Disordered Adsorbed Water Layers on TiO2 Nanoparticles under Subsaturated Humidity Conditions at 235 K
Author(s) -
Fabrizio Orlando,
Luca Artiglia,
Huanyu Yang,
Xiangrui Kong,
Kanak Roy,
Astrid Waldner,
Shuzhen Chen,
Thorsten BartelsRausch,
Markus Ammann
Publication year - 2019
Publication title -
the journal of physical chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.9b02779
Subject(s) - xanes , water vapor , adsorption , nanoparticle , materials science , nucleation , chemical engineering , x ray photoelectron spectroscopy , x ray absorption fine structure , properties of water , hydrogen bond , molecule , spectroscopy , humidity , chemical physics , chemistry , nanotechnology , thermodynamics , organic chemistry , physics , quantum mechanics , engineering
The interaction of water with TiO 2 is of substantial scientific and technological interest as it determines the activity of TiO 2 in photocatalytic and environmental applications in nanoparticle suspensions in water, in complex appliances, or in pure form interacting with water vapor. The influence of TiO 2 nanoparticles on the hydrogen bonding structure of water molecules is an important factor that controls hydration of other species, reactions, or nucleation processes. We use a combination of ambient-pressure X-ray photoelectron spectroscopy and electron yield near-edge X-ray absorption fine structure (NEXAFS) spectroscopy at the oxygen K-edge to investigate the hydrogen bonding structure of adsorbed water on titania nanoparticles in equilibrium with nearly saturated water vapor at 235 K. The results clearly show that the net NEXAFS spectrum of adsorbed water resembles that of liquid, disordered water at 235 K, a temperature at which both homogeneous and heterogeneous freezing of bulk water is anticipated.
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