Self-assembly and wetting properties of gold nanorod–CTAB molecules on HOPG

• Imtiaz Ahmad,
• Floor Derkink,
• Tim Boulogne,
• Pantelis Bampoulis,
• Harold J. W. Zandvliet,
• Hidayat Ullah Khan,
• Rahim Jan and
• E. Stefan Kooij

Beilstein J. Nanotechnol. 2019, 10, 696–705, doi:10.3762/bjnano.10.69

• surface. The self-assembled layers of CTAB molecules on the HOPG terraces prior to nanorod deposition were shown to change the wettability of the surface, and as a result, gold nanorod deposition takes place on nonwetting HOPG terraces. Keywords: CTAB; gold nanorods; micelles; self-assembly; wettability

• ; Introduction In the last few decades there have been many studies that focused on hard colloidal particles and micelles, covering a length scale ranging from nanometers to micrometers. The focus of nanoscience and nanotechnology is increasingly shifting from synthesis to assembly into larger superstructures

• that CTAB surfactant molecules can self-assemble on a highly ordered pyrolytic graphite (HOPG) surface in the form of hemi-cylindrical micelles [43][44][45]. The surface of HOPG is hydrophobic [46][47], while the CTAB molecules have a hydrophilic end group and a hydrophobic tail [48]. Therefore, to

pH-mediated control over the mesostructure of ordered mesoporous materials templated by polyion complex micelles

• Emilie Molina,
• Mélody Mathonnat,
• Jason Richard,
• Patrick Lacroix-Desmazes,
• Martin In,
• Philippe Dieudonné,
• Thomas Cacciaguerra,
• Corine Gérardin and
• Nathalie Marcotte

Beilstein J. Nanotechnol. 2019, 10, 144–156, doi:10.3762/bjnano.10.14

• Coulomb, UMR 5221 CNRS – Université de Montpellier, 34095 Montpellier, France 10.3762/bjnano.10.14 Abstract Ordered mesoporous silica materials were prepared under different pH conditions by using a silicon alkoxide as a silica source and polyion complex (PIC) micelles as the structure-directing agents

• . PIC micelles were formed by complexation between a weak polyacid-containing double-hydrophilic block copolymer, poly(ethylene oxide)-b-poly(acrylic acid) (PEO-b-PAA), and a weak polybase, oligochitosan-type polyamine. As both the micellization process and the rate of silica condensation are highly

• ; hybrid organic–inorganic interface; mesoporous materials; nanostructured materials; polyion complex micelles; polyion electrostatic complexation; Introduction Due to their unique physicochemical properties originating from their uniform pore size and periodically arranged network at the mesoscale

Enhanced antineoplastic/therapeutic efficacy using 5-fluorouracil-loaded calcium phosphate nanoparticles

• Shanid Mohiyuddin,
• Saba Naqvi and
• Gopinath Packirisamy

Beilstein J. Nanotechnol. 2018, 9, 2499–2515, doi:10.3762/bjnano.9.233

• –surfactant molar ratio (MW). By restricting the water–surfactant molar ratio up to 10 (i.e., MW < 10) the reverse micelles can be readily formed with narrow size distribution in a synthetic reaction system [23]. The water molecules restricted inside hydrophilic core resulted in swollen micelles that were

High-throughput micro-nanostructuring by microdroplet inkjet printing

• Hendrikje R. Neumann and
• Christine Selhuber-Unkel

Beilstein J. Nanotechnol. 2018, 9, 2372–2380, doi:10.3762/bjnano.9.222

• densities is highly important in many fields, ranging from nano-optics to biosensor technologies and biomaterials. A well-established method to fabricate quasi-hexagonal patterns of metal nanoparticles is block copolymer micelle nanolithography, which relies on the self-assembly of metal-loaded micelles on

• surfaces by a dip-coating or spin-coating process. Using this method, the spacing of the nanoparticles is controlled by the size of the micelles and by the coating conditions. Whereas block copolymer micelle nanolithography is a high-throughput method for generating well-ordered nanoparticle patterns at

• spacing between a few tens to several hundreds of nanometers is block copolymer micelle nanolithography (BCML) [8]. This technique is based on the self-assembly of metal-containing micelles on surfaces during dip-coating or spin-coating. BCML is very efficient in coating large areas with nanoparticles in

Block copolymers for designing nanostructured porous coatings

• Roberto Nisticò

Beilstein J. Nanotechnol. 2018, 9, 2332–2344, doi:10.3762/bjnano.9.218

• micelles, reverse micelles as well as worm-like structures, lamellar sheets, and vesicles (Figure 5). As mentioned previously, the thermodynamic incompatibility between the blocks forming the polymer chains is the driving force behind the formation of such nanostructures [4][35]. In this context, this

Nanoconjugates of a calixresorcinarene derivative with methoxy poly(ethylene glycol) fragments for drug encapsulation

• Alina M. Ermakova,
• Julia E. Morozova,
• Yana V. Shalaeva,
• Victor V. Syakaev,
• Aidar T. Gubaidullin,
• Alexandra D. Voloshina,
• Vladimir V. Zobov,
• Irek R. Nizameev,
• Olga B. Bazanova,
• Igor S. Antipin and
• Alexander I. Konovalov

Beilstein J. Nanotechnol. 2018, 9, 2057–2070, doi:10.3762/bjnano.9.195

• nanoassociates that are able to encapsulate organic substrates of different hydrophobicity, including drugs (doxorubicin, naproxen, ibuprofen, quercetin). The micelles of the macrocycle slowed down the release of the hydrophilic substrates in vitro. In physiological sodium chloride solution and phosphate

• -buffered saline, the micelles of the macrocycle acquire thermoresponsive properties and exhibit a temperature-controlled release of doxorubicin in vitro. The combination of the low toxicity and the encapsulation properties of the obtained calixresorcinarene–mPEG conjugate shows promising potential for the

• various therapeutics and nanomaterials due to a number of benefits among which its low toxicity the most important [23][24]. PEG has good solubility in water and organic solvents. When being a component of polymeric micelles, it forms the outer hydrophilic shell of the micelle, contributes the colloidal

Self-assembled quasi-hexagonal arrays of gold nanoparticles with small gaps for surface-enhanced Raman spectroscopy

• Emre Gürdal,
• Simon Dickreuter,
• Fatima Noureddine,
• Pascal Bieschke,
• Dieter P. Kern and
• Monika Fleischer

Beilstein J. Nanotechnol. 2018, 9, 1977–1985, doi:10.3762/bjnano.9.188

• /mL and stirred for 2 days. The micelles were loaded with chlorauric acid (HAuCl4, loading parameter (L = 0.5), Sigma-Aldrich) and stirred again for 2 days. Spin-coating was applied to cover the substrate with a monolayer of the gold-loaded micelles (30 s at 2000 rpm). Electroless deposition A quartz

• block [23]. The hydrophobic PS forms the shell, and the hydrophilic P2VP the core of the spherically shaped micelles [24]. Within their core gold salt can be assembled, which is bonded by protonization or complexation [25]. The loaded spherical micelles form a hexagonal array when being deposited on a

• substrate. Exposing them to an aqueous environment promotes a morphological change of the spherical micelles [18]. In the next step, the micelles are treated with UV irradiation, which causes the gold salt particles in the center to grow bigger by photochemical growth [18]. To enlarge the metal precursor

Nanoporous silicon nitride-based membranes of controlled pore size, shape and areal density: Fabrication as well as electrophoretic and molecular filtering characterization

• Axel Seidenstücker,
• Stefan Beirle,
• Fabian Enderle,
• Paul Ziemann,
• Othmar Marti and
• Alfred Plettl

Beilstein J. Nanotechnol. 2018, 9, 1390–1398, doi:10.3762/bjnano.9.131

• . 12 nm) are deposited on the silicon oxide layer with a quasi-hexagonal order by self-organization. This is realized by dip-coating from a solution of Au salt-loaded PS–P2VP diblock copolymer micelles directly on the upper membrane face (coating is done without preceding deposition of appropriate

• self-organization of Au-loaded diblock copolymer micelles followed by plasma treatments. (b) Applying a photochemical growth process the Au NP size can be enlarged in a controlled way. (c) The resulting NP mask is exploited to etch nanopillars by RIE, (d) a Cr layer (black) is evaporated, (e) and the

A simple extension of the commonly used fitting equation for oscillatory structural forces in case of silica nanoparticle suspensions

• Sebastian Schön and
• Regine von Klitzing

Beilstein J. Nanotechnol. 2018, 9, 1095–1107, doi:10.3762/bjnano.9.101

• , aggregates or micelles tend to form a well-ordered layer in close proximity to a confining surface (henceforth called wall) with a density that is higher than that of the bulk. Since the molecules cannot penetrate each other, this layer of increased density is bordering on a region of lower density of

Review on nanoparticles and nanostructured materials: history, sources, toxicity and regulations

• Jaison Jeevanandam,
• Ahmed Barhoum,
• Yen S. Chan,
• Alain Dufresne and
• Michael K. Danquah

Beilstein J. Nanotechnol. 2018, 9, 1050–1074, doi:10.3762/bjnano.9.98

• structures such as dendrimers, micelles, liposomes and polymer NPs. (iv) Composite-based nanomaterials: Composite NMs are multiphase NPs and NSMs with one phase on the nanoscale dimension that can either combine NPs with other NPs or NPs combined with larger or with bulk-type materials (e.g., hybrid

Optical orientation of nematic liquid crystal droplets via photoisomerization of an azodendrimer dopant

• Sergey A. Shvetsov,
• Alexander V. Emelyanenko,
• Natalia I. Boiko,
• Alexander S. Zolot'ko,
• Yan-Song Zhang,
• Jui-Hsiang Liu and
• Alexei R. Khokhlov

Beilstein J. Nanotechnol. 2018, 9, 870–879, doi:10.3762/bjnano.9.81

• different kinds of soft matter, such as light-driven polymers [5][6], elastomers [7][8][9] microgel particles [10][11], micelles [12][13], nematic liquid crystals (NLCs) [7][14], liquid-crystalline (LC) polymers [15][16][17][18] and Langmuir–Blodgett films [19][20] with light-controllable supramolecular

The role of ligands in coinage-metal nanoparticles for electronics

• Ioannis Kanelidis and
• Tobias Kraus

Beilstein J. Nanotechnol. 2017, 8, 2625–2639, doi:10.3762/bjnano.8.263

• particular facets [2]. Their structure-directing action is due to a combination of thermodynamic driving forces (energy differences in facets) and transport modulation, where ligand coverage adjusts diffusion of monomers to the facets [2]. Some ligands also form micelles that can act as templates during the

Fabrication of carbon nanospheres by the pyrolysis of polyacrylonitrile–poly(methyl methacrylate) core–shell composite nanoparticles

• Dafu Wei,
• Youwei Zhang and
• Jinping Fu

Beilstein J. Nanotechnol. 2017, 8, 1897–1908, doi:10.3762/bjnano.8.190

• nanospheres were first fabricated by Kowaleski et al. [31] via successive shell crosslinking, oxidization and carbonization of the micelles resulting from the self-assembly of PAN-b-poly(acrylic acid) (PAA) block copolymer in water. The crosslinked shell can retain the micelle structure during the heat

• treatments, and thus is very crucial to obtain discrete carbon nanospheres after pyrolysis. Jérom et al. [32] obtained discrete carbon nanocapules after pyrolysis of stable PAN-b-PAA micelles with Au-nanoparticle-crosslinked cores. However, the difficulty in synthesis of the block copolymers and the low

• observed in the cavitation of non-covalently-connected micelles composed of carboxyl-ended polybutadiene cores and crosslinked poly(vinyl alcohol) shells in THF/water (9/1, v/v) mixture [44]. It was very possible that the size of PAN chains was too large to diffuse out of the PMMA shell, thus, the

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

• agreement was observed between the DLS data and the microscopy measurements in the case of the compounds 8 and 10 in cone conformation. This is due to the structure of the macrocycles, which formed spherical charged particles (micelles) with inwardly directed hydrophobic parts (thiacalixarene) and outwardly

• oriented hydrophilic positively charged fragments in the solution (Figure 1). The charge on the micelles prevents them from aggregating when we concentrate the solutions for preparation of the SEM experiment. This leads to the preservation of individual particles of similar size to those that exist in

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

• , an anionic surfactant gets adsorbed on the surface of graphene sheets and helps in the dispersion of graphene sheets. Then, the surfactant micelles with graphene sheets bind with metal cations and hence act as building block for self-assembly of metal oxides. Finally metal oxides become crystallized

Spin-chemistry concepts for spintronics scientists

• Konstantin L. Ivanov,
• Alexander Wagenpfahl,
• Carsten Deibel and
• Jörg Matysik

Beilstein J. Nanotechnol. 2017, 8, 1427–1445, doi:10.3762/bjnano.8.143

Synthesis of [Fe(L_eq)(L_ax)]_n coordination polymer nanoparticles using blockcopolymer micelles

• Christoph Göbel,
• Ottokar Klimm,
• Florian Puchtler,
• Sabine Rosenfeldt,
• Stephan Förster and
• Birgit Weber

Beilstein J. Nanotechnol. 2017, 8, 1318–1327, doi:10.3762/bjnano.8.133

• -poly(4-vinylpyridine) (PS-b-P4VP) block copolymer (BCP) micelles as template. Variation of the solvent (THF and toluene) and the rigidity of the axial ligand Lax (Lax = 1,2-di(pyridin-4-yl)ethane) (bpea), trans-1,2-di(pyridin-4-yl)ethene (bpee), and 1,2-di(pyridin-4-yl)ethyne) (bpey); Leq = 1,2

• dynamic light scattering (DLS) in solution, transmission electron microscopy (TEM) and powder X-ray diffraction (PXRD) in the solid. The hydrodynamic diameter of the polymeric micelles loaded with the CP measured by DLS is constant within the error of the measurement throughout all measured samples with

• the measurement, the NP core size is in the same order of magnitude for all samples with an average size of 45 nm (Table 1), demonstrating the excellent size control by the micelles themselves. The NP core size is independent of the number of cycles and independent of the used coordination polymer

The longstanding challenge of the nanocrystallization of 1,3,5-trinitroperhydro-1,3,5-triazine (RDX)

• Florent Pessina and
• Denis Spitzer

Beilstein J. Nanotechnol. 2017, 8, 452–466, doi:10.3762/bjnano.8.49

• substitution using reverse micelles Dabin et al. [22] have developed an ingenious method to prepare nanometer-scale RDX using a simple technique. The crystallization is triggered by a solvent substitution, and the nanometer scale material is obtained by restricting the reactor volume using reverse micelles

• . NaAOT (sodium 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate) with isooctane was used to form reverse micelles. Then RDX in dimethylformamide (DMF) is added to one solution containing these micelles, and water to another solution of micelles. Both are finally mixed together to form the n-RDX with a

Nanoscale isoindigo-carriers: self-assembly and tunable properties

• Tatiana N. Pashirova,
• Andrei V. Bogdanov,
• Lenar I. Musin,
• Julia K. Voronina,
• Irek R. Nizameev,
• Marsil K. Kadirov,
• Vladimir F. Mironov,
• Lucia Ya. Zakharova,
• Shamil K. Latypov and
• Oleg G. Sinyashin

Beilstein J. Nanotechnol. 2017, 8, 313–324, doi:10.3762/bjnano.8.34

• and hydrogen bonding. Another strategy is the use of soft matter (micelles, emulsions, dendrimers, nanospheres, solid lipid nanoparticles or liposomes) as the delivery vehicle. These studies have been encouraged by the possibility to prevent side effects, to increase drug bioavailability, to decrease

• [66]: Data in Table S3 (Supporting Information File 1) show that packing parameters (P) are 0.25 and 0.12 for compounds 1g and 3, respectively, which makes it plausible to assume the occurrence of spherical normal micelles. For derivatives 2a–h P values are close to 0.5, which indicates the formation

• hydropohobic solutes including drugs. Furthermore, the solubilization of organic hydrophobic dyes makes it possible to detect the formation of micelles in solution [67]. In Figure 4a, the dependence of the absorbance of hydrophobic dye (Sudan I) on the concentration of isoindigo derivatives 2g and 2h is shown

Nanocrystalline ZrO₂ and Pt-doped ZrO₂ catalysts for low-temperature CO oxidation

• Amit Singhania and
• Shipra Mital Gupta

Beilstein J. Nanotechnol. 2017, 8, 264–271, doi:10.3762/bjnano.8.29

• nanoparticles such as sol–gel [21], precipitation [22], combustion [23], hydrothermal synthesis [24], solvothermal synthesis [25], reverse micelles [26], chemical vapor synthesis [27], aerosol pyrolysis [28], and sonochemical synthesis [29]. Dongare et al. [30] described the synthesis of ZrO2 by a sol–gel

A dioxaborine cyanine dye as a photoluminescence probe for sensing carbon nanotubes

• Mohammed Al Araimi,
• Petro Lutsyk,
• Anatoly Verbitsky,
• Yuri Piryatinski,
• Mykola Shandura and
• Aleksey Rozhin

Beilstein J. Nanotechnol. 2016, 7, 1991–1999, doi:10.3762/bjnano.7.190

• the PL detection towards the nanotube diameters. The energy diagram shown at the right-hand side of Figure 2a represents a two-component system consisting of the anionic surfactant SDBS and the SWNTs in water, where the anionic surfactant forms micelles around the nanotubes having typical exciton

• mixture at micellar concentration of SDBS does not exhibit new bands in the range of 700–780 nm (in absorption and PL excitation). Thus, no RET from DOB-719 is possible when the micelles of SDBS fully cover the SWNTs. This shows another dissimilarity of the studied system in comparison with SWNT–SDBS

• 735 nm can be used for PL detection of SWNTs in aqueous environment. In the mixture of DOB-719 and SWNTs, the monomeric dye molecules were either in free form and degraded severely, or associated in a complex with the SWNT micelles and became more stable. Thus, the interaction between DOB-719 and the

Antitumor magnetic hyperthermia induced by RGD-functionalized Fe₃O₄ nanoparticles, in an experimental model of colorectal liver metastases

• Oihane K. Arriortua,
• Eneko Garaio,
• Borja Herrero de la Parte,
• Maite Insausti,
• Luis Lezama,
• Fernando Plazaola,
• Jose Angel García,
• Jesús M. Aizpurua,
• Maialen Sagartzazu,
• Mireia Irazola,
• Nestor Etxebarria,
• Ignacio García-Alonso,
• Alberto Saiz-López and
• José Javier Echevarria-Uraga

Beilstein J. Nanotechnol. 2016, 7, 1532–1542, doi:10.3762/bjnano.7.147

• -water micelles, encapsulating iron oxide nanocrystals inside them. The monomeric units of maleic anhydride are easily hydrolyzed to form carboxylic groups, becoming hydrosoluble. Besides, the conjugation of carboxylates to a linker containing both an amino and a triple bond group generates an

Polystyrene-block-poly(ethylene oxide) copolymers as templates for stacked, spherical large-mesopore silica coatings: dependence of silica pore size on the PS/PEO ratio

• Roberto Nisticò,
• Giuliana Magnacca,
• Sushilkumar A. Jadhav and
• Dominique Scalarone

Beilstein J. Nanotechnol. 2016, 7, 1454–1460, doi:10.3762/bjnano.7.137

• critical micellar concentration, CMC) amphiphiles can spontaneously self-organize into well-defined supramolecular aggregates (host) which can be classified as normal and reverse micelles, emulsions, vesicles or liquid crystal phases and can shape or pattern other materials (guest), forming spherical

• concentration dependent. In addition to the amphiphile concentration, the morphology and size of both micelles and micellar aggregates also depend on other solution parameters, such as the type of solvents, the solvent/nonsolvent ratio, the presence of additives, and on molecular parameters, such as the

• films. Thus, by fixing the TEOS/PS-b-PEO weight ratio of the micellar solutions in order to get spherical micelles (that is for TEOS/PS-b-PEO weight ratios of 95/5 or 93/7), we studied the effect of the PS/PEO ratio on the pore size of the templated silica films. Results and Discussion Hybrid TEOS/block

Multiwalled carbon nanotube hybrids as MRI contrast agents

• Nikodem Kuźnik and
• Mateusz M. Tomczyk

Beilstein J. Nanotechnol. 2016, 7, 1086–1103, doi:10.3762/bjnano.7.102

• surfactants seem to enable such water interactions. On the contrary, ionic surfactants tend to form micelles that limit access for the water molecules. Therefore, the results of the SWCNT studies give a general idea of the impact of surfactants on the relaxivity results. When comparing solely r2 measured in

Orientation of FePt nanoparticles on top of a-SiO₂/Si(001), MgO(001) and sapphire(0001): effect of thermal treatments and influence of substrate and particle size

• Martin Schilling,
• Paul Ziemann,
• Zaoli Zhang,
• Johannes Biskupek,
• Ute Kaiser and
• Ulf Wiedwald

Beilstein J. Nanotechnol. 2016, 7, 591–604, doi:10.3762/bjnano.7.52

• particle size, distance and arrangement [11]. Since this preparation is almost independent of the substrate, we successfully deposited the well-separated NPs on a-SiO2/Si(001), sapphire(0001) and magnesium oxide MgO(001). In brief, reverse micelles were formed using a commercial diblock-copolymer (PS-P2VP

• ) solved in water-free toluene and loaded by Zeise’s salt K[PtCl3(C2H4)]·H2O and FeCl2 or FeCl3 in the appropriate ratio for equiatomic FePt NPs. All chemicals were used as received. A self-assembled close-packed monolayer of precursor-loaded micelles forms on the substrates by dip coating at a typical

• velocity of 15 mm/min [11][30]. These deposited precursor-loaded micelles are transformed into FePt NPs by a combination of oxygen and hydrogen plasma treatments: The organic shell is removed by oxygen plasma, followed by a subsequent hydrogen plasma step, necessary to completely reduce the NPs into the