Development of a mucoadhesive drug delivery system and its interaction with gastric cells

• Ahmet Baki Sahin,
• Serdar Karakurt and
• Deniz Sezlev Bilecen

Beilstein J. Nanotechnol. 2025, 16, 371–384, doi:10.3762/bjnano.16.28

• ) nanoparticles, topography, surface composition, size, and charge distribution of the delivery system were determined. The topography of the nanoparticles was studied with SEM (Figure 1). Both Alg and EudAlg nanoparticles are spherical with smooth surfaces (Figure 1A,B). It should be noted that during SEM

• nanoparticles Morphology of nanoparticles The morphological characterization of nanoparticles was done via scanning electron microscopy (SEM, Zeiss, GeminiSEM500) and scanning transmission electron microscopy (STEM, Ziess, GeminiSEM500). For SEM analysis, nanoparticles were air-dried on SEM stabs and coated

• viability testing and particle size measurements were assessed by one-way ANOVA with Tukey post-hoc analysis. A p value ≤ 0.05 was considered statistically significant. Micrographs of nanoparticles. SEM micrographs of (A) Alg NPs and (B) EudAlg NPs. STEM micrographs of (C) Alg NPs and (D) EudAlg NPs. Scale

Pulsed laser in liquid grafting of gold nanoparticle–carbon support composites

• Madeleine K. Wilsey,
• Teona Taseska,
• Qishen Lyu,
• Connor P. Cox and
• Astrid M. Müller

Beilstein J. Nanotechnol. 2025, 16, 349–361, doi:10.3762/bjnano.16.26

• , rapid, scalable, acid-free process to make carbon fiber paper hydrophilic without destroying the carbon network, as other carbon fiber paper oxidation methods do [22], evident from scanning electron microscopy (SEM) imaging (Figure 2A). Hydrophilicity was achieved by graphitic edge carbon oxygenation

• custom-made Teflon tub, in 2.0 mL of commercially available aqueous colloid of citrate-capped gold nanoparticles (100 nm, nanoComposix), followed by drying under a heat lamp at 60 °C for 20 min. Physical characterization Scanning electron microscopy (SEM) images were obtained at UR-Nano. A Zeiss Auriga

• scanning electron microscope with a Schottky field-emission emitter was operated at 20.00 kV with a working distance of 4.9 mm. Energy-dispersive X-ray (EDX) spectroscopy data were collected using an SEM-integrated EDAX Octane elect plus spectrometer with a with silicon drift detector. Double sided carbon

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

• exposed to GO–Chl: A dose-dependent increase in the concentration of cells with compromised cell membranes was observed. Values are expressed as mean ± SEM of three independent experiments. A value of p < 0.05 (*) was considered statistically significant. Flow-cytometry-based cell cycle analysis of A549

• cells exposed to GO–Chl. Different gates were used to represent the cells in various phases of the cell cycle: P2 represents the G1 phase, P3 represents the S phase, P4 represents the G2 phase, and P5 represents the subG1 phase. Values are expressed as mean ± SEM of three independent experiments. A

• –Chl. Values are expressed as mean ± SEM of three independent experiments. A value of p < 0.05 (*) was considered statistically significant. Accumulation of autophagosomes in GO–Chl-exposed A549 lung cancer cells: (a) Representative monodansylcadaverine staining photomicrographs of A549 cells exposed

Fabrication and evaluation of BerNPs regarding the growth and development of Streptococcus mutans

• Tuyen Huu Nguyen,
• Hong Thanh Pham,
• Kieu Kim Thanh Nguyen,
• Loan Hong Ngo,
• Anh Ngoc Tuan Mai,
• Thu Hoang Anh Lam,
• Ngan Thi Kim Phan,
• Dung Tien Pham,
• Duong Thuy Hoang,
• Thuc Dong Nguyen and
• Lien Thi Xuan Truong

Beilstein J. Nanotechnol. 2025, 16, 308–315, doi:10.3762/bjnano.16.23

• prepared using a wet-milling method with zirconium balls to enhance bioavailability and expand potential applications. The particle size and physicochemical properties of the BerNPs were analyzed using field-emission scanning electron microscopy (FE-SEM), UV–vis spectroscopy, X-ray diffraction, and Fourier

• -transform infrared spectroscopy. The broth dilution method was used to determine the antimicrobial activity of the BerNPs against Streptococcus mutans (S. mutans). The impact of the BerNPs on the cell surface of S. mutans was evaluated through FE-SEM analysis, focusing on its ability to inhibit biofilm

• formation of S. mutans. In summary, BerNPs demonstrated a potent inhibitory effect on the activities of S. mutans at selectively applied concentrations. Keywords: antibacterial; berberine nanoparticles; BerNPs; biofilm; FE-SEM; Streptococcus mutans; Introduction According to the Global Burden of Disease

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

• electron microscopy (SEM) and field-emission scanning electron microscopy (FESEM) are more commonly used to analyze the fiber diameter, distribution, and overall surface morphology [144]. Microscopic images obtained from these techniques help to identify defects such as beading or non-uniformity in fibers

• , 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

• diameter measurements from SEM, Hartatiek et al. [148] observed an inversely proportional correlation between fiber diameter and the ultimate tensile strength of the chitosan/PVA/collagen nanofibers, with the smallest average diameter of 154 nm resulting in the highest tensile strength of 5.6 MPa due to

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

• points to surface attachment of FA, although its physical entrapment into the tubes cannot be excluded. After incorporation of TMZ, the mean particle size was increased by 30–40 nm, suggesting again the embedment of TMZ not only into the tubes, but also on the surface of the CNs (as shown in the SEM

• 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

• [48][49][50][51][52][53]. Morphology In the SEM images of the MWCNTs-COOH (presented in our previous study [43]), a dense structure of randomly aggregated, convoluted, and highly tangled tubes was observed. The image of MWCNTs-G shows a hybrid structure of multiwalled nanotubes dispersed within the

Synthesis and the impact of hydroxyapatite nanoparticles on the viability and activity of rhizobacteria

• Bedah Rupaedah,
• Indrika Novella,
• Atiek Rostika Noviyanti,
• Diana Rakhmawaty Eddy,
• Anna Safarrida,
• Abdul Hapid,
• Zhafira Amila Haqqa,
• Suryana Suryana,
• Irwan Kurnia and
• Fathiyah Inayatirrahmi

Beilstein J. Nanotechnol. 2025, 16, 216–228, doi:10.3762/bjnano.16.17

• . The morphology of the analyzed sample, observed through scanning electron microscopy (SEM) at magnifications of 15,000× and 50,000× are depicted in Figure 3. Figure 3 provides a clear view of the sample demonstrating spherical shapes with a consistent particle size distribution. The SEM analysis

• results reveal an average particle size of 68.08 nm, as displayed in Figure 3b. Moreover, a more comprehensive examination of the SEM image using OriginLab software yields a sample porosity of 54.78%, as illustrated in Figure 3d. In this representation, the blue regions correspond to the solid volume of

• nm. SEM analysis revealed a spherical shape with an average particle size of 68.08 nm and a porosity of 54.78%. Rhizobacteria loaded onto the nHA carrier exhibited viability comparable to rhizobacteria incubated without a carrier. Over the observation period, the viability of both types of

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

• MMMs Material characterization techniques are pivotal for the assessment of novel MOF-based MMMs structures. Electron microscopy enables direct imaging of a sample with up to sub-nanometer resolution [139]. Scanning electron microscopy (SEM) is a popular and straightforward method to obtain images of

• 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

TiO₂ immobilized on 2D mordenite: effect of hydrolysis conditions on structural, textural, and optical characteristics of the nanocomposites

• Marina G. Shelyapina,
• Rosario Isidro Yocupicio-Gaxiola,
• Gleb A. Valkovsky and
• Vitalii Petranovskii

Beilstein J. Nanotechnol. 2025, 16, 128–140, doi:10.3762/bjnano.16.12

• complementary characterization techniques, including XRD, SEM-EDX, TGA, N2 sorption, NMR, XPS and UV–vis spectrometry. It was observed that treatment in 70% ethanol solution preserves the ordered layered structure of 2D mordenite because TEOT hydrolysis is slowed down. This, in turn, leads to higher

• ) samples are labeled as Ti-WNh-C and Ti-ENh-C with N = 6, 12, and 24 for materials hydrolyzed in water (W) and 70% ethanol solution (E) for 6, 12, and 24 h, respectively. The non-calcined samples are designated as Ti-WNh and Ti-ENh. XRD, 27Al NMR, and SEM-EDX studies Figure 1a and Figure 1b show small

• treatment. For Ti-E24h-C, the lower TiO2 content compared to TI-E12h-C can be attributed to the formation of 3D mordenite fibers, clearly visible in the SEM images (see below in Figure 3). From the comparison of the surface (XPS) and volume (EDX) content of TiO2, we can not only deduce a fairly uniform

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

• ZnO NPs confirms the XRD results, that is, the hexagonal wurtzite structure (Figure 3). SEM and EDX analysis SEM was used to analyze the surface morphology of a modified nanocomposite film, and the image displays a consistent coverage of a web-like structure. Close-up views revealed a crumpled and

• . 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

Bioinspired nanofilament coatings for scale reduction on steel

• Siad Dahir Ali,
• Mette Heidemann Rasmussen,
• Jacopo Catalano,
• Christian Husum Frederiksen and
• Tobias Weidner

Beilstein J. Nanotechnol. 2025, 16, 25–34, doi:10.3762/bjnano.16.3

• shear stress at the plate is reported in Figure 2D for different angular velocities and corresponding volumetric flow rates. Super-hydrophobicity of SNF coatings on steel Figure 3A shows a scanning electron microscopy (SEM) image of a stainless-steel surface coated with SNFs. The wire-type structures

• – we can conclude that nanofilaments can be deposited on steel surfaces and that the grown structures render the steel surface super-hydrophobic [24]. The morphology and function of the SNF steel coatings remain intact during the shear stress test. The SEM image of the SNF coating after shear exposure

• can be seen in in the optical images in Figure 5A and Figure 5B, no defects are visible after the explosion/decompression test, demonstrating the stability of the SNF coating on steel. This is also borne out by the SEM analysis (Figure 5C), which shows the SNF structures are fully intact after the

Orientation-dependent photonic bandgaps in gold-dust weevil scales and their titania bioreplicates

• Norma Salvadores Farran,
• Limin Wang,
• Primoz Pirih and
• Bodo D. Wilts

Beilstein J. Nanotechnol. 2025, 16, 1–10, doi:10.3762/bjnano.16.1

• . The domains in lattice orientation {100} exhibited polarization conversion. The structure inferred from optical measurements was confirmed using conventional and focused ion beam scanning electron microscopy (FIB-SEM). By averaging the reciprocal space images obtained from different lattice

• cortex is thinner (≈0.5 μm) and flat (Figure 2c). From the FIB-SEM cuts, we estimated the chitin fill fraction of the chitin network to be 0.44 ± 0.06. By adjusting the power and duration of the argon plasma etching, we were able to selectively etch the lower cortex of the scales (Figure 2d), revealing

• was roughly {111}-oriented. SEM images shown in Figure 4d,e confirmed the successful replication with an increased fill fraction, compared to the original material (Figure 2); the two fill fractions, f, were expected to be conserved but exchanged (i.e., titania f ≈ 0.56 and void f ≈ 0.44). The

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

• morphology was analysed using field-emission scanning electron microscopy (FESEM); the composition was determined by EDX attached to the FESEM (Carl Zeiss Smart SEM ULTRA 55). Reflectivity was investigated using a UV–vis–NIR spectrometer (PerkinElmer Lambda 750). For photoluminescence (PL) measurements, a

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

• its composition [14][15][16]. The nanoscale level of the spatial organisation of mucilage observed with scanning electron microscopy (SEM) reveals the complexity of the mucilage with special features, such as 3D organisation of polysaccharides in a net-like structure [7][13]. In the last years, the

• proper characterisation of their micro- and nanostructures. In the last years, SEM visualisation, combined with the critical point drying (CPD) procedure, has been widely used in nanostructural studies of diverse hydrogel-like samples, containing cellulose fibrils, or biofilms [7][40][41]. The CPD method

• 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

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

• the experimental results well. FTIR and Raman spectroscopy confirm the successful capping of silver nanoparticles with ʟ-carnosine. The presence of Ag in ʟ-carnosine-capped AgNPs was also assessed using SEM-EDX. Figure 4d and Figure 4e confirm that Ag is present in ʟ-car-AgNP1 and ʟ-car-AgNP2

• spectroscopy, TEM, SEM-EDX, and XRD. This comprehensive analysis elucidates the optical absorbance, sizes, surface charges, functional group interactions, elemental compositions, and diffraction patterns of ʟ-car-AgNPs. Furthermore, different sizes of ʟ-car-AgNPs (ʟ-car-AgNP1 to ʟ-car-AgNP5) were explored

• -car-AgNP4, and (f) ʟ-car-AgNP5. (a) FTIR spectra of ʟ-carnosine and ʟ-car-AgNPs. Raman spectra of (b) ʟ-carnosine (solid and aqueous solution) and (c) ʟ-car-AgNPs. SEM-EDX data confirms the presence of silver in (d) ʟ-car-AgNP1 and (e) ʟ-car-AgNP2. (f) XRD pattern of ʟ-carnosine AgNP1. Heavy metal ion

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

• sunlight (personal observations). For subsequent analyses, we utilized female specimens collected from Caatinga regions in Pernambuco, Brazil (09°19’44.2’’S, 42°33’30’’W) in February 2022. The specimens were preserved in absolute alcohol. Scanning electron microscopy (SEM) To investigate the internal

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

• the electrode blend, SEM and EDX mapping were used to investigate the distribution of CuBTC and FeBTC on the electrode surface (Figure 4). Figure 4a clearly shows the scattering of bright CuBTC and FeBTC particles on the graphite flakes. Figure 4b confirms the homogenous distribution of Fe, Cu, and O

• 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

Various CVD-grown ZnO nanostructures for nanodevices and interdisciplinary applications

• The-Long Phan,
• Le Viet Cuong,
• Vu Dinh Lam and
• Ngoc Toan Dang

Beilstein J. Nanotechnol. 2024, 15, 1390–1399, doi:10.3762/bjnano.15.112

• down to collect white products formed on Si substrates. They were characterized by scanning electron microscopy (SEM, JEOL-6330F) and energy-dispersive X-ray (EDX) spectroscopy. Renishaw’s RS and PL spectrometers operating with laser wavelengths of 488 and 325 nm were also employed to study phonon

• substrates. The analysis of their EDX spectra in the energy range of E = 0–20 keV shows the presence of Zn and O only, as representatively shown in Figure 1. It means that ZnO crystals were formed, and no impurity was generated during the material fabrication. Recorded SEM images indicate the products grown

• SEM micrographs of some 1D-type nanostructures. They were grown at temperatures T = 620–630 °C. The first structure is typical of hexagonal-prism-shaped nanorods, named R1 and R2 in Figure 2a,b. Their diameter can be of several tens to hundreds of nanometres, and their length is about 10–15 μm. The

A biomimetic approach towards a universal slippery liquid infused surface coating

• Ryan A. Faase,
• Madeleine H. Hummel,
• AnneMarie V. Hasbrook,
• Andrew P. Carpenter and
• Joe E. Baio

Beilstein J. Nanotechnol. 2024, 15, 1376–1389, doi:10.3762/bjnano.15.111

• Microscopy Sciences). Samples were sputter-coated with gold/palladium (Cressington 108A) and imaged on a scanning electron microscope (SEM) (FEI Quanta 600F). ImageJ was used to measure fiber diameter and clot density. Clot density was determined by drawing a line through the image and counting the number of

• buffer were incubated on surfaces in a 96-well plate for 2 h at 37 °C. Surfaces were rinsed with Tyrode’s buffer five times to remove nonadherent and loosely bound platelets. The samples were then fixed and prepared for SEM using the same method as for the clots. At least three spots per sample and two

• fibrin generation time on glass. Samples were isolated from three distinct draws from each of two donors for a total sample size of 14 per sample per donor. Clot fiber diameter and crosslinking density measurements were taken from SEM micrographs. Representative SEM micrographs are shown in Figure 8

Green synthesis of carbon dot structures from Rheum Ribes and Schottky diode fabrication

• Muhammed Taha Durmus and
• Ebru Bozkurt

Beilstein J. Nanotechnol. 2024, 15, 1369–1375, doi:10.3762/bjnano.15.110

• electron microscopy (SEM), I–V/C–V measurements, UV–vis spectroscopy, and steady-state fluorescence spectroscopy, respectively. CDs synthesis 2.5 g of the powdered Rheum ribes plant was placed in an autoclave bottle, and 50 mL of pure water was added to the bottle. This aqueous solution was placed in an

• , the quantum yield of the CDs was calculated as 0.03. Schottky diode fabrication The usability of these newly synthesized CDs in an application area was also discussed. For this purpose, a metal (Au)–semiconductor (CDs) junction-based thin film device was produced. SEM images were taken to determine

• new synthesized CDs were determined, and their structural and optical characterization was performed. The usability of the new CDs in diode fabrication as an application area was discussed. The layer thickness and bandgap energy for the prepared CDs film from SEM and UV–vis absorption measurements

Out-of-plane polarization induces a picosecond photoresponse in rhombohedral stacked bilayer WSe₂

• Guixian Liu,
• Yufan Wang,
• Zhoujuan Xu,
• Zhouxiaosong Zeng,
• Lanyu Huang,
• Cuihuan Ge and
• Xiao Wang

Beilstein J. Nanotechnol. 2024, 15, 1362–1368, doi:10.3762/bjnano.15.109

• . To enrich the basic characterizations of WSe2, we conducted Raman spectroscopy and scanning electron microscopy (SEM) measurements (Supporting Information File 1, Note 5). The broken symmetry leads to an asymmetric distribution of photogenerated carriers, resulting in a non-zero photocurrent even

• probe power. (d) Photoresponse intensity of heterojunction (red dots) and graphene region (black dots) as a function of probe power. Supporting Information Supporting Information File 20: Characterization of structure, SHG image, SEM and EDS images, Raman and PL spectrum of WSe2 and raw TRPC curves for

Investigation of Hf/Ti bilayers for the development of transition-edge sensor microcalorimeters

• Victoria Y. Safonova,
• Anna V. Gordeeva,
• Anton V. Blagodatkin,
• Dmitry A. Pimanov,
• Anton A. Yablokov and
• Andrey L. Pankratov

Beilstein J. Nanotechnol. 2024, 15, 1353–1361, doi:10.3762/bjnano.15.108

• . Finally, we performed a lift-off process using N-methylpyrrolidone followed by a rinse in isopropyl alcohol. The edges of the structures after the lift-off process appeared to be vertical well-defined walls without upward bends, as shown in the SEM image in Figure 2. A thin layer of titanium on top of

• from single quantum vaporized helium atoms, as well as for dark matter search. Photographs of structures taken with an optical microscope. (a) Chip with samples A1–A4 and (b) sample B1. SEM image of the edge of the Hf/Ti bridge structure made with the lift-off process. The dependence of resistance

Hymenoptera and biomimetic surfaces: insights and innovations

• Vinicius Marques Lopez,
• Carlo Polidori and
• Rhainer Guillermo Ferreira

Beilstein J. Nanotechnol. 2024, 15, 1333–1352, doi:10.3762/bjnano.15.107

Mn-doped ZnO nanopowders prepared by sol–gel and microwave-assisted sol–gel methods and their photocatalytic properties

• Cristina Maria Vlăduț,
• Crina Anastasescu,
• Silviu Preda,
• Oana Catalina Mocioiu,
• Simona Petrescu,
• Jeanina Pandele-Cusu,
• Dana Culita,
• Veronica Bratan,
• Ioan Balint and
• Maria Zaharescu

Beilstein J. Nanotechnol. 2024, 15, 1283–1296, doi:10.3762/bjnano.15.104

• crystallization, consistent with the results from XRD and SEM analyses. Additionally, bands at 3437 and 1613 cm−1 correspond to the vibrational modes of hydroxy groups (OH) bonded to the surface of the ZnO powders. X-ray diffraction The crystalline structure of the samples thermally treated at 500 °C was analyzed

• morphologies and the compositions of the calcined samples were evaluated by scanning electron microscopy (SEM-EDS), using a FEI Quanta 3D FEG instrument equipped with the Octane Elect EDS system. The powder samples were placed on double-sided carbon tape and recorded without coating at accelerating voltages of

• , CA, USA) at 25 °C. The samples were prepared in ultrapure water at a concentration of 1.25 mg/mL. FTIR spectra of as-prepared gels. DTA, DTG and TG curves for the as-prepared SG powder. DTA, DTG and TG curves for the as-prepared MW powder. SEM images for (a) SG sample and (b) MW sample. FTIR spectra

New design of operational MEMS bridges for measurements of properties of FEBID-based nanostructures

• Bartosz Pruchnik,
• Krzysztof Kwoka,
• Ewelina Gacka,
• Dominik Badura,
• Piotr Kunicki,
• Andrzej Sierakowski,
• Paweł Janus,
• Tomasz Piasecki and
• Teodor Gotszalk

Beilstein J. Nanotechnol. 2024, 15, 1273–1282, doi:10.3762/bjnano.15.103

• for the desired MEMS measurement platforms are as follows: They should be dimensionally compatible with the nanostructure to be tested and allow for actuation with an embedded actuation mechanism. To operate, MEMS platforms require auxiliary equipment such as a scanning electron microscope (SEM) or

• electrical measurement equipment. The experiments performed in this way belong to the so-called lab-in-SEM (LiS) technologies. The technology for MEMS fabrication comes from microelectronic surface and bulk micromachining methods [31]. MEMS dimensions are typically defined by photolithography and e-beam

• [38], but this technique is difficult to apply in SEM chambers (the ultimate working environment for opMEMS) because of the difficulty of obtaining a controlled magnetic field inside. In the experiments, the resonance of the opMEMS was measured outside the vacuum chamber using a SIOS nano vibration