Interface conditions of roughness-induced superoleophilic and superoleophobic surfaces immersed in hexadecane and ethylene glycol

• Yifan Li,
• Yunlu Pan and
• Xuezeng Zhao

Beilstein J. Nanotechnol. 2017, 8, 2504–2514, doi:10.3762/bjnano.8.250

• concentration of silica nanoparticles in the composite surfaces from 10 to 30 mg·mL−1 leads to an increase in the amplitude parameters, while the pitch parameters remain random. To decouple the individual effect of the amplitude parameters and pitch parameters on slip, surfaces with the same AR roughness were

Synthesis of metal-fluoride nanoparticles supported on thermally reduced graphite oxide

• Alexa Schmitz,
• Kai Schütte,
• Vesko Ilievski,
• Juri Barthel,
• Laura Burk,
• Rolf Mülhaupt,
• Junpei Yue,
• Bernd Smarsly and
• Christoph Janiak

Beilstein J. Nanotechnol. 2017, 8, 2474–2483, doi:10.3762/bjnano.8.247

• ] yielded metal fluoride nanoparticles for Mn, Fe and Co [63]. The reaction of metal acetate (hydrate) precursors in ethylene glycol and an excess of [BMIm][BF4] gave fluoride nanoparticles [67]. Mesoporous carbon/iron carbide hybrids were synthesized using mesoporous silica as template and the ionic liquid

Laser-assisted fabrication of gold nanoparticle-composed structures embedded in borosilicate glass

• Nikolay Nedyalkov,
• Mihaela Koleva,
• Nadya Stankova,
• Rosen Nikov,
• Mitsuhiro Terakawa,
• Yasutaka Nakajima,
• Lyubomir Aleksandrov and
• Reni Iordanova

Beilstein J. Nanotechnol. 2017, 8, 2454–2463, doi:10.3762/bjnano.8.244

• parameters and the optical response was studied. In the nanosecond pulse case, we employed a Nd:YAG laser systems (Lotis) operating at four wavelengths – 1064 nm, 532 nm, 355 nm and 266 nm, with a pulse duration of 12 ns. The laser light was focused by a fused silica lens with a focal length of 200 mm. The

• after laser irradiation can be assigned to oxygen deficiency related to intrinsic defects in the silica matrix [16][28]. Since the photon energy at 226 nm is higher than the Si–O bonding energy (4.5 eV), the laser radiation may cause direct bond breaking. The absorption below 400 nm is related to two

Fabrication of CeO₂–MO_x (M = Cu, Co, Ni) composite yolk–shell nanospheres with enhanced catalytic properties for CO oxidation

• Ling Liu,
• Jingjing Shi,
• Hongxia Cao,
• Ruiyu Wang and
• Ziwu Liu

Beilstein J. Nanotechnol. 2017, 8, 2425–2437, doi:10.3762/bjnano.8.241

• silica sand was loaded into a stainless steel tube. A gas mixture of CO/O2/N2 (1:10:89) with a total flow rate of 50 mL/min flowed through the reactor, equivalent to a weight hourly space velocity (WHSV) of 60000 mL·g−1·h−1. The composition of the gas exiting from the reactor was monitored with an online

Involvement of two uptake mechanisms of gold and iron oxide nanoparticles in a co-exposure scenario using mouse macrophages

• Dimitri Vanhecke,
• Dagmar A. Kuhn,
• Dorleta Jimenez de Aberasturi,
• Sandor Balog,
• Ana Milosevic,
• Dominic Urban,
• Diana Peckys,
• Niels de Jonge,
• Wolfgang J. Parak,
• Alke Petri-Fink and
• Barbara Rothen-Rutishauser

Beilstein J. Nanotechnol. 2017, 8, 2396–2409, doi:10.3762/bjnano.8.239

• microvascular endothelial cells via flotillin-mediated uptake [18]. Flotillin-mediated uptake was also observed for silica NPs in lung epithelial and endothelial cells [19]. The various uptake pathways have one aspect in common: The internalized NP is ultimately located in an intracellular vesicle. Endocytosis

Changes of the absorption cross section of Si nanocrystals with temperature and distance

• Michael Greben,
• Petro Khoroshyy,
• Sebastian Gutsch,
• Daniel Hiller,
• Margit Zacharias and
• Jan Valenta

Beilstein J. Nanotechnol. 2017, 8, 2315–2323, doi:10.3762/bjnano.8.231

• of silicon-rich silicon oxynitride (SRON: SiOxNy) with 4.5 nm thickness and of stoichiometric SiO2 (1, 1.6, 2.2 or 2.8 nm thick) on fused silica substrates by plasma-enhanced chemical vapor deposition (PECVD). On top and below the superlattice stack, 10 nm of SiO2 were deposited as a buffer and

Angstrom-scale flatness using selective nanoscale etching

• Takashi Yatsui,
• Hiroshi Saito and
• Katsuyuki Nobusada

Beilstein J. Nanotechnol. 2017, 8, 2181–2185, doi:10.3762/bjnano.8.217

• incident from the top of the substrate through a chamber with 200 Pa Cl2 for dry etching or a drop of 10 μL Ca(ClO)2 (25 wt %) for wet etching (see Figure 2). The absorption edge of fused silica is approximately 7.9 eV (157 nm) [14]; thus, we could exclude the effect of carrier generation in the fused

• silica. To evaluate the changes in the surface profiles, we used an atomic force microscope (AFM) with a “Sampling Intelligent Scan” mode (Hitachi-Hitech-Science Corp.). The scanning area of the AFM was 10 × 10 μm and 256 × 256 pixels. Results and Discussion Figure 3a–c shows the respective AFM images

Ta₂N₃ nanocrystals grown in Al₂O₃ thin layers

• Krešimir Salamon,
• Maja Buljan,
• Iva Šarić,
• Mladen Petravić and
• Sigrid Bernstorff

Beilstein J. Nanotechnol. 2017, 8, 2162–2170, doi:10.3762/bjnano.8.215

• -assembly of semiconductor quantum dots in amorphous alumina or silica multilayers [18][19]. The key point of this deposition design is the insertion of dielectric layers, so called spacer layers, between all arbitrarily thick active metallic layers. In that way, upon annealing, the growth and final size of

• fused silica substrates held at room temperature. After the deposition, the multilayers were annealed for 1 h in vacuum, at several temperatures Ta ranging from 600 to 900 °C. The spacer layers should suppress the diffusion of Ta atoms between different metallic layers, and thus prevent the formation of

Synthesis and characterization of noble metal–titania core–shell nanostructures with tunable shell thickness

• Bartosz Bartosewicz,
• Marta Michalska-Domańska,
• Malwina Liszewska,
• Dariusz Zasada and
• Bartłomiej J. Jankiewicz

Beilstein J. Nanotechnol. 2017, 8, 2083–2093, doi:10.3762/bjnano.8.208

• [1][2]. This is because the combination of two or more different materials into one structure of controlled size, geometry and morphology can lead to either improved or new properties not observed in the individual constituent materials. CSNs with a silica core and noble metal shell exhibiting

• tunable optical properties depending on the ratio of core radius and shell thickness are an excellent example of such structures [3][4]. The CSNs, with either a silica core or shell, have found many applications due to their useful properties, including surface enhanced spectroscopy or cancer therapy [4

A comparative study of the nanoscale and macroscale tribological attributes of alumina and stainless steel surfaces immersed in aqueous suspensions of positively or negatively charged nanodiamonds

• Colin K. Curtis,
• Antonin Marek,
• Alex I. Smirnov and
• Jacqueline Krim

Beilstein J. Nanotechnol. 2017, 8, 2045–2059, doi:10.3762/bjnano.8.205

• study employed an aqueous dispersion of positively charged NDs, the silica surface is expected to be charged negatively at normal pH (IEP = 3.9, [50]) providing the same short-range electrostatic forces responsible for the ND surface self-assembly. The EIP of SS304 surfaces, however, is somewhat acidic

Imidazolium-based ionic liquids used as additives in the nanolubrication of silicon surfaces

• Patrícia M. Amorim,
• Ana M. Ferraria,
• Rogério Colaço,
• Luís C. Branco and
• Benilde Saramago

Beilstein J. Nanotechnol. 2017, 8, 1961–1971, doi:10.3762/bjnano.8.197

• lubrication of silica surfaces at the macro- and the nanoscale with mixtures of trihexyl(tetradecyl)phosphonium bis(2,4,4-trimethylpentyl)phosphinate and apolar base oils, such as octane and hexadecane. Macroscale studies were done with a pin-on-disk tribometer under loads of 2 N and 10 N, while an atomic

• , it mainly hydrated the substrate surface. However, in both cases, ambient humidity was found to disturb the ion-pair coordination, which resulted in an increase in friction [31]. Tests carried out at macroscale showed the same effect when using hydrophobic imidazolium-based ILs to lubricate silica

• ]. Recently, the same group reported somewhat different results when studying the tribological behavior of silica/silicon pairs lubricated with [EMIM][EtSO4] with a pin-on-disk tribometer at high load (4.5 N) [32]. They studied the effect of ambient humidity and found a decrease in friction and wear of both

Enhancement of mechanical and electrical properties of continuous-fiber-reinforced epoxy composites with stacked graphene

• Naum Naveh,
• Olga Shepelev and
• Samuel Kenig

Beilstein J. Nanotechnol. 2017, 8, 1909–1918, doi:10.3762/bjnano.8.191

• , radiation, modification with rubber, silica, carbon or other nanoparticles, showing interesting enhancements in interlaminar shear strength (ILSS), fracture toughness, fatigue life and related properties [2][3][4][5][6]. Graphite nanoplatelets (GNPs) or stacked graphene (SG) have been developed as a low

Carbon nano-onions as fluorescent on/off modulated nanoprobes for diagnostics

• Stefania Lettieri,
• Marta d’Amora,
• Adalberto Camisasca,
• Alberto Diaspro and
• Silvia Giordani

Beilstein J. Nanotechnol. 2017, 8, 1878–1888, doi:10.3762/bjnano.8.188

• -diisopropylethylamine (DIPEA) (4.9 mL) was added, and after 30 min, boron trifluoride diethyl etherate (BF3OEt2) (5.2 mL) was added. The mixture was stirred for 3 h. The crude was eluted on a silica plug using DCM before purification by column chromatography (SiO2, DCM/hexane 50:50, increasing amount of DCM) to obtain

• , 0.009 mol) in 50 mL of dry toluene and deoxygenated by purging with di-nitrogen (N2). Piperidine (2.4 mL), glacial acetic acid (2.9 mL) and a catalytic amount of Mg(ClO4)2 were added and the reaction mixture was refluxed at 150 °C for 27 h with a Dean–Stark condenser. The crude was eluted on a silica

Application of visible-light photosensitization to form alkyl-radical-derived thin films on gold

• Rashanique D. Quarels,
• Xianglin Zhai,
• Neepa Kuruppu,
• Jenny K. Hedlund,
• Ashley A. Ellsworth,
• Amy V. Walker,
• Jayne C. Garno and
• Justin R. Ragains

Beilstein J. Nanotechnol. 2017, 8, 1863–1877, doi:10.3762/bjnano.8.187

• , atomically flat Au(111) surface. Residual mica was removed from the Au surface by briefly soaking in THF. Size-sorted silica mesospheres with an average diameter of 500 nm (Thermo Scientific) were cleaned by centrifugation and suspension in water (three cleaning cycles). A 10 µL drop of the silica mesosphere

• suspension was placed onto the template-stripped gold substrates, dried in air for 2 h, and then oven-dried for at least 96 h. The final heating step was used to temporarily anneal the silica spheres to the substrate to prevent displacement during immersion in solutions. After completion of the procedures

• , removal of the surface mask was accomplished by sonication in ethanol. Preparation of phthalimide ester compounds. Phthalimide esters were synthesized according to a known procedure [38] and purified with silica gel chromatography. NMR and high-resolution mass spec. data for the new compounds Phth–Me and

Self-assembly of chiral fluorescent nanoparticles based on water-soluble L-tryptophan derivatives of p-tert-butylthiacalix[4]arene

• Pavel L. Padnya,
• Irina A. Khripunova,
• Olga A. Mostovaya,
• Timur A. Mukhametzyanov,
• Vladimir G. Evtugyn,
• Vyacheslav V. Vorobev,
• Yuri N. Osin and
• Ivan I. Stoikov

Beilstein J. Nanotechnol. 2017, 8, 1825–1835, doi:10.3762/bjnano.8.184

• ). The melting points were determined using a Boetius Block apparatus. The purity of the compounds was monitored by melting points, boiling points, 1H NMR and thin layer chromatography (TLC) on 200 μm UV 254 silica gel plate using UV light. All experiments (NMR, UV–vis, CD spectroscopy and DLS) were

Methionine-mediated synthesis of magnetic nanoparticles and functionalization with gold quantum dots for theranostic applications

• Arūnas Jagminas,
• Agnė Mikalauskaitė,
• Vitalijus Karabanovas and
• Jūrate Vaičiūnienė

Beilstein J. Nanotechnol. 2017, 8, 1734–1741, doi:10.3762/bjnano.8.174

• magnetic NPs through biocompatible links such as Au–S– [7]. Iron oxide NPs can be coated with polymeric or silica shells containing incorporated gold NPs [8][9][10]. However, in this case the size of the magnetic NPs increases up to ten times [9], resulting in a significant decrease in the saturation

Near-infrared-responsive, superparamagnetic Au@Co nanochains

• Varadee Vittur,
• Arati G. Kolhatkar,
• Shreya Shah,
• Irene Rusakova,
• Dmitri Litvinov and
• T. Randall Lee

Beilstein J. Nanotechnol. 2017, 8, 1680–1687, doi:10.3762/bjnano.8.168

• various applications, such as energy conversion in solar cells [10][11], biosensing [12], photothermal therapy [13], and biomedical imaging [14]. Surface modification with an inorganic coating, such as silica, can lend biocompatibility to the nanoparticles [15][16][17][18]. A gold shell on magnetic

Two-dimensional carbon-based nanocomposites for photocatalytic energy generation and environmental remediation applications

• Suneel Kumar,
• Ashish Kumar,
• Ashish Bahuguna,
• Vipul Sharma and
• Venkata Krishnan

Beilstein J. Nanotechnol. 2017, 8, 1571–1600, doi:10.3762/bjnano.8.159

Fixation mechanisms of nanoparticles on substrates by electron beam irradiation

• Daichi Morioka,
• Tomohiro Nose,
• Taiki Chikuta,
• Kazutaka Mitsuishi and
• Masayuki Shimojo

Beilstein J. Nanotechnol. 2017, 8, 1523–1529, doi:10.3762/bjnano.8.153

• is caused by the scattering of electrons in the substrate. Silica nanoparticles Electron beam induced fixation can be applied not only to Au but also to other materials. To indicate the versatility of this technique and the possibility of other applications, the fixation of silica nanoparticles was

• also demonstrated. Figure 11 shows silica nanoparticles fixed on a Au-coated Si substrate. As the surface of colloidal silica particles was modified with –COOH groups, a dissociation of the organic shells occurs and the particles are fixed on the substrate. Conclusion The mechanism of fixing

• . Dodecanethiol and ethanol were purchased from Wako Co., Ltd., Japan. The substrate was observed with SEM and the width of the area in which the nanoparticles remained was measured. To show the versatility of this technique silica nanoparticles were also fixed. An Au thin film, the thickness of which was about 5

Low uptake of silica nanoparticles in Caco-2 intestinal epithelial barriers

• Dong Ye,
• Mattia Bramini,
• Delyan R. Hristov,
• Sha Wan,
• Anna Salvati,
• Christoffer Åberg and
• Kenneth A. Dawson

Beilstein J. Nanotechnol. 2017, 8, 1396–1406, doi:10.3762/bjnano.8.141

• capacity of nanoparticles to enter and transport across such barriers. In this work, Caco-2 intestinal epithelial cells were used as a well-established model for the intestinal barrier, and the uptake, trafficking and translocation of model silica nanoparticles of different sizes were investigated using a

• combination of imaging, flow cytometry and transport studies. Compared to typical observations in standard cell lines commonly used for in vitro studies, silica nanoparticle uptake into well-developed Caco-2 cellular barriers was found to be very low. Instead, nanoparticle association to the apical outer

• been achieved [19][20][21]. Caco-2 cells have been used in the literature to investigate the potential toxic effects of a range of nanoparticles, including microporous silicon [22], silica [23][24][25][26][27][28] and zinc oxide [25]. Though such studies have mainly been performed on undifferentiated

Bright fluorescent silica-nanoparticle probes for high-resolution STED and confocal microscopy

• Isabella Tavernaro,
• Christian Cavelius,
• Henrike Peuschel and
• Annette Kraegeloh

Beilstein J. Nanotechnol. 2017, 8, 1283–1296, doi:10.3762/bjnano.8.130

• , fluorescent nanomaterials have gained high relevance in biological applications as probes for various fluorescence-based spectroscopy and imaging techniques. Among these materials, dye-doped silica nanoparticles have demonstrated a high potential to overcome the limitations presented by conventional organic

• dyes such as high photobleaching, low stability and limited fluorescence intensity. In the present work we describe an effective approach for the preparation of fluorescent silica nanoparticles in the size range between 15 and 80 nm based on L-arginine-controlled hydrolysis of tetraethoxysilane in a

• agglomeration and stability) and the fluorescence properties of the obtained particles were compared to particles from commonly known synthesis methods. As a result, the spectroscopic characteristics of the presented monodisperse dye-doped silica nanoparticles were similar to those of the free uncoupled dyes

Preparation of thick silica coatings on carbon fibers with fine-structured silica nanotubes induced by a self-assembly process

• Benjamin Baumgärtner,
• Hendrik Möller,
• Thomas Neumann and
• Dirk Volkmer

Beilstein J. Nanotechnol. 2017, 8, 1145–1155, doi:10.3762/bjnano.8.116

• carbon fibers with a silica shell is presented in this work. By immobilizing linear polyamines on the carbon fiber surface, the high catalytic activity of polyamines in the sol–gel-processing of silica precursors is used to deposit a silica coating directly on the fiber’s surface. The surface

• self-assembles onto the carbon fiber substrate in the form of nanoscopic crystallites, which serve as a template for the subsequent silica deposition. The silicification at close to neutral pH is spatially restricted to the localized polyamine and consequently to the fiber surface. In case of the

• linear poly(ethylenimine), silica shells of several micrometers in thickness can be obtained and their morphology is easily controlled by a considerable number of synthesis parameters. A unique feature is the hierarchical biomimetic structure of the silica coating which surrounds the embedded carbon

Hierarchically structured nanoporous carbon tubes for high pressure carbon dioxide adsorption

• Julia Patzsch,
• Deepu J. Babu and
• Jörg J. Schneider

Beilstein J. Nanotechnol. 2017, 8, 1135–1144, doi:10.3762/bjnano.8.115

• tubes to be obtained. To obtain these materials, a polymer was employed and used as the carbon source and template to mold a spherical structure of silica particles obtained by the Stoeber process. After a carbonization step, a second thermal treatment was employed to obtain either SiC tubes or a

• at 20 W for one minute. Synthesis of silica@polystyrene composite tubes (2) and silica@carbon composite tubes (3) Analogous to our previous work [38], a modified Stoeber method was used to coat the plasma-treated, and thus oxo-functionalized, PS fibres with a silica shell. In a typical reaction, the

• :0.5) was sprayed onto the PS fibres with a commercial air brush gun. The obtained silica@polystyrene composite (2) was treated at 250 °C for 16 h under air and at 950 °C for 4 h under nitrogen atmosphere, yielding the silica@carbon composite tubes (3). Synthesis of carbon tubes (4) An HF solution was

Assembly of metallic nanoparticle arrays on glass via nanoimprinting and thin-film dewetting

• Sun-Kyu Lee,
• Sori Hwang,
• Yoon-Kee Kim and
• Yong-Jun Oh

Beilstein J. Nanotechnol. 2017, 8, 1049–1055, doi:10.3762/bjnano.8.106

• annealing, which turned the imprinted resist into pure silica. The transparent, topographic glass successfully templated the assembly of Au and Ag nanoparticle arrays via thin-film deposition and dewetting at elevated temperatures. The microstructural and mechanical characteristics that developed during the

• temperatures to completely transform them into pure silica by oxidizing and decomposing the CH3 groups in the resist. The maximum annealing temperature was limited to 600 °C, up to which the soda lime glass does not undergo deformation. Noble metals (Au and Ag) were sputter-deposited onto the imprinted resist

• imprinted at 110 °C for 30 min were annealed in the temperature range of ≈400–600 °C to transform them into pure silica. Figure 3 shows an example of the imprinted surface features after annealing at 550 °C for 5 h. The topography of the master mold was mostly transferred onto the silica on glass, although

Bio-inspired micro-to-nanoporous polymers with tunable stiffness

• Julia Syurik,
• Ruth Schwaiger,
• Prerna Sudera,
• Stephan Weyand,
• Siegbert Johnsen,
• Gabriele Wiegand and
• Hendrik Hölscher

Beilstein J. Nanotechnol. 2017, 8, 906–914, doi:10.3762/bjnano.8.92

• a modified, biomimetic investment-casting manufacturing technique [13]. The protective peel was transformed into amorphous silica by bio-templating down to the nanometre-scale, creating a biomorphous inorganic and, therefore, temperature-resistant gradient-foam material . It is well known that