TY - JOUR
T1 - Rich topologies of monolayer ices via unconventional electrowetting
AU - Liu, Yuan
AU - Gao, Yurui
AU - Zeng, Xiao Cheng
N1 - Funding Information:
YL was supported by the National Natural Science Foundation of China (No. 21703006) and the China Postdoctoral Science Foundation (No. 2017M620582). XCZ was supported by the US NSF (CHE-1665324) and Nebraska Center for Energy Sciences Research at UNL, and by University of Nebraska Holland Computing Center.
Publisher Copyright:
© 2020 The Royal Society of Chemistry.
PY - 2020/3
Y1 - 2020/3
N2 - Accurate manipulation of a substance on the nanoscale and ultimately down to the level of a single atom or molecule is an ongoing subject of frontier research. Herein, we show that topologies of water monolayers on substrates, in the complete wetting condition, can be manipulated into rich forms of ordered structures via electrowetting. Notably, two new topologies of monolayer ices were identified from our molecular dynamics simulations: one stable below room temperature and the other one having the ability to be stable at room temperature. Moreover, the wettability of the substrate can be tuned from superhydrophobic to superhydrophilic by uniformly changing the charge of each atomic site of the dipole or quadrupole distributed in an orderly manner on the model substrate. At a certain threshold value of the atomic charge, water droplets on the substrate can spread out spontaneously, achieving a complete electrowetting. Importantly, unlike the conventional electrowetting, which involves application of a uniform external electric field, we proposed non-conventional electrowetting, for the first time, by invoking the electric field of dipoles and quadrupoles embedded in the substrate. Moreover, different topologies of water monolayers can be achieved by using the non-conventional electrowetting. A major advantage of the non-conventional electrowetting is that the contact-angle saturation, a long-standing and known limitation in the field of electrowetting, can be overcome by tuning uniformly the lattice atomic charge at the surface, thereby offering a new way to mitigate the contact-angle saturation for various electrowetting applications.
AB - Accurate manipulation of a substance on the nanoscale and ultimately down to the level of a single atom or molecule is an ongoing subject of frontier research. Herein, we show that topologies of water monolayers on substrates, in the complete wetting condition, can be manipulated into rich forms of ordered structures via electrowetting. Notably, two new topologies of monolayer ices were identified from our molecular dynamics simulations: one stable below room temperature and the other one having the ability to be stable at room temperature. Moreover, the wettability of the substrate can be tuned from superhydrophobic to superhydrophilic by uniformly changing the charge of each atomic site of the dipole or quadrupole distributed in an orderly manner on the model substrate. At a certain threshold value of the atomic charge, water droplets on the substrate can spread out spontaneously, achieving a complete electrowetting. Importantly, unlike the conventional electrowetting, which involves application of a uniform external electric field, we proposed non-conventional electrowetting, for the first time, by invoking the electric field of dipoles and quadrupoles embedded in the substrate. Moreover, different topologies of water monolayers can be achieved by using the non-conventional electrowetting. A major advantage of the non-conventional electrowetting is that the contact-angle saturation, a long-standing and known limitation in the field of electrowetting, can be overcome by tuning uniformly the lattice atomic charge at the surface, thereby offering a new way to mitigate the contact-angle saturation for various electrowetting applications.
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U2 - 10.1039/c9nh00619b
DO - 10.1039/c9nh00619b
M3 - Article
C2 - 32118220
AN - SCOPUS:85081122732
SN - 2055-6756
VL - 5
SP - 514
EP - 522
JO - Nanoscale Horizons
JF - Nanoscale Horizons
IS - 3
ER -