One-step controllable fabrication of superhydrophobic surfaces with special composite structure on zinc substrates

被引:26
作者
Ning, Tao [1 ]
Xu, Wenguo [1 ]
Lu, Shixiang [1 ]
机构
[1] Beijing Inst Technol, Key Lab Cluster Sci, Minist Educ, Sch Sci, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
Superhydrophobic surfaces; Platinum; Composite structure; Wettability; ENHANCED RAMAN-SCATTERING; ELECTROCHEMICAL DEPOSITION; SUPEROMNIPHOBIC SURFACES; REPLACEMENT REACTION; HYDROPHOBIC SURFACE; WATER-REPELLENT; METAL-SURFACES; FILMS; NANOSTRUCTURES; COPPER;
D O I
10.1016/j.jcis.2011.05.060
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Stable superhydrophobic platinum surfaces have been effectively fabricated on the zinc substrates through one-step replacement deposition process without further modification or any other post-treatment procedures. The fabrication process was controllable, which could be testified by various morphologies and hydrophobic properties of different prepared samples. By conducting SEM and water CA analysis, the effects of reaction conditions on the surface morphology and hydrophobicity of the resulting surfaces were carefully studied. The results show that the optimum condition of superhydrophobic surface fabrication depends largely on the positioning of zinc plate and the concentrations of reactants. When the zinc plate was placed vertically and the concentration of PtCl(4) solution was 5 mmol/L, the zinc substrate would be covered by a novel and interesting composite structure. The structure was composed by microscale hexagonal cavities, densely packed nanoparticles layer and top micro- and nanoscale flower-like structures, which exhibit great surface roughness and porosity contributing to the superhydrophobicity. The maximal CA value of about 171 degrees was obtained under the same reaction condition. The XRD, XPS and EDX results indicate that crystallite pure platinum nanoparticles were aggregated on the zinc substrates in accordance with a free deposition way. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:388 / 396
页数:9
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