HUSCAP logo Hokkaido Univ. logo

Hokkaido University Collection of Scholarly and Academic Papers >
Institute of Low Temperature Science >
低温科学 = Low Temperature Science >
第78巻 >


Files in This Item:
09_p061-070.LT78.pdf1.94 MBPDFView/Open
Please use this identifier to cite or link to this item:

Title: 低温基板上に成長させた結晶氷のプロトン秩序と物性に迫る和周波発生振動分光
Other Titles: Observation of proton ordering in crystalline ice films grown on a low-temperature substrate by sum frequency generation spectroscopy
Authors: 杉本, 敏樹1 Browse this author
Authors(alt): Sugimoto, Toshiki1
Keywords: プロトン秩序
Proton ordering
Interfacial water
Low-temperature ice
Ferroelectric ice
Sum-frequency generation spectroscopy
Issue Date: 24-Mar-2020
Publisher: 低温科学第78巻編集委員会
Journal Title: 低温科学
Volume: 78
Start Page: 61
End Page: 70
Abstract: 固体表面に吸着した水分子凝集系においては,水分子の並進構造のみならず配向構造(プロトン配 置)によって化学的特性や物性が大きく変化する.したがって,プロトン配置は水分子凝集系の重要 な構造情報であるが,これをプローブすることは従来の表面科学的実験手法では困難であった.我々 は,プロトン配置に敏感になり得るヘテロダイン検出和周波発生振動分光法を低温Pt(111)基板上の 吸着水や氷の研究に世界に先駆けて応用することで,それらの系のプロトン配置を決定することに成 功した.さらに,氷と基板の界面において形成される異方的なプロトン秩序によって,バルク氷では 発現しない新奇な強誘電物性が氷膜全体に創発されることを見出した.
Interfacial water is ubiquitous in nature and plays crucial roles in a variety of disciplines. In such a symmetrybreaking system, not only adsorption geometry but also anisotropic molecular orientation (i. e., H-up/H-down configuration) is a key structural parameter that determines the unique physicochemical properties of interfacial water systems. However, orientation of water molecules in interfacial hydrogen bond networks has been extremely difficult to investigate with traditional experimental techniques, such as electron diffraction, grazing X-ray scattering, and even scanning probe microscopy because hydrogen has only a single electron and thus respond extremely weakly to the probes used in these techniques. Therefore, the determination of molecular orientation of interfacial water has been an experimental challenge. We have used recently developed heterodyne-detected sum frequency generation (SFG) spectroscopy in our pioneering investigation of the orientation and structure of water molecules on the metal surfaces of the Pt(111). Then, we succeeded in directly demonstrating that the adsorbed first layer water molecules prefer an H-down configuration. The H-down ordering in the first layer was significantly pinned by the Pt (111) substrate and was subsequently propagated to the overlayer during the growth of a multilayer ice film. Temperature dependence of the SFG spectra revealed that such an exotic proton ordering is thermodynamically stable and has an extremely high critical temperature of ~173 K, which is more than twice as large as that of ferroelectric bulk ice XI (Tc = ~72 K). It was demonstrated that anisotropy at the heterointerface is key for stimulating novel exotic proton ordering in many-body proton systems such as ice.
Type: bulletin (article)
Appears in Collections:低温科学 = Low Temperature Science > 第78巻

Export metadata:

OAI-PMH ( junii2 , jpcoar )

MathJax is now OFF:


 - Hokkaido University