterite surfaces as models of interstellar dust grains: An unexpected bathochromic (red) shift of the CO stretching frequency

机译:Forsterite表面的一氧化碳吸附作为星形尘颗粒的模型:CO拉伸频率的意外的沐浴料(红色)偏移

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摘要

Carbon monoxide (CO) is one of the most abundant species in the interstellar medium (ISM). In the colder regions of the ISM, it can directly adsorb onto exposed Mg cations of forsterite (Fo, Mg2SiO4), one of the main constituents of the dust grains. Its energetic of adsorption can strongly influence the chemico-physical evolution of cold interstellar clouds; thus, a detailed description of this process is desirable. We recently simulated the CO adsorption on crystalline Fo surfaces by computer ab initio methods and, surprisingly, reported cases where the CO stretching frequency underwent a bathochromic (red) shift (i.e., it is lowered with respect to the CO gas phase frequency), usually not experimentally observed for CO adsorbed onto oxides with non-d cations, like the present case. Here, we elucidate in deep when and under which conditions this case may happen and concluded that this red shift may be related to peculiar surface sites occurring at the morphologically complex Fo surfaces. The reasons for the red shift are linked to both the quadrupolar nature of the CO molecule and the role of dispersion interactions with surfaces of complex morphology. The present work, albeit speculative, suggests that, at variance with CO adsorption on simple oxides like MgO, the CO spectrum may exhibit features at lower frequencies than the reference gas frequency when CO is adsorbed on complex oxides, even in the absence of transition metal ions.
机译:一氧化碳(CO)是星际培养基(ISM)中最丰富的物种之一。在ISM的较冷区中,它可以直接吸附到暴露的粉末(FO,Mg2SiO 4)的暴露的Mg阳离子上,是粉尘颗粒的主要成分之一。其充满活力的吸附能够强烈影响冷星甲云的化学物理演变;因此,期望对该过程的详细描述。我们最近通过计算机AB初始方法模拟了结晶FO表面的CO吸附,令人惊讶的是报告的病例,其中CO拉伸频率接受了碱度(红色)偏移(即,它相对于CO气相频率降低),通常未通过实验观察到具有非D阳离子的氧化物上的CO,如本案例。在这里,我们在这种情况下可能发生这种情况的阐明和结论是,这种红色移位可能与在形态学复杂的FO表面发生的特殊表面位点有关。红移的原因与CO分子的四汞性质和分散相互作用与复合形态的表面的作用相关联。虽然推测性,但是,当CO在复合氧化物上吸附在复合氧化物上时,CO光谱即使在没有过渡金属上时,CO光谱也可能表现出比参考气体频率低于参考气体频率的CO频率的特征离子。

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