Upcycling agroindustrial waste into graphene oxide supports for gold nanoparticles: toward sustainable nanomaterials

• Juan Marcos Castro-Tapia,
• Selene Acosta,
• Hiram Joazet Ojeda-Galván,
• Elsie Evelyn Araujo-Palomo,
• Edgar Giovanni Villabona-Leal and
• Mildred Quintana

Beilstein J. Nanotechnol. 2026, 17, 489–504, doi:10.3762/bjnano.17.32

• UV–vis, ATR-FTIR, XPS, XRD, and Raman measurements, complemented by TGA and TEM to assess optical properties, surface chemistry, and structural and morphological features. Additionally, gold nanoparticles (AuNPs) were photochemically deposited onto Agro-GO to evaluate its potential for nanotechnology

• , and measurements were carried out under a nitrogen atmosphere with a flow rate of 50 mL·min−1. 3 mg of each sample were used for the analysis. X-ray diffraction (XRD) measurements were carried out using a SmartLab RIGAKU diffractometer operating with a Cu anode X-ray source (Cu Kα radiation, λ

• biomass precursors. Overall, these thermal stability trends are in good agreement with XRD, XPS, Raman, UV–Vis, and TEM characterizations, collectively supporting the coexistence of GO-like domains and amorphous carbon in the agroindustrial waste-derived materials. The corresponding derivative

Eco-efficient materials for agricultural crops based on a mineral rich in MOR- and HEU-type zeolites

• Esperanza Yamile de la Nuez-Pantoja,
• Inocente Rodríguez-Iznaga,
• Gerardo Rodríguez-Fuentes,
• Vitalii Petranovskii,
• Ariel Martínez García,
• José Juan Calvino Gámez and
• Daniel Goma Jiménez

Beilstein J. Nanotechnol. 2026, 17, 381–395, doi:10.3762/bjnano.17.26

• by XRD) and other qualities of these zeolites, highlighting their ion-exchange and adsorption properties for nutrient release and reversible water retention. This is essential for the use of this material as a slow-release fertilizer that efficiently provides nutrients for the agroecological

• ) and other elements (Si) important for agricultural crops. Particular attention was paid to the analysis of the interaction of nitrogen and phosphorus species on this complex multiphase zeolitic carrier, applying Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron

• these experimental materials, studies were conducted using XRD, N2 adsorption isotherms, SEM, TEM, and STEM. However, they will only be presented for the most interesting materials, namely those that were modified with 2.0% and 3.5% DAP and then with a 5 M urea solution, that is, the materials CLIMf2

Durable antimicrobial activity of fabrics functionalized with zeolite ion-exchanged nanomaterials against Staphylococcus aureus and Escherichia coli

• Perla Sánchez-López,
• Kendra Ramirez Acosta,
• Sergio Fuentes Moyado,
• Ruben Dario Cadena-Nava and
• Elena Smolentseva

Beilstein J. Nanotechnol. 2026, 17, 262–274, doi:10.3762/bjnano.17.18

• functionalized textiles. X-ray diffraction XRD patterns of bramante fabrics, composed of 50% cotton and 50% polyester fibers, are shown in Figure 3. The bramante fabrics exhibited a typical cotton cellulose pattern, with three characteristic peaks at 2θ ≈ 14.7°, 16.3°, and 22.4°, corresponding to the

• crystallographic planes (101), (101), and (002), respectively. Modification of the fabrics with nanomaterials led to an increase in the intensity of all peaks, while the position of the signals in XRD patterns remained unchanged (Figure 3). The later may be explained by the increase in crystallinity due to

• , transmission electron microscopy (TEM) images were obtained using a JEOL JEM-2200FS (200 kV), and elemental analysis was performed using EDS. The crystalline structure of the modified fabrics was determined by X-ray diffraction (XRD) in a Panalytical AERIS diffractometer using Cu Kα (λ = 1.54184 Å). The

Gold nanoparticle-decorated reduced graphene oxide as a highly effective catalyst for the selective α,β-dehydrogenation of N-alkyl-4-piperidones

• Brenda Flore Kenyim,
• Mihir Tzalis,
• Marilyn Kaul,
• Robert Oestreich,
• Aysenur Limon,
• Chancellin Pecheu Nkepdep and
• Christoph Janiak

Beilstein J. Nanotechnol. 2026, 17, 218–238, doi:10.3762/bjnano.17.15

• ) reflection of rGO [39]. The crystallite size of the gold nanoparticles (AuNPs) is determined by X-ray diffraction (XRD) analysis using the Scherrer equation (Equation 1) below. The shape factor k, often referred to as the Scherrer constant, is influenced by several factors, including the crystallites’ shape

Reduced graphene oxide paper electrode for lithium-ion cells – towards optimized thermal reduction

• Agata Pawłowska,
• Magdalena Baran,
• Stefan Marynowicz,
• Aleksandra Izabela Banasiak,
• Adrian Racki,
• Adrian Chlanda,
• Tymoteusz Ciuk,
• Marta Wolczko and
• Andrzej Budziak

Beilstein J. Nanotechnol. 2026, 17, 24–37, doi:10.3762/bjnano.17.3

• in the spectra. The data analysis was conducted using PHI MultiPak software (v.9.9.3); the background was removed using the Shirley method. Due to the geometry of the spectrometer, the information depth of this analysis can be estimated at about 5 nm. XRD X-ray diffraction was performed with

• information depth of XPS). It is worth noting that the samples T600 and T800 contain ca. 22% ketone-related bonds, which predispose them for electrochemical applications. The XRD results of rGO paper sheets are depicted in Figure 7. With increasing reduction temperature, the peak of the (002) plane, which

Improving magnetic properties of Mn- and Zn-doped core–shell iron oxide nanoparticles by tuning their size

• Dounia Louaguef,
• Ghouti Medjahdi,
• Sébastien Diliberto,
• Klaus M. Seemann,
• Thomas Gries,
• Joelle Bizeau,
• Damien Mertz,
• Eric Gaffet and
• Halima Alem

Beilstein J. Nanotechnol. 2025, 16, 2285–2295, doi:10.3762/bjnano.16.157

• collected by centrifugation (10,000 rpm, 10 min), washed twice with ethanol, and redispersed in toluene (10 mL) [7]. Characterization methods Structural characterization of the NPs was performed by X-ray diffractometry (XRD) measurements. X-ray diffraction patterns of NPs (Figure S1, Supporting Information

• -background sample holder. The latter was installed on a rotating spinner to allow the highest number of grains to be in diffraction position, and the XRD patterns were recorded at room temperature. The nanoparticles were annealed at 300 °C to remove all the traces of the solvent. in an Anton Paar 1200N oven

• [dT/dt]t=0 is the derivative function of the temperature at t = 0 (K·s−1). Results and Discussion X-ray diffraction analysis The XRD pattern (Supporting Information File 1, Figure S1) displays sharp and intense peaks characteristic of a well-crystallized material. The most intense peak is located at

Optical bio/chemical sensors for vitamin B₁₂ analysis in food and pharmaceuticals: state of the art, challenges, and future outlooks

• Seyed Mohammad Taghi Gharibzahedi and
• Zeynep Altintas

Beilstein J. Nanotechnol. 2025, 16, 2207–2244, doi:10.3762/bjnano.16.153

Rapid synthesis of highly monodisperse AgSbS₂ nanocrystals: unveiling multifaceted activities in cancer therapy, antibacterial strategies, and antioxidant defense

• Funda Ulusu,
• Adem Sarilmaz,
• Yakup Ulusu,
• Faruk Ozel and
• Mahmut Kus

Beilstein J. Nanotechnol. 2025, 16, 2105–2115, doi:10.3762/bjnano.16.145

• gram-negative (Escherichia coli) pathogenic bacteria were evaluated, along with their DPPH scavenging activities. The crystal structure of the synthesized NCs was elucidated through XRD analysis, revealing characteristic diffraction peaks corresponding to the (111), (200), (220), (311), and (222

• Structural and morphological characterization of AgSbS2 NCs The crystal structure and phase of AgSbS2 NCs were investigated by XRD analysis. The obtained diffraction pattern and a schematic representation of the crystal structure are given in Figure 1. As can be seen from the XRD pattern, five dominant peaks

• , indicating robust crystallization. Moreover, the presence of prominent peaks aligning with (220), (311), (420), and (511) planes confirmed alignment with XRD results. Furthermore, utilizing particle size distribution analysis, the crystallite size of average particles was estimated, as illustrated in the

Beyond the shell: exploring polymer–lipid interfaces in core–shell nanofibers to carry hyaluronic acid and β-caryophyllene

• Aline Tavares da Silva Barreto,
• Francisco Alexandrino-Júnior,
• Bráulio Soares Arcanjo,
• Paulo Henrique de Souza Picciani and
• Kattya Gyselle de Holanda e Silva

Beilstein J. Nanotechnol. 2025, 16, 2015–2033, doi:10.3762/bjnano.16.139

• nanofibers The thermal properties and crystallinity of NF-PLA (monolithic), NF-HA/PLA, and NF-HA+NE2/PLA nanofibers were analyzed using thermogravimetric analysis (TGA), X-ray diffraction (XRD), and differential scanning calorimetry (DSC). Thermal behavior and crystallinity of the nanofibers mats of βCp

• nanoemulsion-loaded PLA are displayed in Figure 8. The TGA and DTG curves provide insights into the thermal stability and decomposition behavior of the nanofibers [65]. At the same time, the DSC and XRD analyses complement the study by elucidating the crystallinity and thermal transitions of the samples

• glass transition temperature (Tg) of PLA and related to enthalpic relaxations in the amorphous regions. X-ray diffraction (XRD) analysis was also performed to compare the crystallinity and characteristic peaks of the produced nanofibers. Figure 9 presents the diffractograms of the NF-PLA, NF-HA/PLA, and

On the road to sustainability – application of metallic nanoparticles obtained by green synthesis in dentistry: a scoping review

• Lorena Pinheiro Vasconcelos Silva,
• Joice Catiane Soares Martins,
• Israel Luís Carvalho Diniz,
• Júlio Abreu Miranda,
• Danilo Rodrigues de Souza,
• Éverton do Nascimento Alencar,
• Moan Jéfter Fernandes Costa and
• Pedro Henrique Sette-de-Souza

Beilstein J. Nanotechnol. 2025, 16, 1851–1862, doi:10.3762/bjnano.16.128

• = 36), ultraviolet–visible spectroscopy (UV–vis, 34.69%; n = 35), and X-ray diffraction (XRD, 25.48%; n = 27). They are among the most commonly used techniques for the characterization of metallic nanoparticles synthesized via green routes due to their complementary abilities to elucidate key

• nanoparticle formation in real time by detecting surface plasmon resonance bands, which provide insight into particle size and distribution [57]. XRD offers detailed information on the crystalline structure and phase composition of the nanoparticles, confirming successful synthesis and purity [53]. Together

• potential cytotoxicity of these nanoparticles within the complex and dynamic oral environment [15][20]. A significant number of selected studies (n = 23; 24.1%) also failed to perform advanced physicochemical characterizations, such as FTIR, SEM, or XRD, which are essential for confirming nanoparticle

Piezoelectricity of layered double hydroxides: perspectives regarding piezocatalysis and nanogenerators

• Evgeniy S. Seliverstov,
• Evgeniya A. Tarasenko and
• Olga E. Lebedeva

Beilstein J. Nanotechnol. 2025, 16, 1812–1817, doi:10.3762/bjnano.16.124

• compensated for this deficiency. Second, the presented XRD data are limited to 2θ values below 40°, whereas LDHs characterization is conventionally extended to at least 80° in order to capture the full set of reflections characteristic of the LDHs. Consequently, the data provided do not offer sufficient

• XRD patterns lack the characteristic LDHs reflections, particularly the (003) and (006) peaks typically observed at 2θ values of around 10° and 20°, respectively. The absence of these reflections strongly suggests that the samples do not exhibit the structural features characteristic of LDHs. In

• successful synthesis of a hydrotalcite-like Ni/Fe-LDH. The reported cation ratio of Ni/Fe = 0.56 is unlikely to yield a stable LDH phase. Moreover, the presented XRD data begin only at 2θ values of 20°, thereby omitting the (003) reflection at approximately 10°, which is one of the most critical indicators

Prospects of nanotechnology and natural products for cancer and immunotherapy

• Jan Filipe Andrade Santos,
• Marcela Bernardes Brasileiro,
• Pamela Danielle Cavalcante Barreto,
• Ligiane Aranha Rocha and
• José Adão Carvalho Nascimento Júnior

Beilstein J. Nanotechnol. 2025, 16, 1644–1667, doi:10.3762/bjnano.16.116

• spectroscopy, TEM, DLS, X-ray diffraction (XRD), and Fourier-transform infrared (FTIR) spectroscopy, revealing a polygonal or oval morphology. To evaluate the antitumor effects, cytotoxicity assays, cellular uptake assays, apoptosis detection, ROS production, qRT-PCR, and Western blotting for gene and protein

Photocatalytic degradation of ofloxacin in water assisted by TiO₂ nanowires on carbon cloth: contributions of H₂O₂ addition and substrate absorbability

• Iram Hussain,
• Lisha Zhang,
• Zhizhen Ye and
• Jin-Ming Wu

Beilstein J. Nanotechnol. 2025, 16, 1567–1579, doi:10.3762/bjnano.16.111

• (HRTEM) conducted with a JEM-2100 microscope (Jeol, Tokyo, Japan). Energy-dispersive X-ray (EDX) elemental mapping was performed using the FESEM system to examine the distribution of Ti and O on the carbon cloth substrate. X-ray diffraction (XRD) measurements were conducted using a SmartLab

• the (101) crystal plane of anatase TiO2. Figure 2a shows the XRD patterns of hydrogen titanate nanowires precipitated on carbon cloth (CC/HTNW) and of the sample after air calcination (CC/NW-450 °C). Except for two broad XRD peaks arising from the carbon substrate, a peak located at ca. 8.5° can be

• °, respectively (JCPDS card no. 21-1272). The Raman spectra in Figure 2b are in accordance with the XRD analysis in phase composition. The CC/NW-450 °C spectrum displays prominent peaks at 146, 195, 287, 395, 516, and 637 cm−1, corresponding to the Eg, A1g, B1g, B1g, (A1g + B1g), and Eg modes of the anatase phase

Influence of laser beam profile on morphology and optical properties of silicon nanoparticles formed by laser ablation in liquid

• Natalie Tarasenka,
• Vladislav Kornev,
• Alena Nevar and
• Nikolai Tarasenko

Beilstein J. Nanotechnol. 2025, 16, 1533–1544, doi:10.3762/bjnano.16.108

• structure of the formed NPs were analyzed by means of ultraviolet–visible (UV–vis) spectroscopy, high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), X-ray diffraction (XRD), and Raman and photoluminescence (PL) spectroscopies. Particle size and morphology

Dendrimer-modified carbon nanotubes for the removal and recovery of heavy metal ions from water

• Thao Quynh Ngan Tran,
• Huu Trung Nguyen,
• Subodh Kumar and
• Xuan Thang Cao

Beilstein J. Nanotechnol. 2025, 16, 1522–1532, doi:10.3762/bjnano.16.107

• spectroscopy was specifically used to confirm the Diels–Alder reaction on the surface of CNTs, and other characterization techniques (SEM, EDX, XRD, TGA, and FTIR) were applied to confirm the successive growth of the dendrimers. Highly dendrimerized CNTs were found to be more effective in removing heavy metal

• described in the Experimental section. Finally, all materials were characterized by various other techniques which are discussed thoroughly in the following sections. XRD analysis of CNTs, CNTs-G0, CNTs-G1, CNTs-G2, CNTs-G3, and CNTs-G5 presented two prominent peaks at 2θ ≈ 26° and 43° (Figure 1b). The

• first peak, with higher intensity, corresponds to the (002) plane of graphite indicating a d-spacing (d002) of 0.34 nm, and the second peak ° is associated with the (100) planes of graphite. Both peaks are characteristic to the graphitic crystal lattice of CNTs [44]. Hence, XRD results indicate that the

Laser processing in liquids: insights into nanocolloid generation and thin film integration for energy, photonic, and sensing applications

• Akshana Parameswaran Sreekala,
• Pooja Raveendran Nair,
• Jithin Kundalam Kadavath,
• Bindu Krishnan,
• David Avellaneda Avellaneda,
• M. R. Anantharaman and
• Sadasivan Shaji

Beilstein J. Nanotechnol. 2025, 16, 1428–1498, doi:10.3762/bjnano.16.104

• ]. Figure 10d shows the X-ray diffraction (XRD) measurements of CdS nanoropes. A comparison of spin coating and drop casting for film fabrication on graphene paper was made using Ni/NiO NPs synthesized by LAL. Rutherford backscattering spectrometry measurements revealed that the homogeneity of the NPs was

• , which were clusters of many individual In2O3 NPs. A discrepancy was observed between the grain size measurements from XRD and AFM. This discrepancy arises because AFM directly visualizes the grains but does not account for structural defects, while XRD measurement determines the size of the defect-free

• . This method is widely utilized for forming thin films primarily for characterization purposes such as XRD, AFM, and photoluminescence (PL). However, apart from factors like strain of the substrate or temperature, if any applied to the substrate, no significant control over the film formation is

Photochemical synthesis of silver nanoprisms via green LED irradiation and evaluation of SERS activity

• Tuan Anh Mai-Ngoc,
• Nhi Kieu Vo,
• Cong Danh Nguyen,
• Thi Kim Xuan Nguyen and
• Thanh Sinh Do

Beilstein J. Nanotechnol. 2025, 16, 1417–1427, doi:10.3762/bjnano.16.103

• disappearance of the IPD peak of AgNPs in the UV–vis spectrum in Figure 2. After 72 h, TEM images showed exclusively AgNPrs, which were clearly visible and well defined, in agreement with the corresponding FESEM images. The XRD spectrum of AgNPrs after 72 h of LED irradiation (Figure 5) exhibited four distinct

• performed at an accelerating voltage of 100 kV. The structure of the AgNPrs was analyzed by X-ray diffraction (XRD) using a Bruker D8 Advance instrument equipped with a Cu Kα radiation source (40 kV, 40 mA) at a scanning rate of 4°/min. SERS measurements The SERS properties of the AgNPs and AgNPrs were

• different LED irradiation times. FESEM images of silver nanoparticles after (a) 6 h, (b) 24 h, and (c) 72 h of LED irradiation, and (d) histogram of their size distributions. TEM images of silver nanoparticles after 12, 24, 48, and 72 h of LED irradiation. XRD spectrum of AgNPrs after 72 hours of LED

Enhancing the photoelectrochemical performance of BiOI-derived BiVO₄ films by controlled-intensity current electrodeposition

• Huu Phuc Dang,
• Khanh Quang Nguyen,
• Nguyen Thi Mai Tho and
• Tran Le

Beilstein J. Nanotechnol. 2025, 16, 1289–1301, doi:10.3762/bjnano.16.94

• optimize the crystallinity, surface morphology, and electronic properties of the films. Subsequently, an electrochemical deposition method was developed to facilitate the uniform distribution of V2O5 among Bi–O–I flakes to homogeneously enhance the conversion reaction. The XRD pattern confirms the

• . Characteristics of materials X-ray diffraction (XRD, Bruker D8 Advance) and Raman spectroscopy (LabRAM Odyssey Semiconductor) were used to analyze the crystal structures of photoanodes. UV–vis absorption spectra were obtained using a Cary 60 spectrophotometer. X-ray photoelectron spectroscopy (XPS, VG ESCALAB250

• analysis (XRD) X-ray diffraction (XRD) measurements were conducted to investigate the crystal structures of the BiVO4 photoanodes under various deposition conditions (BiVO4(146), BiVO4(224), BiVO4(226), BiVO4(324), and BiVO4(326)), as shown Figure 1. The diffraction peaks of all photoanodes matched those

Functional bio-packaging enhanced with nanocellulose from rice straw and cinnamon essential oil Pickering emulsion for fruit preservation

• Tuyen B. Ly,
• Duong D. T. Nguyen,
• Hieu D. Nguyen,
• Yen T. H. Nguyen,
• Bup T. A. Bui,
• Kien A. Le and
• Phung K. Le

Beilstein J. Nanotechnol. 2025, 16, 1234–1245, doi:10.3762/bjnano.16.91

• the trapping effect of the polymer matrix on CEO [31]. XRD analysis (Figure 1c) shows that all biopackaging samples exhibit only large peaks at around 22° and 26°, which correspond to the (101) and (200) planes of the PVA structure [40]. It is to note that a slight peak shift to higher angles can be

• visibly lower. This may be related to the disruption of the crystalline structure of PVA after encapsulation of essential oil. For rBP and rCBP, which also contains NC, a small rise in the XRD signal can be seen at around 18°, which may be from the (110) plane of the Iβ cellulose crystalline phase [32

• diffraction (XRD) was performed using an Aeris Minerals Edition from PANalytical (UK) with Co radiation at 40 kV. Biopackaging samples were clipped on a 16 mm holder and the measurement was performed using a 1/8° diffraction slit. Mechanical strength was determined at room temperature using a Testometric X350

Crystalline and amorphous structure selectivity of ignoble high-entropy alloy nanoparticles during laser ablation in organic liquids is set by pulse duration

• Robert Stuckert,
• Felix Pohl,
• Oleg Prymak,
• Ulrich Schürmann,
• Christoph Rehbock,
• Lorenz Kienle and
• Stephan Barcikowski

Beilstein J. Nanotechnol. 2025, 16, 1141–1159, doi:10.3762/bjnano.16.84

• . Nanoparticle characterization is done by high-resolution transmission electron microscopy (HRTEM), energy-dispersive X-ray spectroscopy (STEM-EDX), selected-area electron diffraction (SAED), X-ray diffraction (XRD), and electron energy loss spectroscopy (EELS), complemented by tempering and laser post

• ). This is in good agreement with former ps-LAL studies by Waag et al. and also by Löffler et al., who reported comparable d-values of 2.08 Å (111), 1.81 Å (200), and 1.28 Å (220), determined by both SAED and XRD analysis [18][35]. Conversely, amorphous structures were found during ns-LAL (Figure 1D

• determine whether the structural information obtained from Figure 1 can also be reproduced for a larger fraction of the samples. Thus, XRD measurements were conducted on both ps- and ns-ablated HEA NPs. Figure 2 shows representative diffraction patterns of ps-ablated HEA NPs and ns-ablated HEA NPs (Figure

Influence of ion beam current on the structural, optical, and mechanical properties of TiO₂ coatings: ion beam-assisted vs conventional electron beam evaporation

• Agata Obstarczyk and
• Urszula Wawrzaszek

Beilstein J. Nanotechnol. 2025, 16, 1097–1112, doi:10.3762/bjnano.16.81

• h in ambient atmosphere with a heating ramp of 200 K·h−1, without the use of refrigerants. The effect of ion beam-assisted deposition and additional post-process modification of TiO2 coatings was investigated in detail. XRD measurements (PANalytical Empyrean PIXel3D), Raman spectroscopy (Thermo

• shows a comparison of XRD patterns of as-deposited and annealed TiO2 thin films prepared by EBE and IBAD. All thin films changed their structure from amorphous to anatase after annealing. Mergel et al. [30] and Lu et al. [3] showed that TiO2 films prepared by the EBE method, due to the low substrate

• ion gun current from 3 to 4 A caused a decrease in crystallite size from 34.7 to 30.8 nm after annealing (Figure 1d). The results of the structure analysis are shown in Table 2. Based on the XRD patterns, there is no evidence for the occurrence of TiO2 with the rutile phase, as its specific peaks were

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

• contour map of PG-CDs-AgNPs, which suggests the PL emission in the blue range. The crystalline nature of the PG-CDs-AgNPs was established from the X-ray diffraction pattern. Figure 2a displays an XRD pattern of the PG-CDs-AgNPs synthesized via PG-CDs mediated reduction. According to the XRD pattern, the

• phase composition could be classified according to the face-centered cubic structure of silver. The XRD spectrum showed that the formed PG-CDs-AgNPs were nanocrystals, as confirmed by the peaks at 2θ ≈ 28.20°, 32.66°, 38.61°, 46.60°, and 57.86°. These Bragg diffraction peaks are equivalent to the (110

• ), (111), (121), (200), and (311) planes, which can be seen in the face-centered cubic structure of silver [28][29]. The XRD analysis of the PG-CDs-AgNPs produced via PG-CDs mediated reduction resembles the crystalline phase as referenced by (JCPDS File No. 84-0713) data [30]. Furthermore, the XPS

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

• . nitric acid (HNO3), and ethanol were obtained from Duksan Pure Chemicals Co. Ltd. Graphite powder was supplied by Sigma-Aldrich. Instrumentation and characterization techniques The “PANalytical, X’Pert-PRO MPD” instrument (Cu Kα line; λ = 1.5406 Å) was utilized to carry out the XRD analyses of rGO and

• surfaces through substantial interactions. To confirm the formation of the ternary NC, the XRD analysis of the GVF was performed. As shown in Figure 3a, the characteristic peaks of GVF corresponding to the α phase of Fe2O3 and VO2, along with the signature peak of rGO were observed. To be specific, the

• oxide while oxidizing ferrocene alongside Fe3O4, which is formed as a major iron oxide component during the MW irradiation process. Nevertheless, the XRD pattern of the GV demonstrates the characteristic peaks of VO2, according to the JCPDS card no. 01-072-0514 [32]. Specifically, the peaks at the

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

• potential regarding industrial application. Results and Discussion Crystal structure and phase of the as-synthesized electrodes were verified by X-ray diffraction (XRD) measurements with 2θ ranging from 20° to 80°. Figure 1 displays the XRD patterns of SS, Ni/NiO/SS-5, Ni/NiO/SS-10, Ni/NiO/SS-15, and Ni/NiO

• importantly, the XRD image of Ni/NiO/SS-10 presents peaks at 37.20°, 43.21°, and 62.91°, which correspond to the (111), (200), and (220) planes of the NiO phase (PDF 00-004-0835) [34][35]. Meanwhile, the peak of the Ni metal phase still appeared in the Ni/NiO/SS-10 sample, proving the co-existence of metal

• molecules. In contrast, at high O2 flow rates (15 and 20 sccm), NiO is produced with a large ratio of NiO/Ni, which is indicated by XRD peaks of NiO with high intensity. A high NiO concentration prefers the dissociative adsorption of water molecules, while hydrogen desorption is limited. Besides, the O

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

• by XRD peaks. The microsegregation of Mn can be due to a phenomenon consistent with observations in other CCAs, often attributed to the elastic strain energy [58] or due to the presence of oxygen on the surface forming MnO [59]. As expected, the SEM images and EDX elemental mapping of the polished Al

• ; thus, even small absolute deviations at low concentrations can result in disproportionately high percentage variance. XRD analysis revealed the formation of multiphase alloys, with identifiable peaks corresponding to Al-deficient and Al-rich phases. The Al-deficient phase, Ni2Mn2Si, was found to have a