Exfoliation of titanium nitride using a non-thermal plasma process

• Priscila Jussiane Zambiazi,
• Dolores Ribeiro Ricci Lazar,
• Larissa Otubo,
• Rodrigo Fernando Brambilla de Souza,
• Almir Oliveira Neto and
• Cecilia Chaves Guedes-Silva

Beilstein J. Nanotechnol. 2024, 15, 631–637, doi:10.3762/bjnano.15.53

• temperature to generate ionized particles. These ionized species interact with the ceramic crystal of TiN, resulting in a pronounced structural expansion. The exfoliated TiN products were comprehensively characterized using transmission electron microscopy, X-ray diffraction, and Raman spectroscopy

• microscope operating at 200 kV. X-ray diffraction (XRD) analysis was conducted using a diffractometer (Miniflex II) with Cu Kα radiation over a 2θ range of 20–90°, with a scan speed of 2° per minute. Furthermore, Raman spectra were obtained using a spectrometer (Horiba Scientific MacroRam Raman) equipped

• peak positions, approximately 0.1° less positive, was observed in the X-ray diffractograms for the exfoliated material. This shift aligns with the indications of reduced crystallite size and is consistent with the outcomes reported by de Souza et al. [17], who obtained few layers of hexagonal BN using

Comparative analysis of the ultrastructure and adhesive secretion pathways of different smooth attachment pads of the stick insect Medauroidea extradentata (Phasmatodea)

• Julian Thomas,
• Stanislav N. Gorb and
• Thies H. Büscher

Beilstein J. Nanotechnol. 2024, 15, 612–630, doi:10.3762/bjnano.15.52

• tarsus was dehydrated with an ascending EtOH sequence at 4 °C on a shaker, and subsequently critical point dried using Leica EM CPD300 (Leica, Wetzlar, Germany). The tarsus was scanned using a Skyscan®1172 µCT (Bruker micro‐CT; CT‐scanner settings: X‐ray source: 40 kV, 250 μA, 360 rotation, 0.2 rotation

• the ventral side of the euplantulae revealed a dense hull (lighter grey) and a more X-ray transparent body (darker grey) (Figure 4A). Toluidine blue staining detected a darker blue stained hull and a lighter blue body (Figure 4B). The SEM images unveiled a rather smooth surface topography (Figure 4C

AFM-IR investigation of thin PECVD SiO_x films on a polypropylene substrate in the surface-sensitive mode

• Hendrik Müller,
• Hartmut Stadler,
• Teresa de los Arcos,
• Adrian Keller and
• Guido Grundmeier

Beilstein J. Nanotechnol. 2024, 15, 603–611, doi:10.3762/bjnano.15.51

• with a 5 nm SiOx coating was used and, additionally to the AFM-IR spectra, a hyperspectral image was collected in contact mode. In addition to photothermal AFM-IR measurements in contact mode and surface-sensitive mode, the surface was analyzed with near-ambient pressure X-ray photoelectron

• spectroscopy (NAP-XPS) using a NAP-XPS system with a Phoibos150 NAP analyzer from Specs Surface Nano Analysis GmbH. The setup has a µ-FOCUS 600 X-ray monochromator NAP source working with monochromatic Al Kα radiation at 1468.7 eV. The power was set to 50 W for all measurements. For the environmental charge

Stiffness calibration of qPlus sensors at low temperature through thermal noise measurements

• Laurent Nony,
• Sylvain Clair,
• Daniel Uehli,
• Aitziber Herrero,
• Jean-Marc Themlin,
• Andrea Campos,
• Franck Para,
• Alessandro Pioda and
• Christian Loppacher

Beilstein J. Nanotechnol. 2024, 15, 580–602, doi:10.3762/bjnano.15.50

• used for imaging. At 15 kV, the resolution is 0.6 nm. Energy-dispersive X-ray spectroscopy (EDS) chemical analyses have been performed too, for which an EDAX Octane Silicon Dri Detector (129 eV energy resolution for manganese) coupled to the SEM was used at 15 kV. A large side view (cf. Figure 1a

Radiofrequency enhances drug release from responsive nanoflowers for hepatocellular carcinoma therapy

• Yanyan Wen,
• Ningning Song,
• Yueyou Peng,
• Weiwei Wu,
• Qixiong Lin,
• Minjie Cui,
• Rongrong Li,
• Qiufeng Yu,
• Sixue Wu,
• Yongkang Liang,
• Wei Tian and
• Yanfeng Meng

Beilstein J. Nanotechnol. 2024, 15, 569–579, doi:10.3762/bjnano.15.49

• substituted by O–H. Additionally, other characteristic absorption peaks of CUR and HPS were retained. These findings confirmed the successful synthesis of CUR-Fe@MnO2 NFs. According to the X-ray diffraction (XRD) pattern (Figure 2g), the 2θ diffraction peaks at 30.1° (220), 35.4° (311), 37.0° (222), 43.1

• Scientific, USA) in the range of 400–4000 cm−1. The X-ray diffractometer patterns were characterized by the X-ray diffractometer (D8 ADVANCE, Bruker, Karlsruhe, Germany). The iron and manganese concentrations were determined using an inductively coupled plasma mass spectrometry (ICP‒MS) (7800, Agilent, Santa

Aero-ZnS prepared by physical vapor transport on three-dimensional networks of sacrificial ZnO microtetrapods

• Veaceslav Ursaki,
• Tudor Braniste,
• Victor Zalamai,
• Emil Rusu,
• Vladimir Ciobanu,
• Vadim Morari,
• Daniel Podgornii,
• Pier Carlo Ricci,
• Rainer Adelung and
• Ion Tiginyanu

Beilstein J. Nanotechnol. 2024, 15, 490–499, doi:10.3762/bjnano.15.44

• produced material is investigated by scanning electron microscopy (SEM), while its crystalline and optical qualities are assessed by X-ray diffraction (XRD) analysis and photoluminescence (PL) spectroscopy, respectively. We demonstrate possibilities for controlling the composition and the crystallographic

• sensor applications. Keywords: aeromaterial; crystallographic structure; luminescence; physical vapor transport; scanning electron microscopy (SEM); X-ray diffraction (XRD); Introduction Porous materials represent a class of solid-state networks widely used in adsorptive and photocatalytic removal of

• Instruments. The structural properties were investigated by X-ray diffraction measurements on a Rigaku MiniFlex 600 diffractometer with Cu Kα radiation (λ=1.540598 Å) in a standard 2θ Bragg–Brentano configuration, operating at 45 kV beam voltage and 15 mA beam current. Photoluminescence (PL) was excited by

Photocatalytic degradation of methylene blue under visible light by cobalt ferrite nanoparticles/graphene quantum dots

• Vo Chau Ngoc Anh,
• Le Thi Thanh Nhi,
• Le Thi Kim Dung,
• Dang Thi Ngoc Hoa,
• Nguyen Truong Son,
• Nguyen Thi Thao Uyen,
• Nguyen Ngoc Uyen Thu,
• Le Van Thanh Son,
• Le Trung Hieu,
• Tran Ngoc Tuyen and
• Dinh Quang Khieu

Beilstein J. Nanotechnol. 2024, 15, 475–489, doi:10.3762/bjnano.15.43

• synthesize cobalt ferrite nanoparticles/graphene quantum dots (CF/GQDs). The material was prepared from a homogeneous mixture of iron nitrate, cobalt nitrate, and starch at 140, 180 and 200 °C in a 24 h thermal hydrolysis process. The obtained materials were characterised by using X-ray diffraction, scanning

• benzoquinone (C6H4O2) was provided by Sigma-Aldrich, USA. Sodium hydroxide (NaOH, ≥96%) and hydrogen chloride (HCl, 38%) were purchased from Xilong, China. Instruments X-ray diffraction (XRD) patterns were recorded by using a D8 Advance (Bruker, Germany) with Cu Kα radiation (λ = 0.154 nm). Fourier-transform

• Tristar-3030 system (Micromeritics, USA). The magnetic properties were measured on a Micro Sense vibrating-sample magnetometer (VSM) at room temperature. Scanning electron microscopy (SEM) observations and energy-dispersive X-ray elemental mapping (EDX mapping) were carried out on a Hitachi S-4800 FESEM

Fabrication of nanocrystal forms of ᴅ-cycloserine and their application for transdermal and enteric drug delivery systems

• Hsuan-Ang Tsai,
• Tsai-Miao Shih,
• Theodore Tsai,
• Jhe-Wei Hu,
• Yi-An Lai,
• Jui-Fu Hsiao and
• Guochuan Emil Tsai

Beilstein J. Nanotechnol. 2024, 15, 465–474, doi:10.3762/bjnano.15.42

• improve the bioavailability. In this study, for the first time, DCS, a highly water-soluble compound, has formed nanocrystals and this was confirmed by scanning electronic microscopy and X-ray powder diffraction. Furthermore, DCS nanocrystals were applied to several formulations to test their stability

• ., Ltd.) for 10 min. The collection was vacuum-dried to obtain DCS nanocrystals. Characterization of DCS nanocrystals The DCS nanocrystals were analyzed via scanning electronic microscopy (SEM, JEOL Ltd.) and X-ray powder diffraction (XRPD, Bruker AXS GmbH). For SEM, commercial DCS was spreaded onto a

• formulation in the transdermal delivery system. Scanning electron microscopy images of commercial DCS (A) and DCS nanocrystals (B). The X-ray powder diffraction spectra of DCD nanocrystal and commercial DCS. The pH stability test of DCS in neutral (pH 7.4) and acidic (pH 1.2) environments (p < 0.01). In vitro

Potential of a deep eutectic solvent in silver nanoparticle fabrication for antibiotic residue detection

• Le Hong Tho,
• Bui Xuan Khuyen,
• Ngoc Xuan Dat Mai and
• Nhu Hoa Thi Tran

Beilstein J. Nanotechnol. 2024, 15, 426–434, doi:10.3762/bjnano.15.38

• scholars, the rod-like morphology is better than a spherical one at increasing the extinction coefficient, about 109 to 1011 M−1·cm−1 higher [43][44], which proves the applicability of Ag NPs-DES in SERS biosensors. Furthermore, X-ray fluorescence mapping was used to evaluate the presence of silver in the

• characterization and apparatus The absorbance properties of the sample were recorded using a V-730 UV–vis–NIR spectrophotometer supplied by JASCO, Japan. The crystallinity of the Ag NPs-DES thin film was determined using a D8 Advance diffractometer, Bruker, UK, with a Ni-filtered Cu Kα X-ray source. To evaluate

• the nanostructure and surface morphology of the nanoparticles, as well as the elemental distribution of silver on the substrate, a S4800 field-emission scanning electron microscope purchased from Hitachi, Japan, and an M4 TORNADOPlus Micro X-ray fluorescence spectrometer with a Rh tube at 30 W micro

Controllable physicochemical properties of WO_x thin films grown under glancing angle

• Rupam Mandal,
• Aparajita Mandal,
• Alapan Dutta,
• Rengasamy Sivakumar,
• Sanjeev Kumar Srivastava and
• Tapobrata Som

Beilstein J. Nanotechnol. 2024, 15, 350–359, doi:10.3762/bjnano.15.31

• bias voltage was applied to the p-Si substrates, whereas the WOx films were kept grounded. The crystallinity of the WOx films was examined using X-ray diffraction (XRD) (Bruker) under Bragg–Brentano geometry (θ–2θ) in an angular window of 2θ = 20° to 80°. The chemical composition of the WOx films was

• identified using X-ray photoelectron spectroscopy (XPS) measurements (PHI 5000 VersaProbeII, ULVAC – PHI, INC) with a monochromatic Al Kα source (hν = 1486.6 eV), and a microfocus (100 µm, 15 kV, 25 W) arrangement along with a multichannel detector and a hemispherical analyser. The microstructure of the WOx

Vinorelbine-loaded multifunctional magnetic nanoparticles as anticancer drug delivery systems: synthesis, characterization, and in vitro release study

• Zeynep Özcan and
• Afife Binnaz Hazar Yoruç

Beilstein J. Nanotechnol. 2024, 15, 256–269, doi:10.3762/bjnano.15.24

• -resolution analytical electron microscope (FE-SEM, Thermo Scientific, Apreo 2S LoVac) and a scanning transmission electron microscope (STEM, Phillips XL, 30 ESEM-FEG/EDAX) operating at 120 kV acceleration voltage. The structure of the nanoparticles was analyzed by X-ray diffraction (XRD, PANalytical, Xpert

• between peak broadening and particle size in X-ray analysis. In this equation, the symbols D, K, λ, β, and θ represent the particle size, Scherrer shape factor (here 0.89), X-ray wavelength (0.15418 nm), half-maximum width, and diffraction angle, respectively [43]. Using the X-ray diffraction (XRD

• ) spectrum and Equation 5, the particle size of Fe3O4 NPs was calculated and determined to be 18 nm on average. X-ray patterns showing the distribution of Fe3O4 NPs in their uncoated state are shown in Figure 2a. XRD analysis reveals the presence of seven distinct peaks at 30.13°, 35.48°, 43.12°, 53.6

Exploring disorder correlations in superconducting systems: spectroscopic insights and matrix element effects

• Vyacheslav D. Neverov,
• Alexander E. Lukyanov,
• Andrey V. Krasavin,
• Alexei Vagov,
• Boris G. Lvov and
• Mihail D. Croitoru

Beilstein J. Nanotechnol. 2024, 15, 199–206, doi:10.3762/bjnano.15.19

• kind of X-ray microscopy and has come to the conclusion that such fractal structures boost superconductivity. In particular, the work demonstrates that this material has a small number of very highly ordered regions and larger numbers of disordered regions, with a power-law distribution describing them

Modification of graphene oxide and its effect on properties of natural rubber/graphene oxide nanocomposites

• Nghiem Thi Thuong,
• Le Dinh Quang,
• Vu Quoc Cuong,
• Cao Hong Ha,
• Nguyen Ba Lam and
• Seiichi Kawahara

Beilstein J. Nanotechnol. 2024, 15, 168–179, doi:10.3762/bjnano.15.16

• characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy, contact angle, thermal gravimetric analysis, and scanning electron microscopy. The XRD results showed the appearance of an amorphous region of silica particles at a diffraction angle of 22°. The formation of silica was

• conditions to determine the ideal condition to modify GO for grafting onto NR. The GO-VTES products were characterized using X-ray diffraction (XRD), contact angle, 29Si NMR, Fourier-transform infrared spectroscopy (FTIR), and morphology analysis. The GO-VTES was expected to improve the mechanical properties

• , 200 g of DPNR (DRC 20%, SDS 0.2%), and with the same amount of TEPA/TBHPO as in the preparation of DPNR/GO-VTES. Characterizations X-ray diffraction patterns of graphite and GO were acquired by using a Panalytical X'Pert Pro X-ray diffractometer. The measurements were performed at room temperature

Assessing phytotoxicity and tolerance levels of ZnO nanoparticles on Raphanus sativus: implications for widespread adoptions

• Pathirannahalage Sahan Samuditha,
• Nadeesh Madusanka Adassooriya and
• Nazeera Salim

Beilstein J. Nanotechnol. 2024, 15, 115–125, doi:10.3762/bjnano.15.11

• on Raphanus sativus (R. sativus) concerning its tolerance levels, toxicity, and accumulation. ZnO NPs were synthesized by the wet chemical method and characterized by powder X-ray diffraction (PXRD), Fourier-transform infrared (FTIR) spectroscopy, ultraviolet–visible (UV–vis) spectroscopy, dynamic

• synthesized ZnO NPs were characterized via several techniques such as powder X-ray diffraction (PXRD), Fourier-transform infrared (FTIR) spectroscopy, solid-UV–vis spectroscopy, dynamic light scattering (DLS), and scanning electron microscopy (SEM). Then the potential phytotoxicity of the synthesized ZnO NPs

• ZnO NPs characterization The PXRD technique provides important insights into the chemical composition, physical characteristics of the material and crystallographic structure, and crystalline particle size based on the scattered X-ray beam intensity [20][21]. The PXRD pattern (Figure 1a) of

New application of bimetallic Ag/Pt nanoplates in a colorimetric biosensor for specific detection of E. coli in water

• Azam Bagheri Pebdeni,
• Mohammad N. AL-Baiati and
• Morteza Hosseini

Beilstein J. Nanotechnol. 2024, 15, 95–103, doi:10.3762/bjnano.15.9

• microscopy (FE-SEM) was used to investigate the form and shapes of NPLs. The size of the NPLs is approx. 42 nm. Figure 1a shows a combination of truncated triangular and circular plates of Ag/Pt NPLs. The NPLs were evenly distributed and shaped in the form of discs or triangles. Energy-dispersive X-ray

Berberine-loaded polylactic acid nanofiber scaffold as a drug delivery system: The relationship between chemical characteristics, drug-release behavior, and antibacterial efficiency

• Le Thi Le,
• Hue Thi Nguyen,
• Liem Thanh Nguyen,
• Huy Quang Tran and
• Thuy Thi Thu Nguyen

Beilstein J. Nanotechnol. 2024, 15, 71–82, doi:10.3762/bjnano.15.7

• separation during the electrospinning process [17][38][39], leading to the formation of a BBR-rich phase on the surface of nanofibers. The crystallinity of the PLA pellet and electrospun nanofiber scaffolds were examined by X-ray diffraction (XRD) analysis (Figure 3B). The XRD pattern of the PLA pellet shows

• chemical characteristics of prepared scaffolds in the wavelength range of 200–3200 cm−1. X-ray diffraction measurements of PLA pellets and BBR-loaded PLA nanofiber scaffolds were analyzed with Cu Kα radiation in a 2θ range from 5 to 80° using EQUINOX 5000 – Thermo Scientific X-ray diffractometer. Static

Influence of conductive carbon and MnCo₂O₄ on morphological and electrical properties of hydrogels for electrochemical energy conversion

• Sylwia Pawłowska,
• Karolina Cysewska,
• Yasamin Ziai,
• Jakub Karczewski,
• Piotr Jasiński and
• Sebastian Molin

Beilstein J. Nanotechnol. 2024, 15, 57–70, doi:10.3762/bjnano.15.6

• influence of porosity and conductive properties of these composites on the electrochemical activity of catalyst particles in OER. Elemental mapping by energy-dispersive X-ray spectroscopy (EDS) confirmed the presence of MCO particles inside the hydrogel structure (Figure 2 and Supporting Information File 1

• an accelerating voltage of 10 kV. Before imaging, the hydrogel samples were freeze-dried and coated with a 10 nm gold layer. The chemical composition of the hydrogel was analysed with a Thermo Fisher Scientific silicon drift detector energy-dispersive X-ray spectroscope. For characterisation of the

TEM sample preparation of lithographically patterned permalloy nanostructures on silicon nitride membranes

• Joshua Williams,
• Michael I. Faley,
• Joseph Vimal Vas,
• Peng-Han Lu and
• Rafal E. Dunin-Borkowski

Beilstein J. Nanotechnol. 2024, 15, 1–12, doi:10.3762/bjnano.15.1

• ], transmission electron microscopy (TEM) [1][8][9][10][11], scanning transmission X-ray microscopy [12][13], and magneto-optical Kerr effect microscopy [14][15]. Possible applications of Py nanodisks were proposed for zero-hysteresis magnet sensors, magnetic logic devices, and data storage [16]. Py is a nickel

• Lorentz microscopy and electron holography, along with simultaneous structural and chemical characterization techniques such as electron diffraction, 4D STEM, and energy-dispersive X-ray (EDX) and electron energy loss spectroscopy (EELS), enable a correlative characterization to investigate magnetic

A combined gas-phase dissociative ionization, dissociative electron attachment and deposition study on the potential FEBID precursor [Au(CH₃)₂Cl]₂

• Elif Bilgilisoy,
• Ali Kamali,
• Thomas Xaver Gentner,
• Gerd Ballmann,
• Sjoerd Harder,
• Hans-Peter Steinrück,
• Hubertus Marbach and
• Oddur Ingólfsson

Beilstein J. Nanotechnol. 2023, 14, 1178–1199, doi:10.3762/bjnano.14.98

• precursor (i.e., [Au(CH3)2Cl]2) was used to create FEBID deposits on a SiO2 substrate by using 5 keV and 0.1/0.4 nA in an HV atmosphere [33]. The composition of the structures was checked via energy dispersion X-ray (EDX) mapping and reported to be 29–41 atom % Au, 2–6 atom % Cl, and 53–68 atom % C. The SEM

Sulfur nanocomposites with insecticidal effect for the control of Bactericera cockerelli

• Lany S. Araujo-Yépez,
• Juan O. Tigrero-Salas,
• Vicente A. Delgado-Rodríguez,
• Vladimir A. Aguirre-Yela and
• Josué N. Villota-Méndez

Beilstein J. Nanotechnol. 2023, 14, 1106–1115, doi:10.3762/bjnano.14.91

• rosemary essential oils with the three concentrations of 0.25%, 0.5%, and 0.75%. The samples were characterized by UV–visible spectroscopy, energy-dispersive X-ray spectroscopy, transmission electron microscopy, and scanning electron microscopy. The insecticidal efficacy of the nanocomposites was evaluated

• eucalyptus and rosemary at different concentrations. Characterizations were carried out through UV–visible spectroscopy, energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), and scanning electron microscopy (SEM); also the insecticidal efficacy of the NCMPs for the control of

• stabilizing agent. Characterization techniques and equipment UV–visible spectroscopy was performed on an Analytik Jena SPECORD® S 600 spectrophotometer. Size and morphology of the SNPs were determined using an FEI Tecnai G2 Spirit Twin transmission electron microscope. Energy-dispersive X-ray spectroscopy

Density functional theory study of Au-fcc/Ge and Au-hcp/Ge interfaces

• Olga Sikora,
• Małgorzata Sternik,
• Benedykt R. Jany,
• Franciszek Krok,
• Przemysław Piekarz and
• Andrzej M. Oleś

Beilstein J. Nanotechnol. 2023, 14, 1093–1105, doi:10.3762/bjnano.14.90

• bonds, see Figure 12b. The integrated charge density of the bonding electrons, however, can be expected to be significantly smaller. Also, one can observe that the Au–Ge bond is strongly asymmetrical. Similar bonding states were already observed for Au atoms deposited on a Ge(001) surface using X-ray

Properties of tin oxide films grown by atomic layer deposition from tin tetraiodide and ozone

• Kristjan Kalam,
• Peeter Ritslaid,
• Tanel Käämbre,
• Aile Tamm and
• Kaupo Kukli

Beilstein J. Nanotechnol. 2023, 14, 1085–1092, doi:10.3762/bjnano.14.89

• , the cycle times for SnO2 were kept at 5-2-5-5 s, respectively, for the following sequence: metal precursor pulse, N2 purge pulse, O3 pulse, and N2 purge pulse. The films were grown on Si(100) cleansed and etched prior to the growth. An X-ray fluorescence spectrometer Rigaku ZSX 400 with the program

• grazing incidence X-ray diffractometry (GIXRD), using an X-ray diffractometer SmartLab Rigaku with Cu Kα radiation, which corresponds to an X-ray wavelength of 0.15406 nm. X-ray photoelectron emission and X-ray absorption spectroscopy (XPS and XAS, respectively) measurements were made at the FinEstBeAMS

• ]. The SnO2 films grown at 300 and 500 °C, that is, those with low residual iodine content, were analysed ex situ in terms of surface chemistry using soft X-ray spectroscopy methods. The Sn 3d XPS data (Figure 10a) show almost identical spectra for the samples deposited at 300 and 500 °C, and the narrow

Dual-heterodyne Kelvin probe force microscopy

• Benjamin Grévin,
• Fatima Husainy,
• Dmitry Aldakov and
• Cyril Aumaître

Beilstein J. Nanotechnol. 2023, 14, 1068–1084, doi:10.3762/bjnano.14.88

Experimental investigation of usage of POE lubricants with Al₂O₃, graphene or CNT nanoparticles in a refrigeration compressor

• Kayhan Dağıdır and
• Kemal Bilen

Beilstein J. Nanotechnol. 2023, 14, 1041–1058, doi:10.3762/bjnano.14.86

• nanoparticles is presented separately in the subsequent sections to verify the catalog information provided by the manufacturer. In the characterization of the nanoparticles used in the study, field-emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDS), and X-ray diffraction

• micrograph and b) EDS analysis of Al2O3 nanoparticles. X-ray diffraction pattern of Al2O3 nanoparticles [21]. The a) FE-SEM micrograph with a scale bar of 20 µm, b) FE-SEM micrograph with a scale bar of 10 µm, and c) EDS analysis of the graphene nanoplatelets. The XRD pattern of the graphene nanoplatelets

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