Scanning transmission imaging in the helium ion microscope using a microchannel plate with a delay line detector

• Eduardo Serralta,
• Nico Klingner,
• Olivier De Castro,
• Michael Mousley,
• Santhana Eswara,
• Serge Duarte Pinto,
• Tom Wirtz and
• Gregor Hlawacek

Beilstein J. Nanotechnol. 2020, 11, 1854–1864, doi:10.3762/bjnano.11.167

• studied by detecting the light emitted from the sample during ion bombardment [8][9][10]. Moreover, compositional analyses using secondary ion mass spectrometry (SIMS) can be performed in the HIM with a lateral resolution of the order of 10 nm [11][12][13][14]. Transmission-mode imaging can further

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

• for complete precursor decomposition [14]. Electron-induced decomposition of adsorbed Pt(CO)2Cl2 has been previously studied using X-ray photoelectron spectroscopy (XPS) and mass spectrometry, and some deposits were produced in the ultrahigh vacuum (UHV) environment of an Auger electron spectroscopy

Selective detection of complex gas mixtures using point contacts: concept, method and tools

• Alexander P. Pospelov,
• Victor I. Belan,
• Dmytro O. Harbuz,
• Volodymyr L. Vakula,
• Lyudmila V. Kamarchuk,
• Yuliya V. Volkova and
• Gennadii V. Kamarchuk

Beilstein J. Nanotechnol. 2020, 11, 1631–1643, doi:10.3762/bjnano.11.146

• part of the exhaled breath and, as such, can be used as markers for breath characterization. Hence, it is important to detect single components of the exhaled breath for medical purposes. Mass spectrometry, gas chromatography–mass spectrometry, as well as various optical spectroscopy techniques are

Helium ion microscope – secondary ion mass spectrometry for geological materials

• Matthew R. Ball,
• Richard J. M. Taylor,
• Joshua F. Einsle,
• Fouzia Khanom,
• Christelle Guillermier and
• Richard J. Harrison

Beilstein J. Nanotechnol. 2020, 11, 1504–1515, doi:10.3762/bjnano.11.133

• mass spectrometry (SIMS) attachment, the capabilities of the instrument have expanded to microanalysis of isotopes from Li up to hundreds of atomic mass units, effectively opening up the analysis of all natural and geological systems. However, the instrument has thus far been underutilised by the

• well as practicalities for geological sample analyses of Li alongside a discussion of potential geological use cases of the HIM–SIMS instrument. Keywords: geoscience; helium ion microscopy (HIM); lithium; secondary ion mass spectrometry (SIMS); Introduction The helium ion microscope (HIM) is a

• several suggestions for the possibility of microanalysis on the HIM, the most common of these being Rutherford backscattered ion imaging (RBI) and secondary ion mass spectrometry (SIMS) [7][8][9]. However, the variation of RBI intensity with changing surface chemistry, specifically the atomic number, Z

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

• substrates for deposition and following characterization in CV, the deposited catalyst mass on these small substrates is in the range of 15–30 µg depending on Pt loading. These very low absolute catalyst masses are difficult to handle in inductively-coupled plasma mass spectrometry and prone to high

Plant growth regulation by seed coating with films of alginate and auxin-intercalated layered double hydroxides

• Vander A. de Castro,
• Valber G. O. Duarte,
• Danúbia A. C. Nobre,
• Geraldo H. Silva,
• Vera R. L. Constantino,
• Frederico G. Pinto,
• Willian R. Macedo and
• Jairo Tronto

Beilstein J. Nanotechnol. 2020, 11, 1082–1091, doi:10.3762/bjnano.11.93

• analytical techniques, including powder X-ray diffraction, thermogravimetric analysis coupled to differential scanning calorimetry and mass spectrometry, specific surface area measurement, and scanning electron microscopy. Bioassays were performed with the seeds coated with the composite film to assess the

• agreement with a Zn/Al molar ratio of 2. Figure 2 shows the thermogravimetric analysis-differential scanning calorimetry (TG-DSC) and thermogravimetric analysis mass spectrometry (TG-MS) curves of ZnAl-NAA-LDH, which evidence three main steps of mass loss. The first step occurs from room temperature to 155

Identification of physicochemical properties that modulate nanoparticle aggregation in blood

• Ludovica Soddu,
• Duong N. Trinh,
• Eimear Dunne,
• Dermot Kenny,
• Giorgia Bernardini,
• Ida Kokalari,
• Arianna Marucco,
• Marco P. Monopoli and
• Ivana Fenoglio

Beilstein J. Nanotechnol. 2020, 11, 550–567, doi:10.3762/bjnano.11.44

• were stained in Imperial Protein stain (Thermo Scientific) for 1 h and distained overnight (in ultrapure water). The densitometry analysis was performed using the software ImageJ (NIH). Mass spectrometry analysis The samples were run on a sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS

• surface curvature plays a minor role. This is only apparently in contrast with a previous study showing more significant differences in the protein corona for NPs of different size [34]. In fact, the size range considered here is even larger than in the referenced study. Label-free mass spectrometry

Nanoparticles based on the zwitterionic pillar[5]arene and Ag⁺: synthesis, self-assembly and cytotoxicity in the human lung cancer cell line A549

• Dmitriy N. Shurpik,
• Denis A. Sevastyanov,
• Pavel V. Zelenikhin,
• Pavel L. Padnya,
• Vladimir G. Evtugyn,
• Yuriy N. Osin and
• Ivan I. Stoikov

Beilstein J. Nanotechnol. 2020, 11, 421–431, doi:10.3762/bjnano.11.33

• NMR spectroscopy, two-dimensional 1H,1H-NOESY NMR spectroscopy, IR spectroscopy, MALDI–TOF mass-spectrometry and elemental analysis. Association of decasubstituted pillar[5]arenes with Ag+ In addition, the self-association of the obtained macrocycles 2–4 and their aggregation with AgNO3 in water was

• % residual signal with the maximum gradient strength. The values of δ and Δ were 1.800 μs and 100 ms, respectively. The pulse gradients were incremented from 2 to 95% of the maximum gradient strength in a linear ramp [49]. Electrospray ionization mass spectrometry Electrospray ionization mass spectra (ESI

Interactions at the cell membrane and pathways of internalization of nano-sized materials for nanomedicine

• Valentina Francia,
• Daphne Montizaan and
• Anna Salvati

Beilstein J. Nanotechnol. 2020, 11, 338–353, doi:10.3762/bjnano.11.25

• is also known that the corona composition evolves over time [195][196][197]. Recent studies from Chan and colleagues are trying to explore how the corona composition affects the biological interactions of nanoparticles by performing mass spectrometry screenings and by developing computational models

Bombesin receptor-targeted liposomes for enhanced delivery to lung cancer cells

• Mohammad J. Akbar,
• Pâmela C. Lukasewicz Ferreira,
• Melania Giorgetti,
• Leanne Stokes and
• Christopher J. Morris

Beilstein J. Nanotechnol. 2019, 10, 2553–2562, doi:10.3762/bjnano.10.246

• structure was modified to bear an N terminal ʟ-cysteine residue, which enables subsequent attachment to a functionalised lipid carrier. The peptide, hereafter termed cystabn, was prepared by fluorenylmethoxycarbonyl (Fmoc) solid-phase peptide synthesis and characterised by HPLC and mass spectrometry (data

• peptide affords facile functionalisation of DSPE-PEG2000-maleimide thorough thiol coupling chemistry. Successful conjugation of the peptide was confirmed by MALDI–TOF mass spectrometry (Figure 2a,b). The most abundant mass peak of DSPE-PEG2000-cystabn (calculated mass: 4137.41 Da, assuming perfect

• cystabn (13.3 μmol in 2 mL methanol) and stirred for 24 h at RT under nitrogen gas. After confirmation of successful conjugation by MALDI–TOF mass spectrometry analysis the solvent was evaporated and the reaction mixture re-dissolved in milli-Q water. Unreacted peptide was removed by dialysis against

Label-free highly sensitive probe detection with novel hierarchical SERS substrates fabricated by nanoindentation and chemical reaction methods

• Jingran Zhang,
• Tianqi Jia,
• Yongda Yan,
• Li Wang,
• Peng Miao,
• Yimin Han,
• Xinming Zhang,
• Guangfeng Shi,
• Yanquan Geng,
• Zhankun Weng,
• Daniel Laipple and
• Zuobin Wang

Beilstein J. Nanotechnol. 2019, 10, 2483–2496, doi:10.3762/bjnano.10.239

• food are detected by using many methods including gas chromatography, gas chromatography mass spectrometry, and liquid chromatography. These methods suffer from the need of preprocessing and long analysis time. However, SERS technology is a new option to detect pesticide residues in a fast, simple, and

Mobility of charge carriers in self-assembled monolayers

• Zhihua Fu,
• Tatjana Ladnorg,
• Hartmut Gliemann,
• Alexander Welle,
• Asif Bashir,
• Michael Rohwerder,
• Qiang Zhang,
• Björn Schüpbach,
• Andreas Terfort and
• Christof Wöll

Beilstein J. Nanotechnol. 2019, 10, 2449–2458, doi:10.3762/bjnano.10.235

• . Time-of-flight secondary ion mass spectrometry (TOF-SIMS) measurements were carried out in a TOF-SIMS 5 device (ION-TOF GmbH, Münster, Germany). The spectrometry was performed in static SIMS mode (primary ion beam dose < 2 × 1011 ions/cm2) with Bi3+ primary ions at 25 keV. Spectra were calibrated on

Long-term entrapment and temperature-controlled-release of SF₆ gas in metal–organic frameworks (MOFs)

• Hana Bunzen,
• Andreas Kalytta-Mewes,
• Leo van Wüllen and
• Dirk Volkmer

Beilstein J. Nanotechnol. 2019, 10, 1851–1859, doi:10.3762/bjnano.10.180

•  1). The analysis revealed a gradual mass loss between 150–500 °C. When heated above 500 °C, a second mass loss was observed which corresponded to the framework decomposition. By utilizing mass spectrometry, we analyzed the gaseous products that were released during sample heating. We recorded that

• decomposition, a study of temperature-induced gas release followed by mass spectrometry was carried out. In this measurement only signals corresponding to the SF6 fragments (such as SF5· and SF4·) [41] and no signals of its thermal decomposition products [42] could be detected, confirming that the gas release

• phase by mass spectrometry (Figure S12 in Supporting Information File 1). As expected, upon adding the acid to the reaction vessel, the framework decomposed and an immediate evolution of gas bubbles was observed. The SF6 release could be followed by mass spectrometry; however, a precise quantification

Biocatalytic oligomerization-induced self-assembly of crystalline cellulose oligomers into nanoribbon networks assisted by organic solvents

• Yuuki Hata,
• Yuka Fukaya,
• Toshiki Sawada,
• Masahito Nishiura and
• Takeshi Serizawa

Beilstein J. Nanotechnol. 2019, 10, 1778–1788, doi:10.3762/bjnano.10.173

• structure of the products was analyzed by 1H NMR spectroscopy and MALDI–TOF mass spectrometry. The NMR spectra of the representative products showed proton signals for cellulose oligomers (Figure 5). In addition, the mass spectra further revealed the successful synthesis of cellulose oligomers (Figure 6

• robustness. Experimental Materials αG1P disodium salt n-hydrate and 40% sodium deuteroxide (NaOD)/deuterium oxide (D2O) solution were purchased from Wako Pure Chemical Industries. ProteoMass MALDI–MS standard, 1% trifluoroacetic acid, MeCN used for preparing MALDI–TOF mass spectrometry samples, 2,5

• centrifugation (20,400g)/redispersion cycles to remove more than 99.999% of the soluble fraction of the reaction mixtures. For MALDI–TOF mass spectrometry, the purified product dispersions were stored at 4 °C until use. For the quantification of the insoluble products, a volume of the purified product

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

• samples of copper, silver and gold at 50 eV and 10 eV pass energy and comparison with reference values. Spectra were obtained with an Al Kα X-ray source, using C 1s as a reference for the binding energy [50]. Gas chromatography–mass spectrometry (GC–MS) data were recorded on a Thermo Finnigan Trace DSQ

Serum type and concentration both affect the protein-corona composition of PLGA nanoparticles

• Katrin Partikel,
• Robin Korte,
• Dennis Mulac,
• Hans-Ulrich Humpf and
• Klaus Langer

Beilstein J. Nanotechnol. 2019, 10, 1002–1015, doi:10.3762/bjnano.10.101

• assay, zeta potential measurements, and liquid chromatography–mass spectrometry/mass spectrometry (LC–MS/MS). Additionally, the time-dependent cell interaction of PLGA NPs in the absence or presence of a preformed protein corona was assessed by in vitro incubation experiments with the human liver cancer

• complexes from excess serum proteins we used sodium dodecylsulfate polyacrylamide gel electrophoresis (SDS-PAGE), zeta potential measurements, and liquid chromatography–mass spectrometry/mass spectrometry (LC–MS/MS) to study the composition of adsorbed proteins in detail. A quantitative analysis of corona

• carried out overnight under slight shaking (37 °C, 900 rpm). Finally, the reaction was stopped by adjusting the pH to below 6 with glacial acetic acid and the samples were filled up to a total volume of 2 mL with ultrapure water for the further experimental procedure. Sample preparation for mass

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