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

Non-stoichiometric magnetite as catalyst for the photocatalytic degradation of phenol and 2,6-dibromo-4-methylphenol – a new approach in water treatment

• Joanna Kisała,
• Anna Tomaszewska and
• Przemysław Kolek

Beilstein J. Nanotechnol. 2022, 13, 1531–1540, doi:10.3762/bjnano.13.126

• SEM, X-ray diffraction, and ultraviolet–visible (UV–vis) analysis. The XRD and UV–vis results were published in our previous article [17]. We present this data again in this article as it is necessary for the discussion of the results. Zeta potential measurements were also presented in another

• was performed using a powder X-ray diffractometer (Figure 1a). The XRD spectra revealed that the diffraction peaks at 2θ = 30.2°, 35.3°, 43.7°, 53.9°, 57.1°, and 62.7° (Figure 1a) correspond to those of Fe3O4 (reference code COD 01-089-3854); they belong to a cubic structure system corresponding to

• the facets (220), (311), (400), (422), (511), and (440) of Fe3O4, respectively [21]. The absence of the (210) and (211) peaks confirms that the catalysts were indeed magnetite. The mean size of the catalyst crystallites (D) was calculated from the high-reflection X-ray diffraction profiles by

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

• -scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and linear sweep voltammetry. The results show that the TiO2@MWCNTs nanocomposite has an optical bandgap of 2.5 eV, which is a significant improvement in visible-light absorption capability compared to TiO2 (3.14 eV). The

• nanocomposite characterizations The surface morphology of MWCNTs and the TiO2@MWCNTs nanocomposite is characterized by using field-emission scanning electron microscopy (FE-SEM, S4800) and transmission electron microscopy (TEM, JEOL-1400). The crystallization behavior of the catalysts is analyzed by X-ray

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

• -dispersive X-ray spectroscopy (EDX), and transmission electron microscopy (TEM) techniques were used to characterize nanoparticle development. The breast cancer cell line MCF-7 was used as a test model to study the cytotoxic behavior of Ag/AgCl nanoparticles and, as a counterpart, the nanoparticles were also

• nanoparticles. Crystalline behavior In all of the reactions, the X-ray diffraction patterns shown in Figure 2 confirm the transformation of AgNO3 into metallic Ag. The characteristic peaks of AgNO3 salt and metallic Ag are indicated by short lines and can be used as a reference for comparison with the

Hydroxyapatite–bioglass nanocomposites: Structural, mechanical, and biological aspects

• Olga Shikimaka,
• Mihaela Bivol,
• Bogdan A. Sava,
• Marius Dumitru,
• Christu Tardei,
• Beatrice G. Sbarcea,
• Daria Grabco,
• Constantin Pyrtsac,
• Daria Topal,
• Andrian Prisacaru,
• Vitalie Cobzac and
• Viorel Nacu

Beilstein J. Nanotechnol. 2022, 13, 1490–1504, doi:10.3762/bjnano.13.123

• and porosity were ±0.05 g/cm3 and ±0.05%, respectively. X-ray diffraction With the help of a Bruker D8 ADVANCE X-ray diffractometer, the evolution of the formation of hydroxyapatite and of the intermediate compounds was studied, on samples calcined at different temperatures, as well as after burning

• peak of each diffractogram with the highest intensity, the average size of the crystallite, Dhkl, was calculated using the Scherrer equation: where k is a dimensionless constant called the form factor, usually having a value of 0.9. λ is the X-ray wavelength, in this case λ = 1.54060 Å, FWHM (full

• special cleaning process for 6 min in a nitrogen plasma jet in a FISCHONE Plasma Cleaner. A FEI QUANTA INSPECT S SEM was used to observe structure and morphology of the samples after their treatment in simulated body fluid, as well as to acquire the energy-dispersive X-ray (EDX) spectra and the elemental

Structural studies and selected physical investigations of LiCoO₂ obtained by combustion synthesis

• Monika Michalska,
• Paweł Ławniczak,
• Tomasz Strachowski,
• Adam Ostrowski and
• Waldemar Bednarski

Beilstein J. Nanotechnol. 2022, 13, 1473–1482, doi:10.3762/bjnano.13.121

• reason may be the expected differences in the g-tensor values from nickel complexes on the surface and inside the crystallites. However, as shown in Figure 9 the mutual changes in the concentration of Ni3+(I) and Ni3+(II) complexes are too small in relation to the changes in surface area measured by X

• -ray experiments. Therefore, the assumption that the two different nickel complexes are derived from the crystallites and the surface can probably be rejected. The second reason why two complexes are visible in the EPR spectra is the assumption that two LCO phases are formed during the synthesis: a low

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

• scanning electron microscopy and structural characteristics were analysed by using energy-dispersive X-ray, UV–vis, and Fourier-transform infrared spectroscopy. The electrochemical characteristics of the modified electrodes were studied by cyclic voltammetry, differential pulse voltammetry (DPV), and

• with graphene. The spectrum of Gr in Figure 2c obtained by energy dispersive X-ray spectroscopy (EDX) clearly demonstrates the presence of a high amount of carbon with a minimum amount of oxygen, indicating the purity of Gr. Figure 2d clearly shows the presence of carbon, oxygen, and AuNPs in the

• 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

LED-light-activated photocatalytic performance of metal-free carbon-modified hexagonal boron nitride towards degradation of methylene blue and phenol

• Nirmalendu S. Mishra and
• Pichiah Saravanan

Beilstein J. Nanotechnol. 2022, 13, 1380–1392, doi:10.3762/bjnano.13.114

• times with DI water, and dried overnight at 60 °C. The commercially available HBN was used as a control sample. Characterization techniques A Rigaku Smart Lab high-resolution X-ray diffractometer (HR-XRD) equipped with a HyPix-3000 detector and Cu anode emitting Kα radiation was employed to obtain the

• attachment using BaSO4 as the standard. The electronic arrangement of the studied materials was revealed through a PHI 5000 versa probe III high-resolution X-ray photoelectron spectroscope (HR-XPS). The mineralization efficiency was estimated through the variation in the total organic carbon content by using

Near-infrared photoactive Ag-Zn-Ga-S-Se quantum dots for high-performance quantum dot-sensitized solar cells

• Roopakala Kottayi,
• Ilangovan Veerappan and
• Ramadasse Sittaramane

Beilstein J. Nanotechnol. 2022, 13, 1337–1344, doi:10.3762/bjnano.13.110

• of solar cells. In this study, we synthesized Ag-Zn-Ga-S-Se-based alloyed QDs by colloidal hot injection and characterized them. The X-ray photoelectron spectrum analysis confirms the +1, +2, +3, −2, and −2 oxidation states of, respectively, Ag, Zn, Ga, S, and Se in the QDs, and the energy-dispersive

• X-ray spectrum analysis confirms the 1:1:1:1.5:1.5 stoichiometric ratio of, respectively, Ag, Zn, Ga, S, and Se. These two results indicate the formation of I-II-III-VI3-type alloyed crystals (AgZnGaS1.5Se1.5 nanocrystals). TEM image analysis reveals the QD nature of the synthesized Ag-Zn-Ga-S-Se

• nanocrystals. The X-ray diffraction pattern confirms the hexagonal structure. Due to the near-infrared light absorption capability, the synthesized QDs were used as the sensitizer to fabricate QDSCs. The fabricated QDSCs were characterized by using electrochemical impedance spectroscopy and photovoltaic

Recent trends in Bi-based nanomaterials: challenges, fabrication, enhancement techniques, and environmental applications

• Vishal Dutta,
• Ankush Chauhan,
• Ritesh Verma,
• C. Gopalkrishnan and
• Van-Huy Nguyen

Beilstein J. Nanotechnol. 2022, 13, 1316–1336, doi:10.3762/bjnano.13.109

• intermediates from the synthesis process into photocatalysts to alter the energy band structure and increase photocatalytic activity [89]. A simple two-step technique was used to develop a novel compound photocatalyst of Bi/BiOBr-Bi5+ [90]. X-ray diffraction, field-emission transmission electron microscopy, and

• X-ray photoelectron spectroscopy revealed the coexistence of self-doped Bi5+ and in situ deposited Bi(M). Compared to Bi/BiOBr or BiOBr–Bi5+, the photocatalytic activity of Bi/BiOBr-Bi5+ regarding RhB degradation under visible light was significantly increased. OVs helped in separating photoexcited

Enhanced electronic transport properties of Te roll-like nanostructures

• E. R. Viana,
• N. Cifuentes and
• J. C. González

Beilstein J. Nanotechnol. 2022, 13, 1284–1291, doi:10.3762/bjnano.13.106

• under mild conditions. A large quantity of these polycrystalline nanostructures with a diameter between 100 and 900 nm and a wall thickness around 50 nm were synthesized and characterized by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), transmission electron microscopy

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

• properties of the materials. Scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HR-TEM) were used to assess the morphology of the materials. The crystal phase of the materials was determined by X-ray diffraction (XRD) with a measurement range of 10°–80°. Fourier

• -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

Green synthesis of zinc oxide nanoparticles toward highly efficient photocatalysis and antibacterial application

• Vo Thi Thu Nhu,
• Nguyen Duy Dat,
• Le-Minh Tam and
• Nguyen Hoang Phuong

Beilstein J. Nanotechnol. 2022, 13, 1108–1119, doi:10.3762/bjnano.13.94

• , Vietnam 10.3762/bjnano.13.94 Abstract Zinc oxide nanoparticles (ZnO NPs) were successfully synthesized by a green method using rosin and zinc chloride as salt precursors. The phase structure, morphology, and particle size of ZnO were determined by X-ray powder diffraction, field emission scanning

• reactions that form zinc resinate are shown in Equation 1 and Equation 2. The schematic illustration of the synthesis of ZnO nanoparticles is shown in Figure 1. Methods for determining the characterization of the synthesized material The phase of the synthesized material was determined by X-ray diffraction

• (XRD) using a Bruker D8 advanced X-ray diffractometer equipped with Cu Kα radiation (λ = 1.5418 Å). The morphology and size of the synthesized material were determined by field emission scanning electron microscopy (FESEM) on a Hitachi S-4800 at 15 kV and high-resolution transmission electron

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

Spindle-like MIL101(Fe) decorated with Bi₂O₃ nanoparticles for enhanced degradation of chlortetracycline under visible-light irradiation

• Chen-chen Hao,
• Fang-yan Chen,
• Kun Bian,
• Yu-bin Tang and
• Wei-long Shi

Beilstein J. Nanotechnol. 2022, 13, 1038–1050, doi:10.3762/bjnano.13.91

• . Characterization of the as-prepared catalyst The crystalline structure of the prepared photocatalyst was analyzed by X-ray diffraction spectrometry (Empyrean, Panalytical, Holland) with Cu Kα radiation at a scanning speed of 7 °/min. The morphology of the samples was observed by scanning electron microscopy (SEM

• , FEI-quanta 200, Japan Electronics, Japan), transmission electron microscopy (TEM, FEI-Tecnai F20, USA) and high-resolution transmission electron microscopy (HRTEM, JEOL 2100F, Japan). The element valence and chemical composition was investigated using X-ray photoelectron spectroscopy (XPS, Axis ultra

• photocatalytic activity of the Bi2O3/MIL101(Fe) composite. X-ray photoelectron spectroscopy was performed to explore the elemental compositions and the surface chemical states of BOM-20 and the results are presented in Figure 4. The XPS survey spectrum (Figure 4a) indicates the existence of Fe, Bi, O, and C in

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

• and crystallinity of the assembled binary and ternary metallic oxide NPs, powder X-ray diffraction (PXRD) measurements were carried out. The PXRD patterns of the binary and ternary NPs on rGO showed peaks located at 2θ = 38.1°, 44.2°, 64.3°, and 77.1°, which could be indexed to the (111), (200), (220

• important binding sites, oxidation states, and the elemental composition using X-ray photoelectron spectroscopy. The survey scan of ACC-2 revealed C, O, Cu, Co, and Ag with 54.7, 29.9, 1.0, 8.1, and 6.3 atom % respectively (Figure S10a, Supporting Information File 1). The Ag 3d3/2 and Ag 3d5/2 peaks in the

Effects of focused electron beam irradiation parameters on direct nanostructure formation on Ag surfaces

• Jānis Sniķeris,
• Vjačeslavs Gerbreders,
• Andrejs Bulanovs and
• Ēriks Sļedevskis

Beilstein J. Nanotechnol. 2022, 13, 1004–1010, doi:10.3762/bjnano.13.87

• material greatly affects the growth rate of the nanowires, with the Cu surface providing the fastest growth. Energy-dispersive X-ray spectroscopy (EDX) revealed the presence of both carbon and substrate materials in the nanowires. The effect of substrate material on nanowire growth rate could be attributed

Theoretical investigations of oxygen vacancy effects in nickel-doped zirconia from ab initio XANES spectroscopy at the oxygen K-edge

• Dick Hartmann Douma,
• Lodvert Tchibota Poaty,
• Alessio Lamperti,
• Stéphane Kenmoe,
• Abdulrafiu Tunde Raji,
• Alberto Debernardi and
• Bernard M’Passi-Mabiala

Beilstein J. Nanotechnol. 2022, 13, 975–985, doi:10.3762/bjnano.13.85

• Nanotechnologies, Institut National de Recherche en Sciences Exactes et Naturelles (IRSEN), Brazzaville, Congo 10.3762/bjnano.13.85 Abstract In this study, we present theoretical X-ray absorption near-edge structure (XANES) spectra at the K-edge of oxygen in zirconia containing Ni dopant atoms and O vacancies at

• and magnetic order in a typical diluted magnetic oxide. Such a finding may be crucial for spintronics-related applications. Keywords: defect; ligand field; nickel; oxidation state; oxides; spectroscopy; spintronics; vacancy; X-ray absorption; X-ray absorption near-edge structure (XANES); zirconia

• which is being currently employed in ultra-scaled electronics for its high dielectric constant [24][25] have received significant attention because of its practical applications. Thus, recently, exploiting first principles simulations and X-ray absorption near edge spectroscopy (XANES) in high magnetic

Solar-light-driven LaFe_xNi_1−xO₃ perovskite oxides for photocatalytic Fenton-like reaction to degrade organic pollutants

• Chao-Wei Huang,
• Shu-Yu Hsu,
• Jun-Han Lin,
• Yun Jhou,
• Wei-Yu Chen,
• Kun-Yi Andrew Lin,
• Yu-Tang Lin and
• Van-Huy Nguyen

Beilstein J. Nanotechnol. 2022, 13, 882–895, doi:10.3762/bjnano.13.79

• antibiotics of PPCPs accordinly. Results and Discussion Material characterization of various photocatalysts X-ray powder diffraction (XRD) was used to reveal the structure of the materials. In the synthesis step of LaNiO3, the calcination temperature was set to 500, 600, 700, and 800 °C, respectively, and the

• oxides were prepared ultimately. Photocatalysts characterization The LaFexNi1−xO3 photocatalysts were characterized by D8 advance (Bruker, Germany) to reveal the X-ray powder diffraction (XRD) patterns. The Cu Kα target was facilitated under 40 kV to generate the X-ray with λ = 0.15406 nm. The 2θ

Ultrafast signatures of magnetic inhomogeneity in Pd_1−xFe_x (x ≤ 0.08) epitaxial thin films

• Andrey V. Petrov,
• Sergey I. Nikitin,
• Lenar R. Tagirov,
• Amir I. Gumarov,
• Igor V. Yanilkin and
• Roman V. Yusupov

Beilstein J. Nanotechnol. 2022, 13, 836–844, doi:10.3762/bjnano.13.74

• ferromagnetic resonance techniques (the latter two, because of the large scale, yield volume-averaged signals). Resonant magnetic small-angle X-ray scattering applied to Pd1−xFex alloy films with x = 0.03–0.07 revealed static magnetic fluctuations on the lateral scale of about 100 nm attributed to the magnetic

• beam epitaxy (MBE). The films were 20 nm thick, continuous, and smooth monocrystalline layers. The MBE equipment provided uniformity of the film thickness within 3% on the 1″ lateral size. The film composition x was measured in situ using X-ray photoelectron spectroscopy (all from SPECS, Berlin) with a

Temperature and chemical effects on the interfacial energy between a Ga–In–Sn eutectic liquid alloy and nanoscopic asperities

• Yujin Han,
• Pierre-Marie Thebault,
• Corentin Audes,
• Xuelin Wang,
• Haiwoong Park,
• Jian-Zhong Jiang and
• Arnaud Caron

Beilstein J. Nanotechnol. 2022, 13, 817–827, doi:10.3762/bjnano.13.72

• -/nanotechnology. The surface chemical composition of the liquid alloy was measured by X-ray photoelectric spectroscopy before and after heating to 100 °C for 3 h. Furthermore, we imaged the nanoscopic asperities after measurements on the metallic liquid alloy by SEM to evidence possible liquid residues. For all

• liquid sample by fitting the function to our experimental data. The chemical composition of the eutectic Ga–In–Sn liquid alloy sample was determined by photoelectronic X-ray spectroscopy (XPS) before and after heating in air at 100 °C for 3 h. The spectrograms were recorded with a K-alpha+ XPS system

Optimizing PMMA solutions to suppress contamination in the transfer of CVD graphene for batch production

• Chun-Da Liao,
• Andrea Capasso,
• Tiago Queirós,
• Telma Domingues,
• Fatima Cerqueira,
• Nicoleta Nicoara,
• Jérôme Borme,
• Paulo Freitas and
• Pedro Alpuim

Beilstein J. Nanotechnol. 2022, 13, 796–806, doi:10.3762/bjnano.13.70

• mapping. In the maps, the intensity of D and 2D bands were normalized to the G band intensity. Corresponding statistics were extracted from the maps. X-ray photoelectron spectroscopy The chemical components of PMMA residues were analyzed by X-ray photoelectron spectroscopy (XPS, Thermo Scientific ESCALAB

Efficient liquid exfoliation of KP₁₅ nanowires aided by Hansen's empirical theory

• Zhaoxuan Huang,
• Zhikang Jiang,
• Nan Tian,
• Disheng Yao,
• Fei Long,
• Yanhan Yang and
• Danmin Liu

Beilstein J. Nanotechnol. 2022, 13, 788–795, doi:10.3762/bjnano.13.69

• control the temperature. To prevent sample drift, SiO2 (300 nm)/Si substrates with tested KP15 samples were attached by fixtures to the Linkam THMS600 cryostat. Results and Discussion KP15 bulks, prepared by the gas-phase-transfer method, had a flat and smooth surface shown in Figure 1a. The X-ray

Recent advances in nanoarchitectures of monocrystalline coordination polymers through confined assembly

• Lingling Xia,
• Qinyue Wang and
• Ming Hu

Beilstein J. Nanotechnol. 2022, 13, 763–777, doi:10.3762/bjnano.13.67

• the grown coordination polymers can be distinguished by X-ray diffraction analysis [124][125][126][127]. However, the flexibility of the frameworks brought unexpected phenomena [128][129]. The shell crystal could first yield to the core crystal, making the whole composite present a single phase as the

• are within the length range from 1 to 10 μm, the whole structure of the composites cannot be imaged well by electron microscopy or X-ray based imaging techniques. Second, time-resolved structural changes of the nanoarchitectonics are hard to be observed because of the complex processing environment

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

• the practical content (72.9 wt %) of the Bi2WO6 component in the 70%−Bi2WO6/TiO2-NT nanocomposite. Characterization Powder X-ray diffraction (XRD) patterns of the samples were obtained from the Rigaku Ultima IV diffractometer with a Cu Kα (λ = 0.15405 nm) radiation source. Fourier transform infrared

• (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

• ). Meanwhile, selected area electron diffraction (SAED) patterns and energy dispersive X-ray spectrometry (EDX) mapping images were obtained via HR-TEM. The instrument models used in FE-SEM, TEM, and HR-TEM were Hitachi SU-8010, Hitachi HT-7700, and JEM-2100F, and the working voltages were 5.0, 100, and 200 kV