TY - JOUR
T1 - Ultra-thin self-healing vitrimer coatings for durable hydrophobicity
AU - Ma, Jingcheng
AU - Porath, Laura E.
AU - Haque, Md Farhadul
AU - Sett, Soumyadip
AU - Rabbi, Kazi Fazle
AU - Nam, Sung Woo
AU - Miljkovic, Nenad
AU - Evans, Christopher M.
N1 - Funding Information:
J.M., S.S., and N.M. gratefully acknowledge funding support from the Office of Naval Research (ONR) under grant No. N00014-16-1-2625. N.M. also gratefully acknowledges funding support from the International Institute for Carbon Neutral Energy Research (WPI-I2CNER), sponsored by the Japanese Ministry of Education, Culture, Sports, Science and Technology. J.M. gratefully acknowledges funding support from the PPG-MRL assistantship. C.M.E and L.E.P. gratefully acknowledge support from the Air Force Office of Scientific Research (AFOSR) under support provided by the Organic Materials Chemistry Program (grant FA9550-20-1-0262). This research was partially supported by the NSF through the University of Illinois at Urbana-Champaign Materials Research Science and Engineering Center DMR-1720633. We thank Dr. Richard T. Haasch and Dr. Kathy Walsh at the Materials Research Laboratory at the University of Illinois for their assistance in materials characterizations and insightful discussions.
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/12
Y1 - 2021/12
N2 - Durable hydrophobic materials have attracted considerable interest in the last century. Currently, the most popular strategy to achieve hydrophobic coating durability is through the combination of a perfluoro-compound with a mechanically robust matrix to form a composite for coating protection. The matrix structure is typically large (thicker than 10 μm), difficult to scale to arbitrary materials, and incompatible with applications requiring nanoscale thickness such as heat transfer, water harvesting, and desalination. Here, we demonstrate durable hydrophobicity and superhydrophobicity with nanoscale-thick, perfluorinated compound-free polydimethylsiloxane vitrimers that are self-healing due to the exchange of network strands. The polydimethylsiloxane vitrimer thin film maintains excellent hydrophobicity and optical transparency after scratching, cutting, and indenting. We show that the polydimethylsiloxane vitrimer thin film can be deposited through scalable dip-coating on a variety of substrates. In contrast to previous work achieving thick durable hydrophobic coatings by passively stacking protective structures, this work presents a pathway to achieving ultra-thin (thinner than 100 nm) durable hydrophobic films.
AB - Durable hydrophobic materials have attracted considerable interest in the last century. Currently, the most popular strategy to achieve hydrophobic coating durability is through the combination of a perfluoro-compound with a mechanically robust matrix to form a composite for coating protection. The matrix structure is typically large (thicker than 10 μm), difficult to scale to arbitrary materials, and incompatible with applications requiring nanoscale thickness such as heat transfer, water harvesting, and desalination. Here, we demonstrate durable hydrophobicity and superhydrophobicity with nanoscale-thick, perfluorinated compound-free polydimethylsiloxane vitrimers that are self-healing due to the exchange of network strands. The polydimethylsiloxane vitrimer thin film maintains excellent hydrophobicity and optical transparency after scratching, cutting, and indenting. We show that the polydimethylsiloxane vitrimer thin film can be deposited through scalable dip-coating on a variety of substrates. In contrast to previous work achieving thick durable hydrophobic coatings by passively stacking protective structures, this work presents a pathway to achieving ultra-thin (thinner than 100 nm) durable hydrophobic films.
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U2 - 10.1038/s41467-021-25508-4
DO - 10.1038/s41467-021-25508-4
M3 - Article
C2 - 34471109
AN - SCOPUS:85114175875
SN - 2041-1723
VL - 12
JO - Nature communications
JF - Nature communications
IS - 1
M1 - 5210
ER -