College of Materials Science and Engineering, Nanjing Tech University , Nanjing, Jiangsu 210009, China.
Jiangsu Collaborative Innovation Center for Advanced Inorganic Function Composites , Nanjing 210009, China.
ACS Appl Mater Interfaces. 2017 Feb 1;9(4):4142-4150. doi: 10.1021/acsami.6b12779. Epub 2017 Jan 23.
Any solid surface can spontaneously exhibit variational wettability toward liquids with varied surface tension (γ). However, this correspondence has seldom been proposed or used on an artificial superhydrophobic surface, which should be more remarkable and peculiar. Herein, we fabricated robust, transparent superhydrophobic surfaces utilizing acid- and base-catalyzed silica (AC- and BC-silica) particles combined with candle soot template for structural construction and the CVD process for chemical modification. Three types of porous silica structures were devised, which presented distinctive surface tension responsiveness in wettability. Interestingly, all types of surfaces (i.e., AC-, AC/BC-, and BC-silica) show high repellence to high surface tension liquid (γ > 35 mN/m), and small differences are observed. With decreasing γ of the ethanol-water mixtures (γ < 35 mN/m), the static contact angles (SCAs) on all surfaces have an evident decline, but the features of the decreases are fairly different. As γ decreases, the SCA on the AC-silica surface decreases gradually, but the extent of decline becomes larger when γ < 27.42 mN/m. However, the SCA on the BC-silica surface decreases gradually except for γ ≈ 30.81 mN/m, and the SCA undergoes a sharp decline at γ ≈ 30.81 mN/m. The SCA on the AC/BC-silica surface has a similar variation as that of the SCA on the BC-silica surface, but a lower rate of BC-silica particles, e.g., 1/16, 1/8, 1/1 (AC/BC), further diminishes the critical γ values (where a sharp SCA drop occurs) to 30.16, 29.56, and 28.04 mN/m, respectively. The diversity is believed to be ascribed to the structure-induced selectivity of pore infiltration for the liquid. The tunable responsiveness can be generalized to various classes of organic aqueous solutions including methanol, acetic acid, acetone, and N,N-dimethylformamide. Benefiting from this, we can estimate organics concentration of an organic aqueous solution as well as its liquid surface tension by detecting its wettability on all of the diverse superhydrophobic surfaces.
任何固体表面都可以自发地表现出对具有不同表面张力(γ)的液体的可变润湿性。然而,这种对应关系很少在人工超疏水表面上提出或使用,而人工超疏水表面应该更加显著和特殊。在此,我们利用酸碱催化的二氧化硅(AC 和 BC 二氧化硅)颗粒与蜡烛烟尘模板结合,通过 CVD 工艺进行化学修饰,制备了坚固、透明的超疏水表面。设计了三种类型的多孔二氧化硅结构,它们在润湿性方面表现出独特的表面张力响应。有趣的是,所有类型的表面(即 AC、AC/BC 和 BC 二氧化硅)都对表面张力较高的液体(γ>35 mN/m)表现出高排斥性,并且观察到差异较小。随着乙醇-水混合物表面张力(γ<35 mN/m)的降低,所有表面的静态接触角(SCAs)都明显下降,但下降的特征却大不相同。随着γ的降低,AC-二氧化硅表面的 SCA 逐渐降低,但当γ<27.42 mN/m 时,下降幅度变大。然而,BC-二氧化硅表面的 SCA 逐渐降低,除了γ≈30.81 mN/m 时,SCA 在γ≈30.81 mN/m 时急剧下降。AC/BC-二氧化硅表面的 SCA 变化与 BC-二氧化硅表面的 SCA 变化相似,但由于 BC-二氧化硅颗粒的比例较低,例如 1/16、1/8、1/1(AC/BC),临界γ值(发生急剧 SCA 下降的位置)进一步降低至 30.16、29.56 和 28.04 mN/m。这种多样性被认为归因于孔渗透对液体的结构诱导选择性。这种可调响应可推广到包括甲醇、乙酸、丙酮和 N,N-二甲基甲酰胺在内的各种有机水溶液。有了这个,我们可以通过检测不同超疏水表面上的润湿性来估计有机水溶液的有机物浓度及其液体表面张力。