TY - JOUR
T1 - Nanoporous Substrate-Infiltrated Hydrogels
T2 - A Bioinspired Regenerable Surface for High Load Bearing and Tunable Friction
AU - Ma, Shuanhong
AU - Scaraggi, M.
AU - Wang, Daoai
AU - Wang, Xiaolong
AU - Liang, Yongmin
AU - Liu, Weimin
AU - Dini, Daniele
AU - Zhou, Feng
N1 - Publisher Copyright:
© 2015 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
PY - 2015/12/16
Y1 - 2015/12/16
N2 - Nature has successfully combined soft matter and hydration lubrication to achieve ultralow friction even at relatively high contact pressure (e.g., articular cartilage). Inspired by this, hydrogels are used to mimic natural aqueous lubricating systems. However, hydrogels usually cannot bear high load because of solvation in water environments and are, therefore, not adopted in real applications. Here, a novel composite surface of ordered hydrogel nanofiber arrays confined in anodic aluminum oxide (AAO) nanoporous template based on a soft/hard combination strategy is developed. The synergy between the soft hydrogel fibers, which provide excellent aqueous lubrication, and the hard phase AAO, which gives high load bearing capacity, is shown to be capable of attaining very low coeffcient of friction (<0.01) under heavy load (contact pressures ≈2 MPa). Interestingly, the composite synthetic material is very stable, cannot be peeled off during sliding, and exhibits desirable regenerative (self-healing) properties, which can assure long-term resistance to wear. Moreover, the crosslinked polymethylacrylic acid hydrogels are shown to be able to promptly switch between high friction (>0.3) and superlubrication (≈10-3) when their state is changed from contracted to swollen by means of acidic and basic actuation. The mechanisms governing ultralow and tunable friction are theoretically explained via an in-depth study of the chemomechanical interactions responsible for the behavior of these substrate-infiltrated hydrogels. These findings open a promising route for the design of ultra-slippery and smart surface/interface materials. A novel composite surface of ordered nanohydrogel arrays confined in an anodic aluminum oxide template based on a soft/hard combination strategy is reported. The surface shows a low friction coefficient (<0.01) under 40 N and contact pressures of ≈2 MPa, along with desirable regenerative and antiwear properties, while exhibiting smart switching between high friction (>0.3) and superlubrication (≈10-3) by acidic and basic actuation.
AB - Nature has successfully combined soft matter and hydration lubrication to achieve ultralow friction even at relatively high contact pressure (e.g., articular cartilage). Inspired by this, hydrogels are used to mimic natural aqueous lubricating systems. However, hydrogels usually cannot bear high load because of solvation in water environments and are, therefore, not adopted in real applications. Here, a novel composite surface of ordered hydrogel nanofiber arrays confined in anodic aluminum oxide (AAO) nanoporous template based on a soft/hard combination strategy is developed. The synergy between the soft hydrogel fibers, which provide excellent aqueous lubrication, and the hard phase AAO, which gives high load bearing capacity, is shown to be capable of attaining very low coeffcient of friction (<0.01) under heavy load (contact pressures ≈2 MPa). Interestingly, the composite synthetic material is very stable, cannot be peeled off during sliding, and exhibits desirable regenerative (self-healing) properties, which can assure long-term resistance to wear. Moreover, the crosslinked polymethylacrylic acid hydrogels are shown to be able to promptly switch between high friction (>0.3) and superlubrication (≈10-3) when their state is changed from contracted to swollen by means of acidic and basic actuation. The mechanisms governing ultralow and tunable friction are theoretically explained via an in-depth study of the chemomechanical interactions responsible for the behavior of these substrate-infiltrated hydrogels. These findings open a promising route for the design of ultra-slippery and smart surface/interface materials. A novel composite surface of ordered nanohydrogel arrays confined in an anodic aluminum oxide template based on a soft/hard combination strategy is reported. The surface shows a low friction coefficient (<0.01) under 40 N and contact pressures of ≈2 MPa, along with desirable regenerative and antiwear properties, while exhibiting smart switching between high friction (>0.3) and superlubrication (≈10-3) by acidic and basic actuation.
KW - gel-fiber arrays
KW - nanoporous
KW - regenerable
KW - tunable friction/lubrication
UR - http://www.scopus.com/inward/record.url?scp=84962446767&partnerID=8YFLogxK
U2 - 10.1002/adfm.201503681
DO - 10.1002/adfm.201503681
M3 - 文章
AN - SCOPUS:84962446767
SN - 1616-301X
VL - 25
SP - 7366
EP - 7374
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 47
ER -