TY - JOUR
T1 - Nanoscale viscosity of confined polyethylene oxide
AU - Zhang, Zheng
AU - Ding, Junjun
AU - Ocko, Benjamin M.
AU - Fluerasu, Andrei
AU - Wiegart, Lutz
AU - Zhang, Yugang
AU - Kobrak, Mark
AU - Tian, Ye
AU - Zhang, Honghu
AU - Lhermitte, Julien
AU - Choi, Chang Hwan
AU - Fisher, Frank T.
AU - Yager, Kevin G.
AU - Black, Charles T.
N1 - Publisher Copyright:
© 2019 American Physical Society.
PY - 2019/12/19
Y1 - 2019/12/19
N2 - Complex fluids near interfaces or confined within nanoscale volumes can exhibit substantial shifts in physical properties compared to bulk, including glass transition temperature, phase separation, and crystallization. Because studies of these effects typically use thin film samples with one dimension of confinement, it is generally unclear how more extreme spatial confinement may influence these properties. In this work, we used X-ray photon correlation spectroscopy and gold nanoprobes to characterize polyethylene oxide confined by nanostructured gratings (<100nm width) and measured the viscosity in this nanoconfinement regime to be ∼500 times the bulk viscosity. This enhanced viscosity occurs even when the scale of confinement is several times the polymer's radius of gyration, consistent with previous reports of polymer viscosity near flat interfaces.
AB - Complex fluids near interfaces or confined within nanoscale volumes can exhibit substantial shifts in physical properties compared to bulk, including glass transition temperature, phase separation, and crystallization. Because studies of these effects typically use thin film samples with one dimension of confinement, it is generally unclear how more extreme spatial confinement may influence these properties. In this work, we used X-ray photon correlation spectroscopy and gold nanoprobes to characterize polyethylene oxide confined by nanostructured gratings (<100nm width) and measured the viscosity in this nanoconfinement regime to be ∼500 times the bulk viscosity. This enhanced viscosity occurs even when the scale of confinement is several times the polymer's radius of gyration, consistent with previous reports of polymer viscosity near flat interfaces.
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U2 - 10.1103/PhysRevE.100.062503
DO - 10.1103/PhysRevE.100.062503
M3 - Article
C2 - 31962430
AN - SCOPUS:85077370733
SN - 2470-0045
VL - 100
JO - Physical Review E - Statistical, Nonlinear, and Soft Matter Physics
JF - Physical Review E - Statistical, Nonlinear, and Soft Matter Physics
IS - 6
M1 - 062503
ER -