Microfluidics as tool to prepare size-tunable PLGA nanoparticles with high curcumin encapsulation for efficient mucus penetration

• Nashrawan Lababidi,
• Valentin Sigal,
• Aljoscha Koenneke,
• Konrad Schwarzkopf,
• Andreas Manz and
• Marc Schneider

Beilstein J. Nanotechnol. 2019, 10, 2280–2293, doi:10.3762/bjnano.10.220

• total flow rate. Furthermore, the influence of the length of the focus mixing channel on the size was evaluated in order to better understand the nucleation–growth mechanism. Surprisingly, the channel length was revealed to have no effect on particle size for the chosen settings. In addition, curcumin

• channel, and stabilizer concentration. Furthermore, as our system allows us to cut different lengths of mixing channels, the impact of the length of the mixing channel on the nucleation–growth mechanism of the nanoprecipitation process was evaluated, which is an underestimated aspect of current

• colloidal system, thus minimizing NP agglomeration and nucleation growth [40]. Pluronic F68 was proven to be a muco-inert material [11][47] and was therefore chosen as a stabilizer. The addition of Pluronic F68 (1%) resulted in a slight decrease of the NP diameter to ≈70 nm at 0.05 flow rate ratio in

Nanostructured and oriented metal–organic framework films enabling extreme surface wetting properties

• Andre Mähringer,
• Julian M. Rotter and
• Dana D. Medina

Beilstein J. Nanotechnol. 2019, 10, 1994–2003, doi:10.3762/bjnano.10.196

• the VAC process, namely the surface roughness and the crystallite orientation on the substrate. Antifog coating with MOF films Water condensation on surfaces is a known phenomenon occurring at the dew point on substrates such as glass, which serves as a favorable nucleation site for water droplets

• surface is expected to form, hindering the nucleation of water droplets on the glass surface. For this purpose, we employed the newly developed methodology for the synthesis of nanostructured Ni-CAT-1 films on gold substrates with a slightly modified synthesis procedure in order to address larger

• examine the behavior of the antifog coating under extreme temperature differences, the MOF-modified glass substrates were cooled down to −20 °C and subsequently placed on top of the hot water reservoir. Under all examined conditions, clear vision through the glass was maintained and water vapor nucleation

Porous silver-coated pNIPAM-co-AAc hydrogel nanocapsules

• William W. Bryan,
• Riddhiman Medhi,
• Maria D. Marquez,
• Supparesk Rittikulsittichai,
• Michael Tran and
• T. Randall Lee

Beilstein J. Nanotechnol. 2019, 10, 1973–1982, doi:10.3762/bjnano.10.194

• silver nanocapsules with pNIPAM-co-AAc hydrogel cores. The Au nanoparticles act as nucleation sites (templating agents) for the growth of the Ag shells. Without these templating agents, the core–shell particles fail to form, leading to the exclusive formation of free metal particles and aggregated

• . However, the surface morphology of the porous nanoshells is rough (see Figure 4b). Possible reasons for the roughness include destabilizing intercalation of the salt precursor into the polymer matrix and insufficient nucleation sites, leading to lengthy time periods needed for nanocapsule growth. To

Oblique angle deposition of nickel thin films by high-power impulse magnetron sputtering

• Hamidreza Hajihoseini,
• Movaffaq Kateb,
• Snorri Þorgeir Ingvarsson and
• Jon Tomas Gudmundsson

Beilstein J. Nanotechnol. 2019, 10, 1914–1921, doi:10.3762/bjnano.10.186

• grow on existing columns or repeated nucleation occurs. As the peak discharge current density was increased further to JD,peak = 4 A/cm2 they observed that a film with a featureless morphology developed. Smaller grain sizes in HiPIMS-deposited films than in dcMS-deposited films have been previously

Fabrication and characterization of Si_1−xGe_x nanocrystals in as-grown and annealed structures: a comparative study

• Muhammad Taha Sultan,
• Adrian Valentin Maraloiu,
• Ionel Stavarache,
• Jón Tómas Gudmundsson,
• Andrei Manolescu,
• Valentin Serban Teodorescu,
• Magdalena Lidia Ciurea and
• Halldór Gudfinnur Svavarsson

Beilstein J. Nanotechnol. 2019, 10, 1873–1882, doi:10.3762/bjnano.10.182

• measurements, to explore structural changes and corresponding properties. It is observed that the employment of HiPIMS facilitates the formation of SiGe nanoparticles (2.1 ± 0.8 nm) in the as-grown structure, and that presence of such nanoparticles acts as a seed for heterogeneous nucleation, which upon

• crystals upon annealing. A similar phenomenon may have occurred in our structures, as depicted in Figure 4 and Figure 5. Thus, we can anticipate heterogeneous nucleation to be a dominant process during crystallization rather than conventional homogenous nucleation. This can be due to a better wetting of

• SiGe layer, which in turn reduces the nucleation barrier. It can also be argued that since heterogeneous nucleation occurs at preferential sites (as in our case), small NCs in as-grown MLs or even the crystallites that are under strain [39][40][41][42] will further reduce the surface energy and

Synthesis of nickel/gallium nanoalloys using a dual-source approach in 1-alkyl-3-methylimidazole ionic liquids

• Ilka Simon,
• Julius Hornung,
• Juri Barthel,
• Jörg Thomas,
• Maik Finze,
• Roland A. Fischer and
• Christoph Janiak

Beilstein J. Nanotechnol. 2019, 10, 1754–1767, doi:10.3762/bjnano.10.171

• reduce the Ga3+ precursor, working as a nucleation center for the Ga atoms and prevent uncontrolled coagulation of the liquid metal. Through annealing, the single-phase products can be obtained [27][42]. The all-hydrocarbon precursor GaCp* (Cp* = pentamethylcyclopentadienyl), with the Ga atom in the

Hierarchically structured 3D carbon nanotube electrodes for electrocatalytic applications

• Pei Wang,
• Katarzyna Kulp and
• Michael Bron

Beilstein J. Nanotechnol. 2019, 10, 1475–1487, doi:10.3762/bjnano.10.146

• method allows adjustment of nucleation and growth potential to control the distribution and size of the Fe nanoparticles. A nucleation potential of −1.41 V vs Ag|AgCl|KClsat. and a growth potential of −1.27 V vs Ag|AgCl|KClsat. were applied (compare also Figure S1, Supporting Information File 1). Figure

• . Additionally, the Fe nanoparticles seem to prefer to nucleate on cross junctions between primary CNTs, as observed from Figure S3a, which could be caused by improvement of electron transfer or preferential nucleation sites. The growth of secondary CNTs using the same optimized gas mixture as above and a gas

• transfer resistance with respect to the primary CNTs as determined by electrochemical impedance spectroscopy. Thus, we speculate that the improvement in Pt dispersion is due to a better conductivity within the 3D network and a facilitated electron transfer, which may facilitate Pt nucleation at the CNT

Alloyed Pt₃M (M = Co, Ni) nanoparticles supported on S- and N-doped carbon nanotubes for the oxygen reduction reaction

• Stéphane Louisia,
• Yohann R. J. Thomas,
• Pierre Lecante,
• Marie Heitzmann,
• M. Rosa Axet,
• Pierre-André Jacques and
• Philippe Serp

Beilstein J. Nanotechnol. 2019, 10, 1251–1269, doi:10.3762/bjnano.10.125

• due to the presence of different functional groups at the surface of the CNTs, while un-doped CNTs are relatively inert. With nitrogen or sulfur groups acting as nucleation centers, the distribution of NPs on the CNT walls is better on N-CNTs and S-CNTs than on CNTs. A decrease of the nitrogen content

Green fabrication of lanthanide-doped hydroxide-based phosphors: Y(OH)₃:Eu³⁺ nanoparticles for white light generation

• Tugrul Guner,
• Anilcan Kus,
• Mehmet Ozcan,
• Aziz Genc,
• Hasan Sahin and
• Mustafa M. Demir

Beilstein J. Nanotechnol. 2019, 10, 1200–1210, doi:10.3762/bjnano.10.119

• and TEM images (Figure 1c and Figure 2). The growth mechanism that governs almost the entire nucleation and crystal growth process here was reported already by Hussain et al. [52] in detail, where the authors employed hexamethylenetetramine (HMTA) during the fabrication of La(OH)3:Eu3+ crystals. HMTA

• formed as in a needle-like shape. Such a fast crystal formation may indicate fast nucleation, and here (which is similar to the idea proposed by Hussain et al. [52] where the authors argued that the excessive NH4+ ions may accelerate the reaction between La3+ and OH−), excessive Li+ ions in the reaction

Pure and mixed ordered monolayers of tetracyano-2,6-naphthoquinodimethane and hexathiapentacene on the Ag(100) surface

• Robert Harbers,
• Timo Heepenstrick,
• Dmitrii F. Perepichka and
• Moritz Sokolowski

Beilstein J. Nanotechnol. 2019, 10, 1188–1199, doi:10.3762/bjnano.10.118

• center of the TNAP molecules, possibly related to the comparably electron-rich aromatic core of the molecule. At lower coverages, the nucleation of small TNAP islands (below 50 nm in diameter) at step edges and on terraces was observed. Hardly any mobile molecules could be found between the islands, as

Tailoring the magnetic properties of cobalt ferrite nanoparticles using the polyol process

• Malek Bibani,
• Romain Breitwieser,
• Alex Aubert,
• Vincent Loyau,
• Silvana Mercone,
• Souad Ammar and
• Fayna Mammeri

Beilstein J. Nanotechnol. 2019, 10, 1166–1176, doi:10.3762/bjnano.10.116

• lower for TriEG but not so much regarding the boiling points of the two polyols. Considering the very probable hypothesis that particle nucleation proceeds when the boiling temperature of the reaction medium is reached (leading to the lowest viscosity), one can expect the formation of much more nuclei

A highly efficient porous rod-like Ce-doped ZnO photocatalyst for the degradation of dye contaminants in water

• Binjing Hu,
• Qiang Sun,
• Chengyi Zuo,
• Yunxin Pei,
• Siwei Yang,
• Hui Zheng and
• Fangming Liu

Beilstein J. Nanotechnol. 2019, 10, 1157–1165, doi:10.3762/bjnano.10.115

• affects the formation of ZIF-8. More specifically, it undergoes three main stages: gel formation, nucleation and crystallization [23]. According to Mahmoud’s [35] report, the Ce element which is doped into the lattice of Zn seeds may lower the surface energy, thus leading to a new morphology. Labhane et

In situ AFM visualization of Li–O₂ battery discharge products during redox cycling in an atmospherically controlled sample cell

• Kumar Virwani,
• Younes Ansari,
• Khanh Nguyen,
• Francisco José Alía Moreno-Ortiz,
• Jangwoo Kim,
• Maxwell J. Giammona,
• Ho-Cheol Kim and
• Young-Hye La

Beilstein J. Nanotechnol. 2019, 10, 930–940, doi:10.3762/bjnano.10.94

• those formed due to nucleation on the surface of glassy carbon grow in volume while fresh nucleation and growth of toroidal structures continues on all areas. The total discharge capacity of the cell was measured to be 11.6 µAh. Upon completion of discharge, the cell was allowed to rest at open-circuit

• of electrochemical deposits from solution and nucleation and growth of smaller deposits on the surface of the glassy carbon during discharge. Complementarily, the sudden disappearance of the electrochemical deposits during recharge occurs in a small voltage window of 4.25 V (14% SOC) to 4.35 V (18

• concentration was further increased to ≈4600 ppm. A similar sudden appearance of electrochemical deposits on the surface followed by further nucleation and growth during discharge and disappearance during recharge was also measured with a corresponding increase in the cell capacity to about 24 µAh (Movie 3

Fabrication of silver nanoisland films by pulsed laser deposition for surface-enhanced Raman spectroscopy

• Bogusław Budner,
• Mariusz Kuźma,
• Barbara Nasiłowska,
• Bartosz Bartosewicz,
• Malwina Liszewska and
• Bartłomiej J. Jankiewicz

Beilstein J. Nanotechnol. 2019, 10, 882–893, doi:10.3762/bjnano.10.89

•  2C) is also visible. After 8000 laser pulses, the embedded silver islands are already that large that almost all of them are connected and a semicontinuous layer with an irregular structure is formed (Figure 2D). After 16000 laser pulses the nucleation and growth of silver nanoislands occurs on the

An iridescent film of porous anodic aluminum oxide with alternatingly electrodeposited Cu and SiO₂ nanoparticles

• Menglei Chang,
• Huawen Hu,
• Haiyan Quan,
• Hongyang Wei,
• Zhangyi Xiong,
• Jiacong Lu,
• Pin Luo,
• Yaoheng Liang,
• Jianzhen Ou and
• Dongchu Chen

Beilstein J. Nanotechnol. 2019, 10, 735–745, doi:10.3762/bjnano.10.73

• simultaneous way, into a stable structure possessing a regular geometric appearance. In contrast, electrodeposition involves the nucleation at an electrode surface under the action of an electric field [25]. For example, a high-purity aluminum foil was directly used as a template, on which anodic aluminum

Deposition of metal particles onto semiconductor nanorods using an ionic liquid

• Michael D. Ballentine,
• Elizabeth G. Embry,
• Marco A. Garcia and
• Lawrence J. Hill

Beilstein J. Nanotechnol. 2019, 10, 718–724, doi:10.3762/bjnano.10.71

• potential to impact a number of applications [1][2][3][4]. Deposition of metal nanoparticles onto the nanorod surface competes with homogeneous nucleation of the metal nanoparticles, with the size and number of metal nanoparticles attached to each nanorod controlled by lattice matching of the materials and

• ][15][16][17]. The low surface tension of ionic liquids causes high nucleation rates and allows for the synthesis of small nanoparticles with minimal Ostwald ripening [17]. Further, many ionic liquids consist of a large anion with diffuse negative charge; this lack of strongly binding anionic ligands

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

• ) Sequential AFM images depicting the dynamics of self-assembled CTAB stripes on terraces; for reference, a defect which acts as a vacancy nucleation site is indicated by the white arrows. (E) After the large stripes have completely disappeared, a corrugation of the surface is still observed; the inset depicts

Ultrasonication-assisted synthesis of CsPbBr₃ and Cs₄PbBr₆ perovskite nanocrystals and their reversible transformation

• Longshi Rao,
• Xinrui Ding,
• Xuewei Du,
• Guanwei Liang,
• Yong Tang,
• Kairui Tang and
• Jin Z. Zhang

Beilstein J. Nanotechnol. 2019, 10, 666–676, doi:10.3762/bjnano.10.66

• transformation into Cs4PbBr6 PNCs. This process is related to Ostwald ripening that was found during the nucleation and growth of PNCs [42]. Therefore, the formation of Cs4PbBr6 PNCs is promoted by the capacity of the organic ligands to dissolve PbBr2 and by the dissociation of CsPbBr3 PNCs. A series of TEM

Hydrophilicity and carbon chain length effects on the gas sensing properties of chemoresistive, self-assembled monolayer carbon nanotube sensors

• Juan Casanova-Cháfer,
• Carla Bittencourt and
• Eduard Llobet

Beilstein J. Nanotechnol. 2019, 10, 565–577, doi:10.3762/bjnano.10.58

• oxygen plasma treatment. However, the presence of such defects in CNTs is essential, since it has been shown that they play the role of nucleation centers and help to anchor the Au nanoparticles during the sputtering process [36]. In other words, the defects help to achieve a dense and homogenous

• nucleation centers for the anchoring the Au NPs) was conducted using XPS. The chemical modification caused by the plasma treatment results in the presence of hydroxy, carbonyl and carboxyl groups [36]. Furthermore, Au nucleation centers occur mainly in the proximity of oxygenated defects created during the

• need to be subsequently decorated with Au nanoparticles. Oxygenated defects act as anchoring and nucleation sites. Therefore, high control in the decoration homogeneity and the size of Au nanoparticles (avoiding coalescence effects) have been reported in oxygen-plasma-treated CNTs [37]. Since

Direct observation of the CVD growth of monolayer MoS₂ using in situ optical spectroscopy

• Claudia Beatriz López-Posadas,
• Yaxu Wei,
• Wanfu Shen,
• Daniel Kahr,
• Michael Hohage and
• Lidong Sun

Beilstein J. Nanotechnol. 2019, 10, 557–564, doi:10.3762/bjnano.10.57

• and have inspired many theoretical discussions about the growth mechanisms, they were still unable to provide a clear path to the full understanding of the growth mechanisms [10][15][16][17][18][19]. Several recent efforts aiming at manipulating the nucleation and growth of 2D TMDCs have successfully

• the morphology and crystalline structure of the films. By systematic study using in situ optical spectroscopy assisted with other ex situ characterization techniques, the details of the kinetics including adsorption, dissociation, reaction, nucleation, and growth can be revealed. Differential

Ceria/polymer nanocontainers for high-performance encapsulation of fluorophores

• Kartheek Katta,
• Dmitry Busko,
• Yuri Avlasevich,
• Katharina Landfester,
• Stanislav Baluschev and
• Rafael Muñoz-Espí

Beilstein J. Nanotechnol. 2019, 10, 522–530, doi:10.3762/bjnano.10.53

• group [10][12]. The regular arrangement of functional groups on the nanocapsule surface can provide nucleation and structure-directing centers for the controlled crystallization of metal-oxide particles. We have chosen cerium(IV) oxide nanoparticles to be deposited on the nanocapsule surface in order to

Polymorphic self-assembly of pyrazine-based tectons at the solution–solid interface

• Achintya Jana,
• Puneet Mishra and
• Neeladri Das

Beilstein J. Nanotechnol. 2019, 10, 494–499, doi:10.3762/bjnano.10.50

• between thermodynamic and kinetic effects. During the growth process, kinetic parameters such as nucleation rates and growth rates for each polymorph play a crucial role in determining the arrangement of the molecules on the surface [27]. Non-equilibrium polymorphs can form on the surface provided they

• have faster nucleation or growth rate than the equilibrium structure. Typically such phases are promoted by stronger intermolecular interactions [28]. Availability of additional hydrogen-bonding sites, as discussed previously, thus favors faster nucleation and growth of polymorph II. Once such

Advanced scanning probe lithography using anatase-to-rutile transition to create localized TiO₂ nanorods

• Julian Kalb,
• Vanessa Knittel and
• Lukas Schmidt-Mende

Beilstein J. Nanotechnol. 2019, 10, 412–418, doi:10.3762/bjnano.10.40

• anatase film. In addition, silicon nanoparticles being scraped off the AFM tip might act as nucleation sites such as other dirt particles appearing in the growth solution. However, the absence of nanorods on SiO2 indicates that the growth of rutile nanorods is not triggered by silicon nanoparticles. It

Sub-wavelength waveguide properties of 1D and surface-functionalized SnO₂ nanostructures of various morphologies

• Venkataramana Bonu,
• Binaya Kumar Sahu,
• Arindam Das,
• Sankarakumar Amirthapandian,
• Sandip Dhara and
• Harish C. Barshilia

Beilstein J. Nanotechnol. 2019, 10, 379–388, doi:10.3762/bjnano.10.37

• thermodynamically by considering the Gibbs energy as a measure of structural phase transformation [8]. During VLS growth, the formation of nucleation from the saturated catalyst (Au) is the important step for the shape and structure. As reported earlier, the difference in the Gibbs energy promotes the phase

• transition between two competing phases at the nucleation stage itself and is found to control square and cylindrical shapes [8]. Considering a rectangular shape nucleus for square-shaped NWs (Figure 5a) and a circular-shaped nucleus for cylindrical NWs (Figure 5b), the difference in Gibbs free energy can be

• appropriate value it can be shown that = 2.48 ≈ 1.24(2). After nucleation, a continuous supply of precursor led to axial as well as radial growth. Kwon et al. [21] has shown that axial growth is more favorable than the radial growth and the growth continues until the aspect ratio reaches its limit. However

A Ni(OH)₂ nanopetals network for high-performance supercapacitors synthesized by immersing Ni nanofoam in water

• Donghui Zheng,
• Man Li,
• Yongyan Li,
• Chunling Qin,
• Yichao Wang and
• Zhifeng Wang

Beilstein J. Nanotechnol. 2019, 10, 281–293, doi:10.3762/bjnano.10.27

• flower-like structures may arise from nucleation and coalescence processes [32]. The thickness of the nanopetals rises with immersion time from 0.5 μm (inset of Figure 2b) over 1.0 μm (inset of Figure 2c) to 1.5 μm (inset of Figure 2c). We can see from Figure 2f–h that the curly Ni(OH)2 nanopetals