{"@context":{"@vocab":"https://cir.nii.ac.jp/schema/1.0/","rdfs":"http://www.w3.org/2000/01/rdf-schema#","dc":"http://purl.org/dc/elements/1.1/","dcterms":"http://purl.org/dc/terms/","foaf":"http://xmlns.com/foaf/0.1/","prism":"http://prismstandard.org/namespaces/basic/2.0/","cinii":"http://ci.nii.ac.jp/ns/1.0/","datacite":"https://schema.datacite.org/meta/kernel-4/","ndl":"http://ndl.go.jp/dcndl/terms/","jpcoar":"https://github.com/JPCOAR/schema/blob/master/2.0/"},"@id":"https://cir.nii.ac.jp/crid/1360857593748044288.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.3847/2041-8213/ac3a0e"}},{"identifier":{"@type":"URI","@value":"https://iopscience.iop.org/article/10.3847/2041-8213/ac3a0e"}},{"identifier":{"@type":"URI","@value":"https://iopscience.iop.org/article/10.3847/2041-8213/ac3a0e/pdf"}}],"resourceType":"学術雑誌論文(journal article)","dc:title":[{"@value":"Absolute Absorption Cross Section and Orientation of Dangling OH Bonds in Water Ice"}],"description":[{"type":"abstract","notation":[{"@value":"<jats:title>Abstract</jats:title>\n               <jats:p>The absolute absorption cross section of dangling OH bonds in water ice, a free OH stretch mode by three-coordinated surface water molecules, is derived experimentally as 1.0 ± 0.2 × 10<jats:sup>−18</jats:sup> cm<jats:sup>2</jats:sup> at 3696 cm<jats:sup>−1</jats:sup> for amorphous water at 90 K using infrared multiple-angle incidence resolution spectrometry (IR–MAIRS). The integrated absorption cross section (band strength) of the dangling OH bond at 90 K (1.4 ± 0.3 × 10<jats:sup>−17</jats:sup> cm molecule<jats:sup>−1</jats:sup> at 3710–3680 cm<jats:sup>−1</jats:sup>) is found to be more than 1 order of magnitude smaller than those in bulk ice or liquid water. This indicates that a lack of hydrogen-bonding significantly decreases the band strength of dangling OH bonds. The present study also provides average molecular orientations of dangling OH bonds at 10 K and 90 K, because both the surface-parallel (in-plane) and surface-perpendicular (out-of-plane) vibration spectra of dangling OH bonds are quantitatively measured by IR–MAIRS. The intensity ratio of the dangling-OH peaks between in-plane to out-of-plane spectra shows the isotropic nature (random orientation) of the two- and three-coordinated dangling OH bonds in microporous amorphous water prepared at 10 K; however, the three-coordinated dangling OH bonds in nonporous amorphous water prepared at 90 K are dominantly located at the top ice surface and oriented perpendicular to it. These findings provide fundamental insights into the relationship between the structure and optical properties of ice surfaces, and aid quantitative understanding of the surface structure of interstellar ices and their laboratory analogs.</jats:p>"}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1380857593748044183","@type":"Researcher","foaf:name":[{"@value":"Takumi Nagasawa"}]},{"@id":"https://cir.nii.ac.jp/crid/1380857593748044164","@type":"Researcher","foaf:name":[{"@value":"Reo 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