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

• loading (Figure 2C). The characteristic FTIR peaks were found in both unloaded and drug-loaded nanoparticles, which was confirmed by the PO43− peaks at 1089 and 1046 cm−1 and corresponds to previous reports [32]. The calcium phosphate nanoparticles exhibited FTIR peaks in the range of 1000–1100 cm−1

• , corresponding to the phosphate bending. Evidence of P=O bonds was confirmed by a peak at 1200–1100 cm−1 [32] in the two nanoparticle samples synthesized in addition to P–O bonds in the range of 1100–1000 cm−1. In addition, the FTIR spectrum of 5-FU alone was collected for comparative analysis as shown in Figure

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

Nanoconjugates of a calixresorcinarene derivative with methoxy poly(ethylene glycol) fragments for drug encapsulation

• Alina M. Ermakova,
• Julia E. Morozova,
• Yana V. Shalaeva,
• Victor V. Syakaev,
• Aidar T. Gubaidullin,
• Alexandra D. Voloshina,
• Vladimir V. Zobov,
• Irek R. Nizameev,
• Olga B. Bazanova,
• Igor S. Antipin and
• Alexander I. Konovalov

Beilstein J. Nanotechnol. 2018, 9, 2057–2070, doi:10.3762/bjnano.9.195

• and FTIR. Its molecular weight was measured by static light scattering (SLS) and MALDI-TOF. In the 1H NMR spectrum of 3 signals of ethyleneoxy and methoxy groups at 3.65 and 3.37 ppm, respectively, are observed; signals of bridged methylidene groups and aromatic groups are very broad (Figure 1b). Also

• the NMR time scale and, consequently, to the broadening of the signals of calixresorcinarene platform in the NMR spectra. The same broadening in the spectra of tetraundecylcalix[4]resorcinarene with poly-ε-caprolactone fragments on the upper rim was described earlier [22]. In the FTIR spectrum of 3

• methanol were consecutively applied onto the target and evaporated. An aqueous solution of cesium chloride (CsCl) at a concentration of 1 mg/mL was added to improve the ionization of the analyzed sample. IR spectra were recorded with a Bruker Vector 22 FTIR Spectrometer (Bruker Optics, USA) in KBr pellets

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

• . However, the original characteristic peaks of magnetite are weakened. This indicates that the nano-MnO2 covering on the Fe3O4/diatomite is of low crystallinity or amorphous. Figure 2 shows the FTIR spectra of purified diatomite, Fe3O4/diatomite and MnO2/Fe3O4/diatomite. The broad peaks at 3400 and 1630 cm

• organic pollutants. XRD patterns of the purified diatomite and the prepared diatomite-supported composites. FTIR spectra of the purified diatomite and prepared diatomite-supported composites. The SEM images of diatomite (a), Fe3O4/diatomite (b, d), MnO2/Fe3O4/diatomite (c and e), EDX spectrum (f) and

Uniform cobalt nanoparticles embedded in hexagonal mesoporous nanoplates as a magnetically separable, recyclable adsorbent

• Can Zhao,
• Yuexiao Song,
• Tianyu Xiang,
• Wenxiu Qu,
• Shuo Lou,
• Xiaohong Yin and
• Feng Xin

Beilstein J. Nanotechnol. 2018, 9, 1770–1781, doi:10.3762/bjnano.9.168

• were observed by scanning electron microscopy (SEM, ZEISS, Germany) and transmission electron microscopy (TEM, JEM-2100F, Japan). Energy dispersive X-ray (EDX) analysis was recorded via an EDX spectrometer attached to the SEM. The functional groups on the surface of the samples were measured by FTIR

• spectra on a Nicolet Nexus FTIR spectrometer using the KBr method within the wavelength range of 400–4000 cm−1. Nitrogen adsorption–desorption isotherms were obtained at 77 K on an Autosorb–iQ2–MP nitrogen adsorption apparatus. The Brunauer–Emmett–Teller (BET) specific surface area of the samples was

• carbonization of PDA above 650 °C. After calcination of pure CoAl LDH in a nitrogen atmosphere at 800 °C, only Co3O4 and CoAl2O4 mixtures are obtained (Figure 1f). The successful coating of PDA on the surface of CoAl LDH is verified by FTIR spectra (Figure S1 in Supporting Information File 1). The

Nanocomposites comprised of homogeneously dispersed magnetic iron-oxide nanoparticles and poly(methyl methacrylate)

• Sašo Gyergyek,
• David Pahovnik,
• Ema Žagar,
• Alenka Mertelj,
• Rok Kostanjšek,
• Miloš Beković,
• Marko Jagodič,
• Heinrich Hofmann and
• Darko Makovec

Beilstein J. Nanotechnol. 2018, 9, 1613–1622, doi:10.3762/bjnano.9.153

• NMR and FTIR spectra, respectively (Supporting Information File 1, Figures S1 and S2). The shift of the peak for the methine group, denoted with D, from 3.62 ppm in the 1H NMR spectrum of the original ricinoleic acid to 4.88 ppm in the 1H NMR spectrum of RA-MMA, and a pronounced increase in intensity

• enhanced in the NP-MMA sample when compared to the NP-RA sample (Figure 2), indicating the formation of the methacrylate ester, as depicted in Scheme 1. After polymerization (NP-PMMA-3) the FTIR spectrum shows the characteristic features of PMMA (Figure 2). Based on these results we can conclude that the

• reactions involved in the preparation of the nanocomposites. Supporting Information Additional description of materials used and the synthesis and characterization of nanocomposite materials. Additional FTIR and NMR spectra, TGA curves, a correlation function of the suspensions and TEM images showing the

Closed polymer containers based on phenylboronic esters of resorcinarenes

• Tatiana Yu. Sergeeva,
• Rezeda K. Mukhitova,
• Irek R. Nizameev,
• Marsil K. Kadirov,
• Polina D. Klypina,
• Albina Y. Ziganshina and
• Alexander I. Konovalov

Beilstein J. Nanotechnol. 2018, 9, 1594–1601, doi:10.3762/bjnano.9.151

• the region of 4000–400 cm−1 by using a Bruker Vector-22 FTIR-spectrophotometer with a resolution of 4 cm−1. Samples for the registration of the IR spectra were prepared in KBr pellets. NMR spectroscopic experiments were carried out with an Avance 600 spectrometer (Bruker, Germany) equipped with a

Colorimetric detection of Cu²⁺ based on the formation of peptide–copper complexes on silver nanoparticle surfaces

• Gajanan Sampatrao Ghodake,
• Surendra Krishna Shinde,
• Rijuta Ganesh Saratale,
• Avinash Ashok Kadam,
• Ganesh Dattatraya Saratale,
• Asad Syed,
• Fuad Ameen and
• Dae-Young Kim

Beilstein J. Nanotechnol. 2018, 9, 1414–1422, doi:10.3762/bjnano.9.134

• characterized by high-resolution transmission electron microscopy (HR-TEM), XPS, XRD, and Fourier-transform infrared (FTIR) spectroscopy. The shape of the SPR peak determined the qualitative characterization of the AgNPs, and the size range of the particles in solution concurred with the HR-TEM images. As can

• of AgNPs and to identify their crystalline structure (Figure 3a). The diffraction peaks at scattering angles, 2θ, of 38.25°, 44.42°, 64.51° and 77.55° were assigned to the crystallographic planes (111), (200), (220) and (311), respectively. FTIR was performed to examine the capping of casein peptides

• grids. Shape, size-distribution, and images were observed on Tecnai G2 (FEI Company, USA). The XRD measurements were performed using a thin film sample containing the AgNPs (Rigaku Ultima-IV diffractometer, Cu Kα radiation). The centrifuged AgNPs were examined by FTIR spectroscopy using a Thermo

Induced smectic phase in binary mixtures of twist-bend nematogens

• Anamarija Knežević,
• Irena Dokli,
• Marin Sapunar,
• Suzana Šegota,
• Ute Baumeister and
• Andreja Lesac

Beilstein J. Nanotechnol. 2018, 9, 1297–1307, doi:10.3762/bjnano.9.122

• in controlling the self-organizing processes. Keywords: binary mixture; liquid crystals; smectic phase induction; temperature-dependent FTIR; twist-bend nematogen; Introduction Nowadays liquid crystal (LC) substances possess a wide range of uses. However, it is rather rare that a single organic

• of pure compounds shows no new absorption band (Figure S3, Supporting Information File 1). The peak at 290 nm present in pure CBI shifts toward lower wavelengths as the ratio of BB in the mixture rises, approaching the value of 266 nm characteristic of pure BB. Since FTIR spectroscopy is a sensitive

• technique for determining changes in chemical interactions and molecular geometry in LC phases [37][38][39][40], we investigated the 73 mol % BB mixture using temperature-dependent FTIR measurements. IR spectra were recorded using a KBr pastille method. Since in a binary mixture the cyano group of CBI may

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

• 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

Synthesis and characterization of two new TiO₂-containing benzothiazole-based imine composites for organic device applications

• Anna Różycka,
• Agnieszka Iwan,
• Krzysztof Artur Bogdanowicz,
• Michal Filapek,
• Natalia Górska,
• Damian Pociecha,
• Marek Malinowski,
• Patryk Fryń,
• Agnieszka Hreniak,
• Jakub Rysz,
• Paweł Dąbczyński and
• Monika Marzec

Beilstein J. Nanotechnol. 2018, 9, 721–739, doi:10.3762/bjnano.9.67

• fitting. Temperature evolution of the FTIR spectrum of SP1 imine obtained during heating in two spectral ranges: 1200–650 cm−1 (a) and between 1780–1220 cm−1 (b). Temperature evolution of the FT-MIR spectrum of SP2 imine obtained during heating between: (a) 3080 and 2800 cm−1 (left) and temperature

Cyclodextrin-assisted synthesis of tailored mesoporous silica nanoparticles

• Fuat Topuz and
• Tamer Uyar

Beilstein J. Nanotechnol. 2018, 9, 693–703, doi:10.3762/bjnano.9.64

• smaller particle size than those produced with HP-functional CDs. FTIR, TGA and solid-state 13C NMR demonstrated the adsorption of CDs on the particle surfaces. The proposed concept allows for the synthesis of silica nanoparticles with control over particle shape and size by adjusting the concentration of

• , chemical analysis by FTIR and solid state 13C NMR, thermal properties and composition by TGA, and pore structure by WAXS. Results and Discussion Figure 2 shows the silica particles produced at β-CD concentrations of 0.5 and 1% (w/v) and constant tetraethoxysilane (TEOS) concentration of 1% (v/v). At these

• shape. EDX analysis of particles demonstrated the presence of carbon in addition to oxygen and silicone, suggesting physical attachment of CDs. FTIR was used to confirm adsorbed CDs on silica particles (Figure S1b, Supporting Information File 1). The peaks at 2860 and 2930 cm−1 are associated with the C

Perovskite-structured CaTiO₃ coupled with g-C₃N₄ as a heterojunction photocatalyst for organic pollutant degradation

• Ashish Kumar,
• Christian Schuerings,
• Suneel Kumar,
• Ajay Kumar and
• Venkata Krishnan

Beilstein J. Nanotechnol. 2018, 9, 671–685, doi:10.3762/bjnano.9.62

• 45 kV and 100 mA. The scans were collected over a 2θ range of 10–90° with a scan rate of 2° per minute. Fourier transform infrared (FTIR) spectra were recorded for functional group analysis by using an Agilent K8002AA Carry 660 instrument. Thermogravimetric analysis (TGA) was carried out in order to

• phase purity of CT. Although the (002) peak of g-C3N4 could be evidenced in the diffraction pattern of the CTCN heterojunction, the (001) peak of g-C3N4 could not be seen, which could be attributed to its weak diffraction intensity in comparison to the other peaks. Furthermore, FTIR spectroscopy has

• –C units. The peaks at 1398 cm−1, 1540 cm−1 and 1636 cm−1 correspond to the stretching vibration of aromatic C–N bonds [16][34]. The broad peak from 3000–3600 cm−1 can be assigned to the terminal NH or NH2 groups of the aromatic rings and O–H stretching of surface hydroxyl groups [20]. The FTIR

Anchoring Fe₃O₄ nanoparticles in a reduced graphene oxide aerogel matrix via polydopamine coating

• Błażej Scheibe,
• Radosław Mrówczyński,
• Natalia Michalak,
• Karol Załęski,
• Michał Matczak,
• Mateusz Kempiński,
• Zuzanna Pietralik,
• Mikołaj Lewandowski,
• Stefan Jurga and
• Feliks Stobiecki

Beilstein J. Nanotechnol. 2018, 9, 591–601, doi:10.3762/bjnano.9.55

• reference value. In order to investigate the nature of possible functional groups at the aerogels surface, the samples were analyzed using FTIR spectroscopy. Figure 5a presents FTIR spectra obtained for rGO, rGO-Fe3O4 and rGO-PDA@Fe3O4 aerogels. From this figure one can notice the difference in intensity of

• Fourier Transform Infrared (FTIR) spectroscopy (Bruker Optics, TENSOR 27) equipped with a MCT detector and globar source. The chemical composition of the samples was studied using X-ray photoelectron spectroscopy (XPS). The measurements were performed in an ultra-high vacuum (UHV) chamber using a

• -Fe3O4 and rGO-PDA@Fe3O4 aerogel samples. FTIR absorption (a) and XPS survey (b) spectra of rGO, rGO-Fe3O4 and rGO-PDA@Fe3O4 aerogel samples. XPS C 1s, O 1s, N 1s and Fe 2p spectra of rGO, rGO-Fe3O4 and rGO-PDA@Fe3O4 aerogel samples. The intensity scales are the same for respective elements (in order to

Green synthesis of fluorescent carbon dots from spices for in vitro imaging and tumour cell growth inhibition

• Nagamalai Vasimalai,
• Vânia Vilas-Boas,
• Juan Gallo,
• María de Fátima Cerqueira,
• Mario Menéndez-Miranda,
• José Manuel Costa-Fernández,
• Lorena Diéguez,
• Begoña Espiña and
• María Teresa Fernández-Argüelles

Beilstein J. Nanotechnol. 2018, 9, 530–544, doi:10.3762/bjnano.9.51

• compounds present in the spices will partially remain inside or at the surface of the C-dots after the hydrothermal process, leading to different photoluminescent and biomedical properties. The synthesized C-dots have been extensively characterized with UV–vis, fluorescence, FTIR and Raman spectroscopy, DLS

• literature and it has been reported that they are biocompatible. TEM, DLS, XRD, FTIR and Raman spectra of C-dots TEM images showed that the obtained C-dots are spherical regardless of the starting material. As it can be observed in Figure 3, C-dots are uniform in size and shape. A TEM histogram was plotted

• characteristic peaks of graphene oxide [42][43][44], and they are also in agreement with the HR-TEM lattice distances measured. FTIR spectroscopy of the synthesized C-dots confirms the presence of different functional groups in each sample depending on the starting material. The FTIR spectrum of cinnamon C-dots

Ultralight super-hydrophobic carbon aerogels based on cellulose nanofibers/poly(vinyl alcohol)/graphene oxide (CNFs/PVA/GO) for highly effective oil–water separation

• Zhaoyang Xu,
• Huan Zhou,
• Sicong Tan,
• Xiangdong Jiang,
• Weibing Wu,
• Jiangtao Shi and
• Peng Chen

Beilstein J. Nanotechnol. 2018, 9, 508–519, doi:10.3762/bjnano.9.49

• the carbonization treatment was complete, which is in good agreement with the FTIR and Raman data. Chemical properties The FTIR spectrum of the CNFs, PVA, GO, rGO, CNF/PVA/GO and CNF/PVA/GO carbon aerogels are shown in Figure 3. The CNFs exhibit FTIR absorption bands around 3323 cm−1 (the stretching

• moieties, C–OH and C–O vibrations, respectively. As shown in the spectrum of rGO (Figure 3d), most peaks corresponding to the carbon–oxygen functional groups disappeared, which indicates the complete reduction of GO. Figure 3e shows the FTIR spectrum of the CNF/PVA/GO aerogel. Simultaneously, the

• previous studies [19][29], which is in agreement with the SEM results. FTIR can only be used to detect signals from molecules with infrared activity. Therefore, Raman spectroscopy analysis was studied to detect the stretching vibration characteristic peak of homonuclear diatomic pairs. The Raman spectrum

Facile synthesis of ZnFe₂O₄ photocatalysts for decolourization of organic dyes under solar irradiation

• Arjun Behera,
• Debasmita Kandi,
• Sanjit Manohar Majhi,
• Satyabadi Martha and
• Kulamani Parida

Beilstein J. Nanotechnol. 2018, 9, 436–446, doi:10.3762/bjnano.9.42

• , FESEM, UV–vis DRS, PL, FTIR and photocurrent measurements. The photocatalytic activity of the prepared material is studied with regard to the degradation of rhodamine B (Rh B) and Congo red under solar irradiation. The kinetic study showed that the material exhibits zeroth and first order reaction

• photoluminescence (PL) emission spectra were investigated by a JASCO-FP-8300 fluorescence spectrometer with an excitation wavelength of 330 nm. The chemical composition and vibrational modes of the ZFO samples were analysed by JASCO FTIR-4600. A ZEISS SUPRA 55 was used for FESEM analysis. Morphology and

• highest photocatalytic activity, which is in good agreement with the experimental photocatalytic activity (degradation of Congo red and Rh B) discussed later. FTIR analysis FTIR spectra of the ZFO samples were measured in the range of 4000–400 cm−1 (Figure 6). The bands in the region of 3600–3300 cm−1 and

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

• ]) effects on the application and quality of composites. For this aim, many techniques have been developed such as Raman spectroscopy, Fourier-transforms infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). Raman spectroscopy: Raman spectroscopy is a powerful tool to identify and quantify

• 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

• the CNT structure by adding compounds. It is very difficult to get a good FTIR spectrum of CNTs, thus attenuated total reflection (ATR) FTIR can be used (except with carbon crystal, when germanium is more suitable). The investigation of the intermolecular interaction between the polymer chain and CNT

Electron interaction with copper(II) carboxylate compounds

• Michal Lacko,
• Peter Papp,
• Iwona B. Szymańska,
• Edward Szłyk and
• Štefan Matejčík

Beilstein J. Nanotechnol. 2018, 9, 384–398, doi:10.3762/bjnano.9.38

• FTIR spectrometer and a Spectrum RXI PerkinElmer, using KBr plates (400–4000 cm−1). The Cu content was determined with a Varian Spectr AA-20 Plus spectrophotometer. The content of C and H was determined CHNS Elemental Analyser-Euro Vector model 3018. The yield of the complexes synthesis was about 60

Photocatalytic and adsorption properties of TiO₂-pillared montmorillonite obtained by hydrothermally activated intercalation of titanium polyhydroxo complexes

• Mikhail F. Butman,
• Nikolay L. Ovchinnikov,
• Nikita S. Karasev,
• Nataliya E. Kochkina,
• Alexander V. Agafonov and
• Alexandr V. Vinogradov

Beilstein J. Nanotechnol. 2018, 9, 364–378, doi:10.3762/bjnano.9.36

• , TiO2-PMMх, and TiO2-PMMHх (see Experimental section for abbreviations). XRD patterns of the raw MM and TiO2-PMMx, and TiO2-PMMHx, where М, C, А, and R represent montmorillonite, cristobalite, anatase, and rutile phases, respectively. FTIR spectra of the raw MM, and TiO2-pillared MM. Thermogravimetric

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

• . Characterization of CD/g-C3N4 composites FTIR spectra (Perkin Elmer Spectrum 400 spectrophotometer) were conducted in the range of 400–4000 cm−1 with the samples dispersed in KBr. The XRD analyses were performed using the powder XRD (PANalytical-Empyrean) with Cu Kα radiation at a scanning speed of 0.02 s−1. A

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

• treatments. XRD, FTIR and Raman results suggest that MO2–CNFs were obtained after being calcined at 550 °C and complete removal of the inorganic compound. The SEM images showed that the as-prepared MO2–CNF composite fibers had a smooth surface which turned to rough after calcination, revealing the increased

BN/Ag hybrid nanomaterials with petal-like surfaces as catalysts and antibacterial agents

• Konstantin L. Firestein,
• Denis V. Leybo,
• Alexander E. Steinman,
• Andrey M. Kovalskii,
• Andrei T. Matveev,
• Anton M. Manakhov,
• Irina V. Sukhorukova,
• Pavel V. Slukin,
• Nadezda K. Fursova,
• Sergey G. Ignatov,
• Dmitri V. Golberg and
• Dmitry V. Shtansky

Beilstein J. Nanotechnol. 2018, 9, 250–261, doi:10.3762/bjnano.9.27

• spectroscopy (XPS), and infrared spectroscopy (FTIR). They were also characterized in terms of thermal stability, Ag+ ion release, catalytic and antibacterial activities. The materials synthesized via UV decomposition of AgNO3 demonstrated a much better catalytic activity in comparison to those prepared using

• main features in their FTIR spectra: a sharp low wavenumber peak at 769 cm−1 and a broad high wavenumber mode at 1359 cm−1 (spectra 1 and 3 in Figure 6), which correspond to out-of-plane B–N–B bending and in-plane B–N stretching vibrations, respectively [18][19]. The absorbance bands observed in the

• range of 800–1100 cm−1 were assigned to B–C and B–O–C bonds [20][21][22]. A small peak at 535 cm−1 in the FTIR spectrum of CVD BN/Ag HNMs (Figure 6 (inset)) indicates the oxidized state of Ag [23]. The partial oxidation of Ag during the CVD process appeared to occur during the cooling stage. Considering

Al₂O₃/TiO₂ inverse opals from electrosprayed self-assembled templates

• Arnau Coll,
• Sandra Bermejo,
• David Hernández and
• Luís Castañer

Beilstein J. Nanotechnol. 2018, 9, 216–223, doi:10.3762/bjnano.9.23

• , the reflectance of the fabricated samples has been measured over an area of 36 mm2 using a Fourier transform infrared (FTIR) spectrometer with an integrating sphere. We have conducted characterization measurements on the three steps of our process: (A) after step 1 in Figure 1a, (B) after step 3 in