Nickel nanoparticles supported on a covalent triazine framework as electrocatalyst for oxygen evolution reaction and oxygen reduction reactions

• Secil Öztürk,
• Yu-Xuan Xiao,
• Dennis Dietrich,
• Beatriz Giesen,
• Juri Barthel,
• Jie Ying,
• Xiao-Yu Yang and
• Christoph Janiak

Beilstein J. Nanotechnol. 2020, 11, 770–781, doi:10.3762/bjnano.11.62

• Information File 1). As expected, both CTF-1-400 and CTF-1-600 (as-synthesized) showed limited long-range order according to powder X-ray diffraction (PXRD) measurements (Figure S1, Supporting Information File 1) [32][42]. Nitrogen sorption measurements for CTF-1-400 showed a type-I isotherm with 954 m2/g

• bis(trifluoromethylsulfonyl)imide ([BMIm][NTf2]) was synthesized in two steps following a literature procedure [67]. The anion purity of IL by ion chromatography was found to be above 99% and the water content of the IL by Karl-Fischer titration was less than 10 ppm. Methods Powder X-ray diffraction

Structural optical and electrical properties of a transparent conductive ITO/Al–Ag/ITO multilayer contact

• Aliyu Kabiru Isiyaku,
• Ahmad Hadi Ali and
• Nafarizal Nayan

Beilstein J. Nanotechnol. 2020, 11, 695–702, doi:10.3762/bjnano.11.57

• pure ITO layer (as reference) were prepared by RF and DC sputtering. The microstructural, optical and electrical properties of the ITO/Al–Ag/ITO (IAAI) films were investigated before and after annealing at 400 °C. X-ray diffraction measurements show that the insertion of the Al–Ag intermediate bilayer

• –Ag/ITO) are examined. Moreover, annealing was carried out at 400 °C with an ITO/Al–Ag/ITO (IAAI) multilayer film and a pure ITO film for comparison. Results and Discussion Figure 1 shows the X-ray diffraction (XRD) patterns for as-deposited and annealed IAAI multilayer films. The as-deposited film

• composition of the as-deposited and annealed IAAI films was determined using X-ray diffraction. A PANalytic XPERT-PRO MPD X-ray diffractometer model was used with Cu Kα1 (λ = 1.540598 Å) radiation, 40 kV working voltage and 30 mA filament current, in a range of 2θ = 15–90°. The Scherrer equation was used to

Preparation, characterization and photocatalytic performance of heterostructured CuO–ZnO-loaded composite nanofiber membranes

• Wei Fang,
• Liang Yu and
• Lan Xu

Beilstein J. Nanotechnol. 2020, 11, 631–650, doi:10.3762/bjnano.11.50

• -transform infrared spectroscopy (FTIR, Nicolet5700, Thermo Nicolet Company, Waltham, MA, USA), carrying out 32 scans within the wavenumber range of 400–4000 cm−1 with a resolution of 4 cm−1. X-ray diffraction (XRD) analyses were carried out using a Philips X’Pert-Pro MPD (PANalytical, Almelo & Eindhoven

• analysis of CuO–ZnO-loaded CNFMs The X-ray diffraction spectrum of heterostructured CuO–ZnO-loaded CNFMs is given in Figure 19. The diffraction peaks of PAN and PVDF are located at 17° and 21°, respectively, and the superposition peak of Cu(Ac)2 and Zn(Ac)2 is at 7°, indicating remainders of Cu(Ac)2 and Zn

• CuO–ZnO-loaded CNFMs after different times of hydrothermal synthesis: (a) 6 h; (b) 12 h; (c) 18 h; (d) 24 h. X-ray diffraction pattern of heterostructured CuO–ZnO-loaded CNFMs. Elemental compositions of CNFMs with different CuO–ZnO heterostructures. Morphologies and CA of CNFMs before and after heat

Correction: Photocatalytic antibacterial performance of TiO₂ and Ag-doped TiO₂ against S. aureus. P. aeruginosa and E. coli

• Kiran Gupta,
• R. P. Singh,
• Ashutosh Pandey and
• Anjana Pandey

Beilstein J. Nanotechnol. 2020, 11, 547–549, doi:10.3762/bjnano.11.43

• results of the article. XRD of TiO2 and Ag-doped TiO2 nanoparticles X-ray diffraction (XRD) was used to characterize as-prepared TiO2 and Ag-doped TiO2 nanoparticles. The diameter of crystalline TiO2, 3 wt % Ag-doped TiO2 and 7 wt % Ag-doped TiO2 nanoparticles annealed at 450 °C was calculated by the

Interfacial charge transfer processes in 2D and 3D semiconducting hybrid perovskites: azobenzene as photoswitchable ligand

• Nicole Fillafer,
• Tobias Seewald,
• Lukas Schmidt-Mende and
• Sebastian Polarz

Beilstein J. Nanotechnol. 2020, 11, 466–479, doi:10.3762/bjnano.11.38

• headgroup provides not enough space for the molecule to fit into the structure. The materials were examined by using a combination of methods to study their structure and electronic properties. In Figure 2D the powder X-ray diffraction (PXRD) patterns and the associated scanning electron microscopy (SEM

• . The suspension was stirred for 1 h, then the particles were centrifuged, washed three times with 3 mL DCM and then dried under reduced pressure. The samples were kept under nitrogen atmosphere to prevent decomposition. Characterization X-ray diffraction (XRD) measurements of drop-cast particles on

• , (C) SEM image of 2D-AzoOC12, scale bar = 1 µm. (D) Powder X-ray diffraction (PXRD) pattern of the 2D LHPs with incorporated AzoC2, AzoOC4 and AzoOC12 with a layer thickness of d(001) = 2.48 nm, d(001) = 2.84 nm and d(001) = 3.40 nm, respectively (from top to bottom). (E) 1H NMR spectra in the

Atomic-resolution imaging of rutile TiO₂(110)-(1 × 2) reconstructed surface by non-contact atomic force microscopy

• Daiki Katsube,
• Shoki Ojima,
• Eiichi Inami and
• Masayuki Abe

Beilstein J. Nanotechnol. 2020, 11, 443–449, doi:10.3762/bjnano.11.35

• clean surface is relatively easy. A well-known rutile TiO2(110) surface is the (1 × 1) structure [2]. The (1 × 1) surface has been studied using low-energy electron diffraction (LEED) [3][4], surface X-ray diffraction [5], non-contact atomic force microscopy (NC-AFM) [6][7][8][9], scanning tunneling

Synthesis and enhanced photocatalytic performance of 0D/2D CuO/tourmaline composite photocatalysts

• Changqiang Yu,
• Min Wen,
• Zhen Tong,
• Shuhua Li,
• Yanhong Yin,
• Xianbin Liu,
• Yesheng Li,
• Tongxiang Liang,
• Ziping Wu and
• Dionysios D. Dionysiou

Beilstein J. Nanotechnol. 2020, 11, 407–416, doi:10.3762/bjnano.11.31

• product was named CuO/tourmaline-1:1 (1:1 in mass ratio of the CuO/tourmaline). By controlling the dosage of Cu(CH3COO)2·H2O and NaOH in proportion the CuO/tourmaline composites in different mass ratios of the CuO/tourmaline were acquired. Characterization X-ray diffraction (XRD) patterns were obtained

Facile biogenic fabrication of hydroxyapatite nanorods using cuttlefish bone and their bactericidal and biocompatibility study

• Satheeshkumar Balu,
• Manisha Vidyavathy Sundaradoss,
• Swetha Andra and
• Jaison Jeevanandam

Beilstein J. Nanotechnol. 2020, 11, 285–295, doi:10.3762/bjnano.11.21

• ) nanorods using cuttlefish bone powder as a precursor (CB-Hap NRs). The obtained CB-Hap NRs were investigated using transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA) techniques to evaluate their

• setup via an oil bath approach to synthesize Hap nanorods from cuttlefish bone powders and optimize their synthesis parameters. The systematic characterization using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM) was performed to

• ]. Characterization of cuttlebone-Hap nanorods X-ray diffraction The X-ray diffraction (XRD) was carried out using an X-ray powder diffractometer (Bruker, Model D8 Advance) to study the crystallinity and phase formation of Hap nanorods. CB powder samples (ball milled) and CB-Hap NR powder was gently ground using a

Simple synthesis of nanosheets of rGO and nitrogenated rGO

• Pallellappa Chithaiah,
• Madhan Mohan Raju,
• Giridhar U. Kulkarni and
• C. N. R. Rao

Beilstein J. Nanotechnol. 2020, 11, 68–75, doi:10.3762/bjnano.11.7

• force microscopy (AFM), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). X-ray diffraction patterns of the samples were collected in the range of 10–70° (2θ) using a Bruker D8 diffractometer with a Cu Kα source (λ = 0.154178 nm). The morphology of the samples was examined using a Tescan

Influence of the epitaxial composition on N-face GaN KOH etch kinetics determined by ICP-OES

• Markus Tautz,
• Maren T. Kuchenbrod,
• Joachim Hertkorn,
• Robert Weinberger,
• Martin Welzel,
• Arno Pfitzner and
• David Díaz Díaz

Beilstein J. Nanotechnol. 2020, 11, 41–50, doi:10.3762/bjnano.11.4

• ICP-OES analysis. Methods PLM images were recorded directly after epitaxy on an Olympus BX51 microscope combined with an Olympus U-RFL-T UV light source. For excitation, 408 nm wavelength light was used. X-ray diffraction (XRD) was measured on a Bruker/Jordan Valley QC Velox. Scanning electron

• structure of a GaN layer stack grown by metal organic chemical vapour deposition (MOCVD) was varied in the unintentionally doped u-GaN bulk region. Different sequences of 2D and 3D grown layers led to a variation in dislocation density, which was monitored by photoluminescence microscopy (PLM) and X-ray

• diffraction (XRD). Thin-film processing including laser lift off (LLO) was applied. The influence of epitaxial changes on the N-face etch kinetics was determined in aqueous KOH solution at elevated temperature. Inductively-coupled plasma optical emission spectroscopy (ICP-OES) was used to measure the etch

Synthesis of amorphous and graphitized porous nitrogen-doped carbon spheres as oxygen reduction reaction catalysts

• Maximilian Wassner,
• Markus Eckardt,
• Andreas Reyer,
• Thomas Diemant,
• Michael S. Elsaesser,
• R. Jürgen Behm and
• Nicola Hüsing

Beilstein J. Nanotechnol. 2020, 11, 1–15, doi:10.3762/bjnano.11.1

• %). TEM images (Figure 3a–d) reveal no highly ordered domains (e.g., graphene layers) of the said N-doped carbon spheres, which is in good agreement with the results of the X-ray diffraction measurements (XRD, Figure 4), confirming an amorphous carbon structure for all particles mentioned so far. Upon

• thickness of the graphite layers Lc determined by X-ray diffraction measurements. Similar observation was made by Liu et al. for carbon spheres that were synthesized by hydrothermal treatment of a sucrose solution and subsequently graphitized in the presence of nickel-oxide particles. High-resolution TEM

• (Shirley background; peak shape: 70% Gaussian/30% Lorentzian) was carried out using the CasaXPS software package. X-ray diffraction (XRD) measurements were performed using a Bruker D8 Advance instrument (Bruker Karlsruhe), employing Cu Kα radiation (λ = 0.154 nm) in a 2θ range of 5° to 80° (0.02

Synthesis and acetone sensing properties of ZnFe₂O₄/rGO gas sensors

• Kaidi Wu,
• Yifan Luo,
• Ying Li and
• Chao Zhang

Beilstein J. Nanotechnol. 2019, 10, 2516–2526, doi:10.3762/bjnano.10.242

• of ZnFe2O4 and reduced graphene oxide (rGO) with different rGO content were prepared via a simple solvothermal method followed by a high-temperature annealing process in an inert atmosphere. The X-ray diffraction analysis confirmed that the introduction of rGO had no effect on the spinel structure of

• rate of 5 °C/min to reduce GO to rGO [33][34], and five samples were obtained: hollow spheres of pure ZnFe2O4 and ZnFe2O4/rGO composite spheres with 0.1, 0.25, 0.5 and 1 wt % of rGO. Characterization methods The crystal phases of pure ZnFe2O4 and the ZnFe2O4/rGO composites were characterized by X-ray

• diffraction (XRD, Bruker D8 Advance) using Cu Kα radiation at room temperature. The 2θ range was 10−80°, and the scanning rate was 5°·min−1. The microscopic morphology and the size of all samples were observed using a field-emission scanning electron microscope equipped with an energy-dispersive spectrometer

Air oxidation of sulfur mustard gas simulants using a pyrene-based metal–organic framework photocatalyst

• Ghada Ayoub,
• Mihails Arhangelskis,
• Xuan Zhang,
• Florencia Son,
• Timur Islamoglu,
• Tomislav Friščić and
• Omar K. Farha

Beilstein J. Nanotechnol. 2019, 10, 2422–2427, doi:10.3762/bjnano.10.232

• carbonylation reaction was utilized with 2,7-dibromopyrene as the starting material [46]. Powder X-ray diffraction (PXRD) analysis of the as-synthesized materials revealed that NU-400 is isostructural to the related UiO-67 framework based on 4,4'-biphenyldicarboxylate linkers. Subsequently, the structure of NU

Coating of upconversion nanoparticles with silica nanoshells of 5–250 nm thickness

• Cynthia Kembuan,
• Maysoon Saleh,
• Bastian Rühle,
• Ute Resch-Genger and
• Christina Graf

Beilstein J. Nanotechnol. 2019, 10, 2410–2421, doi:10.3762/bjnano.10.231

• particles of similar sizes [58][60][61]. Since the surface of the particles corresponds to that of particles from a standard Stöber synthesis, the colloids can be functionalized with the same diverse methods as Stöber silica particles [58]. Figure S5 in Supporting Information File 1 shows X-ray diffraction

• , 20 and 40 ppm) or erbium standard for ICP (c(Er3+) = 1, 5 and 10 ppm). X-ray diffraction (XRD) measurements A minimum amount of 10 mg of dried particles were used for the XRD measurements. The XRD device was a Rigaku SmartLab 3 kW with a DTex Ultra 250 detector (40 kV, 30 mA) equipped with a Cu Kα1

Semitransparent Sb₂S₃ thin film solar cells by ultrasonic spray pyrolysis for use in solar windows

• Jako S. Eensalu,
• Atanas Katerski,
• Erki Kärber,
• Lothar Weinhardt,
• Monika Blum,
• Clemens Heske,
• Wanli Yang,
• Ilona Oja Acik and
• Malle Krunks

Beilstein J. Nanotechnol. 2019, 10, 2396–2409, doi:10.3762/bjnano.10.230

• and back contact is needed to attain an AVT in excess of 20% for the complete solar cell. As-deposited Sb2S3 layers on glass/ITO/TiO2 substrate were amorphous (Figure 1d), as only signals of anatase-TiO2 and In2O3 from the substrate were detected by X-ray diffraction (XRD). In contrast, the XRD

• the I–V measurements. Surface views, by scanning electron microscopy (SEM) of 70 nm (a) and 100 nm (b) thick annealed Sb2S3 layers on a glass/ITO/TiO2 substrate. Photograph (c) of a 5 × 5 cm semitransparent (AVT 26%) stack of glass/ITO/TiO2/100 nm annealed Sb2S3, photographed by J. S. Eensalu. X-ray

• diffraction patterns (d) and Raman spectra (e) of as-deposited and vacuum-annealed Sb2S3 layers on glass/ITO/TiO2 substrate. S L2,3 XES spectra of two Sb2S3 films, as-deposited (“as-dep.”, blue) and after post-deposition treatment (“annealed”, red), both on a glass/ITO/TiO2 underlay (excitation energy 180 eV

Polyvinylpyrrolidone as additive for perovskite solar cells with water and isopropanol as solvents

• Chen Du,
• Shuo Wang,
• Xu Miao,
• Wenhai Sun,
• Yu Zhu,
• Chengyan Wang and
• Ruixin Ma

Beilstein J. Nanotechnol. 2019, 10, 2374–2382, doi:10.3762/bjnano.10.228

• SUPRA55. X-ray diffraction (XRD) patterns were collected with a SmartLab from Rigaku at 40 kV and 150 mA by using Cu Kα radiation (λ = 0.15405 nm). The photovoltaic performance of the PSCs was recorded using a Keithley 4200 source meter under one-sun AM 1.5G (100 mW·cm−2) illumination with a solar light

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

• Libra 200). Powder X-ray diffraction (XRD) measurements were conducted to determine the phase of the as-synthesized composites with Cu Kα radiation operated at 40 kV and 30 mA. X-ray photoelectron spectroscopy (XPS) analysis was performed on a Kratos AXIS Ultra DLD instrument using monochromated Al Kα X

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

• saline solution. The presence of cubic spinel CuFe2O4 on HYPS was confirmed through powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR) and diffuse reflectance UV–vis spectroscopy (DR UV–vis) analysis. The HYPS particles showed a surface area of 170 m2/g, pore size of 8.3 nm

• multifunctional biomedical applications. The crystalline phase, morphology, magnetization, and coordination environment of various spinel species were characterized using X-ray diffraction (XRD), BET surface area measurements, vibrating sample magnetometry (VSM), diffuse reflectance UV–vis spectroscopy (DR UV–vis

• and CuFe2O4/silicalite. Characterization techniques Powder X-ray diffraction (PXRD) patterns for the CuFe2O4/HYPS nanoformulation were analyzed using a Miniflex 600 instrument (Rigaku, Japan). The surface textures the formulations were analyzed with a ASAP-2020 plus (Micromeritics, USA) instrument

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

• analysed using X-ray photoelectron spectroscopy (XPS, Kratos AXIS Supra photoelectron spectrometer, Al Kα excitation (1486.6 eV)). Crystalline structure and composition of the samples were characterized by powder X-ray diffraction analysis (XRD, PANaytical MPD) using a Cu Kα (8047.8 eV) radiation source

• energy density of 67.5 Wh·kg−1), and excellent cycling stability and capacity retention. These results can be credited to synergic effects rich and fast redox reactions, high conductivity, as well as highly porous and robust ultrathin nanoflakes structures. (a) X-ray diffraction patterns of Ni1−xCoxS2

BergaCare SmartLipids: commercial lipophilic active concentrates for improved performance of dermal products

• Florence Olechowski,
• Rainer H. Müller and
• Sung Min Pyo

Beilstein J. Nanotechnol. 2019, 10, 2152–2162, doi:10.3762/bjnano.10.208

• loaded active agents, which can be measured by combining differential scanning calorimetry (DSC) with X-ray diffraction. Ruick showed a fast transition from the α modification to the β modification when SLNs were produced with tristearin (Figure 3), while a SmartLipids mixture with eight solid lipids

• ][13] (left) and lidocaine [14] (right). X-ray diffraction patterns of SLNs (pink curve) and SmartLipids mixture (red curve) determined directly after production and after one month (SLNs: blue curve) and one year (SmartLipids: black curve) storage at room temperature [5]. Fast degradation of

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

• others. Natural ternary Cu–Sn–S phases populate the pseudo ternary compositional field mostly along the two CuS–SnS and Cu2S–SnS2 joints [36][44]. Their nanocrystalline counterparts have broadened X-ray diffraction peaks. This limits the discrimination of the different phases and the study of their

• . 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

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

• maximum conversion of 83% after 24 h, the ETS-10-based catalyst reached 100% after 8 h, revealing its higher stability compared to CaO. The following characteristics of the catalysts were experimentally addressed – crystal structure (X-ray diffraction, transmission electron microscopy), crystal shape and

• 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

Nanostructured and oriented metal–organic framework films enabling extreme surface wetting properties

• Andre Mähringer,
• Julian M. Rotter and
• Dana D. Medina

Beilstein J. Nanotechnol. 2019, 10, 1994–2003, doi:10.3762/bjnano.10.196

• reflections at qy = 3.9 nm−1 (100), qy = 7.1 nm−1 (200) and qy = 9.2 nm−1 (210) near qz = 0 were indexed according to the powder X-ray diffraction pattern of Co-CAT-1. The (004) reflection, referred to as the in-plane reflection, is visible as a diffuse arc at qz =19 nm−1 (for further details see Supporting

Magnetic properties of biofunctionalized iron oxide nanoparticles as magnetic resonance imaging contrast agents

• Natalia E. Gervits,
• Andrey A. Gippius,
• Alexey V. Tkachev,
• Evgeniy I. Demikhov,
• Sergey S. Starchikov,
• Igor S. Lyubutin,
• Alexander L. Vasiliev,
• Vladimir P. Chekhonin,
• Maxim A. Abakumov,
• Alevtina S. Semkina and
• Alexander G. Mazhuga

Beilstein J. Nanotechnol. 2019, 10, 1964–1972, doi:10.3762/bjnano.10.193

• nanoparticles designed for use as MRI contrast media are precisely examined by a variety of methods: powder X-ray diffraction (XRD), transmission electron microscopy (TEM), Raman spectroscopy, Mössbauer spectroscopy and zero-field nuclear magnetic resonance (ZF-NMR) spectroscopy. TEM and XRD measurements reveal

• nanoparticles, has been repeatedly emphasized, and the exact composition of the MNPs is usually determined using X-ray diffraction (XRD) or Mössbauer spectroscopy with and without magnetic field [12][13][14]. In this work, we show other options for solving this problem using Raman and nuclear magnetic resonance

• Mössbauer and the Raman spectroscopy, measurements and analysis, by the Ministry of Science and Higher Education of the Russian Federation within the State assignment FSRC “Crystallography and Photonics” RAS concerning the TEM. Powder X-ray diffraction measurements were partly performed using the equipment

Facile synthesis of carbon nanotube-supported NiO//Fe₂O₃ for all-solid-state supercapacitors

• Shengming Zhang,
• Xuhui Wang,
• Yan Li,
• Xuemei Mu,
• Yaxiong Zhang,
• Jingwei Du,
• Guo Liu,
• Xiaohui Hua,
• Yingzhuo Sheng,
• Erqing Xie and
• Zhenxing Zhang

Beilstein J. Nanotechnol. 2019, 10, 1923–1932, doi:10.3762/bjnano.10.188

• -SEM, Hitachi S-4800) and a transmission electron microscope (TEM, FEI Tecnai F30) coupled with an energy dispersive X-ray spectrometer. Crystal structures were tested by X-ray diffraction (XRD, Philips, X’pert Pro, Cu Kα, 0.154056 nm). The vibrational information of chemical bonds of samples was