Journal Article PUBDB-2022-01922

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Structure of Water at Hydrophilic and Hydrophobic Interfaces: Raman Spectroscopy of Water Confined in Periodic Mesoporous (Organo)Silicas

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2022
Soc. Washington, DC

The journal of physical chemistry <Washington, DC> / C 126(7), 3520 - 3531 () [10.1021/acs.jpcc.1c09801]
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Abstract: The temperature dependence of the structure of water confined in hydrophilic mesostructured porous silica (MCM-41) and hydrophobic benzene-bridged periodic mesoporous organosilicas (PMOs) is studied by Raman vibrational spectroscopy. For capillary filled pores (75% relative humidity, RH), the OH stretching region is dominated by the contribution from liquid water situated in the core part of the pore. It adopts a bulklike structure that is modestly disrupted by confinement and surface hydrophobicity. For partially filled pores (33% RH), the structure of the nonfreezable adsorbed film radically differs from that found in capillary filled pores. A first remarkable feature is the absence of the Raman spectral fingerprint of low-density amorphous ice, even at a low temperature (−120 °C). Second, additional bands reveal water hydroxyl groups pointing toward the different water/solid and water/vapor interfaces. For MCM-41, they correspond to water molecules acting as weak H-bond donors with silica and dangling hydroxyl groups oriented toward the empty center of the pore. For benzene-bridged PMO, we found an additional type of dangling hydroxyl groups, which we attribute to water at the hydrophobic solid interface.

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Contributing Institute(s):
  1. CIMMS-RA Center for integr. Multiscale M (CIMMS)
  2. Technische Universität Hamburg-Harburg (TUHH)
Research Program(s):
  1. 631 - Matter – Dynamics, Mechanisms and Control (POF4-631) (POF4-631)
Experiment(s):
  1. No specific instrument

Appears in the scientific report 2022
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 Record created 2022-04-27, last modified 2025-07-15


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