Journal Description
Surfaces
Surfaces
is an international, peer-reviewed, open access journal on all aspects of surface and interface science published quarterly online by MDPI.
- Open Access— free for readers, with article processing charges (APC) paid by authors or their institutions.
- High Visibility: indexed within ESCI (Web of Science), Scopus, Inspec, CAPlus / SciFinder, and other databases.
- Rapid Publication: manuscripts are peer-reviewed and a first decision is provided to authors approximately 15.6 days after submission; acceptance to publication is undertaken in 3.8 days (median values for papers published in this journal in the first half of 2024).
- Journal Rank: CiteScore - Q2 (Materials Science (miscellaneous))
- Recognition of Reviewers: reviewers who provide timely, thorough peer-review reports receive vouchers entitling them to a discount on the APC of their next publication in any MDPI journal, in appreciation of the work done.
Impact Factor:
2.3 (2023);
5-Year Impact Factor:
2.6 (2023)
Latest Articles
Application of High-Surface Tension and Hygroscopic Ionic Liquid-Infused Nanostructured SiO2 Surfaces for Reversible/Repeatable Anti-Fogging Treatment
Surfaces 2024, 7(3), 482-492; https://doi.org/10.3390/surfaces7030031 - 2 Jul 2024
Abstract
Anti-fogging coatings/surfaces have attracted much attention lately because of their practical applications in a wide variety of engineering fields. In this study, we successfully developed transparent anti-fogging surfaces using a non-volatile and hygroscopic ionic liquid (IL), bis(hydroxyethyl)dimethylammonium methanesulfonate ([BHEDMA][MeSO3]), with a
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Anti-fogging coatings/surfaces have attracted much attention lately because of their practical applications in a wide variety of engineering fields. In this study, we successfully developed transparent anti-fogging surfaces using a non-volatile and hygroscopic ionic liquid (IL), bis(hydroxyethyl)dimethylammonium methanesulfonate ([BHEDMA][MeSO3]), with a high surface tension (HST, 66.4 mN/m). To prepare these surfaces, a layer of highly transparent, superhydrophilic silica (SiO2) nano-frameworks (SNFs) was first prepared on a glass slide using candle soot particles and the subsequent chemisorption of tetraethoxysilane (TEOS). This particulate layer of SNFs was then used as the support for the preparation of the [BHEDMA][MeSO3] layer. The resulting IL-infused SNF-covered glass slide was highly transparent, superhydrophilic, hygroscopic, and had self-healing and reasonable reversible/repeatable anti-fogging/frosting properties. This IL-infused sample surface kept its excellent anti-fogging performance in air for more than 8 weeks due to the IL’s non-volatile, HST, and hygroscopic nature. In addition, even if the water absorption limit of [BHEDMA][MeSO3] was reached, the anti-fogging properties could be fully restored reversibly/repeatably by simply leaving the samples in air for several tens of minutes or heating them at 100 °C for a few minutes to remove the absorbed water. Our IL-based anti-fogging surfaces showed substantial improvement in their abilities to prevent fogging when compared to other dry/wet (super)hydrophobic/(super)hydrophilic surfaces having different surface geometries and chemistries.
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(This article belongs to the Special Issue Surface Modification and Coating to Improve Properties of Various Materials)
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Open AccessArticle
Size-Dependence of the Electrochemical Activity of Platinum Particles in the 1 to 2 Nanometer Range
by
Hiroshi Yano and Kouta Iwasaki
Surfaces 2024, 7(3), 472-481; https://doi.org/10.3390/surfaces7030030 - 2 Jul 2024
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Monodisperse Pt nanoparticles supported on carbon (Pt/C) were prepared via an impregnation method. By changing the concentration of the platinum precursor in the initial reagent mixture, the average particle size (d) could be controlled to within a narrow range of less
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Monodisperse Pt nanoparticles supported on carbon (Pt/C) were prepared via an impregnation method. By changing the concentration of the platinum precursor in the initial reagent mixture, the average particle size (d) could be controlled to within a narrow range of less than 2 nm. The specific activity (SA) of these materials, when applied to the oxygen reduction reaction (ORR), increased rapidly with d in the range below 1.8 nm, with a maximum SA at d = 1.3 nm. This value is approximately four times that of a commercial Pt/CB catalyst. The electrochemical active area, ECAA (electrochemical surface area (ECSA)/specific surface area (SSA) × 100), decreased drastically from 100% with decreases in d below 1.3 nm. In this study, we present a correlation between SA and ECAA as a means of determining the appropriate d for polymer electrolyte fuel cells (PEFCs) and propose an optimal size.
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Open AccessArticle
Preparation and Printing Performance of Visible Light Photochromic Paper Based on PMoA-PWA/ZnO/PVP Composite
by
Wanqing Zhao, Hongmei Zhao, Wei Feng and Honggang Zhao
Surfaces 2024, 7(3), 460-471; https://doi.org/10.3390/surfaces7030029 - 1 Jul 2024
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The recyclable paper based on photochromic materials not only reduces the pollution in the paper manufacture process, but also reduces the pollution caused by the use of ink, which receives wide attention. In this paper, a series of phosphomolybdic acid–phosphotungstic acid/ZnO/polyvinylpyrrolidone (PMoA-PWA/ZnO/PVP) hybrid
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The recyclable paper based on photochromic materials not only reduces the pollution in the paper manufacture process, but also reduces the pollution caused by the use of ink, which receives wide attention. In this paper, a series of phosphomolybdic acid–phosphotungstic acid/ZnO/polyvinylpyrrolidone (PMoA-PWA/ZnO/PVP) hybrid films, which had different ratio of PMoA/PWA, was prepared by the ultrasonic composite method. The results indicated that the hybrid film prepared when the ratio of PMoA to PWA was 3 had the best photochromic performance. In this system, ZnO was the photosensitizer, while PMoA/PWA was the chromophore. The photochromic mechanism of the PMoA-PWA/ZnO/PVP hybrid film was based on the photogenerated electron transfer mechanism. ZnO generated photoelectron under the excitation of visible light, then PMoA and PWA obtained the photoelectron and produced photoreduction reaction to generate heteropolyblue. The visible light photochromic paper was prepared by loaded PMoA-PWA/ZnO/PVP hybrid film (A3) on A4 paper. Application tests showed that the prepared paper had extremely stable, excellent and reversible visible light photochromic properties, whether it was printing patterns or words, and could replace ordinary paper to realize the reuse of paper.
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Open AccessReview
Catalytically Active Materials Visualized by Scanning Photoelectron Spectro-Microscopy
by
Matteo Amati, Lada V. Yashina, Philipp Winkler, Kevin Sparwasser, Zygmunt Milosz, Günther Rupprechter and Luca Gregoratti
Surfaces 2024, 7(3), 442-459; https://doi.org/10.3390/surfaces7030028 - 26 Jun 2024
Abstract
Modern catalysts are complex systems whose performance depends both on space and time domains and, most importantly, on the operational environment. As a direct consequence, understanding their functionalities requires sophisticated techniques and tools for measurement and simulation, addressing the proper spatial and temporal
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Modern catalysts are complex systems whose performance depends both on space and time domains and, most importantly, on the operational environment. As a direct consequence, understanding their functionalities requires sophisticated techniques and tools for measurement and simulation, addressing the proper spatial and temporal scale and being capable of mimicking the working conditions of every single component, such as catalyst supports, electrodes, electrolytes, as well as of the entire assembly, e.g., in the case of fuel cells or batteries. Scanning photoelectron spectro-microscopy (SPEM) is one of the approaches that allow combining X-ray photoelectron spectroscopy with sub-micron spatial resolution; in particular, the SPEM hosted at the ESCA Microscopy beamline at Elettra has been upgraded to conduct in situ and operando experiments. Three different case studies are presented to illustrate the capabilities of the SPEM in the investigation of catalytic materials in different conditions and processes.
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(This article belongs to the Special Issue In Situ and Operando Catalyst Characterization)
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Open AccessArticle
Interactions between Cetyltrimethylammonium Bromide Modified Cellulose Nanocrystals and Surfaces: An Ellipsometric Study
by
Xiaoyu Gong, Md Farhad Ismail and Yaman Boluk
Surfaces 2024, 7(2), 428-441; https://doi.org/10.3390/surfaces7020027 - 19 Jun 2024
Abstract
The tailoring of the surface properties of cellulose nanocrystals (CNCs) to meet various requirements in environmental, food, and material areas has always been of great interest. In this study, the surface chemistry of CNCs was noncovalently modified by cetyltrimethylammonium bromide (CTAB), followed by
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The tailoring of the surface properties of cellulose nanocrystals (CNCs) to meet various requirements in environmental, food, and material areas has always been of great interest. In this study, the surface chemistry of CNCs was noncovalently modified by cetyltrimethylammonium bromide (CTAB), followed by characterizations and an investigation into its application as a coating material for interfacial interaction over various substrates. Due to the CTAB modification, the surface charge of the CNCs was neutralized, resulting in an increased size of each nanocrystal at the aqueous status and the aggregated microfibers when dried up. The CTAB modification not only decreased the crystallinity of the samples from 48.57% to 9.12%, but also reasonably hydrophobized the CNCs and decreased their total surface energy. Finally, the adsorption behavior of the CNCs and CTAB-CNCs over nonionic, anionic, and cationic polymers was investigated by ellipsometry. Based on the thickness of the CNC and CTAB-CNC layers over 2-Hydroxyethyl cellulose (HEC), carboxymethyl cellulose (CMC), and polyethyleneimine (PEI), we proposed that the adsorption behavior was overall influenced by electrostatic interaction, hydrogen bonding, and van der Waals forces, and the thickness of the adsorbed layers could be impacted by both the surface charge and the size of the crystals.
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(This article belongs to the Special Issue Surface Modification and Coating to Improve Properties of Various Materials)
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Open AccessArticle
General Method for Predicting Interface Bonding at Various Oxide–Metal Interfaces
by
Michiko Yoshitake
Surfaces 2024, 7(2), 414-427; https://doi.org/10.3390/surfaces7020026 - 3 Jun 2024
Abstract
Interface termination bonding between metal oxide and metals is discussed from the viewpoint of thermodynamics. The method of interface termination prediction proposed by the authors for Al2O3–metal and ZnO–metal interfaces is extended to a general interface between metal-oxide and
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Interface termination bonding between metal oxide and metals is discussed from the viewpoint of thermodynamics. The method of interface termination prediction proposed by the authors for Al2O3–metal and ZnO–metal interfaces is extended to a general interface between metal-oxide and metals. The extension of the prediction method to the interface between metal oxides and elemental semiconductors is also discussed. Information on interface bonding was extracted by carefully examining the experimental results and first-principles calculations in the references. The extracted information on interface bonding from references is compared with the results obtained via the proposed prediction method. It is demonstrated that interface termination bonding can be predicted by extending the method to oxide–metal interfaces in general, when there is no interface reaction such as the reduction of oxide, oxidation of metal, or mixed oxide formation. The method uses only basic quantities of pure elements and the formation enthalpy of oxides. Therefore, it can be applied to most of the metals (including elemental semiconductors) in the periodic table and metal oxides with one stable valence. The method is implemented as a software, “InterChemBond”, and can be used free of charge.
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(This article belongs to the Special Issue Surface Modification and Coating to Improve Properties of Various Materials)
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Open AccessArticle
Adsorption of Gadolinium Bisphthalocyanine on Atomically Flat Surfaces: Comparison of Graphene and Hexagonal Boron Nitride from DFT Calculations
by
Vladimir A. Basiuk and Elena V. Basiuk
Surfaces 2024, 7(2), 404-413; https://doi.org/10.3390/surfaces7020025 - 1 Jun 2024
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We studied the noncovalent interactions of gadolinium bisphthalocyanine (GdPc2) with cluster models for graphene and hexagonal boron nitride (hBN) of variable size by using the PBE functional of the generalized gradient approximation in conjunction with Grimme’s dispersion correction and
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We studied the noncovalent interactions of gadolinium bisphthalocyanine (GdPc2) with cluster models for graphene and hexagonal boron nitride (hBN) of variable size by using the PBE functional of the generalized gradient approximation in conjunction with Grimme’s dispersion correction and a DND double numerical basis set (that is, PBE-D2/DND). We found that in terms of the bonding strength, changes in the Gd-N bond lengths, the charge and spin of the Gd central ion, and the spin of the GdPc2 molecule, the behaviors of the graphene- and hBN-based model systems are rather similar. As expected, when increasing the size of the graphene and hBN cluster models, the strength of the interaction with GdPc2 increases, in which the bonding with the hBN models is usually stronger by a few kcal/mol. One of the main questions addressed in the present work was whether a change in the antiferromagnetic spin alignment to a ferromagnetic one, which is typical for GdPc2, is (at least theoretically) possible, as it has been observed previously for a number of graphene models when a smaller basis set DN was employed. We found that the use of a larger DND basis set dramatically reduces the occurrence of ferromagnetic adsorption complexes but does not exclude this possibility completely.
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Open AccessReview
The Use of Plant Extracts as Green Corrosion Inhibitors: A Review
by
Milad Sheydaei
Surfaces 2024, 7(2), 380-403; https://doi.org/10.3390/surfaces7020024 - 1 Jun 2024
Cited by 1
Abstract
The corrosion of metals is very important, both economically and environmentally, and is a serious concern. Since the past decades, traditional (chemical) corrosion inhibitors to prevent corrosion have been and are still being used. Although these inhibitors can be said to be a
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The corrosion of metals is very important, both economically and environmentally, and is a serious concern. Since the past decades, traditional (chemical) corrosion inhibitors to prevent corrosion have been and are still being used. Although these inhibitors can be said to be a good choice among other protection techniques because of their good efficiency, the toxicity of many of them causes environmental problems, and, due to the change in the laws on the use of chemicals, many of them are no longer allowed. Hence, during the past years, research on green corrosion inhibitors (GCIs) increased and very favorable results were obtained, and now they are very popular. It can be said that biodegradability and easy preparation are their most important factors. Meanwhile, the use of plants, especially their extracts, has been studied a lot. Plant extracts contain compounds that have anti-corrosion properties. In this review, the use of plants as GCIs is investigated, focusing on recent advances in their use. Also, the phenomenon of corrosion, corrosion protection (including coatings, nanoparticles, and chemical inhibitors), and other GCIs are briefly reviewed.
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(This article belongs to the Special Issue Surface Modification and Coating to Improve Properties of Various Materials)
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Open AccessArticle
Optical Characteristics of Directly Deposited Gold Nanoparticle Films
by
Jordi Sancho Parramon, Tilen Švarc, Peter Majerič, Žiga Jelen and Rebeka Rudolf
Surfaces 2024, 7(2), 369-379; https://doi.org/10.3390/surfaces7020023 - 27 May 2024
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The manuscript presents the optical properties of directly deposited films of gold nanoparticles (AuNPs) prepared by the Ultrasonic Spray Pyrolysis (USP) technology. Four samples were produced, with AuNP deposition times on the glass substrate of 15 min, 30 min, 1 h and 4
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The manuscript presents the optical properties of directly deposited films of gold nanoparticles (AuNPs) prepared by the Ultrasonic Spray Pyrolysis (USP) technology. Four samples were produced, with AuNP deposition times on the glass substrate of 15 min, 30 min, 1 h and 4 h. The morphological characterisation of the deposited films showed that the size of the first deposited AuNPs was between 10 and 30 nm, while, with a longer duration of the deposition process, larger clusters of AuNPs grew by coalescence and aggregation. The prepared layers were characterised optically with Ultraviolet–visible spectroscopy (UV–vis) and ellipsometry. The ellipsometric measurements showed an increasingly denser and thicker effective thickness of the AuNP layers. The extinction spectra displayed a clear local surface plasmonic resonance (LSPR) signature (peak 520–540 nm), indicating the presence of isolated particles in all the samples. For all AuNP layers, the imaginary part of the parallel and perpendicular components of the anisotropic dielectric function was dominated by a central peak at around 2.2 eV, corresponding to the LSPR of isolated particles, and a high-energy shoulder due to Au interband transitions. It was shown that, as the density of particles increased, the extinction cross-section grew over the whole spectral range where measurements are taken. Thus, the response can be explained with an enhanced electromagnetic response between the AuNPs that can be connected to the increase in particle density, but also by the formation of clusters and irregular structures.
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Open AccessArticle
Formation of Organic Monolayers on KF-Etched Si Surfaces
by
Tiexin Li, Zane Datson and Nadim Darwish
Surfaces 2024, 7(2), 358-368; https://doi.org/10.3390/surfaces7020022 - 10 May 2024
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Silicon is the most commonly used material in the microelectronics industry, due to its inherent advantages of high natural abundance, low cost, and high purity, coupled with the chemical and electrical stability at the interface with its oxide. For molecular electronics applications, oxide-free
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Silicon is the most commonly used material in the microelectronics industry, due to its inherent advantages of high natural abundance, low cost, and high purity, coupled with the chemical and electrical stability at the interface with its oxide. For molecular electronics applications, oxide-free Si surfaces are widely used because of the relative ease of removing the oxide (SiOx) by chemical means, yielding a surface which forms strong covalent bonds with a wide range of chemical functional groups; another advantage is that these surfaces remain oxide-free in the absence of oxidising agents. Standard procedures require the use of either HF, NH4F, or a mixture of both as the etching solution; however, these two chemicals are highly corrosive and toxic, posing a significant risk to the experimentalist. Here, we report that for silicon wafers etched by using potassium fluoride, a less toxic chemical, the resulting surface is free of oxides and can be functionalized by self-assembled monolayers of 1,8-nonadiyne. To demonstrate this, Si/SiOx wafers were etched by using either KF or NH4F, followed by hydrosilylation with 1,8-nonadiyne and a click reaction of the terminal alkyne with azidomethylferrocene. The surface coverages and electron transfer kinetics of the ferrocene-terminated KF-etched surfaces are comparable to those formed by acidic fluoride etching procedures. This is the first study comparing the differences between surfaces functionalized by self-assembled monolayers of 1,8-nonadiyne which were etched by KF and NH4F. KF could be used as a replacement chemical for etching silicon wafers when a less corrosive and toxic chemical is required.
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Open AccessArticle
Evaluation of the Feasibility of the Prediction of the Surface Morphologiesof AWJ-Milled Pockets by Statistical Methods Based on Multiple Roughness Indicators
by
Nikolaos E. Karkalos, Muthuramalingam Thangaraj and Panagiotis Karmiris-Obratański
Surfaces 2024, 7(2), 340-357; https://doi.org/10.3390/surfaces7020021 - 10 May 2024
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Improvement of the surface quality of machined parts is essential in order to avoid excessive and costly post-processing. Although non-conventional processes can efficiently carry out the machining of difficult-to-cut materials with high productivity, they may also, for various reasons, be related to increased
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Improvement of the surface quality of machined parts is essential in order to avoid excessive and costly post-processing. Although non-conventional processes can efficiently carry out the machining of difficult-to-cut materials with high productivity, they may also, for various reasons, be related to increased surface roughness. In order to optimize the surface quality of generated surfaces in a reliable way, surface profiles obtained during these processes must be adequately modeled. However, given that most studies have focused on Ra or Rz indicators or are based on the assumption of a normal distribution for the profile heights, relevant models cannot accurately represent the surface characteristics that exist in a real machined surface with a high degree of accuracy. Thus, in the present study, a new modeling approach based on the use of a statistical probability distribution for the surface profile height is proposed. After six different distributions were evaluated on the basis of a three-stage procedure involving different roughness indicators pertaining to the abrasive waterjet (AWJ) milling of pockets, it was found that, although it is not possible to model the nominal values of every roughness parameter simultaneously, in several cases, it is possible to approximate the values of critical indicators such as Ra, Rz, Rsk, Rku and Rp/Rv ratio by Weibull distribution with a sufficient degree of accuracy.
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Open AccessReview
Metal–Perovskite Interfacial Engineering to Boost Activity in Heterogeneous Catalysis
by
Christoph Malleier and Simon Penner
Surfaces 2024, 7(2), 296-339; https://doi.org/10.3390/surfaces7020020 - 6 May 2024
Abstract
In this review, we have assessed the possibility of metal–perovskite interfacial engineering to enhance the catalytic activity and selectivity in a range of heterogeneous catalytic reactions. We embarked on a literature screening of different perovskite material classes and reactions to show the versatility
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In this review, we have assessed the possibility of metal–perovskite interfacial engineering to enhance the catalytic activity and selectivity in a range of heterogeneous catalytic reactions. We embarked on a literature screening of different perovskite material classes and reactions to show the versatility of the perovskite structures to induce the formation of such hetero-interfaces and the widespread nature of the phenomenon in catalytic research. There is almost no limitation on the chemical composition of the used perovskites and the nature of the catalyzed reaction, be it under reduction or oxidation conditions. We attempted to classify the perovskite materials, discuss the different strategies leading to the hetero-interfaces, and detail the synergistic action of the components of the respective interfaces. We also provide a critical assessment of the large body of data that is available in terms of a knowledge-based approach to the comparison of differently prepared interfaces with varying interfacial extent to gain a deeper understanding of the bi-functional operation of the interfaces and the urgent necessity to study and characterize such interfaces under realistic operation conditions.
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(This article belongs to the Special Issue In Situ and Operando Catalyst Characterization)
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Open AccessArticle
Fluorine Free Surface Modification of Microfibrillated Cellulose-Clay Composite Films: Effect of Hydrophobicity on Gas Barrier Performance
by
Mohammed Arif Poothanari and Yves Leterrier
Surfaces 2024, 7(2), 283-295; https://doi.org/10.3390/surfaces7020019 - 1 May 2024
Abstract
Diffusion barrier composite films based on microfibrillated cellulose (MFC) and clay were developed with attention paid to the influence of thermal annealing and a fluorine-free surface silylation on their microstructure, water contact angle (WCA), mechanical properties, oxygen transmission rate (OTR), and water vapor
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Diffusion barrier composite films based on microfibrillated cellulose (MFC) and clay were developed with attention paid to the influence of thermal annealing and a fluorine-free surface silylation on their microstructure, water contact angle (WCA), mechanical properties, oxygen transmission rate (OTR), and water vapor transmission rate (WVTR). The OTR of MFC at 23 °C increased from 1.2 to 25.3 cm3/m2/day/bar as relative humidity increased from 50% to 80%. Annealing increased the film’s crystallinity, surface roughness, and hydrophobicity, while decreasing its OTR by 20% at 80%RH. The addition of clay led to a 30% decrease of OTR at 80%RH due to partial exfoliation and to a 50% decrease when combined with annealing. Silylation increased the hydrophobicity of surface of the film and its combination with clay and annealing led to a WCA of 146.5°. The combination of clay, annealing, and silylation considerably reduced the OTR at 80%RH to a value of 8 cm3/m2/day/bar, and the WVTR at 23 °C and 50%RH from 49 g/m2/day for MFC to 22 g/m2/day. The reduction of OTR and WVTR was found to correlate with the increase in surface hydrophobicity of the film, which was attributed to the reduced access of water molecules within the MFC network.
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(This article belongs to the Collection Featured Articles for Surfaces)
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Open AccessReview
Microcalorimetry Techniques for Studying Interactions at Solid–Liquid Interface: A Review
by
Heshu Hu, Jiazhong Wu and Minghui Zhang
Surfaces 2024, 7(2), 265-282; https://doi.org/10.3390/surfaces7020018 - 23 Apr 2024
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Solid–liquid interfacial phenomena play an essential role in our everyday lives and are often regarded as the outcome of interactions at the solid–liquid interface. However, the intricately intrinsic mechanism underlying interfacial interactions renders in situ simulations and direct measurements challenging. As an effective
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Solid–liquid interfacial phenomena play an essential role in our everyday lives and are often regarded as the outcome of interactions at the solid–liquid interface. However, the intricately intrinsic mechanism underlying interfacial interactions renders in situ simulations and direct measurements challenging. As an effective analytic method for studying solid–liquid interfacial interactions, microcalorimetry can provide the most basic thermodynamic information (including changes in enthalpy, entropy, and Gibbs free energy during solid–liquid binding/separation processes), which is extremely crucial for understanding interaction directionality and limitation. This review is dedicated to highlighting the pivotal role of microcalorimetry in studying solid–liquid immersion and adsorption processes. Specifically, we provide an overview of the commonly employed microcalorimetric methods, including differential scanning calorimetry (DSC), isothermal titration calorimetry (ITC), and immersion microcalorimetry (IM), and delve into the influence factors of enthalpy change, and finally discuss the specific applications of microcalorimetry in studying various solid–liquid binding processes. There remains a vast expanse of thermodynamic information regarding solid–liquid interactions that await exploration via calorimetry.
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Graphical abstract
Open AccessArticle
Surface and Aggregation Properties of Rhamnolipids in Water–Bioethanol Mixtures: A Step toward Green Formulation Design
by
Rodolfo Esposito, Francesco Taddeo, Vincenzo Russo, Irene Russo Krauss and Gerardino D’Errico
Surfaces 2024, 7(2), 251-264; https://doi.org/10.3390/surfaces7020017 - 7 Apr 2024
Abstract
Water–ethanol mixtures are largely exploited for many different applications, from industrial processes to pharmaceutical formulations. Surfactants are often added to tune their interfacial properties. Sustainability concerns require redesigning such blends to minimize their environmental impact. A successful approach is to replace synthetic oil-based
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Water–ethanol mixtures are largely exploited for many different applications, from industrial processes to pharmaceutical formulations. Surfactants are often added to tune their interfacial properties. Sustainability concerns require redesigning such blends to minimize their environmental impact. A successful approach is to replace synthetic oil-based components with affordable unpurified bio-derived alternatives. In this respect, we have characterized aqueous mixtures of bioethanol, obtained by the fermentation of algae, and rhamnolipids, biosurfactants of microbial origin. The physico-chemical characterization of water–bioethanol binary mixtures in terms of refractive index, density, viscosity, and surface tension indicates that bioethanol behaves like pure ethanol with negligible effects of impurities. Analysis of tensiometric titrations shows that, at bioethanol contents higher than 20–30% bioethanol mass percent, rhamnolipid aggregation is impaired, whereas surface adsorption at the water–air interface remains poorly affected. Overall, bio-derived components can be proposed as a promising alternative to oil-derived chemicals in eco-sustainable formulations.
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Open AccessArticle
Study on the Sound Absorption Properties of Recycled Polyester Nonwovens through Alkaline Treatment and Dimple Processing
by
Gyeong Cheol Yu, Jeong Jin Park, Eun Hye Kang, Sun Young Lee, Youl Huh and Seung Goo Lee
Surfaces 2024, 7(2), 238-250; https://doi.org/10.3390/surfaces7020016 - 2 Apr 2024
Abstract
This study focused on manufacturing efficient automobile sound-absorbing materials through alkaline treatment and dimple processing of recycled polyethylene terephthalate (rPET) nonwoven fabric. The rPET nonwoven fabric was produced with a sound-absorbing material through compression molding. It was improved through the development of porous
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This study focused on manufacturing efficient automobile sound-absorbing materials through alkaline treatment and dimple processing of recycled polyethylene terephthalate (rPET) nonwoven fabric. The rPET nonwoven fabric was produced with a sound-absorbing material through compression molding. It was improved through the development of porous sound-absorbing materials through alkaline treatment and resonant sound-absorbing materials through dimple processing. As a result of morphological analysis, alkaline treatment showed that pore size and air permeability increased according to temperature and concentration increase conditions. On the other hand, dimple processing caused a decrease in air permeability and a decrease in pores due to yarn fusion, and as the dimple diameter increased, the sound-absorbing coefficient increased in the 5000 Hz band. Finally, it was judged that effective sound absorption performance would be improved through a simple process through alkaline treatment and dimple processing, and thus there would be applicability in various industrial fields.
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(This article belongs to the Special Issue Surface Modification and Coating to Improve Properties of Various Materials)
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Open AccessArticle
A Route towards Durable Underwater Stable Superhydrophobic Surfaces: PET-Reinforced Candle Soot Layers
by
Xinghua Wu, Zhaokang Han, Yuchao Wang, Yutong Pan and Xiaohua Jie
Surfaces 2024, 7(2), 225-237; https://doi.org/10.3390/surfaces7020015 - 2 Apr 2024
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Superhydrophobic coating is widely used due to its waterproof and self-cleaning properties. Carbon soot (CS) nanoparticles are naturally superhydrophobic and non-toxic which are superior to other superhydrophobic coating. However, the weak binding force of the CS nanoparticle layers hinders their practical application. In
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Superhydrophobic coating is widely used due to its waterproof and self-cleaning properties. Carbon soot (CS) nanoparticles are naturally superhydrophobic and non-toxic which are superior to other superhydrophobic coating. However, the weak binding force of the CS nanoparticle layers hinders their practical application. In this study, micro-nanostructured PET-CS superhydrophobic coatings were prepared by a simple method. The obtained coatings presented durable superhydrophobicity and underwater stability, which are superior to PDMS-CS coatings and CS layers. The coating surfaces demonstrated superhydrophobicity under a water pressure of 13.72 kPa for up to 16 days. The surface could withstand water flush for more than 15 min. The coatings also demonstrated good mechanical stability and maintained superhydrophobicity after an abrasion length of 8 m. The stable long-lasting underwater superhydrophobic surface is of great importance for marine applications.
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Open AccessArticle
Preparation of Adsorbent from Mechanochemical Reaction-Based Waste Seashell with Sodium Oxalate and Its Application in Pb Ion Adsorption
by
Hideo Maruyama
Surfaces 2024, 7(2), 208-224; https://doi.org/10.3390/surfaces7020014 - 30 Mar 2024
Abstract
Waste seashell (scallop shell)-based adsorbent was prepared via mechanochemical reaction with sodium oxalate using ball milling. The oxalate-modified seashell-based adsorbents (OS) were prepared by varying the molar ratio of calcium and oxalate to 0.5, 1, and 2. Sodium oxalate was used as the
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Waste seashell (scallop shell)-based adsorbent was prepared via mechanochemical reaction with sodium oxalate using ball milling. The oxalate-modified seashell-based adsorbents (OS) were prepared by varying the molar ratio of calcium and oxalate to 0.5, 1, and 2. Sodium oxalate was used as the aqueous solution in ball milling. Lead ion adsorption was conducted with the prepared adsorbent. The adsorption behavior of lead ions was investigated in terms of adsorption kinetics and adsorption equilibrium. The time course of the amount of Pb adsorbed agreed well with Langmuir rate equation. The adsorption equilibrium relationship of OS adsorbent and Pb agreed well with the Langmuir adsorption isotherm. Increasing with the molar ratio, the saturated amount of Pb adsorbed increased slightly from 5.45 × 10−3 to 6.23 × 10−3 mol/g. Under the present experimental conditions, the maximum equilibrium adsorption was 5.93 × 10−3 mol/g, which is greater than that reported in the literature.
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Microstructure and Properties of Thin-Film Submicrostructures Obtained by Rapid Thermal Treatment of Nickel Films on Silicon
by
Vasilina Lapitskaya, Ruslan Trukhan, Tatyana Kuznetsova, Jaroslav Solovjov, Sergei Chizhik, Vladimir Pilipenko, Karyna Liutsko, Anastasiya Nasevich and Maksim Douhal
Surfaces 2024, 7(2), 196-207; https://doi.org/10.3390/surfaces7020013 - 27 Mar 2024
Abstract
Nickel films of 40 nm thickness were obtained by means of magnetron sputtering on a single-crystalline silicon substrate. The films were subjected to rapid thermal treatment (RTT) for 7 s until the temperature increased from 200 to 550 °C. By means of the
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Nickel films of 40 nm thickness were obtained by means of magnetron sputtering on a single-crystalline silicon substrate. The films were subjected to rapid thermal treatment (RTT) for 7 s until the temperature increased from 200 to 550 °C. By means of the X-ray diffraction method, the structural-phase composition of nickel films before and after RTT was explored. The atomic force microscopy method due to direct contact with the surface under study, made it possible to accurately define the microstructure, roughness, specific surface energy and grain size of the nickel films before and after RTT, as well as to establish the relationship of these parameters with the phase composition and electrical properties of the films. Surface specific resistance was measured using the four-probe method. Based on XRD results, formation of Ni2Si and NiSi phases in the film was ascertained after RTT at 300 °C. At RTT 350–550 °C, only the NiSi phase was formed in the film. The microstructure and grain size significantly depend on the phase composition of the films. A correlation has been established between specific surface energy and resistivity with the average grain size after RTT at 350–550 °C, which is associated with the formation and constant restructuring of the crystal structure of the NiSi phase.
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Open AccessArticle
Etching and Compositional Ratio Effect on the Surface Properties of Bismuth Telluride Thin Films
by
Jeongho Mun, Sangmin Han, Hee-Seung Yoon, Jisoo Kang, Oliver Jonas, Juyun Park and Yong-Cheol Kang
Surfaces 2024, 7(1), 181-195; https://doi.org/10.3390/surfaces7010012 - 15 Mar 2024
Abstract
Bismuth telluride has garnered considerable attention owing to its versatile properties applicable in thermoelectric and antibacterial domains, as well as its intriguing topological insulating properties. In this work, our group fabricated bismuth telluride thin films with various ratios using radio frequency magnetron sputtering.
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Bismuth telluride has garnered considerable attention owing to its versatile properties applicable in thermoelectric and antibacterial domains, as well as its intriguing topological insulating properties. In this work, our group fabricated bismuth telluride thin films with various ratios using radio frequency magnetron sputtering. The surface properties of these thin films were thoroughly analyzed by employing a diverse array of analytical techniques, including X-ray photoelectron spectroscopy (XPS), ultraviolet photoelectron spectroscopy (UPS), scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray diffraction (XRD), four-point probe and contact angle (CA) measurements. Specifically, our XPS findings indicated that Bi is more susceptible to oxidation than Te following Ar+-ion etching. Pure Te thin films exhibited the highest Rq value of 31.2 nm based on AFM and SEM results due to their larger grain sizes. The XRD patterns revealed a peak at 27.75° for thin films with 20% Te, attributed to its rhombohedral structure. Moreover, thin films with 30% Te yielded the highest weighted average work function with a value of 4.95 eV after etching. Additionally, pristine Bi and Te thin films demonstrated the most robust hydrophobic properties compared to intermediate-composition thin films, as determined by CA measurements.
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