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1.
Teisala H Tuominen M Aromaa M Stepien M Mäkelä JM Saarinen JJ Toivakka M Kuusipalo J 《Langmuir : the ACS journal of surfaces and colloids》2012,28(6):3138-3145
Hierarchical roughness is known to effectively reduce the liquid-solid contact area and water droplet adhesion on superhydrophobic surfaces, which can be seen for example in the combination of submicrometer and micrometer scale structures on the lotus leaf. The submicrometer scale fine structures, which are often referred to as nanostructures in the literature, have an important role in the phenomenon of superhydrophobicity and low water droplet adhesion. Although the fine structures are generally termed as nanostructures, their actual dimensions are often at the submicrometer scale of hundreds of nanometers. Here we demonstrate that small nanometric structures can have very different effect on surface wetting compared to the large submicrometer scale structures. Hierarchically rough superhydrophobic TiO(2) nanoparticle surfaces generated by the liquid flame spray (LFS) on board and paper substrates revealed that the nanoscale surface structures have the opposite effect on the droplet adhesion compared to the larger submicrometer and micrometer scale structures. Variation in the hierarchical structure of the nanoparticle surfaces contributed to varying droplet adhesion between the high- and low-adhesive superhydrophobic states. Nanoscale structures did not contribute to superhydrophobicity, and there was no evidence of the formation of the liquid-solid-air composite interface around the nanostructures. Therefore, larger submicrometer and micrometer scale structures were needed to decrease the liquid-solid contact area and to cause the superhydrophobicity. Our study suggests that a drastic wetting transition occurs on superhydrophobic surfaces at the nanometre scale; i.e., the transition between the Cassie-Baxter and Wenzel wetting states will occur as the liquid-solid-air composite interface collapses around nanoscale structures. Consequently, water adheres tightly to the surface by penetrating into the nanostructure. The droplet adhesion mechanism presented in this paper gives valuable insight into a phenomenon of simultaneous superhydrophobicity and high water droplet adhesion and contributes to a more detailed comprehension of superhydrophobicity overall. 相似文献
2.
Cao Y Galoppini E Reyes PI Duan Z Lu Y 《Langmuir : the ACS journal of surfaces and colloids》2012,28(21):7947-7951
A stepwise surface functionalization methodology was applied to nanostructured ZnO films grown by metal organic chemical vapor deposition (MOCVD) having three different surface morphologies (i.e., nanorod layers (ZnO films-N), rough surface films (ZnO films-R), and planar surface films (ZnO films-P). The films were grown on glass substrates and on the sensing area of a quartz crystal microbalance (nano-QCM). 16-(2-Pyridyldithiol)-hexadecanoic acid (PDHA) was bound to ZnO films-N, -R, and -P through the carboxylic acid unit, followed by a nucleophilic displacement of the 2-pyridyldithiol moiety by single-stranded DNA capped with a thiol group (SH-ssDNA). The resulting ssDNA-functionalized films were hybridized with complementary ssDNA tagged with fluorescein (ssDNA-Fl). In a selectivity control experiment, no hybridization occurred upon treatment with non complementary DNA. The ZnO films' surface functionalization, characterized by FT-IR-ATR and fluorescence spectroscopy and detected on the nano-QCM, was successful on films-N and -R but was barely detectable on the planar surface of films-P. 相似文献
3.
Muñoz-Noval Á Hernando Pérez M Torres Costa V Martín Palma RJ de Pablo PJ Manso Silván M 《Langmuir : the ACS journal of surfaces and colloids》2012,28(3):1909-1913
In the present work, we investigate wetting phenomena on freshly prepared nanostructured porous silicon (nPS) with tunable properties. Surface roughness and porosity of nPS can be tailored by controlling fabrication current density in the range 40-120 mA/cm(2). The length scale of the characteristic surface structures that compose nPS allows the application of thermodynamic wettability approaches. The high interaction energy between water and surface is determined by measuring water contact angle (WCA) hysteresis, which reveals Wenzel wetting regime. Moreover, the morphological analysis of the surfaces by atomic force microscopy allows predicting WCA from a semiempiric model adapted to this material. 相似文献
4.
Coadsorption of horseradish peroxidase with thionine on TiO2 nanotubes for biosensing 总被引:4,自引:0,他引:4
In this study, we investigate the coadsorption of protein with thionine on TiO(2) nanotubes for biosensor design. The TiO(2) nanotube arrays fabricated by anodic oxidation of titanium substrate possess large surface areas and good uniformity and conformability and are ready for enzyme immobilization. Electrochemical and spectroscopic measurements show that the TiO(2) nanotube arrays provide excellent matrixes for the coadsorption of horseradish peroxidase (HRP) and thionine and that the adsorbed HRP on these TiO(2) nanotube arrays effectively retains its bioactivity. The immobilized thionine can be electrochemically reduced but cannot be reoxidized in the electrode potential range between -0.7 and 0.0 V. The addition of H(2)O(2) leads to the biocatalytic oxidation of the reduced thionine in the presence of HRP, resulting in developing a novel H(2)O(2) sensor with good stability and reproducibility. The fabricated TiO(2) nanotubes offer a stage for further study of immobilization and electrochemistry of proteins. The proposed method opens a way to develop biosensors using nanostructured materials with low electrical conductivity. 相似文献
5.
The present study is concerned with the structural and electronic properties of the TiO2/SnO2/TiO2 and SnO2/TiO2/SnO2 composite systems. Periodic quantum mechanical method with density functional theory at the B3LYP level has been carried out. Relaxed surface energies, structural characteristics and electronic properties of the (110), (010), (101) and (00) low-index rutile surfaces for TiO2/SnO2/TiO2 and SnO2/TiO2/SnO2 models are studied. For comparison purposes, the bare rutile TiO2 and SnO2 structures are also analyzed and compared with previous theoretical and experimental data. The calculated surface energy for both rutile TiO2 and SnO2 surfaces follows the sequence (110) < (010) < (101) < (001) and the energy increases as (010) < (101) < (110) < (001) and (010) approximately = (110) < (101) < (001) for SnO2/TiO2/SnO2 and TiO2/SnO2/TiO2 composite systems, respectively. SnO2/TiO2/SnO2 presents larger values of surface energy than the individual SnO2 and TiO2 metal oxides and the TiO2/SnO2/TiO2 system renders surface energy values of the same order that the TiO2 and lower than the SnO2. An analysis of the electronic structure of the TiO2/SnO2/TiO2 and SnO2/TiO2/SnO2 systems shows that the main characteristics of the upper part of the valence bands for all the studied surfaces are dominated by the external layers, i.e., by the TiO2 and the SnO2, respectively, and the topology of the lower part of the conduction bands looks like the core layers. There is an energy stabilization of both valence band top and conduction band bottom for (110) and (010) surfaces of the SnO2/TiO2/SnO2 composite system in relation to their core TiO2, whereas an opposite trend is found for the same surfaces of the TiO2/SnO2/TiO2 composite system in relation to the bare SnO2. The present theoretical results may explain the growth of TiO2@SnO2 bimorph composite nanotape. 相似文献
6.
Borras A Barranco A González-Elipe AR 《Langmuir : the ACS journal of surfaces and colloids》2008,24(15):8021-8026
A new type of superhydrophobic material consisting of a surface with supported Ag@TiO(2) core-shell nanofibers has been prepared at low temperature by plasma-enhanced chemical vapor deposition (PECVD). The fibers are formed by an inner nanocrystalline silver thread which is covered by a TiO(2) overlayer. Water contact angles depend on the width of the fibers and on their surface concentration, reaching a maximum wetting angle close to 180 degrees for a surface concentration of approximately 15 fibers microm(-2) and a thickness of 200 nm. When irradiated with UV light, these surfaces become superhydrophilic (i.e., 0 degrees contact angle). The decrease rate of the contact angle depends on both the crystalline state of the titania and on the size of the individual TiO(2) domains covering the fibers. To the best of our knowledge, this is one of the few examples existing in the literature where a superhydrophobic surface transforms reversibly into a superhydrophilic one as an effect of light irradiation. 相似文献
7.
8.
Porous, nanostructured sol gel TiO2 (100 nm) has been sensitized with WS2 quantum sheets (approximately 5 nm) with the help of chemical bath deposition. The absorber has been characterized with help of energy dispersive X-ray (EDX), transmission electron microscopy (TEM), scanning electron microscopy (SEM), Raman spectroscopy, and light absorption measurements. The photosensitization was confirmed via electrochemical measurements. The surface of TiO2 has been modified by a thin Al2O3 film, which significantly enhanced the photocurrent density to 0.4-0.7 mA/cm2. Moiré patterns suggest that the S-W-S layers of WS2 are not perfectly aligned in the direction of the c-axis, emphasizing the role of lateral electron transfer, which is also evidenced by surface passivation experiments. With WS2, a new, cheap, environmentally friendly, and stable absorber material for the sensitization of wide band gap nanomaterials has been introduced. 相似文献
9.
This work demonstrates the process of building optoelectrically cooperative surface wetting in smart and precise way. The superhydrophobic photosensitive film is constructed with TiO(2) nanotube arrays. Compared with conventional organic dyes, CdS quantum dots (QDs) as sensitizer layer are modified on TiO(2) nanotubes surface to improve photosensitivity of the composited surface in visible light region, which offer the benefit for designing and fabricating solid state hetero-junction devices. ITO glass is introduced as top electrode to apply electrical and optical stimuli and the patterned wetting is instantly obtained with masking light through ITO. The optoelectrically cooperative wettability conversion occurred on superhydrophobic TiO(2) nanotube surface at critical voltage of 12 V, which was decreased by 18 V comparing with only using electric stimulus. This study provides potential applications for TiO(2) nanotube arrays to the associated research of liquid reprography, location-controlled microfluidic device and lab-on-chip. 相似文献
10.
以二氧化钛(TiO2)纳米粉(P25)为原料,把它研磨成胶状,用涂敷法制得TiO2纳米多孔膜,并组装成太阳能电池,用100W氙灯作为模拟太阳光,对电池进行光电性能测试.根据电池的短路电流(Isc)、开路电压(Voc)和填充因子(ff)等指标来反映电池的性能.研究表明,分散剂乙酰丙酮、OP乳化剂、研磨时间和热处理后的保温时间长短对TiO2膜的性能均有很大的影响.其结果是,乙酰丙酮0.15mL、OP乳化剂0.10mL、研磨时间1h和保温时间0.5h时,TiO2膜的光电性能较好,Isc、Voc和ff分别为8.85mA、567mV和0.445.并用XRD和比表面及孔隙分析仪对TiO2膜进行了表征. 相似文献
11.
Li Y Sasaki T Shimizu Y Koshizaki N 《Journal of the American Chemical Society》2008,130(44):14755-14762
A hexagonal-close-packed (hcp), hierarchical amorphous TiO2 nanocolumn array was fabricated by pulsed laser deposition (PLD) using a PS colloidal monolayer as a template under a high pressure (6.7 Pa) of background oxygen gas. The formation mechanism was investigated, and a model of multidirection glancing deposition was proposed to explain the formation process. This strategy can be extended to the fabrication of similar structures using different materials. Interestingly, this nanostructured array could be transferred to almost any substrate, avoiding restriction of substrate types in fabrication of nanocolumn arrays, which is helpful in the design and creation of nanodevices on various desired substrates. This hierarchical nanocolumn array exhibits excellent superamphiphilicity with both water and oil contact angles of 0 degrees, without further UV irradiation. More importantly, the amorphous TiO2 nanocolumn array demonstrates better performance in photocatalytic activity than an anatase nanocolumn array due to its large surface area and special microstructures, suggesting that the surface area of the TiO2 is preferable to its crystal structure for enhancing photocatalytic activity. The combination of superamphiphilicity and photocatalytic activity gives the surface an excellent self-cleaning effect. 相似文献
12.
Palladium nanocrystals were grown on a nanostructured SrTiO(3)(001) surface and annealed in ultrahigh vacuum at 620 degrees C. This leads to the so-called strong metal-support interaction (SMSI) state, characterized by encapsulation of the metal clusters with an oxide layer. Scanning tunneling microscopy (STM) of the oxide adlayer on the Pd(111) cluster surface reveals two superstructures with different lattice parameters and crystallographic rotations. Interpretation of the STM images is most readily achieved via noncommensurate TiO(x)() surface layers which result in two distinct Moiré patterns. 相似文献
13.
Villafiorita-Monteleone F Canale C Caputo G Cozzoli PD Cingolani R Fragouli D Athanassiou A 《Langmuir : the ACS journal of surfaces and colloids》2011,27(13):8522-8529
Single-layered photopolymerized nanocomposite films of polystyrene and TiO(2) nanorods change their wetting characteristics from hydrophobic to hydrophilic when deposited on substrates with decreasing hydrophilicity. Interestingly, the addition of a second photopolymerized layer causes a swapping in the wettability, so that the final samples result converted from hydrophobic to hydrophilic or vice versa. The wettability characteristics continue to be swapped as the number of photopolymerized layers increases. In fact, odd-layered samples show the same wetting behavior as single-layered ones, while even-layered samples have the same surface characteristics as double-layered ones. Analytical surface studies demonstrate that all samples, independently of the number of layers, have similar low roughness, and that the wettability swap is due to the different concentration of the nanocomposites constituents on the samples surface. Particularly, the different interactions between the hydrophilic TiO(2) nanorods and the underlying layer lead to different amounts of nanorods exposed on the nanocomposites surface. Moreover, due to the unique property of TiO(2) to reversibly increase its wettability upon UV irradiation and subsequent storage, the wetting characteristics of the multilayered nanocomposites can be tuned in a reversible manner. In this way, a combination of substrate, number of photopolymerized layers, and external UV light stimulus can be used in order to precisely control the surface wettability properties of nanocomposite films, opening the way to a vast number of potential applications in microfluidics, protein assays, and cell growth. 相似文献
14.
Tian ZR Voigt JA Liu J McKenzie B Xu H 《Journal of the American Chemical Society》2003,125(41):12384-12385
We report for the first time a one-step, templateless method to directly prepare large arrays of oriented TiO2-based nanotubes and continuous films. These titania nanostructures can also be easily prepared as conformal coatings on a substrate. The nanostructured films were formed on a Ti substrate seeded with TiO2 nanoparticles. SEM and TEM results suggested that a folding mechanism of sheetlike structures was involved in the formation of the nanotubes. The oriented arrays of TiO2 nanotubes, continuous films, and coatings are expected to have potentials for applications in catalysis, filtration, sensing, photovoltaic cells, and high surface area electrodes. 相似文献
15.
Jiun‐Tai Chen Chih‐Wei Lee Mu‐Huan Chi I‐Chun Yao 《Macromolecular rapid communications》2013,34(4):348-354
We study the solvent‐annealing‐induced nanowetting in templates using porous anodic aluminum oxide membranes. The morphology of polystyrene and poly(methyl methacrylate) nanostructures can be controlled, depending on whether the swollen polymers are in the partial or complete wetting regimes, which are characterized by the spreading coefficient. When the swollen polymers are in the partial wetting regime, polymers wet the nanopores by capillary action, resulting in the formation of polymer nanorods. When the swollen polymers are in the complete wetting regime, polymers form wetting layers in the nanopores, resulting in the formation of polymer nanotubes. The solubility parameters of polymers and solvents are also used to predict the wetting behavior of swollen polymers in cylindrical geometry. 相似文献
16.
Godlewski S Tekiel A Prauzner-Bechcicki JS Budzioch J Gourdon A Szymonski M 《The Journal of chemical physics》2011,134(22):224701
High resolution scanning tunneling microscopy has been applied to investigate adsorption and self-assembly of large organic molecules on the TiO(2)(011) surface. The (011) face of the rutile titania has been rarely examined in this context. With respect to possible industrial applications of rutile, quite often in a powder form, knowledge on behavior of organic molecules on that face is required. In the presented study we fill in the gap and report on experiments focused on the self-assembly of organic nanostructures on the TiO(2)(011) surface. We use three different kinds of organic molecules of potential interest in various applications, namely, PTCDA and CuPc representing flat, planar stacking species, and Violet Landers specially designed for new applications in molecular electronics. In order to reach a complete picture of molecular behavior, extended studies with different surface coverage ranging from single molecule up to 2 monolayer (ML) thick films are performed. Our results show that the adsorption behavior is significantly different from previously observed for widely used metallic templates. Creation of highly ordered molecular lines, quasi-ordered wetting layers, controlled geometrical reorientation upon thermal treatment, existence of specific adsorption geometries, and prospects for tip-induced molecule ordering and manipulation provide better understanding and add new phenomena to the knowledge on the (011) face of rutile titania. 相似文献
17.
Sedona F Rizzi GA Agnoli S Llabrés i Xamena FX Papageorgiou A Ostermann D Sambi M Finetti P Schierbaum K Granozzi G 《The journal of physical chemistry. B》2005,109(51):24411-24426
Ultrathin ordered titanium oxide films on Pt(111) surface are prepared by reactive evaporation of Ti in oxygen. By varying the Ti dose and the annealing conditions (i.e., temperature and oxygen pressure), six different long-range ordered phases are obtained. They are characterized by means of low-energy electron diffraction (LEED), X-ray photoemission spectroscopy (XPS), and scanning tunneling microscopy (STM). By careful optimization of the preparative parameters, we find conditions where predominantly single phases of TiO(x), revealing distinct LEED pattern and STM images, are produced. XPS binding energy and photoelectron diffraction (XPD) data indicate that all the phases, except one (the stoichiometric rect-TiO2), are one monolayer thick and composed of a Ti-O bilayer with interfacial Ti. Atomically resolved STM images confirm that these TiO(x) phases wet the Pt surface, in contrast to rect-TiO2. This indicates their interface stabilization. At a low Ti dose (0.4 monolayer equivalents, MLE), an incommensurate kagomé-like low-density phase (k-TiO(x) phase) is observed where hexagons are sharing their vertexes. At a higher Ti dose (0.8 MLE), two denser phases are found, both characterized by a zigzag motif (z- and z'-TiO(x) phases), but with distinct rectangular unit cells. Among them, z'-TiO(x), which is obtained by annealing in ultrahigh vacuum (UHV), shows a larger unit cell. When the postannealing of the 0.8 MLE deposit is carried out at high temperatures and high oxygen partial pressures, the incommensurate nonwetting, fully oxidized rect-TiO2 is found The symmetry and lattice dimensions are almost identical with rect-VO2, observed in the system VO(x)/Pd(111). At a higher coverage (1.2 MLE), two commensurate hexagonal phases are formed, namely the w- [(square root(43) x square root(43)) R 7.6 degrees] and w'-TiO(x) phase [(7 x 7) R 21.8 degrees]. They show wagon-wheel-like structures and have slightly different lattice dimensions. Larger Ti deposits produce TiO2 nanoclusters on top of the different monolayer films, as supported both by XPS and STM data. Besides the formation of TiO(x) surfaces phases, wormlike features are found on the bare parts of the substrate by STM. We suggest that these structures, probably multilayer disordered TiO2, represent growth precursors of the ordered phases. Our results on the different nanostructures are compared with literature data on similar systems, e.g., VO(x)/Pd(111), VO(x)/Rh(111), TiO(x)/Pd(111), TiO(x)/Pt(111), and TiO(x)/Ru(0001). Similar and distinct features are observed in the TiO(x)/Pt(111) case, which may be related to the different chemical natures of the overlayer and of the substrate. 相似文献
18.
We investigated the formation of bilayer inverse opal TiO(2) (io-TiO(2)) structures via post-treatment with a TiO(2) precursor solution and characterized the photovoltaic performances of the resulting electrodes for use in dye-sensitized solar cells. The post-treatment of TiO(2) inverse opals in a precursor solution grew rutile TiO(2) nanoparticles on anatase crystalline phase io-TiO(2) surfaces, resulting in anatase/rutile bilayer structures. We achieved a maximum photovoltaic conversion efficiency of 4.6% using a 25 μm thick electrode formed with the post-treated io-TiO(2) under simulated AM 1.5 light. This efficiency represents a 183% improvement over the non-post-treated io-TiO(2) electrodes. The shell thickness was controlled by the post-treatment time. The effects of shell thickness on photovoltaic performance were investigated by measuring the morphologies and electrochemical impedance of the post-treated io-TiO(2). We found that post-treatment up to a certain period of time increased the surface area and electron lifetime, but further treatment resulted in decreased area and saturated lifetimes. The optimal post-treatment time was identified, and the optimal io-TiO(2) electrodes were characterized. 相似文献
19.
A class of nanostructured surface phases on SrTiO3(001) is reported and characterized through atomic-resolution scanning tunneling microscopy and Auger electron spectroscopy. These surface phases are created via argon ion sputtering and UHV annealing and form close-packed domains of highly ordered nanostructures. Depending on the type of nanostructures present, the domain ordering exhibit either (6 x 2), (9 x 2), (12 x 2), (6 x 8), or (7 x 4) surface patterning. The nanostructures are composed of TiO2-derived complexes surrounded by a TiO2 surface termination. Such surface ordering phenomena introduce another level of complexity in the chemistry of perovskite oxide surfaces and provide a basis from which potential photocatalytic and molecular-ordering applications may be developed. 相似文献
20.
采用阳极氧化法在钛箔表面制备TiO2纳米管阵列, 并在其表面修饰N3染料(Ruthenium dye)作敏化剂, 用氟硅烷来提高表面疏水性, 获得超疏水薄膜. SEM测定结果表明, 纳米管薄膜具有各向异性浸润结构, 同时阳极氧化的非均匀性增加了表面的粗糙度. UV-Vis吸收光谱及电化学阻抗谱结果表明, 薄膜具有优异的光电性能. 通过施加超过一定阈值的电压, 液滴在薄膜表面由超疏水状态转变为亲水状态. 利用光电协同激励作用时, 阈值电压比单独使用电激励时降低了10 V, 这是使用高效的N3染料光电敏化层的结果. 相似文献