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

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

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

• alloy nanoparticles by LRL with the addition of IPA as a radical scavenger to a solution containing multiple metal ions, and the structure of the synthesized nanoparticles was evaluated by scanning transmission electron microscopy-energy dispersive spectroscopy (STEM-EDS). In this case, we selected an

Quantification of lead through rod-shaped silver-doped zinc oxide nanoparticles using an electrochemical approach

• Ravinder Lamba,
• Gaurav Bhanjana,
• Neeraj Dilbaghi,
• Vivek Gupta and
• Sandeep Kumar

Beilstein J. Nanotechnol. 2025, 16, 422–434, doi:10.3762/bjnano.16.33

• sources of lead exposure [4]. Through contaminated food or drink or through mouth-to-mouth contact, lead can enter the body. Standard techniques for determining lead content involve the use of atomic absorption spectroscopy (AAS) [5] and inductively coupled plasma–mass spectrometry (ICP–MS) [6]. Although

• average diameter of Ag@ZnO NRs is approximately 70 nm. The elemental composition of the fabricated nanorods was examined through energy-dispersive spectroscopy (EDS). Figure 2c depicts the typical EDS spectrum of the produced Ag@ZnO NRs. Observations from the EDS spectrum lead to the conclusion that the

• nanorods are made of zinc and oxygen. The produced nanorods are pure Ag@ZnO NRs with no detectable impurities, as evidenced by the absence of any other peak in the spectrum associated with any impurity. Fourier-transform infrared spectroscopy analysis of Ag@ZnO nanorods Figure 3 presents the typical

ReactorAFM/STM – dynamic reactions on surfaces at elevated temperature and atmospheric pressure

• Tycho Roorda,
• Hamed Achour,
• Matthijs A. van Spronsen,
• Marta E. Cañas-Ventura,
• Sander B. Roobol,
• Willem Onderwaater,
• Mirthe Bergman,
• Peter van der Tuijn,
• Gertjan van Baarle,
• Johan W. Bakker,
• Joost W. M. Frenken and
• Irene M. N. Groot

Beilstein J. Nanotechnol. 2025, 16, 397–406, doi:10.3762/bjnano.16.30

• diffraction/Auger electron spectroscopy system to verify the cleanliness, structure, and composition of the surface. The UHV system is supported by four pneumatic air legs resting on a concrete slab, which is separated from the foundation of the building, and isolated from the main floor in an ultramicroscopy

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

• 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

• with passing energy at 80 eV, and the binding energy spectrum was recorded from 0 to 1,400 eV. The functional group interaction of PEG–PCL nanoparticles was assessed using Fourier-transform infrared (FTIR) spectroscopy (Thermo Scientific, Nicolet 6700). An amout of 5 mg of PEG, PCL, and PEG–PCL

• larger estimate than the dry measurements obtained from TEM and SEM [32]. X-ray photoelectron spectroscopy, also known as electron spectroscopy for chemical analysis (ESCA), was used to analyze the surface chemistry of the PEG–PCL NPs. XPS is a powerful surface-sensitive technique that provides detailed

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

• reflectance Fourier-transform infrared spectroscopy (ATR-FTIR) was used. Freeze-dried nanoparticles were directly placed on an ATR crystal, and the infrared spectrum of the samples was obtained in the range of 4000–400 cm−1 using a FTIR spectrophotometer (Bruker/Vertex70, USA). Particle size and zeta

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

• scattering by the carbon fibers. The pulsed laser-grafted gold nanoparticles exhibited cauliflower morphology with approximately 200 nm diameter and no detectable carbonaceous shells (Figure 2B and cf. X-ray photoelectron spectroscopy (XPS) data below). Assembly of gold nanoparticles by nanosecond laser

• , evident from electrochemical impedance spectroscopy (EIS) data (Figure 5B). Impedance, measured in an electrochemical setup, is the time-dependent opposition to alternating current stemming from the combined effect of ohmic resistance, capacitance, and phase elements in an electronic circuit. Impedance is

• 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

Tailoring of physical properties of RF-sputtered ZnTe films: role of substrate temperature

• Kafi Devi,
• Usha Rani,
• Arun Kumar,
• Divya Gupta and
• Sanjeev Aggarwal

Beilstein J. Nanotechnol. 2025, 16, 333–348, doi:10.3762/bjnano.16.25

• leads to a reduction in microstrain and dislocation density. The optical studies using UV–vis–NIR spectroscopy reveal that the transmittance of films increases with substrate temperature. Further, the shift in transmittance threshold towards lower wavelengths with substrate temperature indicates that

• energy-dispersive X-ray spectroscopy (EDS) operated at 10 keV. The current–voltage (I–V) characteristics of the films were measured in the voltage range from −1 V to 1 V using a two-probe Keithley 4200 A-SCS parametric analyser available at Ion Beam Centre, Kurukshetra University. Results and Discussion

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

• formation of GO–Chl nanoconjugates was confirmed by investigating the optical, functional, structural, and morphological properties employing standard analytical characterization techniques. The optical properties of GO and GO–Chl were assessed using UV–vis spectroscopy (Supporting Information File 1

• characteristic band at around 343 nm, in GO–Chl, could be related to the binding of Chl to GO [42]. The functional groups in GO and GO–Chl nanoconjugates were analyzed by FTIR spectroscopy. Supporting Information File 1, Figure S1b shows the FTIR spectrum of GO, Chl, and GO–Chl in the range of 500–3800 cm−1

• , Raman spectroscopy was utilized to evaluate the formation of GO (after the oxidation of graphite powder) and the GO–Chl nanoconjugate. The structural properties of graphite and GO nanosheets were investigated through the comprehensive analysis of the characteristic graphitic domain band (G band) and