Design and facile synthesis of defect-rich C-MoS₂/rGO nanosheets for enhanced lithium–sulfur battery performance

• Chengxiang Tian,
• Juwei Wu,
• Zheng Ma,
• Bo Li,
• Pengcheng Li,
• Xiaotao Zu and
• Xia Xiang

Beilstein J. Nanotechnol. 2019, 10, 2251–2260, doi:10.3762/bjnano.10.217

• -4, C-MoS2/rGO-6, C-MoS2/rGO-8) with a 3:1 mass ratio was calcined at 155 °C for 12 h in a sealed vessel. Materials characterization The structure and morphology were investigated by field-emission scanning electron microscopy (FE-SEM, INSPECT F50) and transmission electron microscopy (TEM, ZEISS

Nontoxic pyrite iron sulfide nanocrystals as second electron acceptor in PTB7:PC₇₁BM-based organic photovoltaic cells

• Olivia Amargós-Reyes,
• José-Luis Maldonado,
• Omar Martínez-Alvarez,
• María-Elena Nicho,
• José Santos-Cruz,
• Juan Nicasio-Collazo,
• Irving Caballero-Quintana and
• Concepción Arenas-Arrocena

Beilstein J. Nanotechnol. 2019, 10, 2238–2250, doi:10.3762/bjnano.10.216

• tunneling current (It) and the applied potential (U) are A = 50 nm × 50 nm, It = 500 pA and U = 450 mV. The scanning electron microscopy (SEM) image of agglomerated FeS2 NCs is shown in Figure 3b. The results verify that the sizes of the NCs lie within the nanoscale regime (about 15 to 25 nm). The energy

Targeted therapeutic effect against the breast cancer cell line MCF-7 with a CuFe₂O₄/silica/cisplatin nanocomposite formulation

• B. Rabindran Jermy,
• Vijaya Ravinayagam,
• Widyan A. Alamoudi,
• Dana Almohazey,
• Hatim Dafalla,
• Lina Hussain Allehaibi,
• Abdulhadi Baykal,
• Muhammet S. Toprak and
• Thirunavukkarasu Somanathan

Beilstein J. Nanotechnol. 2019, 10, 2217–2228, doi:10.3762/bjnano.10.214

• ), scanning electron microscopy (SEM) equipped with energy dispersive X-ray (EDX) spectroscopy and transmission electron microscopy (TEM) techniques. The study showed the high cisplatin release capability and targeted anticancer efficiency demonstrated in vitro in the breast cancer cell line MCF-7. Materials

Ultrathin Ni_1−xCo_xS₂ nanoflakes as high energy density electrode materials for asymmetric supercapacitors

• Xiaoxiang Wang,
• Teng Wang,
• Rusen Zhou,
• Lijuan Fan,
• Shengli Zhang,
• Feng Yu,
• Tuquabo Tesfamichael,
• Liwei Su and
• Hongxia Wang

Beilstein J. Nanotechnol. 2019, 10, 2207–2216, doi:10.3762/bjnano.10.213

• . Notably, the influence of the substrate on the electrochemical performance can be neglected because of its small area of CV curves under the same scan rate (Figure S1, Supporting Information File 1). Material characterization Field-emission scanning electron microscopy (FESEM, JSM-7001F, JEOL) with energy

Use of data processing for rapid detection of the prostate-specific antigen biomarker using immunomagnetic sandwich-type sensors

• Camila A. Proença,
• Tayane A. Freitas,
• Thaísa A. Baldo,
• Elsa M. Materón,
• Flávio M. Shimizu,
• Gabriella R. Ferreira,
• Frederico L. F. Soares,
• Ronaldo C. Faria and
• Osvaldo N. Oliveira Jr.

Beilstein J. Nanotechnol. 2019, 10, 2171–2181, doi:10.3762/bjnano.10.210

• spectroscopy (FTIR), field-emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDX), and polarization-modulated infrared reflection absorption spectroscopy (PM-IRRAS, Figure S1) is described. The Silhouette coefficients calculated for IDMAP, Sammon’s mapping (SM), principal

Green and scalable synthesis of nanocrystalline kuramite

• Andrea Giaccherini,
• Giuseppe Cucinotta,
• Stefano Martinuzzi,
• Enrico Berretti,
• Werner Oberhauser,
• Alessandro Lavacchi,
• Giovanni Orazio Lepore,
• Giordano Montegrossi,
• Maurizio Romanelli,
• Antonio De Luca,
• Massimo Innocenti,
• Vanni Moggi Cecchi,
• Matteo Mannini,
• Antonella Buccianti and
• Francesco Di Benedetto

Beilstein J. Nanotechnol. 2019, 10, 2073–2083, doi:10.3762/bjnano.10.202

• of nanocrystalline kuramite by means of a simpler, greener and scalable solvothermal synthesis. We exploited a multianalytical characterization approach (X-ray diffraction, extended X-ray absorption fine structure, field emission scanning electron microscopy, Raman spectroscopy and electronic

• (EXAFS) signal. EXAFS spectra were fitted through the use of ARTEMIS, FEFF8 and ATOMS software in the Fourier transform (FT) space [58][60][61]. Results Scanning electron microscopy Typical SEM images are presented in Figure 1 where no appreciable differences among the tens of observations performed on

• . We synthesized three samples using a solvothermal approach, which was carried out under mild conditions in ethylene glycol as a green solvent. We tackled the aforementioned difficulties in phase assignment by means of thorough characterization, including X-ray diffraction (XRD), scanning electron

Incorporation of doxorubicin in different polymer nanoparticles and their anticancer activity

• Sebastian Pieper,
• Hannah Onafuye,
• Dennis Mulac,
• Jindrich Cinatl Jr.,
• Mark N. Wass,
• Martin Michaelis and
• Klaus Langer

Beilstein J. Nanotechnol. 2019, 10, 2062–2072, doi:10.3762/bjnano.10.201

• were confirmed by scanning electron microscopy (SEM) images (Figure 2). Influence of the preparation technique on loading efficiency and drug release Loading efficiencies ranging from 25.5 ± 1.0% to 44.8 ± 5.8% of the applied doxorubicin were detected in the different nanoparticle preparations as shown

• measured at a temperature of 22 °C using a backscattering angle of 173°. The zeta potential was determined with the same instrument and the same diluted nanoparticle suspension by laser Doppler microelectrophoresis. Scanning electron microscopy (SEM) For scanning electron microscopy (SEM), the particle

Synthesis of highly active ETS-10-based titanosilicate for heterogeneously catalyzed transesterification of triglycerides

• Muhammad A. Zaheer,
• David Poppitz,
• Khavar Feyzullayeva,
• Marianne Wenzel,
• Jörg Matysik,
• Radomir Ljupkovic,
• Aleksandra Zarubica,
• Alexander A. Karavaev,
• Andreas Pöppl,
• Roger Gläser and
• Muslim Dvoyashkin

Beilstein J. Nanotechnol. 2019, 10, 2039–2061, doi:10.3762/bjnano.10.200

• size (scanning electron microscopy, laser diffraction), textural properties (N2 sorption, Hg porosimetry), presence of hydroxyl groups and active sites (temperature-programmed desorption of NH3 and CO2, 29Si magic angle spinning nuclear magnetic resonance (NMR)), mesopore accessibility and diffusion

• catalysts were characterized to obtain quantitative information on properties such as crystal structure by X-ray diffraction (XRD), crystal size by laser diffraction, crystal morphology by scanning electron microscopy (SEM) and transmission electron microscopy (TEM), pore width by N2 sorption and Hg

Optimization and performance of nitrogen-doped carbon dots as a color conversion layer for white-LED applications

• Tugrul Guner,
• Hurriyet Yuce,
• Didem Tascioglu,
• Eren Simsek,
• Umut Savaci,
• Aziz Genc,
• Servet Turan and
• Mustafa M. Demir

Beilstein J. Nanotechnol. 2019, 10, 2004–2013, doi:10.3762/bjnano.10.197

• .) attached to a USB2000+ spectrometer (Ocean Optics Inc., Dunedin, FL, USA) with a premium fiber cable. A commercial blue LED chip (CREE, 450 nm, royal blue) was used as the blue light source. The morphology of the produced N-CDot fibers was analyzed by scanning electron microscopy (SEM; Quanta 250, FEI

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

• was 25 cm. We used thermally oxidized Si(001) with an oxide thickness of 100 nm as substrates. However, for the scanning electron microscopy studies, Si(001) substrates with native oxide were used in order to eliminate the charging effect. All films were deposited at room temperature (25 °C) with a

High-tolerance crystalline hydrogels formed from self-assembling cyclic dipeptide

• Yongcai You,
• Ruirui Xing,
• Qianli Zou,
• Feng Shi and
• Xuehai Yan

Beilstein J. Nanotechnol. 2019, 10, 1894–1901, doi:10.3762/bjnano.10.184

• 3317 cm−1, indicating the formation of strong hydrogen bonds between C-WY molecules in the hydrogel (Figure 1B). Further characterization by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) was performed to inspect the morphology of the hydrogel (Figure 1C,D). The fibers in

Charge-transfer interactions between fullerenes and a mesoporous tetrathiafulvalene-based metal–organic framework

• Manuel Souto,
• Joaquín Calbo,
• Samuel Mañas-Valero,
• Aron Walsh and
• Guillermo Mínguez Espallargas

Beilstein J. Nanotechnol. 2019, 10, 1883–1893, doi:10.3762/bjnano.10.183

• needle-like morphology of C60@MUV-2 also remained similar to the one of MUV-2 as confirmed by scanning electron microscopy (SEM) (Figure S1, Supporting Information File 1). Raman and UV–vis spectroscopy Raman spectra of C60, MUV-2 and C60@MUV-2 crystals were measured using a Raman excitation wavelength

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

• included powder X-ray diffraction measurements, thermogravimetric analysis, Fourier-transform infrared spectroscopy, scanning electron microscopy, 19F nuclear magnetic resonance spectroscopy and computational simulations. In addition, the possibility to release the gas guest by applying elevated

• , scanning electron microscopy (SEM) images of the sample (taken before and after the guest loading) did not reveal any detectable changes in the crystal surface and morphology, confirming that the MOF crystals remained intact during the loading (Supporting Information File 1, Figure S1). The presence of SF6

Nanoarchitectonics meets cell surface engineering: shape recognition of human cells by halloysite-doped silica cell imprints

• Elvira Rozhina,
• Ilnur Ishmukhametov,
• Svetlana Batasheva,
• Farida Akhatova and
• Rawil Fakhrullin

Beilstein J. Nanotechnol. 2019, 10, 1818–1825, doi:10.3762/bjnano.10.176

• within the silica shells deposited around perinuclear areas, as shown in Figure 2C. Scanning electron microscopy (SEM) was employed to investigate the morphology of the halloysite-doped and halloysite-free silica shells deposited onto HeLa cells. Suspended cells were deposited onto glass substrates

• . Characterisation Scanning electron microscopy (SEM) imaging of samples sputter-coated with gold was performed with a Hitachi SU8000 microscope equipped with energy-dispersive X-ray (EDX) spectrometer. The interaction of cells with inorganic shapes was also recorded with an atomic-force microscope (Dimension Icon

• ); (B, C) dark-field microscopy images of live HeLa cells coated with halloysite-doped silica shells; scanning electron microscopy images of (D) intact HeLa cells, (E) HeLa cells coated with pure silica shells and (F) HeLa cells coated with halloysite-doped silica shells. Red arrows indicate halloysite

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

• chains [42]. In other words, a higher uniformity of the chain lengths leads to higher integrity of the crystals. Scanning electron microscopy (SEM) was used to uncover the nanomorphology of the gels. The images revealed a well-grown network structure composed of nanoribbon-shaped fibers (Figure 9), which

TiO₂/GO-coated functional separator to suppress polysulfide migration in lithium–sulfur batteries

• Ning Liu,
• Lu Wang,
• Taizhe Tan,
• Yan Zhao and
• Yongguang Zhang

Beilstein J. Nanotechnol. 2019, 10, 1726–1736, doi:10.3762/bjnano.10.168

• structure to accommodate sulfur, but also supplies numerous adsorption and catalytic sites for the polysulfides, thus significantly improving both the specific capacity and cycling performance of Li/S batteries. Figure 3a shows a scanning electron microscopy (SEM) image of as-prepared TiO2, which has been

Doxorubicin-loaded human serum albumin nanoparticles overcome transporter-mediated drug resistance in drug-adapted cancer cells

• Hannah Onafuye,
• Sebastian Pieper,
• Dennis Mulac,
• Jindrich Cinatl Jr.,
• Mark N. Wass,
• Klaus Langer and
• Martin Michaelis

Beilstein J. Nanotechnol. 2019, 10, 1707–1715, doi:10.3762/bjnano.10.166

• 460 and 500 nm and polydispersity indices in the range of 0.153 and 0.213, indicating a narrow but not monodisperse size distribution (Table 1). The spherical shape and narrow size distribution of HSA nanoparticles was confirmed by scanning electron microscopy (SEM) as depicted for nanoparticles

• nanoparticle dilutions described above were transferred into a folded capillary cell and the experiment was conducted at 22 °C. Morphological analysis of nanoparticles by scanning electron microscopy (SEM) 3 µL of diluted HAS nanoparticle suspension (0.25 mg/mL) was applied on a 0.1 µm membrane filter

Tuning the performance of vanadium redox flow batteries by modifying the structural defects of the carbon felt electrode

• Ditty Dixon,
• Deepu Joseph Babu,
• Aiswarya Bhaskar,
• Hans-Michael Bruns,
• Joerg J. Schneider,
• Frieder Scheiba and
• Helmut Ehrenberg

Beilstein J. Nanotechnol. 2019, 10, 1698–1706, doi:10.3762/bjnano.10.165

• scanning electron microscopy (SEM) analysis, it can be seen that the surface morphology of the fibers of both samples looked identical and thus any kind of surface roughening leading to an increase of the surface area can be ignored. This is further supported by our previous study were the BET measurements

• were referenced to the C 1s peak of hydrocarbon at 285.0 eV binding energy, controlled by means of the well-known photoelectron peaks of metallic Cu, Ag, and Au. Scanning electron microscopy (SEM) The carbon surface fiber morphology was investigated in a Zeiss Supra 55 SEM with primary electron

Nanoporous smartPearls for dermal application – Identification of optimal silica types and a scalable production process as prerequisites for marketed products

• David Hespeler,
• Sanaa El Nomeiri,
• Jonas Kaltenbach and
• Rainer H. Müller

Beilstein J. Nanotechnol. 2019, 10, 1666–1678, doi:10.3762/bjnano.10.162

• = 2–60°) was applied and the goniometer was equipped with a Cu anode (Cu Kα, λ= 0.15406 nm) at a voltage of 40 kV and current of 35 mA. Light microscopy (LM) and scanning electron microscopy (SEM) Light microscope imaging was performed using a Motic microscope (BA210, Motic Deutschland GmbH, Germany

• shell of the particles. This was checked by light microscopy and scanning electron microscopy. To study the suitability of the process, silica particles differing in particle size, pore diameter and pore volume were selected (Table 1). The investigation should also provide evidence as to which particle

Subsurface imaging of flexible circuits via contact resonance atomic force microscopy

• Wenting Wang,
• Chengfu Ma,
• Yuhang Chen,
• Lei Zheng,
• Huarong Liu and
• Jiaru Chu

Beilstein J. Nanotechnol. 2019, 10, 1636–1647, doi:10.3762/bjnano.10.159

• into account for a blunt conical tip [34][35]. In our calculations, a half-cone angle of 15° was determined for the adopted probes, which was in accordance with the manufacturer’s specifications. The tip apex radius was averaged to be approximately 50 nm according to scanning electron microscopy

• ]. We have calculated the contact stiffness contrast when the tip radius ranged from 6 to 121 nm. Such a range covers the practical tip radius in experiments according to scanning electron microscopy imaging. The results show that deviations in the evaluated contact stiffness contrast are less than 1

Chiral nanostructures self-assembled from nitrocinnamic amide amphiphiles: substituent and solvent effects

• Hejin Jiang,
• Huahua Fan,
• Yuqian Jiang,
• Li Zhang and
• Minghua Liu

Beilstein J. Nanotechnol. 2019, 10, 1608–1617, doi:10.3762/bjnano.10.156

• 4NCLG assemblies in ethanol was analyzed by scanning electron microscopy (SEM). Figure 2 shows the detailed SEM images of the self-assembled structures. Upon SEM observation, 2NCLG self-assembled into a right-handed helical nanofiber with a helical pitch of about 250 nm and a width of approximately 70

High-temperature resistive gas sensors based on ZnO/SiC nanocomposites

• Vadim B. Platonov,
• Marina N. Rumyantseva,
• Alexander S. Frolov,
• Alexey D. Yapryntsev and
• Alexander M. Gaskov

Beilstein J. Nanotechnol. 2019, 10, 1537–1547, doi:10.3762/bjnano.10.151

• the components in a single homogeneous paste with subsequent thermal annealing. The composition and microstructure of the materials were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy

• Experimental part. The characteristics of the synthesized materials are summarized in Table 1. Figure 2 shows the scanning electron microscopy (SEM) micrographs of SiC (Figure 2a,c) and ZnO (Figure 2b,d) nanofibers in a polymer matrix (Figure 2a,b) and after annealing (Figure 2c,d). The polymeric fibers

• –Halenda) models. The morphology of the nanofibers was studied by scanning electron microscopy (SEM) using a Carl Zeiss NVision 40 electron microscope with an intra-lens detector at an accelerating voltage of 5 kV. The IR spectra (FTIR) of the ZnO/SiC nanocomposites were taken on a Spectrum One (Perkin

Development of a new hybrid approach combining AFM and SEM for the nanoparticle dimensional metrology

• Loïc Crouzier,
• Alexandra Delvallée,
• Sébastien Ducourtieux,
• Laurent Devoille,
• Guillaume Noircler,
• Christian Ulysse,
• Olivier Taché,
• Elodie Barruet,
• Christophe Tromas and
• Nicolas Feltin

Beilstein J. Nanotechnol. 2019, 10, 1523–1536, doi:10.3762/bjnano.10.150

• proposes a new approach of hybrid metrology taking advantage of the complementary nature of atomic force microscopy (AFM) and scanning electron microscopy (SEM) techniques for measuring the main characteristic parameters of nanoparticle (NP) dimensions in 3D. The NP area equivalent, the minimal and the

• budget; Introduction AFM (atomic force microscopy) or SEM (scanning electron microscopy) are considered to be reference techniques for measuring the size of nanoparticles (NPs) because the measurements are based on a direct observation of the imaged NP population. This creates a direct link between the

Rapid thermal annealing for high-quality ITO thin films deposited by radio-frequency magnetron sputtering

• Petronela Prepelita,
• Ionel Stavarache,
• Doina Craciun,
• Florin Garoi,
• Catalin Negrila,
• Beatrice Gabriela Sbarcea and
• Valentin Craciun

Beilstein J. Nanotechnol. 2019, 10, 1511–1522, doi:10.3762/bjnano.10.149

• predefined thickness values. Scanning electron microscopy (SEM) investigations (FEI Quanta) were performed to observe the structures and morphology of the deposited surfaces. Given that the thickness of the quartz substrate is much greater than that of the ITO conductive film, a thin layer of gold was

Flexible freestanding MoS₂-based composite paper for energy conversion and storage

• Florian Zoller,
• Jan Luxa,
• Thomas Bein,
• Dina Fattakhova-Rohlfing,
• Daniel Bouša and
• Zdeněk Sofer

Beilstein J. Nanotechnol. 2019, 10, 1488–1496, doi:10.3762/bjnano.10.147

• -like material by filtration of the mixture on top of a filter. The self-assembled material was denoted as MoS2-based composite paper. A picture of the composite paper is shown in Figure 1. We investigated the morphology of this compound material by scanning electron microscopy (SEM) with results shown

• electron microscopy (SEM) with a FEG electron source (Tescan Lyra dual beam microscope). The elemental composition and mapping were performed using an energy dispersive spectroscopy (EDS) analyzer (X-MaxN) with a 20 mm2 SDD detector (Oxford Instruments) and AZtecEnergy software. A 10 kV beam was used for

• mV·s−1. For the n-butyllithium treated sample, the foil was left in n-butyllithium solution (2.5 M solution) for several days under inert Ar atmosphere. After that, water was added to the solution. The foil was then dried and used. Characterization The morphology was investigated using scanning