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Alignment of the hydrogen molecule under intense laser fields

机译:氢分子在激烈激光田地下的对准

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摘要

Alignment of the electronically excited E,F state of the H-2 molecule is studied using the velocity mapping imaging technique. Photofragment images of H+ due to the dissociation mechanism that follows the 2-photon excitation into the (E,F; nu = 0, J = 0) electronic state show a strong dependence on laser intensity, which is attributed to the high polarizability anisotropy of the H-2 (E,F) state. We observe a marked structure in the angular distribution, which we explain as the interference between the prepared J = 0 and Stark-mixed J = 2 rovibrational states of H-2, as the laser intensity increases. Quantification of these effects allows us to extract the polarizability anisotropy of the H-2 (E,F J = 0) state yielding a value of 312 +/- 82 a.u. (46 angstrom(3)). By comparison, CS2 has 10 angstrom(3), I-2 has 7 angstrom(3), and hydrochlorothiazide (C7H8ClN3O4S2) has about 25 angstrom(3) meaning that we have created the most easily aligned molecule ever measured, by creating a mixed superposition state that is highly anisotropic in its polarizability. Published by AIP Publishing.
机译:使用速度映射成像技术研究了电子激发e,H-2分子的F状态的对准。 H +的光折叠图像由于将2-光子激发沿(e,f; nu = 0,j = 0)电子状态遵循的解离机构显示出对激光强度的强依赖性,这归因于高偏热性各向异性H-2(E,F)状态。我们在角度分布中观察到标记结构,因为激光强度增加,我们在角度分布中解释为所准备的J = 0和STARK混合J = 2振动状态的干扰。这些效果的定量允许我们提取H-2(e,f j = 0)状态的极化性各向异性,其产生312 +/- 82 a.u. (46埃(3))。相比之下,CS2具有10埃(3),I-2具有7埃(3),氢氯噻嗪(C7H8ClN3O4S2)具有约25埃(3),这意味着我们通过创建混合来创建了最容易对准的分子。在其极化性上具有高度各向异性的叠加状态。通过AIP发布发布。

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