大气分子的高分辨率光电VUV截面测量

K. Yoshino, D. E. Freeman, W. Parkinson
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引用次数: 0

摘要

需要精确的舒曼-龙格(S-R)波段的横截面来确定大气对太阳辐射的不透明度,太阳辐射导致平流层成分(如NO)的解离。特别是,NO的主要光解过程分别发生在191 nm和183 nm附近的δ(0,0)和δ(1,0)波段;前者在S-R(5,0)波段范围内,后者在S-R(9,0)和(10,0)波段范围内。为了计算预解离率,需要对这些带的旋转结构进行详细的截面测量。然而,只有当仪器带宽与被测量的线宽相比较小时,才能直接确定准确的横截面。旋转离散线的真实横截面可能在仪器带宽上发生显著变化,这可能导致严重低估峰横截面和扭曲的线轮廓。对这类分子进行高精度横截面测量所需的两个实验条件是达到尽可能高的光谱分辨率和使用光电而不是照相检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High Resolution Photoelectric VUV Cross Section Measurements of Atmospheric Molecules
Accurate cross sections of the Schumann-Runge (S-R) bands of O2 are needed to determine the opacity of the atmosphere to solar radiation that causes the dissociation of stratospheric constituents such as NO. In particular, the principal photodissociation processes for NO occur in the δ(0,0) and δ(1,0) bands near 191 and 183 nm, respectively; the former is in the range of the S-R (5,0) band, and the latter is in the range of the S-R (9,0) and (10,0) bands. Detailed cross section measurements that resolve the rotational structure of these bands are necessary for the calculation of predissociation rates. However, the determination of accurate cross sections is straight-forward only if the instrumental band width is small compared with the line width being measured. The true cross section of rotationally discrete lines may vary significantly over the instrumental band width, and this can lead to seriously underestimated peak cross sections and distorted line profiles. The two experimental conditions required for cross section measurements of high accuracy for such molecules are the attainment of the highest possible spectroscopic resolution and the use of photoelectric rather than photographic detection.
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