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

• processes were discussed. The results are promising for low-cost mass fabrication of devices for several photonic applications. Keywords: dewetting; metal thin films; nanoimprint; nanoparticles; self-assembly; Findings Thin films on nonreactive solid surfaces, having a high surface area relative to their

• as a functional layer. Thus, the applicability of a self-assembly technique that uses dewetting largely depends on how it can be combined with appropriate template materials that have both functionality and dewettability. In this regard, nanoimprint lithography (NIL) is expected to be an effective

Recombinant DNA technology and click chemistry: a powerful combination for generating a hybrid elastin-like-statherin hydrogel to control calcium phosphate mineralization

• Mohamed Hamed Misbah,
• Mercedes Santos,
• Luis Quintanilla,
• Christina Günter,
• Matilde Alonso,
• Andreas Taubert and
• José Carlos Rodríguez-Cabello

Beilstein J. Nanotechnol. 2017, 8, 772–783, doi:10.3762/bjnano.8.80

• polymers (ELPs) or recombinamers (ELRs), which are excellent example of materials that exhibit self-assembly and self-organization [27][28][29]. The majority of ELPs or ELRs consist of simple amino-acid consensus epitopes that are also present in natural elastin, such as (VPGXG)* (see Table 1 for details

• fibrillar morphology. It is known that ELRs undergo hierarchical self-assembly producing a fibrillar structure [27][30][47]. For example, poly(VPGVG) and its analog poly [fv(VPGVG), fx(VPGKG)] (0.1 ≤ fx ≤0.2, fv + fx = 1) interact hydrophobically and self-assemble into nanofilaments that align in parallel

• disassembling ELPs and ELRs [27][29]. Recently, the self-assembly properties of ELRs have been combined with the mineralization capacity of SNA15 using such a biotechnology approach [13]. In that study, Misbah et al. demonstrated that ELRs cannot control the formation of CP in the absence of SNA15. In addition

Synthesis of graphene–transition metal oxide hybrid nanoparticles and their application in various fields

• Arpita Jana,
• Elke Scheer and
• Sebastian Polarz

Beilstein J. Nanotechnol. 2017, 8, 688–714, doi:10.3762/bjnano.8.74

• applications [165]. This aerogel structure exhibits excellent rate capability and outstanding long-term cyclic stability at high current densities. Wang et al. have introduced a solvothermal-induced self-assembly approach to construct the monolithic 3D Fe2O3 and GS hybrids, which have excellent prolonged

• [188]. Guo et al. prepared Co/CoO–graphene by self-assembly of Co NPs on the surface of graphene. This hybrid has similar activity as and better stability than commercial Pt NP catalyst supported on carbon (C–Pt) NPs and may serve as an alternative to C–Pt catalysts for the ORR in alkaline solution

Calculating free energies of organic molecules on insulating substrates

• Julian Gaberle,
• David Z. Gao and
• Alexander L. Shluger

Beilstein J. Nanotechnol. 2017, 8, 667–674, doi:10.3762/bjnano.8.71

• insulating substrates where atomic force microscopy (AFM) provides vital information on film structure and growth modes. Non-contact (NC)-AFM has provided rich information on the adsorption, self-assembly and film structure of various organic molecules on insulators [15][16][17][18][19][20][21]. The current

• ]. In self-assembly processes, the right balance between molecule–molecule (MM) and molecule–surface (MS) interactions is critical to achieve large domains of ordered films. However, forming a molecular complex or a 2D film structure from freely rotating and translating molecules results in a loss in

• entropy as degrees of freedom within the molecules become constrained. This means that free energies can vary significantly from calculated enthalpy values, which may have a direct impact on our understanding of the balance of interactions that govern self-assembly. Methods to compute the free energy from

Computing the T-matrix of a scattering object with multiple plane wave illuminations

• Martin Fruhnert,
• Ivan Fernandez-Corbaton,
• Vassilios Yannopapas and
• Carsten Rockstuhl

Beilstein J. Nanotechnol. 2017, 8, 614–626, doi:10.3762/bjnano.8.66

• experimental data for the dispersive permittivity of silver [43]. Such objects can be fabricated in large quantities by self assembly methods, e.g., by connecting commercially available metal nanospheres with a linker molecule [44]. We set N = 2, because the higher orders do not contribute notably. For general

Formation and shape-control of hierarchical cobalt nanostructures using quaternary ammonium salts in aqueous media

• Ruchi Deshmukh,
• Anurag Mehra and
• Rochish Thaokar

Beilstein J. Nanotechnol. 2017, 8, 494–505, doi:10.3762/bjnano.8.53

• Ruchi Deshmukh Anurag Mehra Rochish Thaokar Department of Chemical Engineering, Indian Institute of Technology Bombay, Powai, Mumbai 400076, India 10.3762/bjnano.8.53 Abstract Aggregation and self-assembly are influenced by molecular interactions. With precise control of molecular interactions

Self-assembly of silicon nanowires studied by advanced transmission electron microscopy

• Marta Agati,
• Guillaume Amiard,
• Vincent Le Borgne,
• Paola Castrucci,
• Richard Dolbec,
• Maurizio De Crescenzi,
• My Alì El Khakani and
• Simona Boninelli

Beilstein J. Nanotechnol. 2017, 8, 440–445, doi:10.3762/bjnano.8.47

• within the plasma reactor. Both the STEM tomography and STEM-EDX analysis contributed to gain further insight into the self-assembly process. In the long-term, this approach might be used to optimize the synthesis of VLS-grown SiNWs via ICP as a competitive technique to the well-established bottom-up

• fabricate ultra-small structures. This concept encompasses the physics and the chemistry of nanostructure formation via a “self-assembly” route. Such ultra-low dimensional systems require appropriate characterization tools, which may lead to further insight in the comprehension of the dynamics of

• chamber and temperatures lower than 1150 °C can be reached at the bottom [16]. It is noteworthy to recall that the ICP process was designed for the synthesis of spherical Si particles. This leads us to suppose that, while the synthesis of spherical Si takes place, the self-assembly of SiNWs via VLS does

Methods for preparing polymer-decorated single exchange-biased magnetic nanoparticles for application in flexible polymer-based films

• Laurence Ourry,
• Delphine Toulemon,
• Souad Ammar and
• Fayna Mammeri

Beilstein J. Nanotechnol. 2017, 8, 408–417, doi:10.3762/bjnano.8.43

• hybrids, one of the main challenges is to avoid NP aggregation. The magnetic response of NPs to external magnetic stimulus depends strongly on their intrinsic properties (composition, size, and shape) but also on their spatial arrangement (self-assembly, dispersion in organic media, compatibility with

Innovations from the “ivory tower”: Wilhelm Barthlott and the paradigm shift in surface science

• Christoph Neinhuis

Beilstein J. Nanotechnol. 2017, 8, 394–402, doi:10.3762/bjnano.8.41

• compiling, to our knowledge, the largest dataset on plant epicuticular surface features. Epicuticular waxes are made up of various soluble lipids and, at least most of them, originate from self-assembly, again a topic studied in various different types of crystals accompanied by recrystallization

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

• structures with tunable morphologies for the use in drug delivery. Amphiphilic long-chain dialkylated isoindigos have the ability to form stable solid nanoparticles via a simple nanoprecipitation technique. Their self-assembly was investigated using tensiometry, dynamic light scattering, spectrophotometry

• ; nanoparticles; self-assembly; surfactants; Introduction Studies of amphiphilic isoindigo derivatives have revealed perspectives and high potential in several fields: (i) Supramolecular assemblies of amphiphilic conjugated π-systems can potentially be useful structures with improved tunable optical and

• . Drug nanostructures thus obtained are single-component systems unlike traditional colloidal drug carriers. The design of building blocks allows for the control of physical and chemical properties of self-assembled systems. Self-assembly [41] and nanoprecipitation [42] are the most common approaches to

Impact of surface wettability on S-layer recrystallization: a real-time characterization by QCM-D

• Jagoba Iturri,
• Ana C. Vianna,
• Alberto Moreno-Cencerrado,
• Dietmar Pum,
• Uwe B. Sleytr and
• José Luis Toca-Herrera

Beilstein J. Nanotechnol. 2017, 8, 91–98, doi:10.3762/bjnano.8.10

• 10 mM CaCl2 (98% Sigma-Aldrich, Germany) and adjusted to pH 9. Sample preparation S-protein preparation: After isolation, the protein solution was centrifuged at 5000 rpm for 5 min in order to separate the S-protein monomers from self-assembly products and was stored at 4 °C. Then, before each

Obtaining and doping of InAs-QD/GaAs(001) nanostructures by ion beam sputtering

• Sergei N. Chebotarev,
• Alexander S. Pashchenko,
• Leonid S. Lunin,
• Elena N. Zhivotova,
• Georgy A. Erimeev and
• Marina L. Lunina

Beilstein J. Nanotechnol. 2017, 8, 12–20, doi:10.3762/bjnano.8.2

• homoepitaxy of silicon on substrates with (001) crystallographic orientation was in parts investigated by Lee and Xue [15]. High-vacuum ion beam heteroepitaxy of nanometer-thick germanium films on silicon substrates was carried out by Alexandrov and co-workers [16]. They were the first to observe the self

• -assembly growth of germanium quantum-dot nanostructures. Furthermore, ion beam sputtering was used for heteroepitaxy of Ge on GaAs substrates [17] and GaAs1−xPx on Si substrates [18]. In addition, the effect of ion beam bombardment of semiconductor surfaces is used at least for two applications. First, it

Solvent-mediated conductance increase of dodecanethiol-stabilized gold nanoparticle monolayers

• Patrick A. Reissner,
• Jean-Nicolas Tisserant,
• Antoni Sánchez-Ferrer,
• Raffaele Mezzenga and
• Andreas Stemmer

Beilstein J. Nanotechnol. 2016, 7, 2057–2064, doi:10.3762/bjnano.7.196

• networks; Self-assembly; Introduction Ordered gold nanoparticle monolayers are increasingly applied as templates for molecular resistor networks [1][2][3][4][5][6][7][8]. Gold nanoparticles serve as conducting nodes and different molecules can bind to the gold nanoparticle using anchoring groups such as

• hexagonally ordered within grain boundaries. Small voids between grains result from the self-assembly process. We masked voids in five SEM images at different sample locations, neglecting voids smaller than 25 nm2, as an upper limit for tolerances in interparticle distance variations. On average, these voids

• monolayers undergoing liquid phase molecular exchange protocols. Solvent induced decreases in lattice constant need to be taken into account for comprehensive interpretation of the electronic measurements on nanoparticle monolayers. We showed here that self-assembly of nanoparticle monolayers on liquid phase

Effect of Anderson localization on light emission from gold nanoparticle aggregates

• Mohamed H. Abdellatif,
• Marco Salerno,
• Gaser N. Abdelrasoul,
• Ioannis Liakos,
• Alice Scarpellini,
• Sergio Marras and
• Alberto Diaspro

Beilstein J. Nanotechnol. 2016, 7, 2013–2022, doi:10.3762/bjnano.7.192

• localization is due to the increase of the radiative process in the localized field. These results suggest that by fabricating special surface patterns using electron beam lithography or by self-assembly, the localization of light can be engineered. The possibility to generate Anderson localization by control

Controlled supramolecular structure of guanosine monophosphate in the interlayer space of layered double hydroxide

• Gyeong-Hyeon Gwak,
• Istvan Kocsis,
• Yves-Marie Legrand,
• Mihail Barboiu and
• Jae-Min Oh

Beilstein J. Nanotechnol. 2016, 7, 1928–1935, doi:10.3762/bjnano.7.184

• linked through hydrogen bonds in the presence of K+ ions. There have been many attempts to synthesize guanosine-based supramolecular assemblies such as ribbon or quadruplex. Spada et al. verified that two kinds of ribbon structures could be obtained by self-assembly of lipophilic deoxyguanosine

• structures result from its self-assembly. GMP makes quadruplex structures in the presence of specific metal as found in the telomere of chromosome [16]. Without metal cations, GMPs make ribbon-type structures through hydrogen bonding between H and electronegative sites (N or O). Two kinds of ribbon phases, I

Graphene-enhanced plasmonic nanohole arrays for environmental sensing in aqueous samples

• Christa Genslein,
• Peter Hausler,
• Eva-Maria Kirchner,
• Rudolf Bierl,
• Antje J. Baeumner and
• Thomas Hirsch

Beilstein J. Nanotechnol. 2016, 7, 1564–1573, doi:10.3762/bjnano.7.150

• packed, two dimensional crystal of polymer particles needs to be formed via self-assembly by a slow evaporation process. Subsequent etching of the particles creates a void between neighbouring particles, generating a non-close packed ordered sphere monolayer. The obtained sphere mask acts as a pattern

Tunable longitudinal modes in extended silver nanoparticle assemblies

• Serene S. Bayram,
• Klas Lindfors and
• Amy Szuchmacher Blum

Beilstein J. Nanotechnol. 2016, 7, 1219–1228, doi:10.3762/bjnano.7.113

• with tunable properties are of great interest for a wide range of applications. The self-assembly of simple nanoparticle building blocks could provide an inexpensive means to achieve this goal. Here, we generate extended anisotropic silver nanoparticle assemblies in solution using controlled amounts of

• one of three inexpensive, widely available, and environmentally benign short ditopic ligands: cysteamine, dithiothreitol and cysteine in aqueous solution. The self-assembly of our extended structures is enforced by hydrogen bonding. Varying the ligand concentration modulates the extent and density of

• and aggregates based on the discrete dipole approximation. The models support the experimental findings and reveal the importance of aggregate size and shape as well as particle polarizability in the plasmon coupling between nanoparticles. Keywords: plasmon coupling; self-assembly; silver

Dielectrophoresis of gold nanoparticles conjugated to DNA origami structures

• Anja Henning-Knechtel,
• Matthew Wiens,
• Mathias Lakatos,
• Andreas Heerwig,
• Frieder Ostermaier,
• Nora Haufe and
• Michael Mertig

Beilstein J. Nanotechnol. 2016, 7, 948–956, doi:10.3762/bjnano.7.87

• Chemistry, University of Alberta, Edmonton, T6G2G2, Canada Kurt-Schwabe-Institut für Mess- und Sensortechnik Meinsberg e.V., 04736 Waldheim, Germany 10.3762/bjnano.7.87 Abstract DNA nanostructures are promising construction materials to bridge the gap between self-assembly of functional molecules and

• hybrid structures. Keywords: gold nanoparticles; dielectrophoresis; DNA nanotechnology; DNA origami; self-assembly; Introduction The DNA origami method facilitates high throughput synthesis of identical and fully addressable two- (2D) or three-dimensional (3D) nanoscaled structures [1][2][3]. Such DNA

• constructs constitute promising template structures to combine different organic and inorganic nanomaterials into tailored hybrid nanodevices, and hence, hold the potential to combine self-assembly of functional molecules with conventional fabrication methods in nanotechnology [4][5][6][7][8][9][10][11]. To

Reconstitution of the membrane protein OmpF into biomimetic block copolymer–phospholipid hybrid membranes

• Matthias Bieligmeyer,
• Franjo Artukovic,
• Stephan Nussberger,
• Thomas Hirth,
• Thomas Schiestel and
• Michaela Müller

Beilstein J. Nanotechnol. 2016, 7, 881–892, doi:10.3762/bjnano.7.80

• for the reconstitution of transmembrane proteins under preservation of protein function, independent of the membrane thickness. Keywords: biomimetics; block copolymer; lipopolymer mixture; OmpF reconstitution; self-assembly; Introduction Protein pores facilitate the transfer of molecules across

• been assessed yet [46][47]. In the present work, we studied the reconstitution of OmpF from Escherichia coli into biomimetic lipopolymer membranes, generated by self-assembly of amphiphilic poly(1,4-isoprene-block-ethylene oxide) block copolymers (PIPEO) and 1,2-diphytanoyl-sn-glycero-3-phosphocholine

• monomer-activated approach [52]. However, an incomplete initiation of the second block could be excluded as side reaction since no tailing within the size exclusion chromatography traces has been observed. Thus, effects on the self-assembly behavior of the block copolymers in aqueous solutions were not

Optical absorption signature of a self-assembled dye monolayer on graphene

• Tessnim Sghaier,
• Sylvain Le Liepvre,
• Céline Fiorini,
• Ludovic Douillard and
• Fabrice Charra

Beilstein J. Nanotechnol. 2016, 7, 862–868, doi:10.3762/bjnano.7.78

• -3,4,9,10-diimide (PTCDI); scanning tunnelling microscopy; self-assembly; self-organization; Introduction Close-packed assemblies of dye molecules exhibit drastically altered photonic properties as compared with the isolated or diluted species [1]. These changes find their origin in near-field optical

• original photonic processes. An atomically precise positioning of self-associated molecular dyes can be achieved either in vacuum or at the solution–substrate interface by self-assembly techniques. In particular, perylene-3,4,9,10-tetracarboxylic-3,4,9,10-diimide (PTCDI) and its sibling molecule perylene

• -packed PTCDA molecules deposited on epitaxial graphene have also been observed [21]. In turn, self-assembly of adsorbed conjugated molecules can influence the electronic properties of its substrate. Such a non-covalent functionalization is especially suitable in the case of graphene because of its

Direct formation of gold nanorods on surfaces using polymer-immobilised gold seeds

• Majid K. Abyaneh,
• Pietro Parisse and
• Loredana Casalis

Beilstein J. Nanotechnol. 2016, 7, 809–816, doi:10.3762/bjnano.7.72

• noble metal NRs or NWs with various techniques, such as electron-beam lithography [14][15], Langmuir–Blodgett (L–B) methods [16], stretched polymer matrices [17], self-assembly [18][19][20], and electric fields [21]. However, both direct and indirect surface-growth approaches present significant

Assembling semiconducting molecules by covalent attachment to a lamellar crystalline polymer substrate

• Rainhard Machatschek,
• Patrick Ortmann,
• Renate Reiter,
• Stefan Mecking and
• Günter Reiter

Beilstein J. Nanotechnol. 2016, 7, 784–798, doi:10.3762/bjnano.7.70

• that the overall thickness CPE45 nanocrystals does not depend solely on the thickness of the crystalline core, which is predefined by the distance between regularly spaced side-groups. Formation of monolayers of nanocrystals Self-assembly of nanocrystals at the air–water interface For electrostatically

• stabilized colloids, self-assembly at the air–water interface has been demonstrated to be an efficient route to generate close packed monolayers with virtually crystalline order up to sizes of square-centimeters [7]. While repulsive forces introduced by surfactants are often used to support the assembly

Magnetic switching of nanoscale antidot lattices

• Ulf Wiedwald,
• Joachim Gräfe,
• Kristof M. Lebecki,
• Maxim Skripnik,
• Felix Haering,
• Gisela Schütz,
• Paul Ziemann,
• Eberhard Goering and
• Ulrich Nowak

Beilstein J. Nanotechnol. 2016, 7, 733–750, doi:10.3762/bjnano.7.65

• -up techniques based on the self-assembly of nanoscale spheres [2][11][12] allow precise control over diameter and distance of the antidots. In the present work, we make use of bottom-up nanosphere lithography in combination with reactive ion etching resulting in hexagonally arranged, non-close packed

• of sphere diameters at relatively narrow size distributions. However, the control of the self-assembly process leading to optimized samples is still challenging. Figure 1 presents the entire preparation process of magnetic antidot arrays. In order to prepare such arrays on a large scale with

• self-assembly of monodisperse PS spheres on the chosen substrate; (b) the homogeneous reduction of the PS sphere diameter by setting the plasma etching time while maintaining their initial positions on the substrate. Then, the nanoscale masks are ready for the deposition of a magnetic film and a

Hierarchical coassembly of DNA–triptycene hybrid molecular building blocks and zinc protoporphyrin IX

• Rina Kumari,
• Sumit Singh,
• Mohan Monisha,
• Sourav Bhowmick,
• Anindya Roy,
• Neeladri Das and
• Prolay Das

Beilstein J. Nanotechnol. 2016, 7, 697–707, doi:10.3762/bjnano.7.62

• composite DNA nanostructures by the self-assembly of complementary symmetrical 2,6,14-triptycenetripropiolic acid (TPA)–DNA building blocks and zinc protoporphyrin IX (Zn PpIX). DNA–organic molecule scaffolds for the composite DNA nanostructure were constructed through covalent conjugation of TPA with 5

• desorption/ionization time-of-flight (MALDI-TOF). The biologically relevant photosensitizer Zn PpIX was used to direct the hybridization-mediated self-assembly of DNA–TPA molecular building blocks as well as a model guest molecule within the DNA–TPA supramolecular self-assembly. The formation of fiber-like

• therapy (PDT) applications as well as photocatalytic reactions. Keywords: DNA nanostructure; DNA–organic hybrid; DNA self-assembly; 2,6,14-triptycenetripropiolic acid; zinc protoporphyrin IX; Introduction Hybrid nanomaterials resulting from the covalent conjugation of DNA with organic molecules [1][2][3

Gold nanoparticles covalently assembled onto vesicle structures as possible biosensing platform

• M. Fátima Barroso,
• M. Alejandra Luna,
• Juan S. Flores Tabares,
• Cristina Delerue-Matos,
• N. Mariano Correa,
• Fernando Moyano and
• Patricia G. Molina

Beilstein J. Nanotechnol. 2016, 7, 655–663, doi:10.3762/bjnano.7.58

• bilayers with the aim of using this nanomaterial as platform for the future design of immunosensors. A novel methodology for the self-assembly of AuNPs onto large unilamellar vesicle structures is described. The vesicles were formed with 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) and 1-undecanethiol

• fulfil performance criteria such as high sensitivity and low limit of detection. In this context, vesicles can be used in the construction of biosensors as supporting film to coat Au or Ag electrodes [3]. Self-assembly of nanoparticles onto organised systems combines the advantages of nanomaterials

• acts as the solvent for the synthesis reaction as well as the reducing agent. Therefore, this work describes the self-assembly of AuNPs photochemically synthesized with two different irradiation times (8 and 13 min) in glycerol onto vesicle structures. After the optimization of some analytical features