A visible-light photodetector based on heterojunctions between CuO nanoparticles and ZnO nanorods

• Doan Nhat Giang,
• Nhat Minh Nguyen,
• Duc Anh Ngo,
• Thanh Trang Tran,
• Le Thai Duy,
• Cong Khanh Tran,
• Thi Thanh Van Tran,
• Phan Phuong Ha La and
• Vinh Quang Dang

Beilstein J. Nanotechnol. 2023, 14, 1018–1027, doi:10.3762/bjnano.14.84

• . The energy-dispersive X-ray spectroscopy (EDS) results in Figure 1c show Zn, Cu, and O, which indicates the presence of ZnO and CuO. No further impurities were found. The results from X-ray diffractometry (XRD) and UV–vis absorption spectroscopy confirm that the nanoparticles covering the surfaces and

• length and 0.02 cm channel width. Characterizations The crystal structure of the materials was investigated by X-ray diffractometry on a Bruker D8 Advance diffractometer with Cu Kα radiation (λ = 1.5406 Å). An energy-dispersive X-ray spectrometer (FEI iQUANTA FEG-200) was used to determine the chemical

Exploring internal structures and properties of terpolymer fibers via real-space characterizations

• Michael R. Roenbeck and
• Kenneth E. Strawhecker

Beilstein J. Nanotechnol. 2023, 14, 1004–1017, doi:10.3762/bjnano.14.83

• , this distinction in fundamental chemistry has significant implications for the structures and properties of the resulting fibers. To date, structure–property characterizations of Technora® in the literature have primarily focused on (i) X-ray diffraction (XRD), (ii) nuclear magnetic resonance (NMR

Isolation of cubic Si₃P₄ in the form of nanocrystals

• Polina K. Nikiforova,
• Sergei S. Bubenov,
• Vadim B. Platonov,
• Andrey S. Kumskov,
• Nikolay N. Kononov,
• Tatyana A. Kuznetsova and
• Sergey G. Dorofeev

Beilstein J. Nanotechnol. 2023, 14, 971–979, doi:10.3762/bjnano.14.80

• nanoparticles with a defective zinc blende structure under mild conditions through thermal annealing of hydrogenated silicon nanoparticles with red phosphorus. The synthesized Si3P4 nanoparticles were analyzed using FTIR, XRD, electron diffraction, EDX, TEM, Raman spectroscopy, X-ray fluorescence spectrometry

• , the less noticeable (400), (331), (422) and (511) signals were observed). Amorphous material is present in the sample, which is most noticeable as a ca. 2 nm layer on the surface of the NPs (Figure 7a). Energy-dispersive X-ray (EDX) elemental maps (Figure 7c,d) for Si Kα and P Kα do not show any

• “WinXPow”. Elemental analysis was carried out on an X-ray fluorescence spectrometer S2 Picofox (Bruker) with total external reflection. Transmission electron microscopy (TEM) samples were dispersed in an ultrasonic bath with hexane and then deposited on copper grids with lacey carbon film (SPI Supplies

Low temperature atomic layer deposition of cobalt using dicobalt hexacarbonyl-1-heptyne as precursor

• Mathias Franz,
• Mahnaz Safian Jouzdani,
• Lysann Kaßner,
• Marcus Daniel,
• Frank Stahr and
• Stefan E. Schulz

Beilstein J. Nanotechnol. 2023, 14, 951–963, doi:10.3762/bjnano.14.78

• saturation behaviour of the process was investigated. X-ray photoelectron spectroscopy measurements could show that the deposited cobalt is in the metallic state. The finally established process in ALD mode shows a homogeneous coating at the wafer level. Keywords: atomic layer deposition (ALD); cobalt; low

• with a deposition rate of approximately 0.1 Å/cycle. The deposited films were analysed by X-ray photoelectron spectroscopy and are well in the metallic state. We also show the optimization of the overall process through varying the pulse times for precursor, purging, and the plasma pulse. Experimental

• metallic cobalt according to Ward [24] combined with a Tauc–Lorentzian model for possible occurrences of oxidised cobalt [25][26]. The film compositions were measured ex situ by X-ray photoelectron spectroscopy (XPS) on a PRECAV sp. Z. o. o. XPS system using a MX-650 Al X-ray source and a R3000 analyser

Upscaling the urea method synthesis of CoAl layered double hydroxides

• Camilo Jaramillo-Hernández,
• Víctor Oestreicher,
• Martín Mizrahi and
• Gonzalo Abellán

Beilstein J. Nanotechnol. 2023, 14, 927–938, doi:10.3762/bjnano.14.76

• identity of the impurity observed in sample x25M, X-ray photoelectron spectroscopy (XPS) was conducted (Figure 1C). In the case of reference x1, the observed main peaks at 781.23 eV (Co 23/2) and 797.36 eV (Co 21/2), as well as their satellites at 783.13 and 798.83 eV, confirm the occurrence of CoII [15

• process and aiming to quantify the amount of this Co-based α-LH impurity, X-ray absorption spectroscopy (XAS) measurements were performed at the CLÆSS BL22 beamline at the ALBA synchrotron. Figure 2A depicts the X-ray absorption near-edge structure (XANES) spectra for the Co K edge. In all samples, the

• of the structural features of the scale-up samples determined by extended X-ray absorption fine structure (EXAFS) measurements, the used model, and the corresponding fits can be found in Supporting Information File 1 (Figure S9 and Table S3). Thermal decomposition in both inert (nitrogen) and

Green SPIONs as a novel highly selective treatment for leishmaniasis: an in vitro study against Leishmania amazonensis intracellular amastigotes

• Brunno R. F. Verçoza,
• Robson R. Bernardo,
• Luiz Augusto S. de Oliveira and
• Juliany C. F. Rodrigues

Beilstein J. Nanotechnol. 2023, 14, 893–903, doi:10.3762/bjnano.14.73

• , arrowheads). The ferrous nature of the observed structures was assessed by chemical element mapping analysis using energy-dispersive X-ray spectroscopy (Figure 2C), confirming that the electron-lucent structures contain iron atoms (Figure 2D). Transmission electron microscopy (TEM) was used to confirm the

• 20 kV equipped with an OXFORD X-MaxN 20 mm2 detector (Oxford Instruments, United Kingdom) for energy-dispersive X-ray spectroscopy. For transmission electron microscopy, after fixation, samples were dehydrated in increasing acetone concentrations and embedded in Epon. Ultrathin sections were obtained

• ). Digital magnification (highlighted rectangular area) showed electron-lucent aggregates even inside intracellular amastigotes (arrowheads). Panels C and D show the X-ray microanalysis mapping of infected macrophages, indicating the presence of iron in the cytosol (red color in Figure 2D). Transmission

N-Heterocyclic carbene-based gold etchants

• Robert B. Chevalier,
• Justin Pantano,
• Matthew K. Kiesewetter and
• Jason R. Dwyer

Beilstein J. Nanotechnol. 2023, 14, 865–871, doi:10.3762/bjnano.14.71

• dissolution of gold. We present scanning electron micrographs and elemental imaging analyses by energy dispersive X-ray spectroscopy to examine the effect of solutions of each species on the gold film. This work highlights the risk of unwanted etching during some routes to NHC-based surface functionalization

• % nitrogen gas. Electron micrographs were recorded using the SE2 detector of a Zeiss SIGMA VP field emission scanning electron microscope (SEM). Energy dispersive X-ray spectroscopy (EDS) spectra were obtained for each sample using an Oxford Instruments X-max 50 mm2 EDS attachment. Peaks were identified

A wearable nanoscale heart sound sensor based on P(VDF-TrFE)/ZnO/GR and its application in cardiac disease detection

• Yi Luo,
• Jian Liu,
• Jiachang Zhang,
• Yu Xiao,
• Ying Wu and
• Zhidong Zhao

Beilstein J. Nanotechnol. 2023, 14, 819–833, doi:10.3762/bjnano.14.67

• . Composition and β-phase content of the piezoelectric composite films were analyzed using X-ray diffraction. The morphology of the composite film fibers was observed through scanning electron microscopy. Finally, the P(VDF-TrFE)/ZnO/graphene composite film was encapsulated in a sandwich-structure heart sound

• underwent characterization through electron microscopy, X-ray diffraction (XRD), and piezoelectric performance testing. The results indicated that the piezoelectric film with a composition ratio of 12% P(VDF-TrFE) + 10% ZnO + 0.1% GR exhibited superior performance regarding various aspects. Consequently, in

• -TrFE)/ZnO flexible piezoelectric composite films without GR. Analysis of X-ray diffraction patterns indicated that the β-phase content of P(VDF-TrFE)/ZnO/GR piezoelectric composite films was higher than that of P(VDF-TrFE)/ZnO and P(VDF-TrFE). P(VDF-TrFE)/ZnO/GR was packaged into a flexible

Nanostructured lipid carriers containing benznidazole: physicochemical, biopharmaceutical and cellular in vitro studies

• Giuliana Muraca,
• María Esperanza Ruiz,
• Rocío C. Gambaro,
• Sebastián Scioli-Montoto,
• María Laura Sbaraglini,
• Gisel Padula,
• José Sebastián Cisneros,
• Cecilia Yamil Chain,
• Vera A. Álvarez,
• Cristián Huck-Iriart,
• Guillermo R. Castro,
• María Belén Piñero,
• Matias Ildebrando Marchetto,
• Catalina Alba Soto,
• Germán A. Islan and
• Alan Talevi

Beilstein J. Nanotechnol. 2023, 14, 804–818, doi:10.3762/bjnano.14.66

• observed by transmission electron microscopy. Fourier-transform infrared spectroscopy, differential scanning calorimetry, thermogravimetric analysis, and small-angle X-ray scattering analyses of the nanoparticles indicated that BNZ might be dispersed in the nanoparticle matrix in an amorphous state. The

• ]. Structural analysis was performed by selecting different angular regions from the small-angle X-ray scattering (SAXS) and wide-angle X-ray scattering (WAXS) patterns. The WAXS patterns (Figure 5) showed contributions of diffraction peaks from BNZ, myristyl myristate, and NLC. The nanostructured lipid

• medium observed after the initial stage could be attributed to the gradual release of drug molecules from the matrix core, where the drug is mainly located according to X-ray diffraction (XRD) results [33]. Remarkably, although our NLC possess a comparatively lower drug load, the maximal accumulated drug

Silver-based SERS substrates fabricated using a 3D printed microfluidic device

• Phommachith Sonexai,
• Minh Van Nguyen,
• Bui The Huy and
• Yong-Ill Lee

Beilstein J. Nanotechnol. 2023, 14, 793–803, doi:10.3762/bjnano.14.65

• NPs. The SEM image of PS@Ag reveals the presence of nanoscale gaps between the Ag NPs, which act as hot spots with a high electric field intensity when exposed to laser irradiation (Figure S10c). To confirm the distribution of chemical elements on the SERS substrate, energy-dispersive X-ray

Silver nanoparticles loaded on lactose/alginate: in situ synthesis, catalytic degradation, and pH-dependent antibacterial activity

• Nguyen Thi Thanh Tu,
• T. Lan-Anh Vo,
• T. Thu-Trang Ho,
• Kim-Phuong T. Dang,
• Van-Dung Le,
• Phan Nhat Minh,
• Chi-Hien Dang,
• Vinh-Thien Tran,
• Van-Su Dang,
• Tran Thi Kim Chi,
• Hieu Vu-Quang,
• Radek Fajgar,
• Thi-Lan-Huong Nguyen,
• Van-Dat Doan and
• Thanh-Danh Nguyen

Beilstein J. Nanotechnol. 2023, 14, 781–792, doi:10.3762/bjnano.14.64

• potential measurements, which were measured on a nanoPartica Horiba SZ-100 (Japan). Fourier-transform infrared (FTIR) spectra were obtained using a Bruker Tensor 27 FTIR spectrophotometer (Germany). X-ray diffraction (XRD) patterns were collected using a Bruker D8 Advance X-ray diffractometer. The

Carboxylic acids and light interact to affect nanoceria stability and dissolution in acidic aqueous environments

• Matthew L. Hancock,
• Eric A. Grulke and
• Robert A. Yokel

Beilstein J. Nanotechnol. 2023, 14, 762–780, doi:10.3762/bjnano.14.63

• produced drastically different TEM images, as expected from the DLS results. The number of nanoceria particles exposed to citric acid was reduced between weeks 0 and 1. By week 2, most of the particles completely disappeared with no evidence of cerium determined by energy-dispersive X-ray spectroscopy (EDS

In situ magnesiothermic reduction synthesis of a Ge@C composite for high-performance lithium-ion batterie anodes

• Ha Tran Huu,
• Ngoc Phi Nguyen,
• Vuong Hoang Ngo,
• Huy Hoang Luc,
• Minh Kha Le,
• Minh Thu Nguyen,
• My Loan Phung Le,
• Hye Rim Kim,
• In Young Kim,
• Sung Jin Kim,
• Van Man Tran and
• Vien Vo

Beilstein J. Nanotechnol. 2023, 14, 751–761, doi:10.3762/bjnano.14.62

• and transferred to a ceramic crucible. The mixture was heated at 750 °C in argon gas flow for 3 h. The obtained solid was re-ground and denoted as Ge/C-SS750. Material characterization X-ray diffraction measurements (XRD, Bruker D8 Advance with Cu Kα radiation (λ = 1.5406 Å) at 40 kV and 40 mA) were

Control of morphology and crystallinity of CNTs in flame synthesis with one-dimensional reaction zone

• Muhammad Hilmi Ibrahim,
• Norikhwan Hamzah,
• Mohd Zamri Mohd Yusop,
• Ni Luh Wulan Septiani and
• Mohd Fairus Mohd Yasin

Beilstein J. Nanotechnol. 2023, 14, 741–750, doi:10.3762/bjnano.14.61

• observed, revealing the agglomeration and sintering of particles during high-temperature growth in the flame. The energy dispersive X-ray (EDX) analysis results in Table 1 indicate a high fraction of nickel. A previous study showed that nickel particles of 5 nm and above can be reactive towards CH4, which

• by field-emission scanning electron microscopy (FESEM, Zeiss Crossbeam 340) coupled with energy-dispersive X-ray analysis (EDX) for morphology and elemental analysis. Raman spectroscopy (HORIBA XploRA PLUS, 532 nm) was done to analyze the signature spectra of the grown CNTs. Line-of-sight images of

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

• synthesized GQDs using the Debye–Scherrer formula, D = 0.9λ/(β·cos θ), where D is the average crystallite size of the synthesized GQDs, λ is the X-ray wavelength, θ is the Bragg diffraction angle, and β is the FWHM. The elemental analysis of GQDs from EDX measurements is shown in Figure 4b. The EDX spectrum

The microstrain-accompanied structural phase transition from h-MoO₃ to α-MoO₃ investigated by in situ X-ray diffraction

• Zeqian Zhang,
• Honglong Shi,
• Boxiang Zhuang,
• Minting Luo and
• Zhenfei Hu

Beilstein J. Nanotechnol. 2023, 14, 692–700, doi:10.3762/bjnano.14.55

• Sciences, Beijing, 100190, China 10.3762/bjnano.14.55 Abstract In situ X-ray diffraction indicates that the structural phase transition from h-MoO3 to α-MoO3 is a first-order transition with a phase transition temperature range of 378.5–443.1 °C. The linear coefficients of thermal expansion of h-MoO3 are

• α-MoO3 is still unclear. Here, to reveal the features of the structural phase transition from h-MoO3 to α-MoO3, we performed in situ X-ray diffraction experiments at temperatures ranging from 30 to 450 °C. The Rietveld refinement results indicate water molecules at the (0 0 0.25) site inside the

• α-MoO3 To observe the crystal structure evolution of h-MoO3 induced by temperature, a thoroughly powdered sample was used to perform in situ X-ray diffraction measurements during heating from 30 to 450 °C, as shown in Figure 1a. At 30 °C, all diffraction peaks can be well indexed to the hexagonal

Titania nanoparticles for photocatalytic degradation of ethanol under simulated solar light

• Evghenii Goncearenco,
• Iuliana P. Morjan,
• Claudiu Teodor Fleaca,
• Florian Dumitrache,
• Elena Dutu,
• Monica Scarisoreanu,
• Valentin Serban Teodorescu,
• Alexandra Sandulescu,
• Crina Anastasescu and
• Ioan Balint

Beilstein J. Nanotechnol. 2023, 14, 616–630, doi:10.3762/bjnano.14.51

• pyrolysis from TiCl4 vapor in air in the presence of ethylene as sensitizer at different working pressures (250–850 mbar) with and without further calcination at 450 °C. The obtained powders were analyzed by energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, X-ray diffractometry, and

• described as: The raw TiO2 powders contain some carbon (from the decomposition of the ethylene sensitizer) and chlorine impurities, whose amount it is greatly diminished by calcination in air at 450 °C for 5 h. To certify this, a composition investigation by energy-dispersive X-ray spectroscopy (EDS) has

• (point defects), there are some deviations. The small oxygen deficiency observed even after calcination is related to remaining chlorine impurities and Ti3+ ions that resisted calcination. Phase composition and crystallites sizes of the TiO2 powders were investigated. The X-ray diffractograms of the

Carbon nanotube-cellulose ink for rapid solvent identification

• Tiago Amarante,
• Thiago H. R. Cunha,
• Claudio Laudares,
• Ana P. M. Barboza,
• Ana Carolina dos Santos,
• Cíntia L. Pereira,
• Vinicius Ornelas,
• Bernardo R. A. Neves,
• André S. Ferlauto and
• Rodrigo G. Lacerda

Beilstein J. Nanotechnol. 2023, 14, 535–543, doi:10.3762/bjnano.14.44

• rapid test, identification, and monitoring of liquid samples in various fields such as fuel adulteration, water quality, solvents, and beverages [6][7][8][9]. Usually, the testing of liquids requires conventional analytical techniques such as absorption/emission spectroscopy (AAS/AES), X-ray

Nanoarchitectonics to entrap living cells in silica-based systems: encapsulations with yolk–shell and sepiolite nanomaterials

• Celia Martín-Morales,
• Jorge Fernández-Méndez,
• Pilar Aranda and
• Eduardo Ruiz-Hitzky

Beilstein J. Nanotechnol. 2023, 14, 522–534, doi:10.3762/bjnano.14.43

• without staining. Electron microscopy imaging was conducted using a field-emission scanning electron microscope FEI-NOVA NanoSEM 230 equipped with an Apollo XL silicon drift detector from EDAX-Ametek or using a high-resolution JEOL IT500HR/LA microscope equipped with an energy dispersive X-ray

On the use of Raman spectroscopy to characterize mass-produced graphene nanoplatelets

• Keith R. Paton,
• Konstantinos Despotelis,
• Naresh Kumar,
• Piers Turner and
• Andrew J. Pollard

Beilstein J. Nanotechnol. 2023, 14, 509–521, doi:10.3762/bjnano.14.42

• %), transmission electron microscopy (TEM) (7.2%) or X-ray photoelectron spectroscopy (XPS) (5.6%). It has the advantages of relatively low cost, simple sample preparation, quick measurements, and automated analysis, offering clear benefits for quality control applications. It has been demonstrated in several

Mixed oxides with corundum-type structure obtained from recycling can seals as paint pigments: color stability

• Dienifer F. L. Horsth,
• Julia de O. Primo,
• Nayara Balaba,
• Fauze J. Anaissi and
• Carla Bittencourt

Beilstein J. Nanotechnol. 2023, 14, 467–477, doi:10.3762/bjnano.14.37

• structure. The pigments are obtained via the addition of coloring ions to boehmite from recycled metallic aluminium. X-ray diffractometry (XRD) and Raman spectroscopy confirmed the crystallographic phase. Additionally, the oxidation state 3+ responsible for the greenish (chromium) and reddish (iron

• obtaining boehmite, we added chromium and iron ions to obtain colored mixed oxides with a corundum-type structure. The stability of the synthesized pigments in acid and alkaline environments was evaluated by colorimetric measurements. Results and Discussion X-ray diffractometry (XRD) The XRD of the pristine

• characteristic of α-Fe2O3 nanoparticles [21]. The same morphology was observed for concentrations of 5 and 20 wt % of coloring ions (Figure S2, Supporting Information File 1). X-ray photoelectron spectroscopy (XPS) The elemental composition of the samples evaluated by the analysis of XPS spectra is shown in

Evaluation of electrosynthesized reduced graphene oxide–Ni/Fe/Co-based (oxy)hydroxide catalysts towards the oxygen evolution reaction

• Karolina Cysewska,
• Marcin Łapiński,
• Marcin Zając,
• Jakub Karczewski,
• Piotr Jasiński and
• Sebastian Molin

Beilstein J. Nanotechnol. 2023, 14, 420–433, doi:10.3762/bjnano.14.34

• magnifications of the morphology of NiFe and CoNiFe after GO addition are presented in Figure S1 and S2, respectively, in Supporting Information File 1. Figure 2 presents the energy-dispersive X-ray (EDX) maps with corresponding SEM images of the catalysts. The analysis confirms the presence of the following

• probably inhibited the electrodeposition process of NiFe and CoNiFe on its surface. This may be the reason for the slower stabilization of the synthesis current density observed in the chronoamperograms (Figure 1a). X-ray diffraction, X-ray photoemission spectroscopy and X-ray absorption spectroscopy

• Figure 3a–d shows the X-ray absorption spectra (XAS) of the L3 edge of nickel (a), iron (b), cobalt (c), and carbon (d) in the studied catalysts. The appearance of a shoulder peak at the L3 edge of the nickel (Figure 3a) at 855 eV indicates the presence of oxides in the structure of the catalysts (Ni in

Recent progress in cancer cell membrane-based nanoparticles for biomedical applications

• Qixiong Lin,
• Yueyou Peng,
• Yanyan Wen,
• Xiaoqiong Li,
• Donglian Du,
• Weibin Dai,
• Wei Tian and
• Yanfeng Meng

Beilstein J. Nanotechnol. 2023, 14, 262–279, doi:10.3762/bjnano.14.24

• anticancer effects [76]. After QT was delivered to tumor tissue by the active targeting ability of the membrane, the sensitivity to radiotherapy was effectively improved, and a strong anticancer effect was exerted under X-ray irradiation [76]. Gong et al. designed a pH-responsive multifunctional biomimetic

A novel approach to pulsed laser deposition of platinum catalyst on carbon particles for use in polymer electrolyte membrane fuel cells

• Bogusław Budner,
• Wojciech Tokarz,
• Sławomir Dyjak,
• Andrzej Czerwiński,
• Bartosz Bartosewicz and
• Bartłomiej Jankiewicz

Beilstein J. Nanotechnol. 2023, 14, 190–204, doi:10.3762/bjnano.14.19

• accelerating voltage of 20 kV and identical work parameters of the EDS detector. The quality of platinum coating on the carbon material was assessed based on images made using a transmission electron microscope (TEM) equipped with an energy-dispersive X-ray spectrometer (EDX). TEM measurements were carried out

• the prepared platinum-coated carbon support, X-ray photoelectron spectroscopy (XPS) was used (Prevac, Poland) with an R3000 VG analyzer (Scienta, Sweden) and an X-ray source with an Al Kα anode (Prevac, Poland) emitting X-rays with a photon energy of 1486.6 eV. The analysis of the XPS spectra

Formation of nanoflowers: Au and Ni silicide cores surrounded by SiO_x branches

• Feitao Li,
• Siyao Wan,
• Dong Wang and
• Peter Schaaf

Beilstein J. Nanotechnol. 2023, 14, 133–140, doi:10.3762/bjnano.14.14

• annealed at 1050 °C was named 15Au5Ni. The morphology was imaged by optical microscopy (OM, Zeiss Axiotech) and high-resolution scanning electron microscopy (HR-SEM, Hitachi S-4800) equipped with energy-dispersive X-ray spectroscopy (EDS, Thermo Scientific). The SEM images were recorded by using mixed

• atomic numbers show brighter contrasts. EDS measurements were performed to obtain the element distribution in the target areas. X-ray diffraction (XRD, Siemens D-5000) analyses were conducted in Bragg–Brentano mode using Cu Kα irradiation at 40 kV. The height distribution of the areas of interest was