Structural and optical properties of penicillamine-protected gold nanocluster fractions separated by sequential size-selective fractionation

• Xiupei Yang,
• Zhengli Yang,
• Fenglin Tang,
• Jing Xu,
• Maoxue Zhang and
• Martin M. F. Choi

Beilstein J. Nanotechnol. 2019, 10, 955–966, doi:10.3762/bjnano.10.96

• -molecule impurities. Based on the results from the mass spectrometry and thermogravimetric analysis, the average composition of the four fractions can be represented by Au38(SR)18, Au28(SR)15, Au18(SR)12, and Au11(SR)8, respectively. This indicates that the SSSP separation is mainly dependent on the core

• synthesized penicillamine-protected AuNCs in aqueous medium. The product was isolated and purified by sequential size-selective precipitation (SSSP) and characterized by mass spectrometry (MS) [20]. In order to further explore the different structures and properties of NCs of different sizes after

• chemical shift at 1.42, 1.51, 1.73, 1.79, 3.77 and 3.98 ppm (Figure 5, spectrum 7), indicating that the main disulfide with a small amount of free ligand and gold(I) complex are separated from other fractions. The assignments are also confirmed by mass spectrometry (vide infra). That is to say that not

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

• surface are still visible. We speculate that under these conditions the cell dies due to the depletion of O2 as a result of slow transport through the electrolyte limited by diffusion in contrast with conventional differential electrochemical mass spectrometry (DEMS) cells where oxygen is bubbled through

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

• pyrazine ring at the para-positions, making an angle of 180° between the two binding sites, giving it a linear shape (Figure 1). Details of the synthesis of the molecule, and its characterization by means of FTIR, 1H and 13C NMR, mass spectrometry, and single crystal X-ray diffraction are provided in

Reduced graphene oxide supported C₃N₄ nanoflakes and quantum dots as metal-free catalysts for visible light assisted CO₂ reduction

• Md Rakibuddin and
• Haekyoung Kim

Beilstein J. Nanotechnol. 2019, 10, 448–458, doi:10.3762/bjnano.10.44

• prepared metal-free GCN-5 is highly stable and can be reused for the photoreduction tests. The photoreduction of CO2 to HCHO is also verified by gas chromatography mass spectrometry (GC–MS). A sample is examined for GC analysis after 4 h of photoirradiation with GCN-5 under identical conditions, and the

• absorbance spectra were measured using a UV–visible spectrophotometer (Thermo Fisher Scientific). Gas chromatography coupled with mass spectrometry (GC–MS) was carried out on an Agilent 7890A instrument with both a thermal conductivity detector and a flame ionization detector and using helium as a carrier

Relation between thickness, crystallite size and magnetoresistance of nanostructured La_1−xSr_xMn_yO_3±δ films for magnetic field sensors

• Rasuole Lukose,
• Valentina Plausinaitiene,
• Milita Vagner,
• Nerija Zurauskiene,
• Skirmantas Kersulis,
• Virgaudas Kubilius,
• Karolis Motiejuitis,
• Birute Knasiene,
• Voitech Stankevic,
• Zita Saltyte,
• Martynas Skapas,
• Algirdas Selskis and
• Evaldas Naujalis

Beilstein J. Nanotechnol. 2019, 10, 256–261, doi:10.3762/bjnano.10.24

• SU70). The structural analysis was performed in cross section geometry by TEM (FEI Tecnai G2 F20 X-TWIN). The elemental composition analysis was performed by inductively coupled plasma high-resolution mass spectrometry (ICP-MS) - Thermo Scientific Element2, where the films were totally dissolved in 2

Mechanism of silica–lysozyme composite formation unravelled by in situ fast SAXS

• Tomasz M. Stawski,
• Daniela B. van den Heuvel,
• Rogier Besselink,
• Dominique J. Tobler and
• Liane G. Benning

Beilstein J. Nanotechnol. 2019, 10, 182–197, doi:10.3762/bjnano.10.17

• water to remove excess lysozyme and salts followed by a 2nd drying step at 40 °C. The amount of lysozyme associated with the composites was quantified by determining the total carbon content in solids by mass spectrometry (DELTAplusXL ThermoFisher) with a Carlo-Erba NC2500. From these analyses the

Scanning probe microscopy for energy-related materials

• Rüdiger Berger,
• Benjamin Grévin,
• Philippe Leclère and
• Yi Zhang

Beilstein J. Nanotechnol. 2019, 10, 132–134, doi:10.3762/bjnano.10.12

• major topic in our daily life. Jonathan Op de Beeck and co-workers identify the ionic processes occurring inside Li-ion composites in order to understand the impact on the entire battery cell [9]. In particular, the authors combine cAFM and secondary-ion mass spectrometry to correlate the presence of

Time-resolved universal temperature measurements using NaYF₄:Er³⁺,Yb³⁺ upconverting nanoparticles in an electrospray jet

• Kristina Shrestha,
• Arwa A. Alaulamie,
• Ali Rafiei Miandashti and
• Hugh H. Richardson

Beilstein J. Nanotechnol. 2018, 9, 2916–2924, doi:10.3762/bjnano.9.270

• -invasively image and measure temperatures in complex systems such as in vivo imaging, cellular biological systems and matrices, whole-blood samples, and electrospray jets used in mass spectrometry [1]. Optical thermometers using UCNPs are well suited for these applications because near-IR excitation of the

Accurate control of the covalent functionalization of single-walled carbon nanotubes for the electro-enzymatically controlled oxidation of biomolecules

• Naoual Allali,
• Veronika Urbanova,
• Mathieu Etienne,
• Xavier Devaux,
• Martine Mallet,
• Brigitte Vigolo,
• Jean-Joseph Adjizian,
• Chris P. Ewels,
• Sven Oberg,
• Alexander V. Soldatov,
• Edward McRae,
• Yves Fort,
• Manuel Dossot and
• Victor Mamane

Beilstein J. Nanotechnol. 2018, 9, 2750–2762, doi:10.3762/bjnano.9.257

• core line and setting adventitious carbon signal (C sp3 signal) to 284.6 eV. For thermogravimetric analyses coupled to mass spectrometry (TGA-MS) experiments, 5–6 mg of the sample powder were placed in an alumina crucible. The TGA-MS instrument included a Setaram Setsys evolution 1750 Thermal

• temperature associated with departure of some chemical groups attached to SWCNT sidewalls. Mass spectrometry channels used to show the departure peaks of the cyclopentadienyl group and its main fragments at m/z = 66 and m/z = 39. Inset: the departure peak of the iron atoms of the ferrocene groups. Raman data

Cytotoxicity of doxorubicin-conjugated poly[N-(2-hydroxypropyl)methacrylamide]-modified γ-Fe₂O₃ nanoparticles towards human tumor cells

• Zdeněk Plichta,
• Yulia Kozak,
• Rostyslav Panchuk,
• Viktoria Sokolova,
• Matthias Epple,
• Lesya Kobylinska,
• Pavla Jendelová and
• Daniel Horák

Beilstein J. Nanotechnol. 2018, 9, 2533–2545, doi:10.3762/bjnano.9.236

• Bruker DPX 300 spectrometer (Billerica; MA, USA) and a Perkin Elmer PARAGON 1000 PC spectrometer (Bucks, UK), respectively. Gas and HPLC SEC chromatography was performed on a Clarus 500 Perkin Elmer gas chromatograph (Shelton, CT, USA) and a Shimadzu HPLC chromatograph (Kyoto, Japan) equipped with a mass

• spectrometry and UV–vis, RID, or DAWN 8 MALS detectors (Wyatt Technology; Santa Barbara, CA, USA), respectively. Agilent DB-35MS GC column (30 m × 0.25 mm id, 0.25 µm film; helium carrier gas) and Chromolith RP-18 e HPLC column (100 mm × 4.6 mm id) with a flow rate of 5 mL acetonitrile/water mixture per min

Non-agglomerated silicon–organic nanoparticles and their nanocomplexes with oligonucleotides: synthesis and properties

• Asya S. Levina,
• Marina N. Repkova,
• Nadezhda V. Shikina,
• Zinfer R. Ismagilov,
• Svetlana A. Yashnik,
• Dmitrii V. Semenov,
• Yulia I. Savinovskaya,
• Natalia A. Mazurkova,
• Inna A. Pyshnaya and
• Valentina F. Zarytova

Beilstein J. Nanotechnol. 2018, 9, 2516–2525, doi:10.3762/bjnano.9.234

• coupled plasma mass spectrometry (ICP-MS). The experimental Si/P value (10.9) showed a reasonable correlation with the calculated data (10.0). The atomic force microscopy (AFM) image of the Si–NH2 nanoparticles was not obtained in a satisfactory quality because of the very small size of the particles

• monomers (Glen Research, USA). The optical absorption of oligonucleotides and their derivatives was measured on a Shimadzu U-1800 spectrophotometer (Shimadzu, Japan). Inductively coupled plasma mass spectrometry (ICP-MS) was performed using an Agilent 7700 ICP MS (USA) spectrometer. The IR spectrum of the

• stirred at this temperature for 15 h and then cooled to the room temperature. The concentration of the product (0.46 M) was evaluated by inductively coupled plasma mass spectrometry (ICP-MS) on an Agilent 7700 ICP-MS spectrometer or by titration of the amino groups with hydrochloric acid. The yield of the

Phosphorus monolayer doping (MLD) of silicon on insulator (SOI) substrates

• Noel Kennedy,
• Ray Duffy,
• Luke Eaton,
• Dan O’Connell,
• Scott Monaghan,
• Shane Garvey,
• James Connolly,
• Chris Hatem,
• Justin D. Holmes and
• Brenda Long

Beilstein J. Nanotechnol. 2018, 9, 2106–2113, doi:10.3762/bjnano.9.199

• the Si substrate. MLD-doped 66 nm SOI was further examined using secondary ion mass spectrometry (SIMS) to attain a more detailed view of total dopant distribution in the substrate, which is complementary to previous measurements of active carrier concentrations through ECV. Data shown in Figure 7

• under neutral conditions. Controlled-voltage etching was carried out with step widths of 2–5 nm. Secondary ion mass spectrometry data was acquired on a Phi Adept 1010 using a 0.5–1.0 keV Cs+ bombardment with negative ion detection. X-ray photoelectron spectroscopy XPS spectra were acquired on an Oxford

• under inert conditions. Secondary ion mass spectrometry analysis of a P-MLD-doped 66 nm silicon on insulator substrate. Blue line: P concentration, red line: O concentration. Hall effect data of 66 nm and 13 nm MLD-doped SOI. Supporting Information Comprehensive Hall effect analysis data and ECV of

Defect formation in multiwalled carbon nanotubes under low-energy He and Ne ion irradiation

• Santhana Eswara,
• Jean-Nicolas Audinot,
• Brahime El Adib,
• Maël Guennou,
• Tom Wirtz and
• Patrick Philipp

Beilstein J. Nanotechnol. 2018, 9, 1951–1963, doi:10.3762/bjnano.9.186

• secondary ion mass spectrometry experiments as described elsewhere, which leads to a modified octagon and pole-pieces [59]. The bright-field (BF) TEM images were recorded in the He+ and Ne+ craters using Gatan on-axis CCD camera with 2k × 2k pixel array (Figure 8). Raman spectroscopy was done prior to TEM

Sulfur-, nitrogen- and platinum-doped titania thin films with high catalytic efficiency under visible-light illumination

• Boštjan Žener,
• Lev Matoh,
• Giorgio Carraro,
• Bojan Miljević and
• Romana Cerc Korošec

Beilstein J. Nanotechnol. 2018, 9, 1629–1640, doi:10.3762/bjnano.9.155

• dispersions [45]. The prepared samples were analyzed using thermogravimetric analysis–differential scanning calorimetry–mass spectrometry (TGA-DSC-MS), X-ray diffraction spectroscopy (XRD), specific surface area measurements via Brunauer–Emmett–Teller method (BET), X-ray photoelectron spectroscopy (XPS

• durations of illumination with visible light. The concentration of the dye was calculated using the Beer–Lambert law. Thermogravimetric analysis–differential scanning calorimetry–mass spectrometry (TGA-DSC-MS) curves of different xerogel samples: a) REF, b) S1 and c) S3. X-ray diffraction patterns for

Nanoscale electrochemical response of lithium-ion cathodes: a combined study using C-AFM and SIMS

• Jonathan Op de Beeck,
• Nouha Labyedh,
• Alfonso Sepúlveda,
• Valentina Spampinato,
• Alexis Franquet,
• Thierry Conard,
• Philippe M. Vereecken,
• Wilfried Vandervorst and
• Umberto Celano

Beilstein J. Nanotechnol. 2018, 9, 1623–1628, doi:10.3762/bjnano.9.154

• established nanoscale analysis techniques namely conductive atomic force microscopy (C-AFM) and secondary ion mass spectrometry (SIMS). We present a platform to study Li-ion composites with nanometer resolution that allows one to sense a multitude of key characteristics including structural, electrical and

• indicated. Keywords: all-solid-state microbatteries (ASB); conductive atomic force microscopy (C-AFM); Li-ion kinetics; secondary ion mass spectrometry (SIMS); 3D thin-film batteries; Findings Conventional Li-ion battery technology is undergoing continuous improvements in order to fulfil the increasing

• conductive atomic force microscopy (C-AFM) and secondary ion mass spectrometry (SIMS). As model systems, we focus on LiMn2O4 (LMO) as cathode material [7] deposited by wet electrodeposition (thickness 260 nm) and RF-sputtered (thickness 100 nm) and compare their properties on a local (sub-100 nm) scale. In

Absence of free carriers in silicon nanocrystals grown from phosphorus- and boron-doped silicon-rich oxide and oxynitride

• Daniel Hiller,
• Julian López-Vidrier,
• Keita Nomoto,
• Michael Wahl,
• Wolfgang Bock,
• Tomáš Chlouba,
• František Trojánek,
• Sebastian Gutsch,
• Margit Zacharias,
• Dirk König,
• Petr Malý and
• Michael Kopnarski

Beilstein J. Nanotechnol. 2018, 9, 1501–1511, doi:10.3762/bjnano.9.141

• measurements were post-annealed in the same furnace in pure H2 gas at 450 °C for 1 h to enable the passivation of dangling bond defects [18]. For electrical measurements, MOS capacitors were processed by thermal evaporation of Al-contacts. Molecular Cs+ secondary ion mass spectrometry (MCs+-SIMS [19]; Cameca

Effect of annealing treatments on CeO₂ grown on TiN and Si substrates by atomic layer deposition

• Silvia Vangelista,
• Rossella Piagge,
• Satu Ek and
• Alessio Lamperti

Beilstein J. Nanotechnol. 2018, 9, 890–899, doi:10.3762/bjnano.9.83

• distribution as in [26]. Time-of-flight secondary ion mass spectrometry (ToF-SIMS) investigation of the compositional depth profile of the CeO2/TiN/Si and CeO2/Si structures has been performed by means of a Cs+ ion beam (energy of 0.5 keV, ion current 38.0 nA) sputtering a 200 μm × 200 μm area, and a Ga+ ion

Electron interactions with the heteronuclear carbonyl precursor H₂FeRu₃(CO)₁₃ and comparison with HFeCo₃(CO)₁₂: from fundamental gas phase and surface science studies to focused electron beam induced deposition

• Ragesh Kumar T P,
• Paul Weirich,
• Lukas Hrachowina,
• Marc Hanefeld,
• Ragnar Bjornsson,
• Helgi Rafn Hrodmarsson,
• Sven Barth,
• D. Howard Fairbrother,
• Michael Huth and
• Oddur Ingólfsson

Beilstein J. Nanotechnol. 2018, 9, 555–579, doi:10.3762/bjnano.9.53

• ), reflection-absorption IR spectroscopy (RAIRS), and/or high-resolution electron energy loss spectroscopy (HREELS), while mass spectrometry has been used to identify gas phase species generated as a result of electron irradiation. As such the surface science experiments represent an increased level of

• monitored in situ by X-ray photoelectron spectroscopy (XPS) and mass spectrometry. Figure 9 shows the evolution of the O 1s, Fe 2p and Ru 3d/C 1s XPS regions of a nanometer-thick film of H2FeRu3(CO)13 adsorbed onto a gold substrate at 213 K, plotted as a function of increasing electron dose. Area analysis

Green synthesis of fluorescent carbon dots from spices for in vitro imaging and tumour cell growth inhibition

• Nagamalai Vasimalai,
• Vânia Vilas-Boas,
• Juan Gallo,
• María de Fátima Cerqueira,
• Mario Menéndez-Miranda,
• José Manuel Costa-Fernández,
• Lorena Diéguez,
• Begoña Espiña and
• María Teresa Fernández-Argüelles

Beilstein J. Nanotechnol. 2018, 9, 530–544, doi:10.3762/bjnano.9.51

• involved in the toxicity in both cell types. Black pepper C-dots showed the most noticeable effect on the LN-229 cells. Thus, in order to elucidate whether the black pepper C-dots effect might be attributed to the presence of molecules existing in the starting material, mass spectrometry measurements of

• , Germany) and the C-dots samples were prepared on a glass substrate. Fourier transform infrared (FTIR) spectra were recorded using a Perkin Elmer Spectra 100 FTIR Spectrometer (Perkin Elmer, USA). Electrospray ionization coupled to quantitative time of flight mass spectrometry measurements were performed

Electron interaction with copper(II) carboxylate compounds

• Michal Lacko,
• Peter Papp,
• Iwona B. Szymańska,
• Edward Szłyk and
• Štefan Matejčík

Beilstein J. Nanotechnol. 2018, 9, 384–398, doi:10.3762/bjnano.9.38

• Toruń, Gagarina 7, 87-100 Toruń, Poland 10.3762/bjnano.9.38 Abstract In the present study we have performed electron collision experiments with copper carboxylate complexes: [Cu2(t-BuNH2)2(µ-O2CC2F5)4], [Cu2(s-BuNH2)2(µ-O2CC2F5)4], [Cu2(EtNH2)2(µ-O2CC2F5)4], and [Cu2(µ-O2CC2F5)4]. Mass spectrometry was

BN/Ag hybrid nanomaterials with petal-like surfaces as catalysts and antibacterial agents

• Konstantin L. Firestein,
• Denis V. Leybo,
• Alexander E. Steinman,
• Andrey M. Kovalskii,
• Andrei T. Matveev,
• Anton M. Manakhov,
• Irina V. Sukhorukova,
• Pavel V. Slukin,
• Nadezda K. Fursova,
• Sergey G. Ignatov,
• Dmitri V. Golberg and
• Dmitry V. Shtansky

Beilstein J. Nanotechnol. 2018, 9, 250–261, doi:10.3762/bjnano.9.27

• The rates of Ag+ ion release from BN/Ag HNMs were studied by means of inductively coupled plasma mass spectrometry (ICP–MS) using an X-Series II unit. 15 mg powder mixtures of BN/Ag HNMs were immersed in flasks filled with 40 mL of distilled water at room temperature and then sonicated for 1 min. To

Electron-driven and thermal chemistry during water-assisted purification of platinum nanomaterials generated by electron beam induced deposition

• Ziyan Warneke,
• Markus Rohdenburg,
• Jonas Warneke,
• Janina Kopyra and
• Petra Swiderek

Beilstein J. Nanotechnol. 2018, 9, 77–90, doi:10.3762/bjnano.9.10

• (methylcyclopentadienyl)platinum(IV) (MeCpPtMe3). The experiments performed under ultrahigh vacuum conditions apply a combination of different desorption experiments coupled with mass spectrometry to analyse reaction products. Electron-stimulated desorption monitors species that leave the surface during electron exposure

• present and previous [10] surface studies, precursor fragmentation is driven by electron impact ionization (EI). In this regime, loss of CH4 from the precursors has in fact been observed in gas phase mass spectrometry [11][20]. Nonetheless, the abundances of specific fragment ions observed in the positive

Response under low-energy electron irradiation of a thin film of a potential copper precursor for focused electron beam induced deposition (FEBID)

• Leo Sala,
• Iwona B. Szymańska,
• Céline Dablemont,
• Anne Lafosse and
• Lionel Amiaud

Beilstein J. Nanotechnol. 2018, 9, 57–65, doi:10.3762/bjnano.9.8

• spontaneously lose amine ligands under vacuum. This loss can be enhanced by mild heating. The combination of mass spectrometry and low-energy electron irradiation (0–15 eV) shows that full amine ligands can be released upon irradiation, and that fragmentation of the perfluorinated ligands is induced by

Synthesis of [{AgO₂CCH₂OMe(PPh₃)}_n] and theoretical study of its use in focused electron beam induced deposition

• Jelena Tamuliene,
• Julian Noll,
• Peter Frenzel,
• Tobias Rüffer,
• Alexander Jakob,
• Bernhard Walfort and
• Heinrich Lang

Beilstein J. Nanotechnol. 2017, 8, 2615–2624, doi:10.3762/bjnano.8.262

• ), thermogravimetry-coupled mass-spectrometry (TG–MS) and by differential scanning calorimetry (DSC). The corresponding TG/DTG and DSC traces of 1 (argon, temperature range 100–500 °C, heating rate 10 °C min−1) are depicted in Figure 2. The decomposition of 1 occurs in consecutive steps, which were quantified with a

• the different structure of both complexes. The mechanism of dissociation for both species was studied using thermogravimetry-coupled mass spectrometry confirming that 1 decarboxylates at first followed by Ag–C, C–C and C–O bond cleavages. The remaining residue was characterized as elemental silver by

Fabrication of CeO₂–MO_x (M = Cu, Co, Ni) composite yolk–shell nanospheres with enhanced catalytic properties for CO oxidation

• Ling Liu,
• Jingjing Shi,
• Hongxia Cao,
• Ruiyu Wang and
• Ziwu Liu

Beilstein J. Nanotechnol. 2017, 8, 2425–2437, doi:10.3762/bjnano.8.241

• and Ce 3d XPS peaks. As shown in Table 1, the surface M/(M + Ce) ratio calculated from XPS data is 37%, 22% and 28% for CeO2–CuOx, CeO2–CoOx and CeO2–NiO, respectively. Compared with 11.3%, 8.3% and 6.6% for the actual concentration measured by inductively coupled plasma mass spectrometry (ICP-MS

• analyzed by inductively coupled plasma mass spectrometry (ICP-MS, Agilent NWR 213-7900). Hydrogen temperature programmed reduction (H2-TPR) experiment was performed on a PCA-1200 instrument, equipped with a thermal conductivity detector (TCD) to detect H2 consumption. Typically, 50 mg of the sample was