Tailoring the stability/aggregation of one-dimensional TiO₂(B)/titanate nanowires using surfactants

• Atiđa Selmani,
• Johannes Lützenkirchen,
• Kristina Kučanda,
• Dario Dabić,
• Engelbert Redel,
• Ida Delač Marion,
• Damir Kralj,
• Darija Domazet Jurašin and
• Maja Dutour Sikirić

Beilstein J. Nanotechnol. 2019, 10, 1024–1037, doi:10.3762/bjnano.10.103

• mixed phase, TiO2(B) and trititanate layered TNW structure was confirmed by powder X-ray diffraction (PXRD) as well as Fourier-transform infrared spectroscopy (FTIR) and Raman spectroscopy. The details can be found in Supporting Information File 1. High-resolution scanning electron microscopy (HR-SEM

Synthesis of novel C-doped g-C₃N₄ nanosheets coupled with CdIn₂S₄ for enhanced photocatalytic hydrogen evolution

• Jingshuai Chen,
• Chang-Jie Mao,
• Helin Niu and
• Ji-Ming Song

Beilstein J. Nanotechnol. 2019, 10, 912–921, doi:10.3762/bjnano.10.92

• , CISCCN5 and CISCCN10, respectively. Pure CdIn2S4 (CIS) was also synthesized by the same hydrothermal method but without adding CCN. Characterization The as-prepared products were characterized by transmission electron microscopy (TEM) (JEM-2100, JEOL, Japan), Fourier-transform infrared spectroscopy (FTIR

The systemic effect of PEG-nGO-induced oxidative stress in vivo in a rodent model

• Qura Tul Ain,
• Samina Hyder Haq,
• Abeer Alshammari,
• Moudhi Abdullah Al-Mutlaq and
• Muhammad Naeem Anjum

Beilstein J. Nanotechnol. 2019, 10, 901–911, doi:10.3762/bjnano.10.91

• polyethylene glycol (PEG). PEGylation of nGO was confirmed by Fourier-transform infrared spectroscopy (FTIR), UV spectroscopy and TEM. The average size distribution of nGO and PEG-nGO was determined by using dynamic light scattering (DLS). Subsequently, an in vivo study measuring a marker for oxidative stress

• ° according to a d-spacing of 2.13 Å, confirming the successful GO synthesis [42]. Fourier-transform infrared spectroscopy The surface functional groups of nGO and PEG-nGO were investigated by Fourier-transform infrared spectroscopy (FTIR). The infrared spectra of nGO and PEG-nGO were processed using Origin

Rapid, ultraviolet-induced, reversibly switchable wettability of superhydrophobic/superhydrophilic surfaces

• Yunlu Pan,
• Wenting Kong,
• Bharat Bhushan and
• Xuezeng Zhao

Beilstein J. Nanotechnol. 2019, 10, 866–873, doi:10.3762/bjnano.10.87

• MERLIN Compact SEM, operated at a 20 kV acceleration voltage, Carl Zeiss Jena, Germany), and the surface roughness was measured with a laser confocal microscope (LCM, OLS5000, Olympus, Japan). The chemical modification and the end group changes on the surfaces was studied by Fourier transform infrared

• spectroscopy (FTIR, Nicolet iS50, Thermo Scientific, USA). The contact angles were measured at room temperature with an optical contact angle meter (DropMeterTM Element A-60, Maist, Ningbo, China), where the static CAs of the droplets (6 µL) placed onto the surfaces were measured five times at different

Outstanding chain-extension effect and high UV resistance of polybutylene succinate containing amino-acid-modified layered double hydroxides

• Adam A. Marek,
• Vincent Verney,
• Christine Taviot-Gueho,
• Grazia Totaro,
• Laura Sisti,
• Annamaria Celli and
• Fabrice Leroux

Beilstein J. Nanotechnol. 2019, 10, 684–695, doi:10.3762/bjnano.10.68

• medium wavelength range of the ultraviolet C (UVC) and ultraviolet B (UVB) regions. In the present work, Mg2Al LDH materials were first organo-modified with histidine and phenylalanine using a co-precipitation method and then characterized by X-ray diffraction (XRD), Fourier transform infrared

• spectroscopy (FTIR) and thermogravimetric analysis (TGA). As expected, the UV–vis spectra showed absorbance in the UVC and UVB regions and the potential role as UV stabilizers. In a second part, PBS composites were prepared with 5 wt % of LDH filler by melt blending and once again fully characterized (XRD, TGA

Ultrathin hydrophobic films based on the metal organic framework UiO-66-COOH(Zr)

• Miguel A. Andrés,
• Clemence Sicard,
• Christian Serre,
• Olivier Roubeau and
• Ignacio Gascón

Beilstein J. Nanotechnol. 2019, 10, 654–665, doi:10.3762/bjnano.10.65

• OPD/MOF ultrathin films have been fabricated onto glass, calcium fluoride, quartz crystal microbalance (QCM), Si(100) substrates and mica and characterized using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), atomic force microscopy (AFM

Removal of toxic heavy metals from river water samples using a porous silica surface modified with a new β-ketoenolic host

• Said Tighadouini,
• Smaail Radi,
• Abderrahman Elidrissi,
• Khadija Haboubi,
• Maryse Bacquet,
• Stéphanie Degoutin,
• Mustapha Zaghrioui and
• Yann Garcia

Beilstein J. Nanotechnol. 2019, 10, 262–273, doi:10.3762/bjnano.10.25

• characterized by elemental analysis, Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) images, thermogravimetric analysis (TGA) and nitrogen adsorption–desorption isotherms. Physical methods. Atomic adsorption measurements were performed on a Varian A.A. 400 spectrophotometer

Hybrid Au@alendronate nanoparticles as dual chemo-photothermal agent for combined cancer treatment

• Anouchka Plan Sangnier,
• Romain Aufaure,
• Laurence Motte,
• Claire Wilhelm,
• Erwann Guenin and
• Yoann Lalatonne

Beilstein J. Nanotechnol. 2018, 9, 2947–2952, doi:10.3762/bjnano.9.273

• estimated values for other NPs coated with HMBP molecules (i.e., 3.4 HMBPene/nm2) [18]. Indeed, alendronate is a zwitterion, capable of forming pairs of ions that generate multilayers around the gold NP. The chemisorption of alendronate was qualitatively assessed (Figure 1c) by Fourier-transform infrared

• spectroscopy (FTIR) comparing the coated gold NPs (red curve) with free alendronate (black curve). Large modifications were observed within the PO region (900–1200 cm−1). The free alendronate spectrum exhibits two sharp peaks at 1211 and 957 cm−1, assigned to P=O and P–OH, respectively [31]. The broad band at

Enhanced antineoplastic/therapeutic efficacy using 5-fluorouracil-loaded calcium phosphate nanoparticles

• Shanid Mohiyuddin,
• Saba Naqvi and
• Gopinath Packirisamy

Beilstein J. Nanotechnol. 2018, 9, 2499–2515, doi:10.3762/bjnano.9.233

• -transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). The antineoplastic potential of the CaP@5-FU NPs against colorectal and lung cancer cells was reported. The CaP@5-FU NPs were found to inhibit half the population (IC50) of lung adenocarcinoma (A549) cells at 32 μg/mL and colorectal (HCT

• with an approximate diameter of 160–180 nm was confirmed by different methods. The physicochemical characterization of the synthesized CaP@5-FU NPs was done with transmission electron microscopy (TEM), dynamic light scattering (DLS), field emission scanning electron microscopy (FE-SEM), Fourier

Electrospun one-dimensional nanostructures: a new horizon for gas sensing materials

• Muhammad Imran,
• Nunzio Motta and
• Mahnaz Shafiei

Beilstein J. Nanotechnol. 2018, 9, 2128–2170, doi:10.3762/bjnano.9.202

Synthesis of a MnO₂/Fe₃O₄/diatomite nanocomposite as an efficient heterogeneous Fenton-like catalyst for methylene blue degradation

• Zishun Li,
• Xuekun Tang,
• Kun Liu,
• Jing Huang,
• Yueyang Xu,
• Qian Peng and
• Minlin Ao

Beilstein J. Nanotechnol. 2018, 9, 1940–1950, doi:10.3762/bjnano.9.185

• Fourier transform infrared spectroscopy (FTIR) using a Nicolet Nexus 670 spectrometer. The morphology of samples was observed with a TESCAN MIRA3 LMU scanning electron microscope (SEM) and a JEOL JEM-1200EX transmission electron microscope (TEM). The X-ray photoelectron spectroscopy (XPS) measurements

Heavy-metal detectors based on modified ferrite nanoparticles

• Urszula Klekotka,
• Ewelina Wińska,
• Elżbieta Zambrzycka-Szelewa,
• Dariusz Satuła and
• Beata Kalska-Szostko

Beilstein J. Nanotechnol. 2018, 9, 762–770, doi:10.3762/bjnano.9.69

• metals Cd, Cu and Pb. The obtained nanoparticles were structurally characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and Mössbauer spectroscopy. The amounts of Cd, Cu and Pb were measured out by atomic absorption spectroscopy

A review of carbon-based and non-carbon-based catalyst supports for the selective catalytic reduction of nitric oxide

• Shahreen Binti Izwan Anthonysamy,
• Syahidah Binti Afandi,
• Mehrnoush Khavarian and
• Abdul Rahman Bin Mohamed

Beilstein J. Nanotechnol. 2018, 9, 740–761, doi:10.3762/bjnano.9.68

• ACFN produced higher activity than those on ACFP. This is because the surface of CeO2/ACFN is more acidic as it was treated with nitric acid and the reaction between NO and the catalyst surface became more active. Using several characterisation techniques, such as Fourier transform infrared

• spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and temperature-programmed desorption (TPD), the comparison of the properties for both ACFP and ACFN was clarified. Chuang et al. [18] considered three different methods, i.e., impregnation, polyol, and microwave-heated polyol methods for the

Engineering of oriented carbon nanotubes in composite materials

• Razieh Beigmoradi,
• Abdolreza Samimi and
• Davod Mohebbi-Kalhori

Beilstein J. Nanotechnol. 2018, 9, 415–435, doi:10.3762/bjnano.9.41

• signals that mask the signals of other organic components. In such cases, tunable UV Raman spectroscopy may be used, although this technique is rarely used. Fourier-transform infrared spectroscopy: FTIR is often used to characterize molecular bonding on the CNT surface and to determine the modification of

Sugarcane juice derived carbon dot–graphitic carbon nitride composites for bisphenol A degradation under sunlight irradiation

• Lan Ching Sim,
• Jing Lin Wong,
• Chen Hong Hak,
• Jun Yan Tai,
• Kah Hon Leong and
• Pichiah Saravanan

Beilstein J. Nanotechnol. 2018, 9, 353–363, doi:10.3762/bjnano.9.35

• degradation of endocrine disrupting chemicals (EDCs). Bisphenol A (BPA) was chosen as a model pollutant under natural sunlight irradiation. Herein, the structural and optical properties of samples were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), photoluminescence

• lattice fringes of the CDs were found to be about 0.24 nm (Figure 1f), which correlated with the (100) in-plane lattice spacing of graphene [45]. X-ray diffraction (XRD) and Fourier-transform infrared spectroscopy (FTIR) Figure 2a shows the XRD patterns of all CD/g-C3N4 composites. A major diffraction

Synthesis and characterization of electrospun molybdenum dioxide–carbon nanofibers as sulfur matrix additives for rechargeable lithium–sulfur battery applications

• Ruiyuan Zhuang,
• Shanshan Yao,
• Maoxiang Jing,
• Xiangqian Shen,
• Jun Xiang,
• Tianbao Li,
• Kesong Xiao and
• Shibiao Qin

Beilstein J. Nanotechnol. 2018, 9, 262–270, doi:10.3762/bjnano.9.28

• using an electrospinning technique followed by calcination, using sol–gel precursors and polyacrylonitrile (PAN) as a processing aid. The resulting samples were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, Brunauer–Emmet–Teller (BET

• MoO2–CNF was successfully prepared through electrospinning. The Fourier transform infrared spectroscopy (FTIR) spectra of PAN fibers, as-prepared composite PAN/PMA fibers, and composite fibers calcined at different temperatures are illustrated in Figure 2. The FTIR spectra of PAN fibers and as-prepared

Preparation and characterization of polycarbonate/multiwalled carbon nanotube nanocomposites

• Claudio Larosa,
• Niranjan Patra,
• Marco Salerno,
• Lara Mikac,
• Remo Merijs Meri and
• Mile Ivanda

Beilstein J. Nanotechnol. 2017, 8, 2026–2031, doi:10.3762/bjnano.8.203

• characterized by UV–vis spectrometry using a Cary 6000i spectrometer by Varian, UK, in double beam configuration with empty reference sample position. Fourier-transform infrared spectroscopy (FTIR) of PC/MWCNT composites with different loadings was carried out in the range of 600–4000 cm−1 on a Bruker Vertex 70

Fluorination of vertically aligned carbon nanotubes: from CF₄ plasma chemistry to surface functionalization

• Claudia Struzzi,
• Mattia Scardamaglia,
• Jean-François Colomer,
• Alberto Verdini,
• Luca Floreano,
• Rony Snyders and
• Carla Bittencourt

Beilstein J. Nanotechnol. 2017, 8, 1723–1733, doi:10.3762/bjnano.8.173

• carbon nanotubes (vCNT) exposed to the fluorine-rich glow discharge. In situ residual gas analysis (RGA) mass spectrometry is performed to probe the chemistry of the plasma phase and to individuate the plasma products that are simultaneously explored by Fourier transform infrared spectroscopy (FTIR). The

• by Fourier transform infrared spectroscopy (FTIR). The spectra are recorded using a Varian FTIR-670 spectrometer. The multipass cell consists of a cylindrical section of 120 cm length and 25 cm in diameter, crossing the chamber. One side of the section is connected to the FTIR spectrometer through a

• infrared spectroscopy (FTIR) analysis are used for the plasma phase study, while the fluorinated vCNT surfaces are investigated using X-ray photoelectron (XPS) and Raman spectroscopies. For plasma power higher than P = 80 W, a considerable fragmentation of the parent CF4 molecule is observed, while the

Surface functionalization of 3D-printed plastics via initiated chemical vapor deposition

• Christine Cheng and
• Malancha Gupta

Beilstein J. Nanotechnol. 2017, 8, 1629–1636, doi:10.3762/bjnano.8.162

• PLA and flat PPFDA due to surface roughness [34]. Penetration of polymer through the lattice was also confirmed by deposition on the silicon wafer piece underneath the lattice. We used Fourier transform infrared spectroscopy (FTIR) (Figure 2b) to compare the spectra of the PPFDA film deposited on the

Oxidative chemical vapor deposition of polyaniline thin films

• Yuriy Y. Smolin,
• Masoud Soroush and
• Kenneth K. S. Lau

Beilstein J. Nanotechnol. 2017, 8, 1266–1276, doi:10.3762/bjnano.8.128

• pentachloride as oxidant. Microscopy and spectroscopy indicate that oCVD processing conditions influence the PANI film chemistry, oxidation, and doping level. Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS) indicate that a substrate

• components that might lead to unfavorable electrochemical properties. Thin film characterization As-deposited and washed PANI films were analyzed by Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and scanning electron microscopy (SEM). FTIR spectra were acquired using

Vapor-phase-synthesized fluoroacrylate polymer thin films: thermal stability and structural properties

• Paul Christian and
• Anna Maria Coclite

Beilstein J. Nanotechnol. 2017, 8, 933–942, doi:10.3762/bjnano.8.95

• Supporting Information File 1, while a full description of the setup can be found in a previous publication [17]. As substrates, silicon wafers with a native oxide layer (thickness 1.7 nm) were used after being cut into 2 × 2 cm2 pieces. Fourier transform infrared spectroscopy (FTIR) was performed on a

Optical and photocatalytic properties of TiO₂ nanoplumes

• Viviana Scuderi,
• Massimo Zimbone,
• Maria Miritello,
• Giuseppe Nicotra,
• Giuliana Impellizzeri and
• Vittorio Privitera

Beilstein J. Nanotechnol. 2017, 8, 190–195, doi:10.3762/bjnano.8.20

• reported in [21] indicated that the nanoplumes are made of TiO2. In addition, an accurate characterization of the nanoplumes performed by X-ray diffraction (XRD) measurements, X-ray Fourier transform infrared spectroscopy (FTIR), and photoelectron spectroscopy (XPS), revealed that after the etching the

A novel electrochemical nanobiosensor for the ultrasensitive and specific detection of femtomolar-level gastric cancer biomarker miRNA-106a

• Maryam Daneshpour,
• Kobra Omidfar and
• Hossein Ghanbarian

Beilstein J. Nanotechnol. 2016, 7, 2023–2036, doi:10.3762/bjnano.7.193

• , Freescale) analysis. In order to study structural and elemental properties, X-ray diffraction (XRD) (Philips, pw 1800, Netherlands) and energy-dispersive X-ray diffraction (EDX) were carried out. These NPs were also characterized using Fourier transform infrared spectroscopy (FTIR) to study the chemical

Organoclay hybrid materials as precursors of porous ZnO/silica-clay heterostructures for photocatalytic applications

• Marwa Akkari,
• Pilar Aranda,
• Abdessalem Ben Haj Amara and
• Eduardo Ruiz-Hitzky

Beilstein J. Nanotechnol. 2016, 7, 1971–1982, doi:10.3762/bjnano.7.188

• diffractometer using monochromatic Cu Kα radiation, scanning from 2 to 70° in 2θ degrees with steps of 0.02 degrees. The average size of the crystallites was calculated by using the Debye–Scherrer formula [33]. Fourier transform infrared spectroscopy (FTIR) was performed in a Bruker IFS 260 66v/S

Ammonia gas sensors based on In₂O₃/PANI hetero-nanofibers operating at room temperature

• Qingxin Nie,
• Zengyuan Pang,
• Hangyi Lu,
• Yibing Cai and
• Qufu Wei

Beilstein J. Nanotechnol. 2016, 7, 1312–1321, doi:10.3762/bjnano.7.122

• morphology of In(NO3)3/PVP, In2O3/PANI composite nanofibers and pure PANI were investigated by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), transmission electron microscopy (TEM) and current–voltage (I–V) measurements. The gas sensing properties