Morphology and properties of pyrite nanoparticles obtained by pulsed laser ablation in liquid and thin films for photodetection

• Akshana Parameswaran Sreekala,
• Bindu Krishnan,
• Rene Fabian Cienfuegos Pelaes,
• David Avellaneda Avellaneda,
• Josué Amílcar Aguilar-Martínez and
• Sadasivan Shaji

Beilstein J. Nanotechnol. 2025, 16, 785–805, doi:10.3762/bjnano.16.60

• nanocolloid in this work. The optical properties of nanocolloids and their thin films were evaluated using UV–visible (UV–vis) spectroscopy. The nanoparticle characterization and surface morphology were studied using transmission electron microscopy (TEM), scanning electron microscopy (SEM), and the

• temperatures and amounts of sulfur. Characterization The morphological analyses of pyrite NPs were recorded using the FEI Titan G2 80–300 for TEM, high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM), high-resolution TEM (HRTEM) and selected area electron diffraction (SAED). The

• SEM analysis of pyrite thin films was performed using a Hitachi Model SU 8020. The NPs were deposited on carbon-coated copper grids for TEM analysis and on silicon substrates for SEM analysis. Using monochromatic Al Kα radiation with an energy of 1486.68 eV, X-ray photoelectron spectroscopy (XPS

Changes of structural, magnetic and spectroscopic properties of microencapsulated iron sucrose nanoparticles in saline

• Sabina Lewińska,
• Pavlo Aleshkevych,
• Roman Minikayev,
• Anna Bajorek,
• Mateusz Dulski,
• Krystian Prusik,
• Tomasz Wojciechowski and
• Anna Ślawska-Waniewska

Beilstein J. Nanotechnol. 2025, 16, 762–784, doi:10.3762/bjnano.16.59

• transmission electron microscopy (TEM). Composition studies using XRD, magnetic properties using dc and ac magnetometry, and extensive spectral analysis using Fourier-transform infrared spectroscopy (FTIR), Raman, and electron paramagnetic resonance (EPR) were also performed. Considering that the AB-Fortis

• . This unknown quantity of core–shell nanoparticles is encapsulated within a Ca alginate coating. SEM and TEM studies were conducted to compare the postulated structure of the microcapsule with its actual image. Figure 2 shows representative SEM micrographs of the FS0 sample. The observed grains exhibit

• cellulose, while the latter is speculated to be vitamins and SiO2. Figure 3 illustrates TEM images of the samples FS0 and FST. For the FS0 sample (Figure 3a,b) groups of the nanoparticles are distributed in a porous structure (a) recognized as calcium alginate, but also attached to thin, elongated stripes

High-temperature epitaxial growth of tantalum nitride thin films on MgO: structural evolution and potential for SQUID applications

• Michelle Cedillo Rosillo,
• Oscar Contreras López,
• Jesús Antonio Díaz,
• Agustín Conde Gallardo and
• Harvi A. Castillo Cuero

Beilstein J. Nanotechnol. 2025, 16, 690–699, doi:10.3762/bjnano.16.53

• diffraction database was used for the qualitative search–match phase identification. To determine the epitaxy of the films, TEM was carried out with a Jeol JEM 2100F. Finally, the resistivity, R, was measured as a function of the temperature T using the van der Pauw method in a DynaCool Quantum Design

• nitrogen concentration reached its highest value, and oxygen and carbon impurities were minimized. These results also align with the results from XRD and TEM, as the film deposited under these conditions exhibited the best crystallinity and epitaxial growth. The combination of optimal stoichiometry and

• temperature on the structural evolution of TaN thin films deposited on MgO(100) substrates was investigated using XRD and TEM. Figure 3 shows the XRD patterns of TaN films deposited at various temperatures, revealing critical insights into phase development, crystallinity, and epitaxial growth as the

Colloidal few layered graphene–tannic acid preserves the biocompatibility of periodontal ligament cells

• Teissir Ben Ammar,
• Naji Kharouf,
• Dominique Vautier,
• Housseinou Ba,
• Nivedita Sudheer,
• Philippe Lavalle and
• Vincent Ball

Beilstein J. Nanotechnol. 2025, 16, 664–677, doi:10.3762/bjnano.16.51

• granules, each being hundreds of micrometers in size (Figure 1A). In contrast, the obtained FLG–TA colloid has a layered structure, and sheets seem to have been peeled off from the graphite surface (Figure 1B,C). Transmission electron microscopy (TEM) micrographs of the flakes’ edges (Figure 1D,E) reveal

• more in-depth its layered structure, consisting of approximately four layers. Quantitative analysis of SEM and TEM images enabled the determination of the FLG–TA sheets’ average lateral size distribution, presented in Figure 1F, indicating an average lateral size of approximately 2 µm. Note that the

• determination of the size distribution was attempted by means of dynamic light scattering but was unsuccessful owing to the lack of transparency of the suspensions even after strong dilution. The TEM images also reveal visible granules atop the layers (Figure 1D,E). Additional analysis of these granules (Figure

Feasibility analysis of carbon nanofiber synthesis and morphology control using a LPG premixed flame

• Iftikhar Rahman Bishal,
• Muhammad Hilmi Ibrahim,
• Norikhwan Hamzah,
• Mohd Zamri Mohd Yusop,
• Faizuan Bin Abdullah,
• I Putu Tedy Indrayana and
• Mohd Fairus Mohd Yasin

Beilstein J. Nanotechnol. 2025, 16, 581–590, doi:10.3762/bjnano.16.45

• three stainless steel inlet tubes for LPG, oxygen, and nitrogen was used to synthesize CNTs. TEM images revealed a 0.35 nm interplanar spacing, showing high crystallinity and a thin amorphous layer [11]. In a separate study, CNFs were synthesized using acetylene and plasma-enhanced chemical vapor

• deposition with nickel as the catalyst and hydrogen as the plasma source. SEM and TEM characterization showed vertically aligned CNFs. This method highlights the impact of plasma conditions and gas ratios on CNF morphology and alignment [12]. An experiment by Li et al. showed CNT growth at decomposition

• room temperature, the product was purified with 1% HCl solution, distilled water, and ethanol, then vacuum-dried at 50 °C for about 4 h. The final product was nearly pure CNFs, as shown by FESEM images. TEM images indicated an average CNF diameter of 100 nm. Raman spectra showed a strong, narrow peak

Nanomaterials in targeting amyloid-β oligomers: current advances and future directions for Alzheimer's disease diagnosis and therapy

• Shiwani Randhawa,
• Trilok Chand Saini,
• Manik Bathla,
• Rahul Bhardwaj,
• Rubina Dhiman and
• Amitabha Acharya

Beilstein J. Nanotechnol. 2025, 16, 561–580, doi:10.3762/bjnano.16.44

Electron beam-based direct writing of nanostructures using a palladium β-ketoesterate complex

• Chinmai Sai Jureddy,
• Krzysztof Maćkosz,
• Aleksandra Butrymowicz-Kubiak,
• Iwona B. Szymańska,
• Patrik Hoffmann and
• Ivo Utke

Beilstein J. Nanotechnol. 2025, 16, 530–539, doi:10.3762/bjnano.16.41

• oxygen signal of the native oxide layer is separated from the signal of oxygen from ligand residues of [Pd(tbaoac)2] in the deposit. Nanostructural observations were performed with transmission electron microscopy (TEM) using a probe-corrected ThermoFisher Scientific Titan Themis 200 G3 operating at an

• accelerating voltage of 200 kV. For this purpose, the FEB deposits were prepared on an ultrathin carbon support layer of less than 3 nm thickness supported by a lacey carbon membrane (PELCO) on a TEM grid. The TEM grid was fixed to the heatable stage. The deposition process was carried out in a Philips XL30

• diffusion process taking place. TEM analysis revealed metal nanograins embedded in a carbonaceous matrix. The deposits contained up to 30 atom % Pd, with a prominent reduction of about 90% of the 23 carbon atoms in the precursor. Using a continuum model, the calculated upper limit of the desorption rate

Performance optimization of a microwave-coupled plasma-based ultralow-energy ECR ion source for silicon nanostructuring

• Joy Mukherjee,
• Safiul Alam Mollick,
• Tanmoy Basu and
• Tapobrata Som

Beilstein J. Nanotechnol. 2025, 16, 484–494, doi:10.3762/bjnano.16.37

• the transformative impact of nanopatterning through low-energy inert ions. Keywords: optimization of ion current; surface topography; TEM; ultralow-energy ECR-based ion source; UV–vis spectroscopy; Introduction Ion sources serve as fundamental components in numerous scientific and industrial

• formation of well-defined nanoscale ripple patterns. The prominence of ripple structures increases with prolonged irradiation time, while bombardment at 72.5° with the same ion beam parameters leads to the coarsening of nanostructures. Cross-sectional transmission electron microscopy (TEM) measurements

• context of optimization of inert Ar-ion beam and subsequent ion-induced silicon nanopatterning. The TEM used for this work is a FEI Tecnai G2 12 Twin model, which operates at a voltage range of 20–120 kV. It employs a LaB6 emitter as the electron source and offers a line resolution of 0.2 nm with a

Effect of additives on the synthesis efficiency of nanoparticles by laser-induced reduction

• Rikuto Kuroda,
• Takahiro Nakamura,
• Hideki Ina and
• Shuhei Shibata

Beilstein J. Nanotechnol. 2025, 16, 464–472, doi:10.3762/bjnano.16.35

• solution without IPA. On the other hand, when 10 vol % IPA was added (red line in Figure 1), an increase in absorbance was immediately seen after the start of laser irradiation, and the absorbance levelled off after 5 min of laser irradiation. Figure 2 shows the transmission electron microscopy (TEM

• ) images of the samples extracted from solutions with and without and IPA after 10 and 30 min of laser irradiation. In the case of the sample without IPA, in the TEM image of the sample after 10 min of laser irradiation, which is the initial stage of laser fragmentation, in addition to spherical particles

• % IPA, even in the TEM image of the sample after 10 min of laser irradiation, nanoparticles with a narrow particle size distribution of less than 10 nm in diameter were observed. This suggests that the nanoparticle synthesis reaction finished after 10 min of irradiation. This is due to the fact that the

Engineered PEG–PCL nanoparticles enable sensitive and selective detection of sodium dodecyl sulfate: a qualitative and quantitative analysis

• Soni Prajapati and
• Ranjana Singh

Beilstein J. Nanotechnol. 2025, 16, 385–396, doi:10.3762/bjnano.16.29

• performed using SEM (FEI Quanta 250, Netherlands). Transmission electron microscopy (TEM) was also performed to measure nanoparticle mean size and their distribution. The sample was diluted 1000-fold from the stock solution, and 5 µL of the sample was placed onto a carbon-coated copper grid with 200 mesh

• size. The imaging was performed using TEM at 120 kV (Jeol JEM1400, Germany). The surface elements and their composition in the nanoparticle were analyzed using X-ray photoelectron spectroscopy (PHI 5000 Versa Probe II, FEI Inc) regarding their binding energy. The fixed transmission mode was utilized

• physicochemical properties, such as size, shape, surface charge, and elemental composition using DLS, TEM, SEM, and XPS (Figure 2). The PEG–PCL NPs were characterized using a zetasizer (Nano ZS, Malvern, UK) to comprehensively assess their size, surface charge, monodispersity, and average hydrodynamic size

Graphene oxide–chloroquine conjugate induces DNA damage in A549 lung cancer cells through autophagy modulation

• Braham Dutt Arya,
• Sandeep Mittal,
• Prachi Joshi,
• Alok Kumar Pandey,
• Jaime E. Ramirez-Vick,
• Govind Gupta and
• Surinder P. Singh

Beilstein J. Nanotechnol. 2025, 16, 316–332, doi:10.3762/bjnano.16.24

• of vacuoles were observed in the treated cells (Figure 4a, black arrows). Furthermore, TEM micrographs reveal the presence and effective cellular internalization of the GO–Chl nanoconjugate in A549 cells (Figure 4a; red arrows and Figure 4b), corroborating our previous findings [25]. To investigate

• presence of autophagosomes via TEM. Figure 8b reveals the appearance of autophagosomes in GO–Chl-exposed A549 cells. The MDC staining assay and TEM analysis together show the appearance of autophagosomes, which could be due to inhibition of autophagy. Furthermore, we performed confocal microscopy with GFP

• microscopy using GFP-LC3 transfected cells, and TEM analysis. A significant dose-dependent increase accumulation of autophagosomes was observed, suggesting inhibition of autophagy and the possible connection between DNA-damage response and autophagy. Finally, elevated expression levels of key autophagy

Enhancing mechanical properties of chitosan/PVA electrospun nanofibers: a comprehensive review

• Nur Areisman Mohd Salleh,
• Amalina Muhammad Afifi,
• Fathiah Mohamed Zuki and
• Hanna Sofia SalehHudin

Beilstein J. Nanotechnol. 2025, 16, 286–307, doi:10.3762/bjnano.16.22

• , which can adversely affect mechanical performance. Besides SEM and FESEM, transmission electron microscopy (TEM) has the additional ability to visualize fiber cross sections and can be employed to examine core–shell, encapsulated, and particle-incorporated fiber structures [112][145][146]. Atomic force

• concentration because of improved coverage of the chitosan shell layer as observed from TEM images of the fiber. The different methods used in the measurement of chitosan/PVA nanofiber properties are summarized in Table 6. These methods allow for comprehensive characterization of the mechanical properties of

Preferential enrichment and extraction of laser-synthesized nanoparticles in organic phases

• Theo Fromme,
• Maximilian L. Spiekermann,
• Florian Lehmann,
• Stephan Barcikowski,
• Thomas Seidensticker and
• Sven Reichenberger

Beilstein J. Nanotechnol. 2025, 16, 254–263, doi:10.3762/bjnano.16.20

• glycerol carbonate and 1-nonanol for copper and iron. Zeta potential of copper nanoparticles in (a) 1-nonanol and (b) propylene carbonate obtained by LAL at 85 °C in the monophasic TMS of 1-nonanol and propylene carbonate. Size distribution and TEM images of the respective (c, d) copper and (e, f) iron

Radiosensitizing properties of dual-functionalized carbon nanostructures loaded with temozolomide

• Radmila Milenkovska,
• Nikola Geskovski,
• Dushko Shalabalija,
• Ljubica Mihailova,
• Petre Makreski,
• Dushko Lukarski,
• Igor Stojkovski,
• Maja Simonoska Crcarevska and
• Kristina Mladenovska

Beilstein J. Nanotechnol. 2025, 16, 229–251, doi:10.3762/bjnano.16.18

• images in this study and the SEM and TEM images in [43]). In all series, a relatively unimodal particle size distribution was observed, with PDI values not higher than 0.541. In the irradiated series, the mean particle size ranged from 222 nm (I-MWCNTs-PEG6000-FA) to 347 nm (I-MWCNTs-G-PEG6000-FA-TMZ

• graphene sheets, formed by interactions between the hydrophobic regions of graphene and the side walls of MWCNTs. Also, in the SEM and TEM images of TMZ-loaded non-modified CNs, entrapment of TMZ into the tubes and wrapping around the CNs was visible [43]. In the present study, the covalent PEGylation and

A review of metal-organic frameworks and polymers in mixed matrix membranes for CO₂ capture

• Charlotte Skjold Qvist Christensen,
• Nicholas Hansen,
• Mahboubeh Motadayen,
• Nina Lock,
• Martin Lahn Henriksen and
• Jonathan Quinson

Beilstein J. Nanotechnol. 2025, 16, 155–186, doi:10.3762/bjnano.16.14

• MOF-based MMMs [113][118][122][124][125][128][131][132]. Often, the membrane is broken apart to enable a cross-sectional view of the MOF-based MMM, which may effortlessly reveal interfacial defects as in Figure 8 [132]. In addition to SEM, TEM and HRTEM are often used to obtain information about MOF

• distribution within the MMM [122][125][128]. However, TEM analysis of MOF-based MMMs usually involves diluting the MOF–polymer precursor slurry in a volatile solvent and dispersing it on a conductive metal grid. The sample is then dried in air or under vacuum [122][125]. Consequently, the ultrathin membrane

Characterization of ZnO nanoparticles synthesized using probiotic Lactiplantibacillus plantarum GP258

• Prashantkumar Siddappa Chakra,
• Aishwarya Banakar,
• Shriram Narayan Puranik,
• Vishwas Kaveeshwar,
• C. R. Ravikumar and
• Devaraja Gayathri

Beilstein J. Nanotechnol. 2025, 16, 78–89, doi:10.3762/bjnano.16.8

• nanoparticles (ZnO NPs), utilizing lactic acid bacteria isolated from curd as the key biological agent. Bacteria function as agents for both reduction and capping processes, which aids the synthesis of ZnO NPs. Various characterization techniques including XRD, FTIR, UV–vis, TEM, SEM-EDX, and zeta potential

• produce hydroxyl radicals (•OH−). These radicals degrade the dye molecules into harmless substances; the degradation is shown in Figure 2d. TEM analysis The size of the ZnO NPs, which was determined from TEM using Image J software, varied from 7 to 98 nm, with an average size of 10 nm. The SAED pattern of

• . Microscopic examination via TEM and SEM offered details about nanoparticle size and shape. Our study reported a size range from 7 to 98 nm, with an average size of 10 nm. Suba et al. [22] reported an average size of 32 nm, while Mohd Yusof et al. [23] synthesized ZnO NPs with a size of 291 nm (flower-like

A nanocarrier containing carboxylic and histamine groups with dual action: acetylcholine hydrolysis and antidote atropine delivery

• Elina E. Mansurova,
• Andrey A. Maslennikov,
• Anna P. Lyubina,
• Alexandra D. Voloshina,
• Irek R. Nizameev,
• Marsil K. Kadirov,
• Anzhela A. Mikhailova,
• Polina V. Mikshina,
• Albina Y. Ziganshina and
• Igor S. Antipin

Beilstein J. Nanotechnol. 2025, 16, 11–24, doi:10.3762/bjnano.16.2

• through dialysis for 1.5 h using a 12000 Da pore dialysis bag. The size of p(Hist-CA) is approximately 12 ± 3 nm according to TEM, and it forms aggregates ranging in size from 80 to 150 nm (Figure 1a,b). The molecular weight of p(Hist-CA) was determined using gel permeation chromatography (GPC). The GPC

• electron microscopy (TEM) images were taken with a Libra 120 EFTEM (A Carl Zeiss SMT AG Company, Oberkochen, Carl Zeiss, Germany) at 100 kV. Samples were spread on a 300 mesh copper grid with a carbon/formvar support film. 1H and 13C NMR spectra were obtained using a Bruker Avance 600 spectrometer with an

• dilution was tested in two parallel wells. The samples were then incubated for 1 h at 37 °C, followed by hemagglutination observation with the naked eye (Figure 3) [39]. Images of the samples were captured using a Nikon Eclipse Ci-S microscope (Nikon, Japan) (Figure 4). Data for p(Hist-CA): (a, b) TEM

Attempts to preserve and visualize protein corona on the surface of biological nanoparticles in blood serum using photomodification

• Julia E. Poletaeva,
• Anastasiya V. Tupitsyna,
• Alina E. Grigor’eva,
• Ilya S. Dovydenko and
• Elena I. Ryabchikova

Beilstein J. Nanotechnol. 2024, 15, 1654–1666, doi:10.3762/bjnano.15.130

• that, in addition to EVs, other “natural” NPs are present in the blood, namely, lipoproteins (LPs), which are not vesicles. The content of LPs in blood is incomparably higher than that of EVs [5][16]. Previously, we detected LPs using transmission electron microscopy (TEM) in various biological fluids

• prevent the corona loss, we fixed it on the surface of the bio-NPs by the photomodification method. We developed this method recently for fixing a full protein corona on model NPs with lipid envelope. One of the proofs of protein corona formation on the particle surface was its visualization using TEM [23

• -NPs from FBS and NBS. Results and Discussion Isolation of bio-NPs by ultracentrifugation To obtain samples of intact bio-NPs, we used single or double ultracentrifugation (UC) of 10% FBS, and the resulting samples were negatively stained and examined in TEM. The largest share of bio-NPs observed in

Fabrication of hafnium-based nanoparticles and nanostructures using picosecond laser ablation

• Abhishek Das,
• Mangababu Akkanaboina,
• Jagannath Rathod,
• R. Sai Prasad Goud,
• Kanaka Ravi Kumar,
• Raghu C. Reddy,
• Ratheesh Ravendran,
• Katia Vutova,
• S. V. S. Nageswara Rao and
• Venugopal Rao Soma

Beilstein J. Nanotechnol. 2024, 15, 1639–1653, doi:10.3762/bjnano.15.129

• techniques The synthesised NPs were drop-cast on carbon-coated copper grids to record transmission electron microscopy (TEM) images and selected area electron diffraction (SAED) patterns using a FEI Tecnai G2 S-Twin operating at 200 kV. Further, these NPs were drop-cast on cleaned Si substrates, and their

• Horiba LabRAM HR Evolution (Excitation: 325 nm, Lens: 40×, spot size: 1 μm) was used. Image J software was used to extract spatial periodicities and to generate 2D fast Fourier transform images (2D FFT) of the Hf surface structures. Results and Discussion Nanoparticles Figure 3 shows TEM images, the

• corresponding particle size distributions, and the SAED patterns of NPs obtained in DW (Figure 3a–c), toluene (Figure 3d–f), and anisole (Figure 3g–i). The TEM image corresponding to HfNPs in DW shows the formation of nanofibres of diameters ranging from 5 to 65 nm along with spherical NPs (marked with red

Natural nanofibers embedded in the seed mucilage envelope: composite hydrogels with specific adhesive and frictional properties

• Agnieszka Kreitschitz and
• Stanislav N. Gorb

Beilstein J. Nanotechnol. 2024, 15, 1603–1618, doi:10.3762/bjnano.15.126

• atomic force microscopy (AFM), transmission electron microscopy (TEM), SEM, or cryo-SEM [45][57][63][64][65][66]. Very often, the procedures for preparing mucilage envelope samples can destroy and/or influence the organisation of polysaccharides, making the analysis of spatial structure of the mucilage

• structure. This technique is very effective for sample imagining in TEM and SEM [7][41][67][68]. CPD minimises the negative pressure differences during drying. The comparison of CPD and air-drying techniques of plant material, for example, parenchymatic cells [69] and the mucilage envelope [7][13], clearly

• in Ocimum basilicum [7]. TEM and SEM [45][65][78][79] showed the size of cellulose microfibrils in a range of 3–50 nm, depending on cell wall type. This wide range of size can be also a result of bundles formed by cellulose fibrils (Figure 4h) [80]. The results of our research [7][13] confirmed the

Liver-targeting iron oxide nanoparticles and their complexes with plant extracts for biocompatibility

• Shushanik A. Kazaryan,
• Seda A. Oganian,
• Gayane S. Vardanyan,
• Anatolie S. Sidorenko and
• Ashkhen A. Hovhannisyan

Beilstein J. Nanotechnol. 2024, 15, 1593–1602, doi:10.3762/bjnano.15.125

• Sonic-150W, MRC, Israel) at 80% power with an on/off cycle of 5/4 s. During the synthesis of the nanoparticles, a black precipitate with paramagnetic properties formed. Nature and morphology of this precipitate were determined using electron diffraction and transmission electron microscopy (TEM, LEO-912

Facile synthesis of size-tunable L-carnosine-capped silver nanoparticles and their role in metal ion sensing and catalytic degradation of p-nitrophenol

• Akash Kumar,
• Ridhima Chadha,
• Abhishek Das,
• Nandita Maiti and
• Rayavarapu Raja Gopal

Beilstein J. Nanotechnol. 2024, 15, 1576–1592, doi:10.3762/bjnano.15.124

• ʟ-carnosine in synthesizing tunable plasmonic silver nanoparticles (ʟ-car-AgNPs). The formation of ʟ-car-AgNPs was confirmed via UV–vis optical absorption spectroscopy, showing single and double plasmonic peaks, depending on the synthesis conditions. Physicochemical characterization using TEM, FTIR

• (Nano ZS, Malvern, UK). The hydrodynamic size of ʟ-car-AgNPs was measured by placing them in 1 mL disposable cuvettes (DTS0012), while the zeta potential was measured using zeta cuvettes (ZEN1020). The ʟ-car-AgNPs samples were observed under a transmission electron microscope (TEM, 120 kV, FEI Tecnai

• towards the positively charged surfaces of silver. The morphology and size of silver nanoparticles capped with ʟ-carnosine were measured using TEM (Figure 3b–f). The TEM micrograph of ʟ-car-AgNP1 (Figure 3b) indicates the formation of spherical particles with high monodispersity and is consistent with the

Ultrablack color in velvet ant cuticle

• Vinicius Marques Lopez,
• Wencke Krings,
• Juliana Reis Machado,
• Stanislav Gorb and
• Rhainer Guillermo-Ferreira

Beilstein J. Nanotechnol. 2024, 15, 1554–1565, doi:10.3762/bjnano.15.122

• of the ultrablack cuticle in Traumatomutilla bifurca, an enigmatic and visually striking species of velvet ants (Hymenoptera, Mutillidae). Using a combination of scanning electron microscopy (SEM), transmission electron microscopy (TEM), confocal laser scanning microscopy (CLSM), and optical

• spectroscopy, we conducted a comprehensive analysis of the cuticle to elucidate its unique optical properties. SEM imaging provided a detailed surface morphology, while TEM provided insights into the internal structure. CLSM showed that the cuticle exhibits no autofluorescence. Our findings reveal a highly

• different magnifications, starting at 15,000× and adjusted as needed. Transmission electron microscopy (TEM) TEM was utilized to examine the internal cuticle morphology at high resolution at a nanometer scale. The apparatus was configured to operate at 50 kV with a minimum vacuum column pressure of 5.10

Electrochemical nanostructured CuBTC/FeBTC MOF composite sensor for enrofloxacin detection

• Thi Kim Ngan Nguyen,
• Tien Dat Doan,
• Huy Hieu Luu,
• Hoang Anh Nguyen,
• Thi Thu Ha Vu,
• Quang Hai Tran,
• Ha Tran Nguyen,
• Thanh Binh Dang,
• Thi Hai Yen Pham and
• Mai Ha Hoang

Beilstein J. Nanotechnol. 2024, 15, 1522–1535, doi:10.3762/bjnano.15.120

•  2e), the binding energy peak of Cu 2p3/2 (934.9 eV) can be attributed to Cu2+. Characterization of (Cu)(Fe)BTC@CPE Morphology The TEM image of the (Cu)(Fe)BTC sample shows unevenly distributed particles with different particle sizes fluctuating in the range of 40 to 100 nm (Figure 3). After mixing

• room temperature (25 ± 1 °C). (a) XRD pattern and (b) N2 adsorption/desorption isotherms of the (Cu)(Fe)BTC sample. Full-scan (a) and high-resolution C 1s (b), O 1s (c), Fe 2p (d), and Cu 2p (e) XPS spectra of the (Cu)(Fe)BTC sample. TEM image of (Cu)(Fe)BTC sample. SEM images of (Cu)(Fe)BTC@CPE (a

Strain-induced bandgap engineering in 2D ψ-graphene materials: a first-principles study

• Kamal Kumar,
• Nora H. de Leeuw,
• Jost Adam and
• Abhishek Kumar Mishra

Beilstein J. Nanotechnol. 2024, 15, 1440–1452, doi:10.3762/bjnano.15.116

• ), and density functional theory (DFT) study suggests that the hydrogenation of graphene with atomic hydrogen leads to the formation of graphone [8]. The full hydrogenation of graphene (graphane) was experimentally obtained by Elias et al., and their TEM and Raman spectroscopy results evidence the