Nickel nanoparticle-decorated reduced graphene oxide/WO₃ nanocomposite – a promising candidate for gas sensing

• Ilka Simon,
• Alexandr Savitsky,
• Rolf Mülhaupt,
• Vladimir Pankov and
• Christoph Janiak

Beilstein J. Nanotechnol. 2021, 12, 343–353, doi:10.3762/bjnano.12.28

• 99.996 vol %) atmosphere by using standard Schlenk techniques. Samples were prepared and stored in a MBraun Glovebox. Solvents (acetonitrile, n-hexane, and methylene chloride) were dried by using a MBraun solvent purification system or distilled (1-methylimidazole and 1-chlorobutane) and stored over 4 Å

Differences in surface chemistry of iron oxide nanoparticles result in different routes of internalization

• Barbora Svitkova,
• Vlasta Zavisova,
• Veronika Nemethova,
• Martina Koneracka,
• Miroslava Kretova,
• Filip Razga,
• Monika Ursinyova and
• Alena Gabelova

Beilstein J. Nanotechnol. 2021, 12, 270–281, doi:10.3762/bjnano.12.22

• characteristics of these nanoparticles in the solvent and culture medium are shown in Table 1. Dynamic light scattering (DLS) Particle size distribution and zeta potential of the surface-modified MNPs in stock solution and culture medium were determined by DLS using a Zetasizer Nano-ZS (Malvern Instruments, UK

Gold(I) N-heterocyclic carbene precursors for focused electron beam-induced deposition

• Cristiano Glessi,
• Aya Mahgoub,
• Cornelis W. Hagen and
• Mats Tilset

Beilstein J. Nanotechnol. 2021, 12, 257–269, doi:10.3762/bjnano.12.21

• unless specified otherwise. NMR spectra were recorded on Bruker Advance DPX200, DPX300, AVII400, AVIII400 and AVII600 instruments at ambient temperature. 1H and 13C NMR spectra were referenced relative to the residual solvent system (CD2Cl2). 19F NMR spectra were referenced to hexafluorobenzene (−164.9

• . [(Cl,Et)AuBr] (4): A solution of 2 (100.6 mg, 0.24 mmol, 1 equiv) and LiBr (211.6 mg, 2.4 mmol, 10 equiv) in dried acetone (10 mL) was stirred in the dark under Ar for 20 h. Solvent was removed by rotary evapouration and the resulting white solid was partially dissolved in dichloromethane (DCM) and

• analysis: calcd. for C7H10AuBrCl2N2: C, 17.89; H, 2.14; N, 5.96; found: C, 17.76; H, 2.13; N, 5.82%. [(Cl,Et)AuI] (5): A suspension of 2 (100.3 mg, 0.24 mmol, 1 equiv) and NaI (358.2 mg, 2.4 mmol, 10 equiv) in dried acetone (10 mL) was stirred in the dark under Ar for 20 h. Solvent was removed by rotary

A review on the green and sustainable synthesis of silver nanoparticles and one-dimensional silver nanostructures

• Sina Kaabipour and
• Shohreh Hemmati

Beilstein J. Nanotechnol. 2021, 12, 102–136, doi:10.3762/bjnano.12.9

• . Another physical method widely used for the synthesis of AgNPs is the arc discharge method. In this method, two electrodes – a cathode and an anode – are connected in a high current DC circuit and submerged in a solvent – mostly deionized water – to run the process [129][131]. These electrodes can be

• ]. In the sol–gel method, a gel-like mixture is first prepared by mixing the silver precursor solution with a metal complex compound (i.e. comprised of Ca, Ti, Sr, etc.) [143][144] in a solvent such as water or alcohol. Then the product is heated in order for the nucleation and reaction to take place

• –gel technique at 100 °C and produced particles with an average diameter of 25 nm with hexagonal cross section. In the sol–gel process, besides temperature and gel composition, the solvent plays an important role in determining the size, morphology, and surface characteristics of the synthesized AgNPs

Fusion of purple membranes triggered by immobilization on carbon nanomembranes

• René Riedel,
• Natalie Frese,
• Fang Yang,
• Martin Wortmann,
• Raphael Dalpke,
• Daniel Rhinow,
• Norbert Hampp and
• Armin Gölzhäuser

Beilstein J. Nanotechnol. 2021, 12, 93–101, doi:10.3762/bjnano.12.8

• between the capacitor plates using a syringe. For an incubation time of 5 min, a voltage of 5 V was applied, and then the drop was removed. Since the substrate was not completely dry after removal of the solvent, it was found that the surface tension pulls the deposited patches apart forming quasi

Unravelling the interfacial interaction in mesoporous SiO₂@nickel phyllosilicate/TiO₂ core–shell nanostructures for photocatalytic activity

• Bridget K. Mutuma,
• Xiluva Mathebula,
• Isaac Nongwe,
• Bonakele P. Mtolo,
• Boitumelo J. Matsoso,
• Rudolph Erasmus,
• Zikhona Tetana and
• Neil J. Coville

Beilstein J. Nanotechnol. 2020, 11, 1834–1846, doi:10.3762/bjnano.11.165

• 20 min. TEOS (10 mL) was added to the solvent mixture, and the solution was stirred further at room temperature for 4 h. C18-TMS (2 mL) together with 5 mL of TEOS were thereafter added to the reaction mixture and the solution was stirred for 24 h [81]. The resulting product was centrifuged at 5000

Nanocasting synthesis of BiFeO₃ nanoparticles with enhanced visible-light photocatalytic activity

• Thomas Cadenbach,
• Maria J. Benitez,
• A. Lucia Morales,
• Cesar Costa Vera,
• Luis Lascano,
• Francisco Quiroz,
• Alexis Debut and
• Karla Vizuete

Beilstein J. Nanotechnol. 2020, 11, 1822–1833, doi:10.3762/bjnano.11.164

• . The phase purity of the product depends on the type of carboxylic acid used in the synthesis of the metal precursors, the type of solvent in the wet impregnation process, and the calcination procedure. By using tartaric acid in the synthesis of the metal precursors, acidified 2-methoxyethanol in the

• -15 in Supporting Information File 1. The influence of different complexing agents was investigated using slightly acidified H2O as a solvent. In a typical experiment, 1.010 g (2.5 mmol) of Fe(NO3)3·9H2O, 1.249 g (2.58 mmol) of Bi(NO3)3·5H2O, and 2.5 mmol of the respective organic acid were dissolved

• in 30 mL of HNO3-acidified water at pH 3. After stirring the solution for 4 h at room temperature the solvent was removed by evaporation using a membrane pump vacuum on a rotary evaporator at 75 °C. Then, the sample was dried for 16 h in a ventilated oven at 75 °C until a dry powder was obtained

Electron beam-induced deposition of platinum from Pt(CO)₂Cl₂ and Pt(CO)₂Br₂

• Aya Mahgoub,
• Hang Lu,
• Rachel M. Thorman,
• Konstantin Preradovic,
• Titel Jurca,
• Lisa McElwee-White,
• Howard Fairbrother and
• Cornelis W. Hagen

Beilstein J. Nanotechnol. 2020, 11, 1789–1800, doi:10.3762/bjnano.11.161

• temperature under N2 for six additional hours, during which the black suspension became a dark purple solution. Anhydrous n-heptane (30 mL) was added into the solution and the flask was stored in the freezer overnight. The product was obtained as pale white crystals. The solvent was removed by cannulation and

• suspension was transferred into a Schlenk flask and the solvent was removed on a Schlenk line. A light yellow solid (0.47 g, yield 80%) was collected after purification by sublimation at 30–35 °C at 125 ± 1 mTorr. The compound was identified by comparison to literature data [25]. 13C NMR (CDCl3): δ 152.34

Out-of-plane surface patterning by subsurface processing of polymer substrates with focused ion beams

• Serguei Chiriaev,
• Luciana Tavares,
• Vadzim Adashkevich,
• Arkadiusz J. Goszczak and
• Horst-Günter Rubahn

Beilstein J. Nanotechnol. 2020, 11, 1693–1703, doi:10.3762/bjnano.11.151

• spin coater, in the same manner described in [4]. After the deposition, the samples were annealed at 200 °C for 90 s to remove solvent residuals. The PDMS polymer used was a two-component Dow Sylgard™184 silicone elastomer with a hardness value of 43 in the Durometer Shore scale. After mixing the

Electrokinetic characterization of synthetic protein nanoparticles

• Daniel F. Quevedo,
• Cody J. Lentz,
• Adriana Coll de Peña,
• Yazmin Hernandez,
• Nahal Habibi,
• Rikako Miki,
• Joerg Lahann and
• Blanca H. Lapizco-Encinas

Beilstein J. Nanotechnol. 2020, 11, 1556–1567, doi:10.3762/bjnano.11.138

• synthetic protein nanoparticles SPNPs were synthesized using a modification of the well-established EHD co-jetting technique [51][52][53]. Generally, SPNPs are generated by dissolving a protein of interest and a copolymer of choice into a co-solvent system of water and an organic solvent, such as ethanol or

Cu₂O nanoparticles for the degradation of methyl parathion

• Juan Rizo,
• David Díaz,
• Benito Reyes-Trejo and
• M. Josefina Arellano-Jiménez

Beilstein J. Nanotechnol. 2020, 11, 1546–1555, doi:10.3762/bjnano.11.137

• deionized water. Preparation of Cu2O NPs For the preparation of Cu2O nanoparticles Benedict’s reagent was used [35], with the variation of a water/dimethyl sulfoxide (DMSO) solvent mixture in order to obtain different NPs sizes. The modified Benedict’s reagent was prepared as follows: In 50 mL of distilled

• and consequently methyl parathion is also removed and therefore absent in the NMR spectra. Figure 6 is the 1H NMR spectrum of the degradation products obtained with Cu2O NPs of 29 nm using D2O as solvent. The chemical shifts at 6.8 and 8.1 ppm belong to the coupled protons (d, J = 9 Hz) of 4

• -nitrophenol. The peaks at 3.45 and 3.48 ppm are the methyl groups of phosphate, which show coupling to phosphorous, and the peak at 4.65 ppm is due to the HDO produced by the deuterium interchange with the hydroxyl group of 4-nitrophenol. D2O was used as solvent for 1H NMR instead, of CDCl3 like in 31P NMR

Self-assembly and spectroscopic fingerprints of photoactive pyrenyl tectons on hBN/Cu(111)

• Domenik M. Zimmermann,
• Knud Seufert,
• Luka Ðorđević,
• Tobias Hoh,
• Sushobhan Joshi,
• Tomas Marangoni,
• Davide Bonifazi and
• Willi Auwärter

Beilstein J. Nanotechnol. 2020, 11, 1470–1483, doi:10.3762/bjnano.11.130

• fluorescence quantum yields were then calculated according to Equation 1: Therein, I is the measured integrated fluorescence emission intensity, η is the refractive index of the solvent, and ϕ is the quantum yield. Computational methods DFT calculations were performed using the Gaussian 09 (Revision D.01

• Information File 1). b) Time-dependent DFT (TDDFT)-calculated excitation energy in explicit solvent reflecting the UV–vis measurements in toluene solution (see Tables S1–S3). The units are in Volt. P: pore area, W: wire area. High-resolution STM images revealing the bias-dependent intramolecular contrast of

• oscillator strengths (f), as determined by TDDFT (CAM-B3LYP, 6-31G**, explicit solvent: toluene). Supporting Information Supporting Information File 137: Additional computational results (including electronic transitions, electrostatic potential, Cartesian coordinates of optimized structures) and additional

Antimicrobial metal-based nanoparticles: a review on their synthesis, types and antimicrobial action

• Matías Guerrero Correa,
• Fernanda B. Martínez,
• Cristian Patiño Vidal,
• Camilo Streitt,
• Juan Escrig and
• Carol Lopez de Dicastillo

Beilstein J. Nanotechnol. 2020, 11, 1450–1469, doi:10.3762/bjnano.11.129

• stabilizer or protective agent [42]. Occasionally, a catalyst can be added to accelerate the reaction, as well as a solvent, which can favor the interaction of the chemicals. As an example, we highlight the work of Wang et al. in which well-dispersed spherical nanoparticles with sizes ranging from 20 to 80

• temperature well above their boiling point, facilitating the interaction of the precursors during synthesis. Some examples are Y2O3 [58] and ZnO [59] nanoparticles with different morphologies and sizes. When water is used as the solvent, the method is called the hydrothermal technique, which is an easy and

Growth of a self-assembled monolayer decoupled from the substrate: nucleation on-command using buffer layers

• Robby Reynaerts,
• Kunal S. Mali and
• Steven De Feyter

Beilstein J. Nanotechnol. 2020, 11, 1291–1302, doi:10.3762/bjnano.11.113

• understanding of this already enigmatic process is further impaired by the nature of the solution–solid interface. A number of factors such as the temperature [6][7][8][9], the solvent [10][11][12][13][14][15], the substrate [16][17][18] and the concentration of the building block in solution [19][20][21][22

• proposed molecular model (red and green circles, Figure 2h). Due to this shift, the two (parallel) dimers with a different propagation direction are closer to each other. The molecular model also reveals that the space between four benzene rings may host a molecule of solvent adsorbed edge-on (black arrow

Role of redox-active axial ligands of metal porphyrins adsorbed at solid–liquid interfaces in a liquid-STM setup

• Thomas Habets,
• Sylvia Speller and
• Johannes A. A. W. Elemans

Beilstein J. Nanotechnol. 2020, 11, 1264–1271, doi:10.3762/bjnano.11.110

• single-molecule level, employing scanning tunneling microscopy (STM) [7][8][9]. Since our aim was to stay as close as possible to the laboratory conditions at which catalysis takes place (typically in an organic solvent under ambient conditions), we carried out our STM studies at a solid–liquid interface

• varying the experimental conditions in terms of type of substrate, solvent, solute, and concentration of the solute, we will demonstrate that the ligand can in fact be involved in redox processes in the liquid-STM setup. Results and Discussion One of the possible mechanisms for axial ligand dissociation

• no direct metal atom coordination from the substrate is possible. To our surprise we found a strong influence of the solvent on the success of imaging the molecules with STM. When n-tetradecane was used as the solvent, monolayers of MnTUPCl readily formed on Au(111) (Figure 1c), while poorly

Gas sorption porosimetry for the evaluation of hard carbons as anodes for Li- and Na-ion batteries

• Yuko Matsukawa,
• Fabian Linsenmann,
• Maximilian A. Plass,
• George Hasegawa,
• Katsuro Hayashi and
• Tim-Patrick Fellinger

Beilstein J. Nanotechnol. 2020, 11, 1217–1229, doi:10.3762/bjnano.11.106

• market share of HC and graphite was still 52% and 43%, respectively, and today graphite is almost exclusively used as negative electrode material in commercial LIBs [11]. Graphite with an interlayer distance of 0.335 nm cannot be intercalated by sodium without solvent co-intercalation [9][12][13

• either the reversible or the irreversible capacity [25]. Pores that can be accessed by solvent molecules of the electrolyte will contribute to the irreversible capacity, while smaller ones are suitable for the adsorption of alkali metal ions protected from side reactions with solvent molecules from the

• –electrolyte interphase, HCs can act as molecular sieves. Here, Na ions are adsorbed in the pores in a metal-plating-like mechanism and separated from bigger solvent molecules that suffer from electrochemical reductive decomposition at potentials below ca. 0.8 VLi or towards the alkali metal, respectively

Thermophoretic tweezers for single nanoparticle manipulation

• Jošt Stergar and
• Natan Osterman

Beilstein J. Nanotechnol. 2020, 11, 1126–1133, doi:10.3762/bjnano.11.97

• refraction between the particle and the surrounding solvent is also required. For manipulation of smaller particles and molecules, typically, electrophoretic [4] and electrokinetic [5] forces are used, but they need sophisticated electrode geometries. A combination of optical tweezers and an array of

• , diffusion coefficient D = kBT/6πηa, and thermodiffusion coefficient DT = STD (here ST is the Soret coefficient) in a solvent of viscosity η we dynamically created high-temperature gradients. To limit diffusion of the particle, one has to create an appropriate temperature gradient ∇T to produce a

Straightforward synthesis of gold nanoparticles by adding water to an engineered small dendrimer

• Sébastien Gottis,
• Régis Laurent,
• Vincent Collière and
• Anne-Marie Caminade

Beilstein J. Nanotechnol. 2020, 11, 1110–1118, doi:10.3762/bjnano.11.95

• , yielding compound 3 as a white powder. The 31P NMR spectra of compound 3 were different depending on the solvent used. When D2O was used as the solvent, only the expected set of doublets was observed (21.3 (P=N) ppm and 50.6 (P=S) ppm, JPP = 29 Hz, Figure S5, Supporting Information File 1). However, when

• DMSO was the solvent used, several sets of doublets were observed within the same region (Supporting Information File 1, Figure S6) presumably due to the presence of both the Z and E-isomers of the hydrazones [51]. These isomers were also detected in the 1H NMR spectra as two signals corresponding to

• the CH=N groups (8.13 ppm and 8.42 ppm) when DMSO was used as the solvent. The reaction completion was confirmed by the disappearance of the signal corresponding to the aldehydes in the 1H and 13C NMR spectra. The presence of isomers resulting from the CH=N–NHC(O)CH2NMe3 linkage was confirmed in the

Applications of superparamagnetic iron oxide nanoparticles in drug and therapeutic delivery, and biotechnological advancements

• Maria Suciu,
• Corina M. Ionescu,
• Alexandra Ciorita,
• Septimiu C. Tripon,
• Dragos Nica,
• Hani Al-Salami and
• Lucian Barbu-Tudoran

Beilstein J. Nanotechnol. 2020, 11, 1092–1109, doi:10.3762/bjnano.11.94

• also measures the layer of solvent and solutes permanently or transiently retained on the nanoparticle surface. For example, ultrasmall SPIONs of 10 nm or less (synthesis dimension) can measure a hydrodynamic diameter of 300 nm in water when uncoated, and around 100–150 nm when functionalized. If the

Microwave-induced electric discharges on metal particles for the synthesis of inorganic nanomaterials under solvent-free conditions

• Vijay Tripathi,
• Harit Kumar,
• Anubhav Agarwal and
• Leela S. Panchakarla

Beilstein J. Nanotechnol. 2020, 11, 1019–1025, doi:10.3762/bjnano.11.86

• ]. However, the microwave discharge technique, which is fast, solvent-free, and easy to set up technically, has not been explored to its fullest potential to synthesize different nanomaterials with controlled morphology. In this communication, we report on the microwave-induced electric discharge synthesis

A 3D-polyphenylalanine network inside porous alumina: Synthesis and characterization of an inorganic–organic composite membrane

• Jonathan Stott and
• Jörg J. Schneider

Beilstein J. Nanotechnol. 2020, 11, 938–951, doi:10.3762/bjnano.11.78

• ) in porous alumina membranes (ALOX-membranes) with respect to different solvent mixtures (tetrahydrofuran (THF) and dichloromethane (DCM)). It was found that increasing the volume fraction of DCM leads to an increasing amount of fibrillar polymer structures within the porous ALOX-membrane. A three

• -grafted gel might be interesting in membrane separation technology or supported drug release/adsorption systems. We investigate the ability of polyphenylalanine to form organo-gels in situ within a porous inorganic environment with respect to different volume fractions of DCM in the solvent mixture. We

• prefunctionalized with (3-aminopropyl)trimethoxysilane (APTMS) to enable surface-initiated polymerization. The polymerization of PA-NCA was performed in solvent mixtures of THF and DCM, employing different volume fractions of these solvent mixtures. We mainly investigate the morphology of the grafted polypeptitde

Three-dimensional solvation structure of ethanol on carbonate minerals

• Hagen Söngen,
• Ygor Morais Jaques,
• Peter Spijker,
• Christoph Marutschke,
• Stefanie Klassen,
• Ilka Hermes,
• Ralf Bechstein,
• Lidija Zivanovic,
• John Tracey,
• Adam S. Foster and
• Angelika Kühnle

Beilstein J. Nanotechnol. 2020, 11, 891–898, doi:10.3762/bjnano.11.74

• experimental studies exist addressing the interfacial arrangement of other solvent molecules [8][9][10]. This is unfortunate given the relevance of the interaction between organic molecules and carbonate surfaces, for example, in the field of biomineralization [11]. Moreover, by changing the solvent molecule

• , the same feature appears to be a saddle point rather than a maximum in the case of magnesite. At this short tip–sample distance, the solvent–tip approximation [19][20] alone cannot explain the data, but instead the chemical nature and macroscopic shape of the tip plays a crucial role. Hence, the

• from the OH group switch the hydrogen bond back and forth to a neighboring carbonate group within a very similar distance during the simulation run, which we further discuss in Supporting Information File 1. To compare the MD simulations with the AFM data, we use the well-established “solvent–tip

Simulations of the 2D self-assembly of tripod-shaped building blocks

• Łukasz Baran,
• Wojciech Rżysko and
• Edyta Słyk

Beilstein J. Nanotechnol. 2020, 11, 884–890, doi:10.3762/bjnano.11.73

• this research, several factors have been established that can help to control the self-assembly process, such as precursor design [4][5], substrate nature and symmetry [6][7], type of solvent and its concentration, and thermodynamic conditions. The knowledge of the influence of these variables is

• computer modeling, which allows for a versatile examination of various thermodynamic conditions in acceptable time frames. Additionally, it is also a convenient tool to vary multiple factors such as the shape of the molecules, and the type of solvent and substrate. The insight gained from the simulations

Transition from freestanding SnO₂ nanowires to laterally aligned nanowires with a simulation-based experimental design

• Jasmin-Clara Bürger,
• Sebastian Gutsch and
• Margit Zacharias

Beilstein J. Nanotechnol. 2020, 11, 843–853, doi:10.3762/bjnano.11.69

• , diluted in a solvent and deposited on a new substrate [6][10][11][12]. The deposited NWs will be randomly oriented and have to be individually contacted [10][12]. Laterally aligned NWs have the advantage that no transfer from the growth substrate to a new substrate is necessary [10]. Due to their

Quantitative determination of the interaction potential between two surfaces using frequency-modulated atomic force microscopy

• Nicholas Chan,
• Carrie Lin,
• Tevis Jacobs,
• Robert W. Carpick and
• Philip Egberts

Beilstein J. Nanotechnol. 2020, 11, 729–739, doi:10.3762/bjnano.11.60

• with acetone and subsequently ethanol for 20 min with each solvent. The samples were then transferred into the vacuum chamber and baked at 120 °C for 8 h. A non-reflective silicon AFM probe (PPP-NCL, Nanosensors) was used in AFM measurements. TEM images were taken of the AFM tip apex before mounting