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

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

• domains (red regions) (Figure 2B) and beta-sheet secondary structures (blue regions) (Figure 2C). Intriguingly, the X-ray diffraction (XRD) results showed the presence of sharp peaks, indicating that the hydrogel has long-range, ordered, crystal patterns (Figure 2D). The crystal patterns were further

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

• three days at 60 °C. Then, the material was exhaustively washed with o-dichlorobenzene in order to remove the physisorbed C60 on the MOF surface, washed with methanol and dried at 150 °C for 2 h. The powder X-ray diffraction (PXRD) pattern of C60@MUV-2 shows that the principal peak remains at 3.4

• and solvents employed for the syntheses were of high purity and were purchased from Sigma-Aldrich Co., and TCI. Powder X-ray diffraction patterns were recorded using 0.7 mm borosilicate capillaries that were aligned on an Empyrean PANalytical powder diffractometer, using Cu Kα radiation (λ = 1.54056 Å

• red spheres represent C, S, Fe and O atoms, respectively. Powder X-ray diffraction (PXRD) patterns of simulated and experimental desolvated MUV-2 and C60@MUV-2. a) Raman spectra of C60, MUV-2 and C60@MUV-2. b) Solid-state UV–vis spectra of MUV-2 and C60@MUV-2. The spectra were recorded by dispersing

Fabrication and characterization of Si_1−xGe_x nanocrystals in as-grown and annealed structures: a comparative study

• Muhammad Taha Sultan,
• Adrian Valentin Maraloiu,
• Ionel Stavarache,
• Jón Tómas Gudmundsson,
• Andrei Manolescu,
• Valentin Serban Teodorescu,
• Magdalena Lidia Ciurea and
• Halldór Gudfinnur Svavarsson

Beilstein J. Nanotechnol. 2019, 10, 1873–1882, doi:10.3762/bjnano.10.182

• impulse magnetron sputtering (HiPIMS). The as-grown structures subsequently underwent rapid thermal annealing (550–900 °C for 1 min) in N2 ambient atmosphere. The structures were investigated using X-ray diffraction, high-resolution transmission electron microscopy together with spectral photocurrent

• incidence X-ray diffraction (GIXRD) and high-resolution transmission electron microscopy (HRTEM). Strain relaxation and its effect on the formation of NCs and the resulting interface integrity was studied and compared with structures having a thicker (ca. 200 nm) SiGe layer [23], deposited by radio

• grazing incidence XRD (GIXRD) and X-ray reflectometry (XRR) via Philips X'pert diffractometer (Cu Kα, 0.15406 nm, precision of 0.00001°) and Jeol ARM 200F transmission electron microscopy (TEM). For the X-ray diffraction scans, a 2×Ge(220) asymmetrical hybrid monochromator utilizing line focus, with a 1/4

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

• molecules left in the pores, thus ensuring that the whole pore volume was available for trapping the SF6 guest. The bulk sample was analyzed before and after the gas loading by conventional analytical methods, including FTIR, powder X-ray diffraction (XRD) and thermogravimetric analysis (TGA). SF6-loading

• SF6. Bands attributed to SF6 are marked with an asterisk. Powder X-ray diffraction analysis of MFU-4 before (black) and after (Sample 3a, blue) the loading of SF6. 19F MAS NMR spectrum of MFU-4 (Sample 3b) loaded with SF6 recorded at room temperature. The spectrum was referenced against CFCl3. (a) MFU

Lipid nanostructures for antioxidant delivery: a comparative preformulation study

• Elisabetta Esposito,
• Maddalena Sguizzato,
• Markus Drechsler,
• Paolo Mariani,
• Federica Carducci,
• Claudio Nastruzzi,
• Giuseppe Valacchi and
• Rita Cortesi

Beilstein J. Nanotechnol. 2019, 10, 1789–1801, doi:10.3762/bjnano.10.174

• transmission electron microscopy, small-angle X-ray diffraction, encapsulation efficiency, preliminary stability, in vitro cytotoxicity and protection against cigarette smoke. Nanostructured lipid carriers were found to reduce agglomerate formation and provided better dimensional stability, as compared to

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

• discussed further below. The crystal structure of the representative products was analyzed by X-ray diffraction (XRD) measurements and attenuated total reflection Fourier-transform infrared (ATR-FTIR) absorption spectroscopy. The XRD profiles showed three peaks at 2θ (θ is the Bragg angle) of 12.2, 19.9

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

• at 230 °C, a black powder was obtained after 10 min. The TEM measurements show spherical and non-aggregated nanoparticles with a narrow size distribution of 3.0 ± 0.5 nm (Figure 1). To validate the intermetallic 1:1 NiGa phase of the obtained nanoparticles, powder X-ray diffraction pattern (P-XRD) or

• column). The water content measured by coulometric Karl-Fischer titration was below 10 ppm. Powder X-ray diffraction. PXRD data were obtained at ambient temperature on a Bruker D2 Phaser using a flat sample holder and Cu Kα radiation (λ = 1.54182 Å, 35 kV). Samples had been precipitated with acetonitrile

The impact of crystal size and temperature on the adsorption-induced flexibility of the Zr-based metal–organic framework DUT-98

• Simon Krause,
• Volodymyr Bon,
• Hongchu Du,
• Rafal E. Dunin-Borkowski,
• Ulrich Stoeck,
• Irena Senkovska and
• Stefan Kaskel

Beilstein J. Nanotechnol. 2019, 10, 1737–1744, doi:10.3762/bjnano.10.169

• fragmentation of the crystals. In a series of samples, the average crystal size of DUT-98 crystals was varied from 120 µm to 50 nm and the obtained solids were characterized by X-ray diffraction, infrared spectroscopy, as well as scanning and transmission electron microscopy. We analyzed the adsorption behavior

• -dependent steep water uptake of up to 20 mmol g−1 at 0.5 p/p0 with potential for water harvesting and heat pump applications. We furthermore investigate the temperature-induced structural transition by in situ powder X-ray diffraction. At temperatures beyond 110 °C, the open-pore state of the nanometer

• were analyzed by powder X-ray diffraction (PXRD), illustrating the phase purity of the desired DUT-98op (open pore) phase (Figure 4). A significant peak broadening is observed for samples 3 and 4, which is indicative of the presence of nanometer-sized crystals. Quantitative analysis of the mean crystal

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

• , which guarantees the excellent cyclic stability and desirable rate performance of Li/S batteries. Figure 2a shows X-ray diffraction (XRD) patterns of the as-spun and as-dealloyed sample. The TiAl foil exhibits Al3Ti (JCPDS 65-2667) and Al (JCPDS 65-2869) phases. After dealloying, the specimen shows a

Novel hollow titanium dioxide nanospheres with antimicrobial activity against resistant bacteria

• Carol López de Dicastillo,
• Cristian Patiño,
• María José Galotto,
• Yesseny Vásquez-Martínez,
• Claudia Torrent,
• Daniela Alburquenque,
• Alejandro Pereira and
• Juan Escrig

Beilstein J. Nanotechnol. 2019, 10, 1716–1725, doi:10.3762/bjnano.10.167

• and titanium dioxide, and after a calcination process, hollow nanospheres were obtained with a radius of approximately 345 nm and shell thickness of 17 nm. The structural characterization was performed using electron microscopy, and X-ray diffraction and small-angle X-ray diffraction evidenced an

Layered double hydroxide/sepiolite hybrid nanoarchitectures for the controlled release of herbicides

• Ediana Paula Rebitski,
• Margarita Darder and
• Pilar Aranda

Beilstein J. Nanotechnol. 2019, 10, 1679–1690, doi:10.3762/bjnano.10.163

• following alginate–zein (A-Z) bionanocomposite beads were prepared: A-Z@MCPA-LDH and A-Z@MCPA-LDH/Sep0.5:1_60C, incorporating the intercalation compound or the hybrid nanoarchitecture, respectively. Characterization Powder X-ray diffraction (XRD) data were collected on a Bruker D8 Advance diffractometer

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

• a heating rate of 20 K/min between 25 and 300 °C under 80 mL/min nitrogen purge. X-ray diffraction (XRD) To determine the amorphous state and possible residual crystal fractions of rutin in smartPearls, XRD was performed using a Bruker D8 (Bruker, USA) instrument (n = 1). A scan rate of 0.02°/s (2θ

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

• monitored by CD did not show inversion. X-ray diffraction analysis To understand the different structure of the three NCLG compounds, X-ray diffraction (XRD) measurements were further adopted to evaluate the assembled structures of the three gelators. As shown in Figure 4a, for 2NCLG xerogels, a series of

Materials nanoarchitectonics at two-dimensional liquid interfaces

• Katsuhiko Ariga,
• Michio Matsumoto,
• Taizo Mori and
• Lok Kumar Shrestha

Beilstein J. Nanotechnol. 2019, 10, 1559–1587, doi:10.3762/bjnano.10.153

• the MOF formation to the liquid interface. The interfacially grown BHT–Ni network film of 1–2 µm thickness exhibited X-ray diffraction patterns corresponding to a crystalline network structure. Takada et al. adopted a similar technique to form electrochromic bis(terpyridine)metal complex nanosheets

• water phase, yielding a monolayer sheet of the two-dimensional nickel–iron cyanide grid network. Characterizations of the extended network by X-ray photoelectron spectroscopy (XPS), FTIR spectroscopy, SQUID magnetometry, X-ray absorption fine structure (XAFS), and grazing incidence synchrotron X-ray

• diffraction (GIXD) revealed a face-centred square grid structure with an average domain size of 3600 Å2. Makiura et al. employed a similar method to form multilayers of an oriented porphyrin-based MOF film on top of substrates by repeating transfer and washing of interfacially grown MOF layers (Figure 10

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

• quasi-one-dimensional structure of ZnO wires is retained. The X-ray diffraction data indicate (Figure 3a) that the annealing of polymer fibers leads to the formation of crystalline phases of ZnO (wurtzite, ICDD 36-1451) and SiC (3C polytype, ICDD 29-1129). The crystallite size (dXRD), estimated from the

• × 0.5 mm in size with the thickness of 5–7 μm. The list of the samples is given in Table 1. Materials characterization The phase composition was determined by X-ray diffraction (XRD) using a DRON-3 diffractometer (radiation Co Kα, λ = 1.7903 Å). The crystallite size (dXRD) of SiC and ZnO phases in