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

• detection is described using a silver/platinum nanoplate (Ag/Pt NPL) that interacts with an oligonucleotide aptamer as a bioreceptor. The size of the Ag/Pt NPLs was about 42 nm according to the FE-SEM images. The EDS result indicates that a thin layer of Pt ions was coated on the surface of the Ag NPLs

• 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

• that, one drop of the E. coli-contaminated sample was put onto a paper chip. The final stage in the paper evaluation was to add 6 µL of H2O2 and 6 µL of TMB to paper chips. The ImageJ software was utilized to evaluate the intensity of the resulting blue color. a) The SEM image AND b) EDS analysis of Ag

Study of the reusability and stability of nylon nanofibres as an antibody immobilisation surface

• Inés Peraile,
• Matilde Gil-García,
• Laura González-López,
• Nushin A. Dabbagh-Escalante,
• Juan C. Cabria-Ramos and
• Paloma Lorenzo-Lozano

Beilstein J. Nanotechnol. 2024, 15, 83–94, doi:10.3762/bjnano.15.8

• measured as relative fluorescence unit (RFU) (index explained in the Experimental section). Results are expressed as the mean RFU of the replicates, and the variation is expressed as the standard error of the mean (SEM). When the immunocapture system had been reconstituted after the stripping procedure

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

• observed by scanning electron microscopy (SEM, Figure 1). The BBR powder appeared as aggregates of rods in the micrometer size (Figure 1a), while BBR NPs were formed as nanoscale rectangles (Figure 1b). The electrospun PLA nanofibers showed bead-free and uniform morphology with fiber diameter in the range

• conducted for 6 h to obtain the PLA, BBR/PLA, and BBR NPs/PLA nanofiber scaffolds. Characterization of prepared scaffolds The morphology of PLA and BBR-loaded PLA nanofiber scaffolds was observed by a scanning electron microscope (JSM-6510LV). Fiber diameters were measured from the SEM images by using the

• inverted microscope every 24 h. Statistical analysis The data were reported as mean values ± standard deviations. Statistical analysis of antibacterial data was performed using one-way analysis of variance (ANOVA). A p-value of less than 0.05 was considered statistically significant. (a) SEM image of BBR

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

• structures were examined in terms of their morphology, electrical properties, and catalytic layers in the OER process. Results and Discussion Characterisation of hydrogel-based polymer composites with dispersed catalytic and conductive particles Scanning electron microscopy (SEM) analysis of hydrogel samples

• temperature above LCST results in shrinkage of the hydrogel structure and formation of inhomogeneities. Such a hydrogel ceases to be transparent and loses most of its water [42]. Morphological and physicochemical characterisation Scanning electron microscopy was performed with an FE-SEM FEI Quanta FEG 250 at

• 1 V to 1.7 V vs RHE). SEM micrographs of freeze-dried nanostructures of pure (a, d) and composite hydrogel samples: Hgel-MCO-cCB 1:3 (b, e) and Hgel-MCO-cCB 1:6 (c, f). EDS analysis of hydrogel composites: Hgel-MCO (a, d, g), Hgel-MCO-cCB 1:3 (b, e, h), Hgel-MCO-cCB 1:6 (c, f, i). Transmittance plot

Measurements of dichroic bow-tie antenna arrays with integrated cold-electron bolometers using YBCO oscillators

• Leonid S. Revin,
• Dmitry A. Pimanov,
• Alexander V. Chiginev,
• Anton V. Blagodatkin,
• Viktor O. Zbrozhek,
• Andrey V. Samartsev,
• Anastasia N. Orlova,
• Dmitry V. Masterov,
• Alexey E. Parafin,
• Victoria Yu. Safonova,
• Anna V. Gordeeva,
• Andrey L. Pankratov,
• Leonid S. Kuzmin,
• Anatolie S. Sidorenko,
• Silvia Masi and
• Paolo de Bernardis

Beilstein J. Nanotechnol. 2024, 15, 26–36, doi:10.3762/bjnano.15.3

• sensitivity. Scanning electron microscopy (SEM) images of the sample LSPE VB 210/240 SINS1 No. 43 deposited at NNSTU were obtained using an electron microscope at the Collective Use Center of the IPM RAS (Figure 4a,b). The dimensions of the junctions can be precisely measured using SEM and compared with the

• a substrate thickness of 0.29 mm seem to be closer to the experimental results, see Measurement results section below. (a) Design of the sample of LSPE VB 210/240 from the SINS1 series. (b) Optical photo of the sample of LSPE VB 210/240 from the SINS1 series. (a) SEM image of the LSPE sample; bow

• -tie antennas are visible. (b) SEM image where the required elements are painted with pseudocolors; red: normal metal absorber, green: SN contact, and blue: SIN tunnel junctions. I–V characteristics of two receiving structures of a sample receiving system from the LSPE VB 210/240 SINS1 series. Measured

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

• lower dose than the main exposure so that it does not induce chain scission in the top resist layer, but only in the bottom resist layer, which is more sensitive. The result of the multi-dose exposure was controlled by observing a cross section of the developed bilayer resist using a SEM in snapshot

• lithographically patterned nanostructures to be examined using TEM. The results of the fabrication methods mentioned above were examined using SEM. This is important because the structural information (disk dimensions and deformation from fences) later correlates to the magnetic properties. A magnetic vortex

• results are consistent with the observations from LTEM. Conclusion Electron beam lithography in combination with lift-off and IBE methods for the preparation of Py nanodisks has been optimized. The results have been compared using SEM and TEM. In addition, the application of stencil lithography for the

Determination of the radii of coated and uncoated silicon AFM sharp tips using a height calibration standard grating and a nonlinear regression function

• Perawat Boonpuek and
• Jonathan R. Felts

Beilstein J. Nanotechnol. 2023, 14, 1200–1207, doi:10.3762/bjnano.14.99

• for 30 nm depth to obtain sufficient data of force curves. The blunted tips were imaged by SEM immediately after running the nanoindentation process in the AFM program. Then, each tip radius was determined by fitting the force loading curves with the Hertz model equation using the indentation depth

• . Figure 1 shows SEM images of the three different tips. The calibration standard grating used in this experiment is a HS-20MG height calibration standard (supplied by Budget Sensor) with an external size of 1 mm × 1 mm and an inner size of 500 µm × 500 µm [15]. The rectangular height grate pattern is made

• calibration grating as imaged by SEM [17]. The lines in the lower panel of Figure 3 were created through connecting the point-to-point data of the AFM tip position while the tip was moved along the calibration grate. The height of the lines indicates the height of the grate. At this point, we were interested

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

• (500 nm)/Si(111) In this experiment, 4 × 4 µm2 FEBID structures were written with [Au(CH3)2Cl]2 as the precursor using an acceleration voltage of 5 keV and a beam current of 1.5 nA. The fabricated structures were examined with scanning electron microscopy (SEM) and Auger electron spectroscopy (AES

• ). Figure 1a depicts an SEM image of the FEBID deposit created with an electron exposure of 7.80 C/cm2. The position of the corresponding AES analysis is marked in Figure 1a by a green-colored star. The AES spectra acquired on the bare substrate and the deposit are shown in Figure 1b. On the pristine SiO2

• selected area of the SEM image shown in Figure 1a is depicted in Figure 1c, where nanoparticles in the deposition are noticeable, although the picture is somewhat blurry. To better visualize the observed nanoparticles, a background subtraction was performed with the image enhancement program ImageJ [35

Hierarchically patterned polyurethane microgrooves featuring nanopillars or nanoholes for neurite elongation and alignment

• Lester Uy Vinzons,
• Guo-Chung Dong and
• Shu-Ping Lin

Beilstein J. Nanotechnol. 2023, 14, 1157–1168, doi:10.3762/bjnano.14.96

• Supporting Information File 1, Figure S2). Scanning electron microscopy (SEM) images (Figure 1C–E) confirm the featureless surface of flat PU and the ordered arrays of nanopillars and nanoholes on the nanopatterned films. For the PU nanopillar substrate, some short pillars occassionally appeared (Figure 1D

• dimensions of high-aspect-ratio nanostructures [16], we re-measured some dimensions using SEM images (Supporting Information File 1, Figure S4). The nanopillars were around 860 nm high and 350 nm wide at the base and had a rounded tip. The nanoholes were around 960 nm deep and 860 nm wide at the opening and

• flat substrate for neurite extension despite higher cell and primary neurite counts (Figure 2A). SEM images of the PC12 cells on PU samples (Figure 2G–I) show that the neurites grew unimpeded on both the flat and nanostructured substrates. On the nanopillar array (Figure 2H), the neurites and neurite

Curcumin-loaded albumin submicron particles with potential as a cancer therapy: an in vitro study

• Nittiya Suwannasom,
• Netsai Sriaksorn,
• Chutamas Thepmalee,
• Krissana Khoothiam,
• Ausanai Prapan,
• Hans Bäumler and
• Chonthida Thephinlap

Beilstein J. Nanotechnol. 2023, 14, 1127–1140, doi:10.3762/bjnano.14.93

• together with evasion from recognition by macrophages and the immune system because of the low binding of proteins on the particles’ surface [32]. Representative SEM images of HSA-MPs and CUR-HSA-MPs are displayed in Figure 2C,D. The results reveal that the submicron particles displayed a “hairy” surface

• morphology of the particles was examined in a JSM-5910 SEM (JEOL USA, Peabody, MA, USA). The microparticle samples were diluted in distilled water, and a drop of the particle suspension was applied on copper tape and then allowed to dry at RT overnight. The dried samples were then sputter-coated with gold

• . SEM images were obtained under high-vacuum conditions at an operation voltage of 15 kV. Fourier-transform infrared spectroscopy Chemical characteristics of CUR, HSA, HSA-MPs, and CUR-HSA-MPs were examined using Fourier-transform infrared spectroscopy (FTIR, Thermo Scientific, NICOLET IS5, Waltham, MA

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

• 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

• distribution were calculated. UV–vis spectrum of SNPs. (a) SEM micrograph and (b) EDS spectrum of synthesized SNPs. (a) TEM micrograph of synthesized SNPs and (b) density function. STEM micrographs (left) and density plots (right) of eucalyptus nanocomposites with oil concentrations of (a) 0.25%, (b) 0.5%, and

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

• (XRD) analyses were performed. Characterization of Al2O3 nanoparticles The morphological features of the Al2O3 nanoparticles were investigated with the help of FE-SEM micrograph (Figure 2a). It is seen that the Al2O3 nanoparticles exhibit amorphous nature. Thus, it can be stated that the particle size

• cannot be clearly determined in FE-SEM micrograph, but the primary particle size is smaller than 50 nm. On the other hand, EDS analysis was conducted on the Al2O3 sample to determine the elemental composition and purity of Al2O3 nanoparticles. The result of the EDS analysis is given in Figure 2b and it

Prediction of cytotoxicity of heavy metals adsorbed on nano-TiO₂ with periodic table descriptors using machine learning approaches

• Joyita Roy,
• Souvik Pore and
• Kunal Roy

Beilstein J. Nanotechnol. 2023, 14, 939–950, doi:10.3762/bjnano.14.77

• XGBoost gives the highest R2 (0.99) for the training set, while AdaBoost gives the lowest R2 (0.88) with the highest MAEtest (0.33). Cross-validation (CV) statistics were obtained based through 20 times fivefold repetitive CV along with 1000 times shuffle split CV (mean ± SEM) method. This is done to

• . SHAP summary plot. Cross-validation statistics based on 20 times fivefold repetitive CV and 1000 times shuffle split CV method (mean ± SEM). General mechanism of toxicity to HK-2 cell by heavy metals. Different concentrations of heavy metal salt samples in µmol/L. Statistical parameters and selected

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

• CoAl-LDH synthesis method. We thoroughly study the effects of the mass scale-up (25-fold: up to 375 mM) and the volumetric scale-up (20-fold: up to 2 L). For this, we use a combination of several structural (XRD, TGA, and N2 and CO2 isotherms), microscopic (SEM, TEM, and AFM), magnetic (SQUID), and

• CoAl-based LDH synthesis through an ARR method had been demonstrated, morphological aspects were addressed by means of scanning electron microscopy (SEM), transmission electron microscopy (TEM), and atomic force microscopy (AFM) (Figure 4 and Figure 5). For reference x1, well-defined hexagonal single

• experimental conditions extracted from SEM analysis. Besides slight differences in size and morphology (sharpness of the edges), the AFM comparison of single hexagonal platelets of reference x1 and sample x20V shows a similar thickness of around 85 nm (Figure 5A,B and Supporting Information File 1, Figure S15

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

• of etching observed in Figure 3d. Figure 4 shows the effect of species 2–4 in solutions of THF and DCM. Species 2 at a concentration of 3.25 × 10−2 M in THF in Figure 4a shows the most aggressive etching across species 1–4 in all solvents. After only 30 min there was no evidence by SEM of extant gold

• maps in Figure S5 (Supporting Information File 1) support that the black sections of the SEM images in Figure 3 and Figure 4 correspond to the absence of gold, that is, to complete loss of gold to the action of the etchant solution. We mixed, with 10 min of vortexing, citrate-capped AuNPs in 10 mL

• % 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

Biomimetics on the micro- and nanoscale – The 25th anniversary of the lotus effect

• Matthias Mail,
• Kerstin Koch,
• Thomas Speck,
• William M. Megill and
• Stanislav N. Gorb

Beilstein J. Nanotechnol. 2023, 14, 850–856, doi:10.3762/bjnano.14.69

• with a super depth-of-field microscope, measure cross-sections of veins of wings via SEM, and characterize the nanomechanical structural and elastic behaviour of the structures using a nanoindenter. The authors use the detailed observations obtained to explore the relative aerodynamical performance of

• Mail, Kerstin Koch, Thomas Speck, William M. Megill and Stanislav N. Gorb Eggenstein-Leopoldshafen, Kleve, Freiburg, and Kiel, July 2023 Biological archetype and eponym of the lotus effect: The sacred lotus (Nelumbo nucifera). a) Photo of a lotus plant. b) Scanning electron microscopy (SEM) image of

Ultralow-energy amorphization of contaminated silicon samples investigated by molecular dynamics

• Grégoire R. N. Defoort-Levkov,
• Alan Bahm and
• Patrick Philipp

Beilstein J. Nanotechnol. 2023, 14, 834–849, doi:10.3762/bjnano.14.68

• substantially more controllable at low energies [10][11], which also makes such beams valid candidates for these processes. Another application includes lamella preparation for transmission electron microscopy (TEM). TEM and scanning electron microscopy (SEM) have high constraints regarding cleanliness [12

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

• utilized to analyze the composition and β-phase content of the composite piezoelectric nanofilms, while scanning electron microscopy (SEM) was employed to observe the morphology of the thin film filaments. Figure 6 displays the XRD patterns of the three composite piezoelectric nanofilms. In the P(VDF-TrFE

• is in agreement with the XRD findings. The thickness of the piezoelectric film was determined to be approximately 120 μm using a Vernier caliper with a precision of 0.02 mm. The SEM images in Figure 8 reveal that the microstructure of the nanofilms consists of fibrous filaments at the micro/nanoscale

• . SEM images of a pure PVDF film in Figure 8a and Figure 8b exhibit filamentous fibers with a relatively smooth surface. In contrast, Figure 8c and Figure 8d show that the addition of ZnO to the P(VDF-TrFE) filaments leads to a rough and granular surface, caused by the aggregation of ZnO particles that

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

• (USA). Deionized water with a resistivity of 18 MΩ·cm−1, provided by a Milli-Q water purification system (Millipore Corp., MA, USA), was used throughout all the experiments. The morphologies of Ag NPs and SERS substrates were examined using a field-emission scanning electron microscope (FE-SEM, Mira II

•  2). FE-SEM micrographs of the samples are shown in Figure 3. The average sizes of Ag nanoparticles were estimated to be 24.10 ± 0.15, 27.07 ± 0.16, 28.07 ± 0.17, and 30.88 ± 0.31 nm by using the ImageJ program. Based on the calculated data, it is evident that the average size of Ag NPs increases

• with an increase in the concentration of reactants. Structural characterization of the SERS substrate In Supporting Information File 1, Figure S10a shows the SEM image of the SAM of Ag NPs on the surface of methanol, while Figure S10b displays the image of the PS substrate after covering with the Ag

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

• demonstrate the enhanced contact between the in situ formed Ge and the carbon matrix, which promotes conductivity, accommodates volume variation, and ultimately improves the electrochemical performance of the material. The morphology of the materials was observed using FE-SEM and HR-TEM. As shown in Figure 2a

• carried out for structural and phase information. Infrared (IR, Shimadzu IRAffinity-1S) and Raman (LabRAM HR evolution confocal Raman microscope) spectra were measured for bond analysis. Field-emission scanning electron microscopy (FE-SEM, Hitachi S-4800) and high-resolution transmission electron

• spectra, and (c) Raman spectra of pure Ge, Ge/C-iM750, Ge/C-HT180, Ge/C-SS750, and BC-800 (see Experimental section for sample denominations). SEM images of (a) Ge and (b) Ge/C-iM750; TEM images of (c) Ge, (d) Ge/C-iM750, (e) Ge/C-HT180, and (f) Ge/C-SS750. CV measurements of (a) pure Ge, (b) Ge/C-iM750

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

• the ⟨001⟩α direction, and the neighbouring chains share corners to form an octahedron layer along the ⟨100⟩α direction. The octahedron layer grows along the ⟨100⟩α, ⟨101⟩α, and ⟨010⟩α directions to crystalize into the tabular structure seen in the SEM experiment (Figure 1d). The structural phase

• , respectively. (b) Mass fraction of the α-MoO3 phase and the microstrain in the h-MoO3 phase. (c,d) SEM microstructures of samples calcinated at 300 and 450 °C, respectively. Crystal structure of the hexagonal phase MoO3·H2O from the sample calcinated at 375 °C. (a) Result of the Rietveld refinement; (b

Humidity-dependent electrical performance of CuO nanowire networks studied by electrochemical impedance spectroscopy

• Jelena Kosmaca,
• Juris Katkevics,
• Jana Andzane,
• Raitis Sondors,
• Liga Jasulaneca,
• Raimonds Meija,
• Kiryl Niherysh,
• Yelyzaveta Rublova and
• Donats Erts

Beilstein J. Nanotechnol. 2023, 14, 683–691, doi:10.3762/bjnano.14.54

• (Figure 1b,c,e). The average diameters of the individual CuO nanowires, determined from the SEM images, were 50–100 nm, and their lengths varied between 2 and 20 µm (Figure 1a). To optimize the dielectrophoretic alignment of nanowires of such lengths and to maximize the number of the nanowire

• electron microscopy (SEM, Hitachi S4800) and atomic force microscopy (AFM, Asylum Research MFP-3D). Electrochemical impedance measurements were performed under various atmospheric conditions in a custom-made system described elsewhere [28]. The main system parameters were RH from 4% to 97%, gas flow from

SERS performance of GaN/Ag substrates fabricated by Ag coating of GaN platforms

• Magdalena A. Zając,
• Bogusław Budner,
• Malwina Liszewska,
• Bartosz Bartosewicz,
• Łukasz Gutowski,
• Jan L. Weyher and
• Bartłomiej J. Jankiewicz

Beilstein J. Nanotechnol. 2023, 14, 552–564, doi:10.3762/bjnano.14.46

• morphology of fabricated Ag layers examined by scanning electron microscopy (SEM). Then, we present the results of their optical properties determined using UV–vis spectroscopy. Finally, we compare the SERS performance of the GaN/Ag substrates toward 4-mercaptobenzoic acid (pMBA) molecules adsorbed on them

• intense Raman signal. SEM images of the GaN platforms with MS-deposited silver layers of different thicknesses are shown in Figure 2. The morphology of MS-fabricated SERS substrates does not change significantly with the change in Ag layer thickness. With a larger amount of deposited Ag, the thickness of

• in the temperature of the platform. Determination of a numerical value describing the thickness of the Ag layer on nanostructured GaN platforms as a function of the temperature would be complicated because of the complex 3D morphology of the GaN platforms. SEM images of the GaN platforms with PLD

Observation of multiple bulk bound states in the continuum modes in a photonic crystal cavity

• Rui Chen,
• Yi Zheng,
• Xingyu Huang,
• Qiaoling Lin,
• Chaochao Ye,
• Meng Xiong,
• Martijn Wubs,
• Yungui Ma,
• Minhao Pu and
• Sanshui Xiao

Beilstein J. Nanotechnol. 2023, 14, 544–551, doi:10.3762/bjnano.14.45

• carried out to compensate for deviations between fabricated and designed values. To obtain devices with larger Q factors and higher scattering power, cavities with larger Na = 30 and Nb = 10 were fabricated. Optical and scanning electron microscopy (SEM) images are given in Figure 3a. A microscope was