Structural and optical characteristics determined by the sputtering deposition conditions of oxide thin films

• Petronela Prepelita,
• Florin Garoi and
• Valentin Craciun

Beilstein J. Nanotechnol. 2021, 12, 354–365, doi:10.3762/bjnano.12.29

• dielectric properties (e.g., SiO2 and ZnO) exhibit a dependence of the electrical resistance with temperature [22][23]. SiO2 and ZnO films are obtained by various deposition techniques, such as matrix-assisted pulsed laser evaporation (MAPLE) [24][25], spin coating of sol–gel precursor solutions [26], radio

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

• can be easily synthesized from the precursor material bis(1,5-cyclooctadiene)nickel(0) (Ni(COD)2) in different ionic liquids without any additional stabilizing or reducing agents [46]. Ionic liquids have the ability to exfoliate graphene oxide into single sheets. Thus, a higher surface area can be

• supported on reduced graphene oxide paves the way for their application as dopant in other metal oxide gas sensors. Experimental Due to the sensitivity of the precursor substances towards moisture and oxidation, all experiments were carried out in a purified argon (grade 99.998 vol %) or nitrogen (grade

Exploring the fabrication and transfer mechanism of metallic nanostructures on carbon nanomembranes via focused electron beam induced processing

• Christian Preischl,
• Linh Hoang Le,
• Elif Bilgilisoy,
• Armin Gölzhäuser and
• Hubertus Marbach

Beilstein J. Nanotechnol. 2021, 12, 319–329, doi:10.3762/bjnano.12.26

• ” approach for the fabrication of arbitrarily shaped nanostructures [1][2][3][4][5]. The most prominent method within the FEBIP family is electron beam-induced deposition (EBID). In EBID, a focused electron beam is used to locally dissociate adsorbed precursor molecules. Thus, a localized deposit of the non

• satisfying results [4][9]. However, for certain precursors, EBID yields clean deposits when carried out under ultrahigh vacuum (UHV) conditions. It was shown that in UHV, for some precursors, an autocatalytic growth (AG) process occurs already at room temperature, which leads, upon further precursor dosage

• , to the dissociation of the precursor molecules on top of the initial EBID deposit. In the case of Fe(CO)5 this AG process results in the formation of deposits consisting of pure iron [10]. A second method from the FEBIP family, namely electron beam-induced surface activation (EBISA), also largely

The patterning toolbox FIB-o-mat: Exploiting the full potential of focused helium ions for nanofabrication

• Victor Deinhart,
• Lisa-Marie Kern,
• Jan N. Kirchhof,
• Sabrina Juergensen,
• Joris Sturm,
• Enno Krauss,
• Thorsten Feichtner,
• Sviatoslav Kovalchuk,
• Michael Schneider,
• Dieter Engel,
• Bastian Pfau,
• Bert Hecht,
• Kirill I. Bolotin,
• Stephanie Reich and
• Katja Höflich

Beilstein J. Nanotechnol. 2021, 12, 304–318, doi:10.3762/bjnano.12.25

• combination with a thermal stability up to 2600 K [50], renders graphene an exciting candidate for room-temperature bolometry [51]. Single-layer graphene was grown by chemical vapor deposition onto a multicrystalline copper foil using methane as precursor gas at 1035 °C. For the transfer process, the graphene

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

• substitutions on deposit composition and growth rate indicates that the most suitable organic ligand for the gold precursor is triazole-based, with the best deposit composition of 15 atom % gold, while the most suitable anionic ligand is the trifluoromethyl group, leading to a growth rate of 1 × 10−2 nm3/e

• the deposit. A major challenge is therefore to achieve control over the composition of the deposited material through a proper design of the precursor molecule [17][18]. Gold deposition has been one of the earliest interests in FEBID [19], as gold 3D-nanostructures can find a wide range of

• gold(I) complexes has been explored, such as Au(PF3)Cl [27][28][29][30] and Au(CO)Cl [31], which gave high-purity deposits. Unfortunately, the high instability of these precursor molecules has severely hindered their use as FEBID precursors. For the compounds [AuMe2Cl]2 and Au(PMe3)Me [32], it was

Scanning transmission helium ion microscopy on carbon nanomembranes

• Daniel Emmrich,
• Annalena Wolff,
• Nikolaus Meyerbröker,
• Jörg K. N. Lindner,
• André Beyer and
• Armin Gölzhäuser

Beilstein J. Nanotechnol. 2021, 12, 222–231, doi:10.3762/bjnano.12.18

• ) [35]. Thin CNMs were prepared from terphenylthiol precursor molecules, thick CNMs were obtained from CNM Technologies GmbH (Bielefeld, Germany). The CNMs used for this experiment offer a low conductivity to give a negligible SE contribution. Monte Carlo simulations of the ion trajectories were run

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

• type, reagent type, precursor concentration, temperature, process duration, and pH. Physical and chemical methods have been among the most common methods to synthesize silver nanostructures; however, they possess substantial disadvantages and short-comings, especially compared to green synthesis

• reaction parameters, such as temperature, pH, precursor, and reagent concentration, on silver nanostructure size and morphology are discussed. Also, green synthesis techniques used for the synthesis of one-dimensional (1D) silver nanostructures have been reviewed, and the potential of alternative green

• either composed of an inert metal, such as titanium, or any metal of interest of which the nanoparticles will be produced, for instance, silver for the synthesis of AgNPs [129][131]. In the case of titanium electrodes, AgNO3 is used as the precursor, an electric discharge takes place between cathode and

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

• stable freestanding monolayers produced from irradiation-induced cross-linking of self-assembled monolayers (SAMs) [35]. They have a thickness in the range of 1–2 nm and can be made from a variety of carbon precursor molecules [36]. They are well characterized in terms of their permeability [37][38] and

• performed to obtain both optimal orientations of the PM patches and coverage of the CNM substrate. Due to the limited availability of c-His PM, wild-type PM (WT PM) has been used for all preliminary experiments. It has been found that the most appropriate CNM precursor for this purpose is NBPT since the

Atomic layer deposited films of Al₂O₃ on fluorine-doped tin oxide electrodes: stability and barrier properties

• Hana Krýsová,
• Michael Neumann-Spallart,
• Hana Tarábková,
• Pavel Janda,
• Ladislav Kavan and
• Josef Krýsa

Beilstein J. Nanotechnol. 2021, 12, 24–34, doi:10.3762/bjnano.12.2

• precursor was 0.1 s with a purge time of 5 s and the pulse of H2O was 0.1 s with a purge time of 10 s. TMA and water were maintained at 22 °C. Nitrogen (99.999%, Linde) was used as a carrier gas. The deposition of aluminium oxide films on silicon or FTO was carried out by performing 30, 60, 120, and 200

Towards 3D self-assembled rolled multiwall carbon nanotube structures by spontaneous peel off

• Jonathan Quinson

Beilstein J. Nanotechnol. 2020, 11, 1865–1872, doi:10.3762/bjnano.11.168

• individual nanomaterials can be a challenging task. However, it opens up opportunities for the production of increasingly complex nanostructures. Unusual rolled multiwall carbon nanotube structures are synthesized here by simply inducing a change of precursor composition during the growth of multiwall carbon

• during sample preparation. Nevertheless, on MWCNT structures with only one junction a change in structure can still be related to the precursor used. In the case of N1/C2 junctions (Figure 4a and Figure 4b) the interface between the two expected sections is conveniently marked by darker features, which

• . First, a liquid precursor consisting of toluene (99.9%, Sigma-Aldrich) and 5 wt % of ferrocene (98%, Aldrich, purified via sublimation at 90 °C prior to use) was injected into the furnace with Ar gas flow at 2000 sccm in a first precursor line (Supporting Information File 1, Figure S3) for 3 min. In a

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

• reactions, methane reforming, and hydrogen evolution [35][36][37][38][39][40]. Wang et al. [38] reported the growth of nickel phyllosilicate by simultaneous reaction of a silica precursor (tetraethylorthosilicate), nickel chloride, water, and urea in a hydrothermal reactor at 210 °C for 12 h. They obtained

• NiPS nickel phyllosilicate structure Si2Ni3O5(OH)4 [42][43]. Basically, NiPS is formed upon the precipitation of nickel species onto a silica surface after basification of a nickel(II) solution [44]. Depending on the deposition-precipitation time, the molar ratio between urea and nickel precursor, and

• °C, urea hydrolysis took place reducing the nickel precursor to nickel species, which diffused into the silica layers through the mesoporous shell. The nickel species reacted with the surface hydroxides to give nickel phyllosilicate via a Ni–O–Si polymerization reaction. TiO2 (dTiO2 = 30 ± 9 nm) was

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

• hygroscopic nature of bismuth nitrate, we observed higher yields and the formation of pure-phase BiFeO3 powders when fresh Bi(NO3)3·5H2O was used. The influence of different calcination conditions was then analyzed. It should be noted that precursor powder resulting from the synthesis of bismuth and iron

Self-standing heterostructured NiC_x-NiFe-NC/biochar as a highly efficient cathode for lithium–oxygen batteries

• Shengyu Jing,
• Xu Gong,
• Shan Ji,
• Linhui Jia,
• Bruno G. Pollet,
• Sheng Yan and
• Huagen Liang

Beilstein J. Nanotechnol. 2020, 11, 1809–1821, doi:10.3762/bjnano.11.163

• the previous literatures [40][41][42]. However, a hydrothermal process was introduced here as a new treatment step prior to the precursor calcination in order to modify the properties of the prepared electrode materials. Heterostructured NiCx-NiFe-NC derived from bimetallic Prussian blue supported on

• structure. As shown in the inset of Figure 2d, the main diffraction peaks of the Ni–Fe PBA precursor are consistent with the standard patterns of Ni3[Fe(CN)6]2 (JCPDS: 51-1897). During a hydrothermal pretreatment, the ion-exchange reaction of OH−/[Fe(CN)6]3− occurred at the interface between NiFe-PBA cubes

• . Conclusion In this investigation, heterostructured NiCx-NiFe-NC derived from bimetallic Prussian blue supported on biochar was successfully synthesized to improve the electronic conductivity and electrocatalytic activity, and was used as the cathode material for Li–O2 batteries. When the precursor was heated

Nanomechanics of few-layer materials: do individual layers slide upon folding?

• Ronaldo J. C. Batista,
• Rafael F. Dias,
• Ana P. M. Barboza,
• Alan B. de Oliveira,
• Taise M. Manhabosco,
• Thiago R. Gomes-Silva,
• Matheus J. S. Matos,
• Andreij C. Gadelha,
• Cassiano Rabelo,
• Luiz G. L. Cançado,
• Ado Jorio,
• Hélio Chacham and
• Bernardo R. A. Neves

Beilstein J. Nanotechnol. 2020, 11, 1801–1808, doi:10.3762/bjnano.11.162

• material and the precursor layered material. As a result of the variational procedure, we obtain (see Supporting Information File 1): and Equation 1 and Equation 2 can be used to determine either the geometry of the folded edge from the properties of the 2D material (κ/α and thickness) or vice versa. In

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

• scanning electron microscope (SEM), wherein series of pillars were successfully grown from both precursors. The growth of the pillars was studied as a function of the electron dose and compared to deposits grown from the commercially available precursor MeCpPtMe3. The composition of the deposits was

• precursor gas into the vacuum chamber of an electron microscope [2][3]. At specific locations on the substrate exposed to the electron beam, the transiently adsorbed precursor molecules decompose, forming a deposit while the volatile byproducts of the reaction desorb into the vacuum [4][5][6][7]. One of the

• main challenges associated with FEBID is the typical low purity of the deposits. Many FEBID precursors are organometallic, leading to high carbon content in the deposit [6][8][9]. Often, unwanted fragments of the precursor molecules remain in the deposits [10]. Some precursors perform better in this

The influence of an interfacial hBN layer on the fluorescence of an organic molecule

• Christine Brülke,
• Oliver Bauer and
• Moritz M. Sokolowski

Beilstein J. Nanotechnol. 2020, 11, 1663–1684, doi:10.3762/bjnano.11.149

• out in an ultrahigh-vacuum chamber with a base pressure of 2.3 × 10−10 mbar. The Cu(111) sample could be heated up to 1100 K via a tungsten filament and electron bombardment and cooled down to 20 K by using liquid helium. The hBN layer was grown by dosing the precursor borazine [(HBNH)3] into the

High-responsivity hybrid α-Ag₂S/Si photodetector prepared by pulsed laser ablation in liquid

• Raid A. Ismail,
• Hanan A. Rawdhan and
• Duha S. Ahmed

Beilstein J. Nanotechnol. 2020, 11, 1596–1607, doi:10.3762/bjnano.11.142

• bromide (CTAB) surfactant-assisted hydrothermal method [15]. Zhang et al. synthesized monodisperse Ag2S NPs using thermolysis of harmless silver xanthates as a single-source molecular precursor and controlled the particle size by changing the alkyl chain length in the precursors [16]. Recently, Kang et al

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

• diameters ranging between 80 and 180 nm and length values that can reach several tens of micrometers. The chemical reduction method was initially proposed by Michael Faraday in 1856–1857 while investigating the properties of colloidal gold. This method generally uses a precursor, a reducing agent, and a

• ) and controlling the NP size. Green synthesis Generally, the procedures for obtaining nanoparticles are physical and/or chemical methods in which a precursor material reacts with reducing agents, as mentioned earlier. Nevertheless, both methods have been proven to be harmful for the environment and

One-step synthesis of carbon-supported electrocatalysts

• Sebastian Tigges,
• Nicolas Wöhrl,
• Ivan Radev,
• Ulrich Hagemann,
• Markus Heidelmann,
• Thai Binh Nguyen,
• Stanislav Gorelkov,
• Stephan Schulz and
• Axel Lorke

Beilstein J. Nanotechnol. 2020, 11, 1419–1431, doi:10.3762/bjnano.11.126

• process at a substrate temperature as low as 350 °C using platinum acetylacetonate as a single-source precursor was established for the deposition of a Pt/C electrocatalyst. Platinum in the form of NPs is homogeneously distributed in a carbon support structure due to the simultaneous deposition of both

• by cyclic voltammetry (CV) measurements. Results and Discussion One-step synthesis and its product Platinum acetylacetonate was used as a single-source precursor for the deposition of Pt-NPs embedded in the supporting CNW matrix. CNWs are vertically aligned, graphitic, multilayer carbon sheets, which

• degree of oxidation of the Pt-NPs can be found. Other elemental signals besides carbon, oxygen, or platinum were not detected, which is expected, as the precursor Pt(acac)2 only consists of these elements and hydrogen. The Pt4f signal is divided into elemental Pt (Pt0) at ≈71 eV and oxidized Pt (PtII

Analysis of catalyst surface wetting: the early stage of epitaxial germanium nanowire growth

• Owen C. Ernst,
• Felix Lange,
• David Uebel,
• Thomas Teubner and
• Torsten Boeck

Beilstein J. Nanotechnol. 2020, 11, 1371–1380, doi:10.3762/bjnano.11.121

• dewetting process, since the name of the resulting structures are nanoparticles or clusters but rarely droplets. Nevertheless, the origin of these structures from fluid-like states offers the opportunity for novel bottom-up techniques to produce precursor materials for functional materials, such as

Structural and electronic properties of SnO₂ doped with non-metal elements

• Jianyuan Yu,
• Yingeng Wang,
• Yan Huang,
• Xiuwen Wang,
• Jing Guo,
• Jingkai Yang and
• Hongli Zhao

Beilstein J. Nanotechnol. 2020, 11, 1321–1328, doi:10.3762/bjnano.11.116

• (substituting O) can effectively increase the carrier concentration and improve the conductivity. Majumder successfully prepared SnO2:F thin films using spray pyrolysis with SnF2 as the precursor. By adjusting the concentration of the precursor solution, doped SnO2 films with different properties were obtained

• . When the concentration of the precursor solution was adjusted to 0.15 M and the substrate temperature was 773 K, a film with a resistivity of 1.2 × 10−4 Ω·cm was obtained [10]. Theoretical calculations, based on first principles, show that the doping of N into the SnO2 crystal structure can introduce

Structure and electrochemical performance of electrospun-ordered porous carbon/graphene composite nanofibers

• Yi Wang,
• Yanhua Song,
• Chengwei Ye and
• Lan Xu

Beilstein J. Nanotechnol. 2020, 11, 1280–1290, doi:10.3762/bjnano.11.112

• nanofibers have been widely used as a material to synthesize electrodes upon a carbonization step [13][14]. Polyacrylonitrile (PAN) is often used as a precursor to synthesize carbon nanofibers. It can be obtained from a variety of sources and it has good spinnability [14][15]. However, carbon-based materials

Magnetic-field-assisted synthesis of anisotropic iron oxide particles: Effect of pH

• Andrey V. Shibaev,
• Petr V. Shvets,
• Darya E. Kessel,
• Roman A. Kamyshinsky,
• Anton S. Orekhov,
• Sergey S. Abramchuk,
• Alexei R. Khokhlov and
• Olga E. Philippova

Beilstein J. Nanotechnol. 2020, 11, 1230–1241, doi:10.3762/bjnano.11.107

• ][30][31][32], solvothermal [33] and hydrothermal [34] reactions, the polyol method [35], dehydration or reduction of precursor rod-like particles [8][11], sonochemical oxidation [36], thermal decomposition [23][26], sol–gel reactions [37], synthesis in worm-like surfactant micellar solutions [38][39

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

• ]. The first step was a hydrothermal synthesis of a precursor, followed by a pyrolytic carbonization to get the final HC product. At first, a 25 wt % solution of ᴅ-fructose (Sigma-Aldrich, Germany) in deionized water (Millipore, Merck, Germany) was prepared. Similar to a synthesis reported by Fellinger

• precursor overnight at 70 °C under vacuum, it was carbonized in a tube furnace with argon flow at a rate of higher than 0.5 L min−1 at 1000 °C for 1, 5, or 10 h. The carbons produced by this hydrothermal method (HT carbons) will be called HTx, where x is an integer. The synthesis conditions (temperature of

Influence of the magnetic nanoparticle coating on the magnetic relaxation time

• Mihaela Osaci and
• Matteo Cacciola

Beilstein J. Nanotechnol. 2020, 11, 1207–1216, doi:10.3762/bjnano.11.105

• additional step in which the hydrothermal method or thermal decomposition technique are used. The method used to obtain nanoparticles by thermal decomposition of an iron precursor in the presence of NaBH4 in a polyol was found to be suitable for size control in both chemical approaches [1][2][3][4][6]. Since