Time-resolved probing of laser-induced nanostructuring processes in liquids

• Maximilian Spellauge,
• David Redka,
• Mianzhen Mo,
• Changyong Song,
• Heinz Paul Huber and
• Anton Plech

Beilstein J. Nanotechnol. 2025, 16, 968–1002, doi:10.3762/bjnano.16.74

• . Ultrafast time-resolved probing approaches are key to revealing the transient states and pathways that govern material transformation in LSPC. Keywords: electron diffraction; laser processing in liquids; optical imaging; optical spectroscopy; pump–probe; single objects; time-resolved probing; X-ray

• parameters, improving reproducibility, and tailoring material properties for specific applications. Ultrafast optical techniques such as transient absorption spectroscopy (TAS) [84][85][86][87] have been applied to investigate the influence of the liquid environment on the energy relaxation processes of

Synthesis of biowaste-derived carbon-dot-mediated silver nanoparticles and the evaluation of electrochemical properties for supercapacitor electrodes

• Navya Kumari Tenkayala,
• Chandan Kumar Maity,
• Md Moniruzzaman and
• Subramani Devaraju

Beilstein J. Nanotechnol. 2025, 16, 933–943, doi:10.3762/bjnano.16.71

• using UV–vis spectroscopy. Supporting Information File 1, section S1 contains the details of the material characterization techniques. Results and Discussion Plant extract-mediated production of nanoparticles from noble metal precursors are well reported. In the present work, waste P. pinnata leaf

• evidenced from the progressive color change of the solution as shown by surface plasmon resonance (SPR). Structural and morphological analysis The optical properties of PG-CDs and PG-CDs-AgNPs were studied using UV–visible spectroscopy and photoluminescence (PL) spectroscopy. An absorption peak at 275 nm

• PG-CDs exhibited intense blue fluorescence (inset in Figure 1a), indicating the successful formation and photoluminescent nature of CDs. The formation of PG-CDs-AgNPs in the nanoscale is established by UV–visible spectroscopy by the appearance of SPR peaks at 475 nm [26]. The gradual emergence of

Structural and magnetic properties of microwave-synthesized reduced graphene oxide/VO₂/Fe₂O₃ nanocomposite

• Sumanta Sahoo,
• Ankur Sood and
• Sung Soo Han

Beilstein J. Nanotechnol. 2025, 16, 921–932, doi:10.3762/bjnano.16.70

• graphite oxide to form rGO, the reduction of V2O5 to form VO2, and the formation of Fe2O3 from ferrocene. X-ray diffraction and X-ray photoelectron spectroscopy analyses confirm the formation of distinct metal oxides in the presence of rGO. Furthermore, the morphological analysis reveals the deposition of

• the NCs. The Raman spectra of rGO and the related NCs were recorded through the “XploRA plus HORIBA” instrument with a laser excitation of 532 nm. Additionally, the surface analysis was performed using X-ray photoelectron spectroscopy measurements (XPS, Thermofisher Scientific) functioning at 12 kV

Focused ion beam-induced platinum deposition with a low-temperature cesium ion source

• Thomas Henning Loeber,
• Bert Laegel,
• Meltem Sezen,
• Feray Bakan Misirlioglu,
• Edgar J. D. Vredenbregt and
• Yang Li

Beilstein J. Nanotechnol. 2025, 16, 910–920, doi:10.3762/bjnano.16.69

• merits of ion sources based on alkali metals. Also, Cs+ is a preferred species of ions over Ga+ for secondary ion mass spectroscopy (SIMS) applications because Cs+ can induce higher secondary ion yields for several elements such as carbon (C), oxygen (O), and hydrogen [17][18][19], which provides higher

• energy-dispersive X-ray spectroscopy (EDS), lamellas for transmission electron microscopy (TEM) were prepared. Experimental The Ga+ FIB is a ThermoFisher Helios NanoLab 650 and uses a gas injection system (GIS). ZeroK NanoTech Corporation has created commercially available Cs+ FIB systems based on

Heat-induced transformation of nickel-coated polycrystalline diamond film studied in situ by XPS and NEXAFS

• Olga V. Sedelnikova,
• Yuliya V. Fedoseeva,
• Dmitriy V. Gorodetskiy,
• Yuri N. Palyanov,
• Elena V. Shlyakhova,
• Eugene A. Maksimovskiy,
• Anna A. Makarova,
• Lyubov G. Bulusheva and
• Aleksandr V. Okotrub

Beilstein J. Nanotechnol. 2025, 16, 887–898, doi:10.3762/bjnano.16.67

• thin nickel film deposited by thermal evaporation. The graphitization of diamond with and without a nickel coating as a result of high-vacuum annealing at a temperature of about 1100 °C was studied in situ using synchrotron-based X-ray photoelectron spectroscopy (XPS) and near-edge X-ray absorption

• crystallites; however, the layer defectiveness increased in areas with fine-dispersed crystallites. According to NEXAFS and Raman spectroscopy data, the most ordered atomic structure of graphitic layers was obtained by annealing nickel-coated SCD. The angular dependence of NEXAFS C K-edge spectra of nickel

• . Keywords: graphitization; near-edge X-ray absorption fine structure spectroscopy; nickel coating; polycrystalline diamond film; single-crystal diamond; X-ray photoelectron spectroscopy; Introduction Diamond and graphite, both composed entirely of carbon atoms, exhibit vastly different properties due to

Ar⁺ implantation-induced tailoring of RF-sputtered ZnO films: structural, morphological, and optical properties

• Manu Bura,
• Divya Gupta,
• Arun Kumar and
• Sanjeev Aggarwal

Beilstein J. Nanotechnol. 2025, 16, 872–886, doi:10.3762/bjnano.16.66

• , defects, and interstitials are induced through the interaction between energetic ions and the host material, resulting in structural modification and thus alteration in lattice dynamics of the host material [10]. The implantation-induced disorder can be qualitatively examined using Raman spectroscopy

• studied using field-emission scanning electron microscopy (FESEM) along with energy dispersive X-ray spectroscopy (EDS). Cross-sectional images are also obtained to evaluate the thickness of ZnO film. The optical properties of pristine and implanted ZnO films are investigated using a Shimadzu UV–visible

• fluence, which can be attributed to the fact that an enormous amount of energy is transferred to the lattice when the ion beam travels through the sample quickly, which generates dislocations. Raman spectroscopy Figure 4 reveals the Raman spectra of pristine and 30 keV argon-implanted ZnO films at various

Insights into the electronic and atomic structures of cerium oxide-based ultrathin films and nanostructures using high-brilliance light sources

• Paola Luches and
• Federico Boscherini

Beilstein J. Nanotechnol. 2025, 16, 860–871, doi:10.3762/bjnano.16.65

• light sources, such as synchrotrons and free-electron lasers, allow researchers to probe the structural, electronic, and dynamic properties of functional materials at an unprecedented level of detail. Techniques like X-ray photoelectron spectroscopy and X-ray absorption spectroscopy, can reveal atomic

• applications, examining the application of high-brilliance light sources on model systems such as supported thin films and epitaxial nanostructures. We review selected studies exploiting the high energy resolution and sensitivity of synchrotron radiation-based X-ray photoelectron spectroscopy and X-ray

• absorption spectroscopy to explain the factors influencing the material’s reducibility, with particular focus on dimensionality effects and on metal–oxide interaction, and the interaction with molecules. The potential of studies conducted under ambient pressure conditions is highlighted, and, finally, the

Synchrotron X-ray photoelectron spectroscopy study of sodium adsorption on vertically arranged MoS₂ layers coated with pyrolytic carbon

• Alexander V. Okotrub,
• Anastasiya D. Fedorenko,
• Anna A. Makarova,
• Veronica S. Sulyaeva,
• Yuliya V. Fedoseeva and
• Lyubov G. Bulusheva

Beilstein J. Nanotechnol. 2025, 16, 847–859, doi:10.3762/bjnano.16.64

• . In this work, to reveal the effect of carbon coating on the interaction of sodium with the MoS2 layers located vertically relative to the substrate, model experiments were carried out using synchrotron-radiation-induced X-ray photoelectron spectroscopy (XPS). Sodium vapor obtained by heating a sodium

• surface correspond to Pt nanoparticles, the presence of which is confirmed by energy-dispersive X-ray (EDX) spectroscopy (Supporting Information File 1, Figure S1). These nanoparticles have a uniform size and are densely distributed on the sample surface, in contrast to the polysulfide particles of

• deposited on a SiO2/Si substrate using magnetron sputtering. Raman spectroscopy and SEM revealed the vertical orientation of the MoS2 layers relative to the substrate surface. According to XPS data, the surface of the MoS2 film is enriched with sulfur even after its annealing at 1073 K in hydrogen. PyC

Facile one-step radio frequency magnetron sputtering of Ni/NiO on stainless steel for an efficient electrode for hydrogen evolution reaction

• Ha Huu Do,
• Khac Binh Nguyen,
• Phuong N. Nguyen and
• Hoai Phuong Pham

Beilstein J. Nanotechnol. 2025, 16, 837–846, doi:10.3762/bjnano.16.63

• is increased, determined by energy-dispersive X-ray spectroscopy (EDX), as shown in Table 1. Ni/NiO/SS-5 displayed the lowest O content (4.69 wt %). In contrast, Ni/NiO/SS-20 showed the highest O content (22.69 wt %), attributed to the highest O2 flow rate in the sputtering process. Ni/NiO/SS-10

• distribution of the primary elements (Ni, O) in the Ni/NiO/SS-10 sample. This outcome revealed that catalytic sites were also uniformly distributed on the electrode’s surface. Figure 5a exhibits the X-ray photoelectron spectroscopy (XPS) survey of the Ni/NiO/SS-10 sample. It can be seen that Ni/NiO/SS gives Ni

• spectroscopy (EIS) was carried out at a voltage of −200 mV to confirm the HER kinetics. Figure 6c shows the Nyquist plots of the various electrodes accompanied by an equivalent circuit (inset of Figure 6c). Ni/NiO/SS-10 has a charge transfer resistance (Rct) of 5.35 Ω, which is much smaller than that of SS

Synthesis and magnetic transitions of rare-earth-free Fe–Mn–Ni–Si-based compositionally complex alloys at bulk and nanoscale

• Shabbir Tahir,
• Tatiana Smoliarova,
• Carlos Doñate-Buendía,
• Michael Farle,
• Natalia Shkodich and
• Bilal Gökce

Beilstein J. Nanotechnol. 2025, 16, 823–836, doi:10.3762/bjnano.16.62

• ground, polished, and analyzed by SEM (JEOL JSM-7600 F, Japan). The chemical composition was determined using energy-dispersive X-ray spectroscopy (EDX) with an Oxford Inca spectrometer. The crystal structure of bulk CCAs was characterized by X-ray diffraction (XRD) using a DRON-4–07 diffractometer with

Supramolecular hydration structure of graphene-based hydrogels: density functional theory, green chemistry and interface application

• Hon Nhien Le,
• Duy Khanh Nguyen,
• Minh Triet Dang,
• Huyen Trinh Nguyen,
• Thi Bang Tam Dao,
• Trung Do Nguyen,
• Chi Nhan Ha Thuc and
• Van Hieu Le

Beilstein J. Nanotechnol. 2025, 16, 806–822, doi:10.3762/bjnano.16.61

• GO-SG-ZH powder. The graphene-based nanocomposites in hydrogel form and in powder form were comparatively characterized using moisture analysis, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and aqueous dispersibility. Brush coating of graphene oxide–nanosilica–zinc

• microscopy and energy-dispersive X-ray spectroscopy were performed using a JSM-IT200 system (JEOL). Samples were coated with Pt before the SEM-EDS analysis. X-ray diffraction was performed on a D8 Advance instrument (Bruker). Fourier-transform infrared spectroscopy (FTIR) was characterized with a FT/IR-6600

• instrument (Jasco). Ultraviolet–visible absorption spectroscopy (UV–vis) and light transmittance spectroscopy were recorded using a V-670 spectrophotometer (Jasco). Microscopic texture and imaging were observed by a stereo zoom microscope (Optika SZM). Agar diffusion assays were used for testing

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

• microscopy, scanning electron microscopy, X-ray photoelectron spectroscopy, and ultraviolet–visible spectroscopy. The morphology of the NPs in different solvents varied from spherical, rice-like to rod-like particles which demonstrates the effect of the solvent on the morphology/composition of NPs

• 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

• 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

• AC) performed on the undissolved sample revealed the presence of a low temperature blocking process ( ≈ 10 K), and confirmed its superparamagnetic state between 70– 250 K. X-ray photoelectron spectroscopy and Raman studies showed a varied composition of the undissolved sample in which organic

• completely dissolved sample. Keywords: calcium alginate; dissolution; iron oxyhydroxide nanoparticles; magnetic properties; saline; spectroscopy; Introduction Hematinic are substances such as iron, vitamin B12, and folic acid that are essential in the production of blood [1]. Iron deficiency drugs, which

• 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

Thickness dependent oxidation in CrCl₃: a scanning X-ray photoemission and Kelvin probe microscopies study

• Shafaq Kazim,
• Rahul Parmar,
• Maryam Azizinia,
• Matteo Amati,
• Muhammad Rauf,
• Andrea Di Cicco,
• Seyed Javid Rezvani,
• Dario Mastrippolito,
• Luca Ottaviano,
• Tomasz Klimczuk,
• Luca Gregoratti and
• Roberto Gunnella

Beilstein J. Nanotechnol. 2025, 16, 749–761, doi:10.3762/bjnano.16.58

• importance, limited experimental research has been conducted on the electronic structure of CrX3 [5][6]. According to previously published photoelectron spectroscopy results, CrX3 belongs to metal compounds in which the 3d states are very close to the Fermi level, significantly above the 3p/4p/5p states of

• showed that oxygen adsorption on cleaved surfaces facilitates the formation of a stable structure with charge transfer signatures, as identified by high-resolution photoemission spectroscopy [8]. It remains unclear whether similar effects occur in exfoliated thin flakes. Like in other materials, the

• effect) [19][20][21]. A well-known and suitable technique to investigate the electronic structure of surfaces is X-ray photoemission spectro-microscopy [22][6]; in order to obtain the necessary spatial resolution, the beam size must be reduced to tens of nanometers. The Electron Spectroscopy for Chemical

Synthesis of a multicomponent cellulose-based adsorbent for tetracycline removal from aquaculture water

• Uyen Bao Tran,
• Ngoc Thanh Vo-Tran,
• Khai The Truong,
• Dat Anh Nguyen,
• Quang Nhat Tran,
• Huu-Quang Nguyen,
• Jaebeom Lee and
• Hai Son Truong-Lam

Beilstein J. Nanotechnol. 2025, 16, 728–739, doi:10.3762/bjnano.16.56

• were characterized, and the TC adsorption efficiency of PGC was assessed using high-performance liquid chromatography–mass spectroscopy (HPLC-MS). Elemental analysis of PGC identified four key mechanisms governing its endothermic TC adsorption mechanism: surface complexation, electrostatic interactions

• , ‒C=O, and ‒COOH), which confer a negative charge, enabling electrostatic interactions (Figure 6b). FTIR spectroscopy (Figure 2g) confirms the presence of these oxygen-containing functional groups on PGC, supporting this explanation. Thus, electrostatic attraction between the positively charged TC–N

• ‒desorption isotherms at 77.3 K under controlled pressure conditions. Before analysis, the sample was degassed at 150 °C for 2 h and 30 min under an N2 atmosphere. High-performance liquid chromatography-mass spectroscopy (HPLC–MS/MS) The HPLC-MS/MS system consisted of an AB Sciex 4000 QTRAP mass spectrometer

Efficiency of single-pulse laser fragmentation of organic nutraceutical dispersions in a circular jet flow-through reactor

• Tina Friedenauer,
• Maximilian Spellauge,
• Alexander Sommereyns,
• Verena Labenski,
• Tuba Esatbeyoglu,
• Christoph Rehbock,
• Heinz P. Huber and
• Stephan Barcikowski

Beilstein J. Nanotechnol. 2025, 16, 711–727, doi:10.3762/bjnano.16.55

• yield of submicrometer particles and nanoparticles was quantified using UV–vis extinction spectroscopy, scanning electron microscopy, and analytical centrifugation, while high-performance liquid chromatography determined degradation. We found improved fragmentation efficiency at lower mass

• chemical degradation [29]. Other purely organic materials, such as vitamin C and capsaicin (an alkaloid in chili), were also fragmented using a femtosecond laser with a wavelength of 800 nm, and the yield was determined based on an increase in extinction using UV–vis extinction spectroscopy. It was shown

• enhancement in the colloidally stable supernatants of particle dispersions after sedimentation of the colloidally unstable, unfragmented MP educts, determined by UV–vis extinction spectroscopy, which is proportional to the amount of SMPs and NPs [2][22][49]. This extinction enhancement from the unirradiated

Nanostructured materials characterized by scanning photoelectron spectromicroscopy

• Matteo Amati,
• Alexey S. Shkvarin,
• Alexander I. Merentsov,
• Alexander N. Titov,
• María Taeño,
• David Maestre,
• Sarah R. McKibbin,
• Zygmunt Milosz,
• Ana Cremades,
• Rainer Timm and
• Luca Gregoratti

Beilstein J. Nanotechnol. 2025, 16, 700–710, doi:10.3762/bjnano.16.54

• , environmental reliability, and operando capabilities. Scanning photoelectron spectromicroscopy (SPEM) is one of the characterization tools that combine high spectral resolution X-ray photoelectron spectroscopy with submicron spatial resolution. In particular, the SPEM equipment hosted at the ESCA microscopy

• enhanced sensitivities are examples of capabilities that modern techniques of characterization in nanotechnology must possess. X-ray photoelectron spectroscopy (XPS) is still one of the fundamental tools for chemical and electronic characterization of surfaces and subsurface layers. In the last three to

• several improvements have been developed at synchrotron light facilities where unique properties of X-ray radiation can be found. Scanning photoelectron microscopy (SPEM) combines XPS analysis with lateral resolution; chemical imaging as well as XPS spectroscopy at nanoscale sized areas can be performed

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

• using pulsed laser deposition (PLD). This research investigates the influence of varying deposition parameters, including substrate temperature and ambient gas composition, on the structural, morphological, and superconducting properties of the films. X-ray photoelectron spectroscopy, X-ray diffraction

• nitrogen pressure between 10 and 90 mTorr. The experiment was performed in a laser ablation system “RIBER LDM 32”. It consists of three stainless steel ultrahigh-vacuum (UHV) chambers for sample introduction, PLD deposition, and X-ray photoelectron spectroscopy (XPS) analysis, isolated by UHV gate valves

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

• of graphene confers antioxidant properties The arrangement of TA molecules on graphene layers and their antioxidant effects were analyzed through three experimental methods. The concentration of TA in the FLG suspension was measured using UV–vis spectroscopy, surface composition changes from graphite

• to the FLG–TA colloid were analyzed using X-ray photoelectron spectroscopy (XPS), and the antioxidant properties of FLG–TA were evaluated using the DPPH free radical scavenging assay. XPS analysis (Figure 2 and Table S1, Supporting Information File 1) shows a significant increase in the O-to-C ratio

• provided DPPH (Figure S4B0–B2 of Supporting Information File 1). These findings indicate significant oxygen enrichment due to TA adsorption on FLG sheets, supporting earlier Raman spectroscopy results and colloidal stability observations (Figure S3A1, Supporting Information File 1). Both free and adsorbed

Aprepitant-loaded solid lipid nanoparticles: a novel approach to enhance oral bioavailability

• Mazhar Hussain,
• Muhammad Farooq,
• Muhammad Asad Saeed,
• Muhammad Ijaz,
• Sherjeel Adnan,
• Zeeshan Masood,
• Muhammad Waqas,
• Wafa Ishaq and
• Nabeela Ameer

Beilstein J. Nanotechnol. 2025, 16, 652–663, doi:10.3762/bjnano.16.50

• analysis. APT-loaded SLNs were prepared by the precipitation method and characterized by physicochemical studies including particle size and zeta potential measurements, drug content, encapsulation efficiency and solubility studies, Fourier-transform infrared spectroscopy (FTIR), scanning electron

• , and zeta potential measurements. Also Fourier-transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), solubility, in vitro dissolution, and in vivo and stability studies were carried out. Result and Discussion Physicochemical evaluation The solubility of APT in the SLNs was 24-fold higher

• solvents were stronger and minimized the formation of cracks. However, APT-loaded SLNs formulations in the aqueous phase appeared as nonspherical granules. FTIR studies FTIR spectroscopy was applied to estimate any interaction between APT and β-CD or poloxamer 407 in APT-CD-NP4 and APT-PX-NP8. Figure 4a

Nanoscale capacitance spectroscopy based on multifrequency electrostatic force microscopy

• Pascal N. Rohrbeck,
• Lukas D. Cavar,
• Franjo Weber,
• Peter G. Reichel,
• Mara Niebling and
• Stefan A. L. Weber

Beilstein J. Nanotechnol. 2025, 16, 637–651, doi:10.3762/bjnano.16.49

• nanoscale systems across materials science, biology, and nanotechnology, complementing established methods in the field. Keywords: atomic force microscopy; capacitance gradients; dielectric constant; dielectric spectroscopy; heterodyne frequency mixing; Kelvin probe force microscopy; multifrequency AFM

• ; quantitative force spectroscopy; scanning capacitance force microscopy; Introduction Technological progress in fields including electronics, energy storage, photonics, and biomedical devices would not have been possible without the development of new materials. Progress in these areas requires a detailed

• ][56][57][58][59][60][61][62][63][64][65][66][67][68][69][70][71][72][73]. Compared to optical ellipsometry or reflectance spectroscopy, SCM and SCFM can map surface properties such as film thickness [35][39] and dielectric constants [35][74], with superior spatial resolution. However, in particular

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

• revealed nanofiber morphology, and Raman spectroscopy showed the characteristic IG and ID bands of CNFs [18]. Catalytic chemical vapor deposition was conducted by Hammel et al. to synthesize CNFs using a tube furnace. The experiment used a nickel-based catalyst and diluted acetylene as the source of carbon

• microscopy (FESEM, Zeiss Crossbeam 340) for morphological analysis. Raman spectroscopy (HORIBA XploRA PLUS, 532 nm) was carried out to analyze the signature spectra of the grown CNFs. Results and Discussion Flame characterization and temperature The flames were characterized regarding flame shape and

• . A higher presence of defects was found before in CNFs via Raman spectroscopy [12]. A slightly elevated defect density was also observed in CNTs derived from LPG [16][31]. The D band and G band intensities show an ID/IG ratio of more than 1.13, which is a clear indicator for high disorder and

Retrieval of B1 phase from high-pressure B2 phase for CdO nanoparticles by electronic excitations in Cd_xZn_1−xO composite thin films

• Arkaprava Das,
• Marcin Zając and
• Carla Bittencourt

Beilstein J. Nanotechnol. 2025, 16, 551–560, doi:10.3762/bjnano.16.43

• oxygen ion irradiation, while it entirely disappears with silver ion irradiation, confirming the amorphization of the Zn2SiO4 phase. Complementary observations from X-ray photoelectron spectroscopy (XPS), specifically O 1s and Si 2p peaks in XPS spectra, support these findings. Additionally, the track

• diverse characterization techniques, demonstrating the potential reversibility of the B1 to B2 phase transformation induced by ion irradiation. Keywords: irradiation; phase transformation; thermal spike; track diameter; X-ray absorption near edge spectroscopy; X-ray photoelectron spectroscopy

• irradiated thin films was performed with X-ray diffraction and Raman spectroscopy. Additionally, X-ray absorption near-edge structure (XANES) spectroscopy was conducted at the Zn L3,2 and O K edges for all the thin films. X-ray photoelectron spectroscopy (XPS) on Si 2p and O 1s core levels provided direct

Functionalized gold nanoflowers on carbon screen-printed electrodes: an electrochemical platform for biosensing hemagglutinin protein of influenza A H1N1 virus

• Carlos Enrique Torres-Méndez,
• Sharmilee Nandi,
• Klara Martinovic,
• Patrizia Kühne,
• Yifan Liu,
• Sam Taylor,
• Maria Lysandrou,
• Maria Ines Berrojo Romeyro Mascarenhas,
• Viktoria Langwallner,
• Javier Enrique Sebastián Alonso,
• Ivana Jovanovic,
• Maike Lüftner,
• Georgia-Vasiliki Gkountana,
• David Bern,
• Abdul-Raouf Atif,
• Ehsan Manouchehri Doulabi,
• Gemma Mestres and
• Masood Kamali-Moghaddam

Beilstein J. Nanotechnol. 2025, 16, 540–550, doi:10.3762/bjnano.16.42

• , followed by blocking with bovine serum albumin to minimize nonspecific hydrophobic binding. The electrodes were characterized by cyclic voltammetry and electrochemical impedance spectroscopy experiments in the presence of [Fe(CN)6]3−/4−. Differential pulse voltammetry was used to measure the change in

• was coupled to an automated microfluidics system, and no significant decrease of the electrochemical signal was observed. Keywords: charge transfer; cyclic voltammetry; differential pulse voltammetry; electrochemical impedance spectroscopy; electrodeposition; Introduction Viral infections pose a

• nanohybrids of MoSe2−CsPbBr3 with a size range between 60 and 80 nm [38]. This effect has been relevant to enhance the Raman scattering vibrational modes in surface-enhanced Raman spectroscopy measurements. It has also been noticed that the shape of the nanostructure can be used to tune the magnitude of the

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

• effective dwell time with a 600 nm FWHM of the electron beam), and 2000 cycles. For deposit morphology observation, a high-resolution Hitachi S4800 FESEM was used. The chemical composition of the deposits was confirmed through energy-dispersive X-ray spectroscopy (EDX) using a silicon drift detector from