TY - JOUR
T1 - Ultrasonication-Assisted Waterborne Synthesis of Self-Restorable Superhydrophobic Surfaces with Prolonged Lifespan in Oil Collection
AU - Liu, Songyu
AU - Gao, Yunshan
AU - Ma, Yanlin
AU - Meng, Tingting
AU - Yi, Changfeng
AU - Xu, Zushun
AU - Peng, Bo
AU - Deng, Ziwei
PY - 2020/12/3
Y1 - 2020/12/3
N2 - Self‐restorable superhydrophobic surfaces have attracted increasing attention due to their important applications. However, great challenges in an easy and rapid way to accomplish superhydrophobic surfaces with tunable self‐restorability are retained. Here, a facile yet fast strategy is presented to endow commercial substrates with self‐restorable superhydrophobic surfaces irrespective of their surface chemistry and geometry. By ultrasonicating an aqueous solution comprising poly(dimethylsiloxane), bis(3‐aminopropyl)‐terminated (H2N‐PDMS‐NH2) and dopamine hydrochloride (DA) with substrates for 30 min, superhydrophobic surfaces are yielded. Under ultrasonication, H2N‐PDMS‐NH2 is dispersed as the microdroplets and produces a weakly alkaline environment to enhance self‐polymerization of DA to polydopamine (PDA). In turn, PDA reacts with microdroplets and simultaneously anchors them to substrates, creating hierarchical morphology. The diffusion of hydrophobic H2N‐PDMS‐NH2 from the interior to the surface of the coating leads to superhydrophobic surface. This superhydrophobicity is self‐restorable after it is destroyed by air‐plasma or amphiphilic molecules, presumably because the H2N‐PDMS‐NH2 diffusion from the interior to the particles’ surface minimizes the overall interfacial‐energy. The self‐restoration is significantly accelerated by heating or rubbing the substrates. This self‐restoration offers superhydrophobic materials with a considerably prolonged life‐span, promising a wide range of applications, e.g., sustainable oil/water separation.
AB - Self‐restorable superhydrophobic surfaces have attracted increasing attention due to their important applications. However, great challenges in an easy and rapid way to accomplish superhydrophobic surfaces with tunable self‐restorability are retained. Here, a facile yet fast strategy is presented to endow commercial substrates with self‐restorable superhydrophobic surfaces irrespective of their surface chemistry and geometry. By ultrasonicating an aqueous solution comprising poly(dimethylsiloxane), bis(3‐aminopropyl)‐terminated (H2N‐PDMS‐NH2) and dopamine hydrochloride (DA) with substrates for 30 min, superhydrophobic surfaces are yielded. Under ultrasonication, H2N‐PDMS‐NH2 is dispersed as the microdroplets and produces a weakly alkaline environment to enhance self‐polymerization of DA to polydopamine (PDA). In turn, PDA reacts with microdroplets and simultaneously anchors them to substrates, creating hierarchical morphology. The diffusion of hydrophobic H2N‐PDMS‐NH2 from the interior to the surface of the coating leads to superhydrophobic surface. This superhydrophobicity is self‐restorable after it is destroyed by air‐plasma or amphiphilic molecules, presumably because the H2N‐PDMS‐NH2 diffusion from the interior to the particles’ surface minimizes the overall interfacial‐energy. The self‐restoration is significantly accelerated by heating or rubbing the substrates. This self‐restoration offers superhydrophobic materials with a considerably prolonged life‐span, promising a wide range of applications, e.g., sustainable oil/water separation.
UR - http://www.scopus.com/inward/record.url?scp=85097026880&partnerID=8YFLogxK
U2 - 10.1002/admi.202001886
DO - 10.1002/admi.202001886
M3 - Article
VL - 8
JO - Advanced Materials Interfaces
JF - Advanced Materials Interfaces
SN - 2196-7350
IS - 1
M1 - 2001886
ER -