A graphene quantum dots–glassy carbon electrode-based electrochemical sensor for monitoring malathion

• Sanju Tanwar,
• Aditi Sharma and
• Dhirendra Mathur

Beilstein J. Nanotechnol. 2023, 14, 701–710, doi:10.3762/bjnano.14.56

• hydrothermal process with glucose as a precursor undergoing carbonization. Different spectroscopic techniques were used to analyze the optical characteristics of GQDs, including UV–visible, photoluminescence, FTIR, and Raman spectroscopy. Atomic force microscopy, transmission electron microscopy, and X-ray

• obtained, which will be used as an electrochemical nanosensor in further studies for malathion detection (Figure 1). Characterization FTIR, Raman, UV–vis, and fluorescence spectroscopy measurements were carried out to determine the optical properties of GQDs. A Perkin Elmer LAMBDA 750 spectrophotometer was

• used to record the UV–visible absorbance spectrum. The luminescence characteristics of the GQDs were investigated using a Perkin Elmer LS 55 fluorescence spectrometer. On a Perkin Elmer FT-IR Spectrum 2, FTIR spectra were measured in the range of 500–4000 cm−1 by making KBr pellets of the sample. At

Quercetin- and caffeic acid-functionalized chitosan-capped colloidal silver nanoparticles: one-pot synthesis, characterization, and anticancer and antibacterial activities

• Akif Hakan Kurt,
• Elif Berna Olutas,
• Fatma Avcioglu,
• Hamza Karakuş,
• Mehmet Ali Sungur,
• Cansu Kara Oztabag and
• Muhammet Yıldırım

Beilstein J. Nanotechnol. 2023, 14, 362–376, doi:10.3762/bjnano.14.31

• infrared (FTIR) spectroscopy, and transmission electron microscopy (TEM). The characteristic surface plasmon resonance (SPR) absorption band has been found at 417 and 424 nm for Ch/Q- and Ch/CA-Ag NPs, respectively. The formation of a chitosan shell comprising quercetin and caffeic acid, which surround the

• colloidal core Ag NPs, was confirmed by UV–vis, and FTIR analyses, and monitored by TEM microscopy. The size of nanoparticles has been determined as 11.2 and 10.3 nm for Ch/Q- and Ch/CA-Ag, respectively. The anticancer activity of Ch/Q- and Ch/CA-Ag NPs has been evaluated against U-118 MG (human

• first time the one-pot synthesis of Ch/Q- and Ch/CA-Ag NPs and their biological properties (anticancer and antibacterial). Ag NPs have been prepared and characterized by UV–vis, FTIR, and TEM measurements. In another study of ours, Lomustine, a common drug against glioblastoma cancer, was applied at a

Structural, optical, and bioimaging characterization of carbon quantum dots solvothermally synthesized from o-phenylenediamine

• Zoran M. Marković,
• Milica D. Budimir,
• Martin Danko,
• Dušan D. Milivojević,
• Pavel Kubat,
• Danica Z. Zmejkoski,
• Vladimir B. Pavlović,
• Marija M. Mojsin,
• Milena J. Stevanović and
• Biljana M. Todorović Marković

Beilstein J. Nanotechnol. 2023, 14, 165–174, doi:10.3762/bjnano.14.17

• characterization methods (AFM, TEM, EDS, FTIR, photoluminescence, and EPR) indicate the significant influence of the precursor on structural, chemical, and optical properties. Antibacterial and cytotoxicity tests showed that these dots did not have any antibacterial potential, because of the low extent of reactive

• nm (Figure S1c,d in Supporting Information File 1). Figure 1 shows the surface morphology of neat PU and a CQDs/PU sample. The RMS roughness values of these samples are 4.45 and 14.04 nm, respectively. FTIR, UV–vis, and PL spectra of CQDs and CQDs/PU To study the chemical and optical properties of

• CQDs, FTIR, UV–vis, and PL spectra were measured. A FTIR spectrum of the CQDs is presented in Figure S2a (Supporting Information File 1). The spectrum contains many peaks associated with the following bonds: Peaks at 3634 and 3448 cm−1 stem from O–H stretching vibrations. A peak at 3367 cm−1 could be

Two-step single-reactor synthesis of oleic acid- or undecylenic acid-stabilized magnetic nanoparticles by thermal decomposition

• Mykhailo Nahorniak,
• Pamela Pasetto,
• Jean-Marc Greneche,
• Volodymyr Samaryk,
• Sandy Auguste,
• Anthony Rousseau,
• Nataliya Nosova and
• Serhii Varvarenko

Beilstein J. Nanotechnol. 2023, 14, 11–22, doi:10.3762/bjnano.14.2

• oleate and formation of undecylate complexes, Fourier-transform infrared spectroscopy (FTIR) studies of the reaction mixtures were carried out at the beginning and at the end of the first stage of NPM synthesis prior to removing acetylacetone under vacuum (see Figures S2 and S3 in Supporting Information

• , thereby proving their partial oxidation [39][40]. The Fourier-transform infrared spectroscopy/attenuated total reflectance (ATR-FTIR) and TGA techniques were used for surface characterization in terms of the presence of higher fatty acids, which play an essential role in the stability and future

• functionality of the particles. ATR-FTIR studies confirmed the presence of characteristic bands that could be assigned to the organic (stabilizing) layer on the surface of the nanoparticles synthesized with both OA (TMO-I) and UA (TMU-II) (Figure 7). The peaks at 2850 and 2920 cm−1 were attributed to symmetric

Photoelectrochemical water oxidation over TiO₂ nanotubes modified with MoS₂ and g-C₃N₄

• Phuong Hoang Nguyen,
• Thi Minh Cao,
• Tho Truong Nguyen,
• Hien Duy Tong and
• Viet Van Pham

Beilstein J. Nanotechnol. 2022, 13, 1541–1550, doi:10.3762/bjnano.13.127

• of materials The morphology, the phase, and the vibrational characteristics of the surface functional groups of the materials were observed by field-emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), and Fourier-transform infrared spectroscopy (FTIR). Diffuse reflectance

• determined by using FTIR spectroscopy, as shown in Figure 3b. The formation of TiO2 on the Ti foil is indicated by the vibrations of the Ti–O bond in the wavenumber region from 450 to 750 cm−1 [47]. The bonding characteristics in the MoS2 material are presented by Mo–S vibration peaks between 1620 and 420 cm

• −1 [48]. Also, FTIR spectroscopy is used as an extremely effective technique for studying the vibrational states of organic bonds in g-C3N4 materials using the vibrational peaks of C–N bonds between 1640 and 1200 cm−1. A very strong absorption peak at 807.2 cm−1 characterizes the fluctuation of tri-s

A TiO₂@MWCNTs nanocomposite photoanode for solar-driven water splitting

• Anh Quynh Huu Le,
• Ngoc Nhu Thi Nguyen,
• Hai Duy Tran,
• Van-Huy Nguyen and
• Le-Hai Tran

Beilstein J. Nanotechnol. 2022, 13, 1520–1530, doi:10.3762/bjnano.13.125

• diffraction (XRD, D2 PHASER). The chemical structure of the samples is characterized using Fourier-transform infrared spectroscopy (FTIR, Brucker 27). The electrochemical measurements are carried out on a MPG2 Biologic system with a three-electrode cell controlled by ECLab® software. Diffuse reflectance

• defects in the initial MWCNTs are hardly affected by the TiO2 nanoparticles. The TEM image also confirms that TiO2 nanoparticles only attach to some defects on the MWCNTs (Figure 3c) [17]. FTIR spectra of MWCNTs, TiO2, and the TiO2@MWCNTs nanocomposite are shown in Figure 6a. Regarding the spectrum of

• MWCNTs and TiO2@MWCNTs. Raman spectra of MWCNTs and TiO2@MWCNTs. FTIR spectra of (a) MWCNTs, TiO2, and TiO2@MWCNTs, and (b) UV–vis DRS of TiO2 and TiO2@MWCNTs (Inset: Tauc plots). XRD patterns of MWCNTs, TiO2 and TiO2@MWCNTs nanocomposite. (a) Cyclic voltammograms in 0.1 M KCl at 50 mV/s of scan rate, (b

In search of cytotoxic selectivity on cancer cells with biogenically synthesized Ag/AgCl nanoparticles

• Mitzi J. Ramírez-Hernández,
• Mario Valera-Zaragoza,
• Omar Viñas-Bravo,
• Ariana A. Huerta-Heredia,
• Miguel A. Peña-Rico,
• Erick A. Juarez-Arellano,
• David Paniagua-Vega,
• Eduardo Ramírez-Vargas and
• Saúl Sánchez-Valdes

Beilstein J. Nanotechnol. 2022, 13, 1505–1519, doi:10.3762/bjnano.13.124

• pineapple peel extracts and their behavior on the breast cancer cell line MCF-7 is shown. Bioreactions were monitored at different temperatures. Fourier-transform infrared spectroscopy (FTIR), ultraviolet–visible spectroscopy (UV–vis), thermogravimetric analysis (TGA), X-ray diffraction (XRD), energy

• for Ag nanoparticle formation using extracts from Cucurbita maxima, Moringa oleifera, and Acorus calamus. The FTIR results are shown in Figure 5. The spectra of the precursor salt and pineapple peel extract are shown for signal comparison. In the spectrum of the AgNO3 salt, some signals were observed

• absorption bands of the reaction products are also a consequence of the capacity of the extract metabolites to act as capping agents for the formation of nanoparticles. Morphological characterization Although the data obtained by XRD and FTIR do not show significant differences in the formation of

Rapid and sensitive detection of box turtles using an electrochemical DNA biosensor based on a gold/graphene nanocomposite

• Abu Hashem,
• M. A. Motalib Hossain,
• Ab Rahman Marlinda,
• Mohammad Al Mamun,
• Khanom Simarani and
• Mohd Rafie Johan

Beilstein J. Nanotechnol. 2022, 13, 1458–1472, doi:10.3762/bjnano.13.120

• the composite (Figure 2f) indicated the presence of AuNPs. Fourier-transform infrared spectroscopy (FTIR) was used to investigate the vibrational spectrum of the functional groups present in the nanoparticles and their composites. The FTIR spectra of Gr, AuNPs, and DNA/AuNPs/Gr were fused in Figure 2g

• Oxford Instrument energy dispersive X-ray spectrometer. UV–vis was performed on a Libra S80 Biochrom spectrophotometer and FTIR was performed on a Spectrum 400 PerkinElmer spectrometer (U.S.). Electrochemical studies of the electrodes The electrochemical behaviour of different modified SPCE surfaces was

• of different nanoparticles and their composites. FESEM images of (a) Gr and (b) AuNPs/Gr; EDX of images of (c) Gr and (d) AuNPs/Gr; UV–vis spectra of (e) Gr and (f) AuNPs/Gr; and FTIR spectra of (g) Gr, AuNPs/Gr, and DNA/AuNPs/Gr. AuNPs were taken (33.33%, 1:3) in the AuNPs/Gr nanocomposite

Supramolecular assembly of pentamidine and polymeric cyclodextrin bimetallic core–shell nanoarchitectures

• Alexandru-Milentie Hada,
• Nina Burduja,
• Marco Abbate,
• Claudio Stagno,
• Guy Caljon,
• Louis Maes,
• Nicola Micale,
• Massimiliano Cordaro,
• Angela Scala,
• Antonino Mazzaglia and
• Anna Piperno

Beilstein J. Nanotechnol. 2022, 13, 1361–1369, doi:10.3762/bjnano.13.112

• stable Ag NPs. In the framework of our research on BMNPs, we collected several experimental data, including FTIR spectra, which suggested strong interactions between PolyCD and Au@Ag BMNPs [14]. In this paper we partially clarify the role of PolyCD in the formation/stabilization of Au@Ag BMNPs by

Role of titanium and organic precursors in molecular layer deposition of “titanicone” hybrid materials

• Arbresha Muriqi and
• Michael Nolan

Beilstein J. Nanotechnol. 2022, 13, 1240–1255, doi:10.3762/bjnano.13.103

• 180 °C to 0.49 Å/cycle at 300 °C. This reduction was attributed to the increased thermal motion and desorption of molecules on the growth surface. FTIR spectra indicated that the hybrid film shows a stable bridging bonding mode between Ti and the acid group at temperatures under 200 °C and a high

Design of surface nanostructures for chirality sensing based on quartz crystal microbalance

• Yinglin Ma,
• Xiangyun Xiao and
• Qingmin Ji

Beilstein J. Nanotechnol. 2022, 13, 1201–1219, doi:10.3762/bjnano.13.100

• resonance [10], Fourier transform infrared spectrometry (FTIR) [11], UV–vis absorption spectrometry [12], mass spectrometry (MS) [13], titration microcalorimetry [14], high-performance liquid chromatography (HPLC) [15], gas chromatography (GC), capillary electrophoresis (CE) [16], and electrochemical chiral

Rapid fabrication of MgO@g-C₃N₄ heterojunctions for photocatalytic nitric oxide removal

• Minh-Thuan Pham,
• Duyen P. H. Tran,
• Xuan-Thanh Bui and
• Sheng-Jie You

Beilstein J. Nanotechnol. 2022, 13, 1141–1154, doi:10.3762/bjnano.13.96

• -transform infrared spectroscopy (FTIR) was used to determine the chemical bond composition of the materials. Differential reflectance spectroscopy (DRS) determined the change in the bandgap of the materials. The elements of the materials were identified by high-resolution X-ray photoelectron spectroscopy

• cycles, respectively. The photocatalytic NO degradation efficiency decreased by 7% after five cycles. The FTIR spectra and the XRD patterns of the 3% MgO@g-C3N4 before and after the recycling test are shown in Figure S1a and Figure S1b of Supporting Information File 1, respectively. The results indicate

• values of g-C3N4, MgO, 1% MgO@g-C3N4, 3% MgO@g-C3N4, and 5% MgO@g-C3N4 are −201.6%, −58.2%, −160.8%, 47.4%, and −25.8%, respectively. XRD and FTIR analyses XRD patterns of the synthesized materials are shown in Figure 4a. There are two distinct diffraction peaks at 2θ = 13° and 27.4°, which were assigned

Recent advances in green carbon dots (2015–2022): synthesis, metal ion sensing, and biological applications

• Aisha Kanwal,
• Naheed Bibi,
• Sajjad Hyder,
• Arif Muhammad,
• Hao Ren,
• Jiangtao Liu and
• Zhongli Lei

Beilstein J. Nanotechnol. 2022, 13, 1068–1107, doi:10.3762/bjnano.13.93

• cerasifera fruit was used to synthesize highly luminescent CDs via a hydrothermal method. The reaction temperature and time used were 200 °C and 20 h, respectively. Characterization techniques such as TEM, FTIR, and XPS were used to study the CDs which were almost spherical and had high nitrogen content [49

Electrocatalytic oxygen reduction activity of AgCoCu oxides on reduced graphene oxide in alkaline media

• Iyyappan Madakannu,
• Indrajit Patil,
• Bhalchandra Kakade and
• Kasibhatta Kumara Ramanatha Datta

Beilstein J. Nanotechnol. 2022, 13, 1020–1029, doi:10.3762/bjnano.13.89

• microwave-assisted approach with different fractions of Ag, Cu, and Co, that is, Ag0.6Co1.5Cu1.5 (ACC-1), Ag2.0Co1.0Cu1.0 (ACC-2), and Ag6.0Co1.0Cu1.0 (ACC-3). Our method is convenient and efficient for designing a sustainable electrode material for the ORR in alkaline media. XRD, FTIR, and SEM were used to

• the trimetallic oxide NPs. The graphene oxide support provides the necessary functional groups for the cohesion of binary and ternary metallic oxide NPs (Figure S2a, Supporting Information File 1). The functional groups and the metal oxygen bonds were determined by FTIR spectroscopy, besides the

• shown in Figure 7b. Following the stability investigation, another assessment of functional groups and morphology of ACC-2 was carried out by FTIR and SEM (Figure S11, Supporting Information File 1). There is no considerable change in the morphological integrity of the catalyst (before and after 10,000

Hierarchical Bi₂WO₆/TiO₂-nanotube composites derived from natural cellulose for visible-light photocatalytic treatment of pollutants

• Zehao Lin,
• Zhan Yang and
• Jianguo Huang

Beilstein J. Nanotechnol. 2022, 13, 745–762, doi:10.3762/bjnano.13.66

• (FTIR) spectra of the samples were recorded on the Nicolet iS10 spectrometer. The X-ray photoelectron spectroscopy (XPS) experiment was performed on the Thermo Scientific ESCALAB 250Xi spectrometer equipped with an Al Kα X-ray source at an energy value of 1486.6 eV. The XPS spectra were calibrated by

• presence of the hierarchical TiO2 nanotubes influences and inhibits the crystallinity of Bi2WO6 in between the interface of the two phases, revealing the strong interaction between TiO2 and Bi2WO6 phases [35][36]. Figure 2b displays the FTIR spectra of the hierarchical Bi2WO6/TiO2-NT nanocomposites, pure

• TiO2-NT, and pure Bi2WO6 powder samples, where all present two similar absorption bands at 1625 and 3420 cm−1 which can be indexed to the stretching vibration of adsorbed H2O and –OH group on the sample surface [37]. Apart from the 30%−Bi2WO6/TiO2-NT nanocomposite, the FTIR spectra of the other Bi2WO6

A nonenzymatic reduced graphene oxide-based nanosensor for parathion

• Sarani Sen,
• Anurag Roy,
• Ambarish Sanyal and
• Parukuttyamma Sujatha Devi

Beilstein J. Nanotechnol. 2022, 13, 730–744, doi:10.3762/bjnano.13.65

• (ULVAC-PHI, U.S.) with monochromatic Al Kα (hν = 1486.6 eV) radiation, and a beam size of 100 μm. The Fourier transform infrared (FTIR) absorption spectra of GO and ERGO were collected in the 4000–400 cm−1 region on a Perkin Elmer spectrometer as KBr (Sigma-Aldrich, Germany) pellets. The crystalline

• , has been chosen for an efficient conversion of GO to ERGO. Figure 1C shows the characteristic FTIR spectra of GO and ERGO (in PBS, pH 4.5) to identify the change of functional groups due to electrolytic reduction of GO. The predominant characteristic absorption peaks of GO include a broad peak at 3426

• and/or epoxy C–O stretching vibration. The significant reduction of the FTIR signal intensity of ERGO for –OH, –C=O, and –C–O suggests the successful formation of ERGO due to the electrochemical deoxygenation of GO, which corroborates the Raman analysis. Figure 1D depicts a characteristic XRD peak of

Antibacterial activity of a berberine nanoformulation

• Hue Thi Nguyen,
• Tuyet Nhung Pham,
• Anh-Tuan Le,
• Nguyen Thanh Thuy,
• Tran Quang Huy and
• Thuy Thi Thu Nguyen

Beilstein J. Nanotechnol. 2022, 13, 641–652, doi:10.3762/bjnano.13.56

• of glycerol on the physicochemical properties of BBR NPs was investigated by UV–vis absorption and FTIR spectroscopy. The UV–vis absorption spectra of pure BBR and BBR NP solutions in distilled water at the same concentration are shown in Figure 1. Glycerol has no absorption band in the UV–vis

• , whereas the solubility of BBR NPs was significantly enhanced. The chemical characteristics of BBR and BBR NPs were analyzed through FTIR spectroscopy (Figure 2). In the FTIR spectrum of glycerol (Figure 2a), the absorption band appearing at 3287 cm−1 is characteristic for stretching vibrations of the –OH

• group. The two bands with maxima at 2934 and 2880 cm−1 are ascribed to symmetrical and asymmetrical –CH2 vibrations. The band at 1032 cm−1 is attributed to C–H deformation vibrations and C–C stretching vibrations. In the FTIR spectrum of pure BBR (Figure 2c), an intense broad band at 3414 cm−1 appeared

Detection and imaging of Hg(II) in vivo using glutathione-functionalized gold nanoparticles

• Gufeng Li,
• Shaoqing Li,
• Rui Wang,
• Min Yang,
• Lizhu Zhang,
• Yanli Zhang,
• Wenrong Yang and
• Hongbin Wang

Beilstein J. Nanotechnol. 2022, 13, 549–559, doi:10.3762/bjnano.13.46

• the GSH and Rh6G2 were successfully bound to the surface of GNPs. FTIR spectra of GNPs, GSH, GNPs-GSH, and GNPs-GSH-Rh6G2 are presented in Figure 2e. As citrate ions are attached on the surface of GNP, C=O, and C–O stretching vibration modes occur at 1655 and 1443 cm−1, respectively. The peaks of GSH

• Fluorescence spectrophotometer (Hitachi, Japan). Mean particle size and the zeta potential were recorded using a Zetasizer Nano ZS90 (Malvern, UK). A Nicolet iS10 infrared spectrometer (Nicolet, USA) was used to gather FTIR spectra in a scanning range of 400–4000 cm−1. Fluorescence images of cells were

• GNPs-GSH-Rh6G2; (e) FTIR spectra of GNPs, GSH, GNPs-GSH, and GNPs-GSH-Rh6G2. (a) Fluorescence intensity of GNPs-GSH-RH6G2 as function of the ratio between nGSH and nRh6G2 (nGNPs is 0.0726 µmol); (b) fluorescence intensity of GNPs-GSH-Rh6G2 synthesized using different amounts of GSH (nGNPs and nRH6G2

Coordination-assembled myricetin nanoarchitectonics for sustainably scavenging free radicals

• Xiaoyan Ma,
• Haoning Gong,
• Kenji Ogino,
• Xuehai Yan and
• Ruirui Xing

Beilstein J. Nanotechnol. 2022, 13, 284–291, doi:10.3762/bjnano.13.23

• component co-assembles with Myr and GSH. Fourier-transform infrared (FTIR) spectra were used to further confirm the self-assembly of the MZG nanoparticles. In Figure 2d, the two bands at 2522 cm−1 and 3350 cm−1 were assigned to the mercapto group (–SH) and the stretching vibration of the amino group (–NH2

• ) FTIR spectra of MZG, GSH, and Myr. (e) Stability evaluation of MZG nanoparticles during incubation in aqueous solution at 37 °C for 24 h. (f) Stability evaluation of MZG nanoparticles during incubation in the mixture medium of PBS containing 9% DMEM and 1% FBS (v/v) at 37 °C for 24 h (equivalent

Enhancement of the piezoelectric coefficient in PVDF-TrFe/CoFe₂O₄ nanocomposites through DC magnetic poling

• Marco Fortunato,
• Alessio Tamburrano,
• Maria Paola Bracciale,
• Maria Laura Santarelli and
• Maria Sabrina Sarto

Beilstein J. Nanotechnol. 2021, 12, 1262–1270, doi:10.3762/bjnano.12.93

• influenced by magnetic poling, we performed FTIR analyses of six different samples. Figure 1 shows the FTIR spectra of the nanocomposite specimen produced with a CoFe2O4 nanoparticle content of 5 wt %, poled for increasing time (from 60 to 120 min) at increasing strengths of the DC magnetic field (50 and 110

• nanoparticles, the measured FTIR spectra show a broadband shoulder close to the α phase peak located at 763 cm−1 (probably due to the interaction between polymer and nanoparticles), making the evaluation of the relative fraction of β phase by using Equation 1 difficult. By deconvolving the shoulder from the

• to what has been reported in [25], where an increase of F(β) was observed, with a maximum increase for magnetic fields around 400 Oe. Furthermore, analyzing the FTIR data in the range of 1600–1900 cm−1, as reported in Figure 1, we observed that a broad peak at 1740 cm−1 appears in the spectra of all

Electrical, electrochemical and structural studies of a chlorine-derived ionic liquid-based polymer gel electrolyte

• Ashish Gupta,
• Amrita Jain,
• Manju Kumari and
• Santosh K. Tripathi

Beilstein J. Nanotechnol. 2021, 12, 1252–1261, doi:10.3762/bjnano.12.92

• . We are also grateful to Dr. J.K. Bera, Department of Chemistry, IIT Kanpur for providing FTIR facilities, Dr. Kamlesh Pandey, NCEMP, Allahabad for providing SEM facilities, Dr. Ajay Gupta and Dr. Mukul Gupta, UGC-DAE Consortium for Scientific Research, Indore-centre for providing the XRD facility and

pH-driven enhancement of anti-tubercular drug loading on iron oxide nanoparticles for drug delivery in macrophages

• Karishma Berta Cotta,
• Sarika Mehra and
• Rajdip Bandyopadhyaya

Beilstein J. Nanotechnol. 2021, 12, 1127–1139, doi:10.3762/bjnano.12.84

• the interaction of water molecules with the Fe ions on the surface of IONPs, which in turn facilitates protonation and deprotonation with varying pH [33]. Characteristic iron oxide and NOR peaks were observed in their respective FTIR spectra and were used as a reference for comparison with the coated

• samples (Figure 2e,f). FTIR peaks observed at 587–590 cm−1, 1630 cm−1 and 3420 cm−1 in Figure 2e correspond to Fe–O vibrations and O–H bending and stretching vibrations, respectively [34]. The O–H vibrations present in the iron oxide nanoparticles possibly arise from the association of oxygen from the

• individual nanoparticles (Figure 3b), clearly indicating a reduced aggregate size in comparison to the UIONPs which was also indicated by the reduced FWHM, i.e., 40.72 nm. The XRD pattern confirmed the presence of iron oxide nanoparticles (Figure 3c). The FTIR spectrum of NOR@IONPpH5 indicated the presence

Comprehensive review on ultrasound-responsive theranostic nanomaterials: mechanisms, structures and medical applications

• Sepand Tehrani Fateh,
• Lida Moradi,
• Elmira Kohan,
• Michael R. Hamblin and
• Amin Shiralizadeh Dezfuli

Beilstein J. Nanotechnol. 2021, 12, 808–862, doi:10.3762/bjnano.12.64

The preparation temperature influences the physicochemical nature and activity of nanoceria

• Robert A. Yokel,
• Wendel Wohlleben,
• Johannes Georg Keller,
• Matthew L. Hancock,
• Jason M. Unrine,
• D. Allan Butterfield and
• Eric A. Grulke

Beilstein J. Nanotechnol. 2021, 12, 525–540, doi:10.3762/bjnano.12.43

• 900 °C at 10 °C/min. Fourier-transform infrared spectroscopy (FTIR) (Nicolet 6700 FTIR with a diamond ATR crystal) was used to detect organic functional groups on the ENM surface. Thirty-two scans were completed. Nanoceria calcination Two samples (6.5 and 6.7 mg) of solvothermally synthesized

• ), indicative of some organic surface coating, as previously reported [7]. The TGA weight loss for the solvothermally synthesized nanoceria was much greater (ca. 15%) due to its citrate coating (Figure 8 of [35]). FTIR, not previously reported for NM-212, showed small peaks at ca. 1630, 1420, and 1320 cm−1

• , attributed to N–O, –COOH, or hydroxy groups; probably COOH and the stretching mode of O–H bonds; and either –CH or C–O–C, respectively [16][49][50] (Figure 4). Due to the citrate coating on the solvothermally synthesized nanoceria, the FTIR spectrum shows additional large peaks at 1535 and 1365 cm−1 (Figure

Boosting of photocatalytic hydrogen evolution via chlorine doping of polymeric carbon nitride

• Malgorzata Aleksandrzak,
• Michalina Kijaczko,
• Wojciech Kukulka,
• Daria Baranowska,
• Martyna Baca,
• Beata Zielinska and
• Ewa Mijowska

Beilstein J. Nanotechnol. 2021, 12, 473–484, doi:10.3762/bjnano.12.38

• the interlayers of PCN and not on its π-conjugated planes as it is in the case with other commonly used metal/non-metal (Cu, Ni, C, N or O) modifications [42][43][44][45][46]. Fourier-transform infrared (FTIR) spectroscopy was used to obtain the molecular structure information of the carbon nitride

• materials. The FTIR absorption analysis was recorded in the spectral range of 600–3600 cm−1 to examine the surface of the prepared materials (Figure 3a). The FTIR spectra of both samples (before and after doping) reveal that the positions of the vibration peaks are nearly the same, indicating a similar

• packing motif of the tri-s-triazine units. The shift from 27.38° to 27.30° is caused by the increased internal distance of PCN by Cl doping, which is in good agreement with AFM data and suggests that Cl is located at the interlayers of carbon nitride. Moreover, the XRD and FTIR analyses confirmed that the