The role of biochar in combating microplastic pollution: a bibliometric analysis in environmental contexts

• Tuan Minh Truong Dang,
• Thao Thu Thi Huynh,
• Guo-Ping Chang-Chien and
• Ha Manh Bui

Beilstein J. Nanotechnol. 2025, 16, 1401–1416, doi:10.3762/bjnano.16.102

• utilizing silica sand and corn straw biochar for 10 µm PS particles [38]. For particles larger than 75 µm, mechanisms such as hydrogen bonding and hydrophobic interactions dominate, while smaller particles (<75 µm) are removed through π–π interactions between the benzene rings of PS and biochar surfaces

• , surface adsorption, hydrogen bonding, and surface complexation [67]. These findings highlight the potential of diverse biochar configurations for efficient MP removal under various conditions. Recent studies on biochar derived from coffee waste modified with amino-functionalized zeolite/phosphoric acid

Synthesis and antibacterial properties of nanosilver-modified cellulose triacetate membranes for seawater desalination

• Lei Wang,
• Shizhe Li,
• Kexin Xu,
• Wenjun Li,
• Ying Li and
• Gang Liu

Beilstein J. Nanotechnol. 2025, 16, 1380–1391, doi:10.3762/bjnano.16.100

• the C/O ratio of the PCTA film. This decrease in the C/O ratio is likely attributed to hydrogen bonding interactions between the –OH groups in Ag(NH3)2OH and the PDA layer. These interactions enhance the oxygen content relative to carbon, thereby reducing the C/O ratio. Collectively, these results

• primary factors. First, the abundant –OH and amino groups in PDA promote hydrogen bonding with water molecules, thereby enhancing the hydrophilicity of the membrane surface. This effect is further amplified by the dopamine coating, which not only increases the membrane thickness but also augments its

Ferroptosis induction by engineered liposomes for enhanced tumor therapy

• Alireza Ghasempour,
• Mohammad Amin Tokallou,
• Mohammad Reza Naderi Allaf,
• Mohsen Moradi,
• Hamideh Dehghan,
• Mahsa Sedighi,
• Mohammad-Ali Shahbazi and
• Fahimeh Lavi Arab

Beilstein J. Nanotechnol. 2025, 16, 1325–1349, doi:10.3762/bjnano.16.97

• reactions of hydrogen peroxides in LIPs under the name of the Fenton reaction [59][60]. In addition, iron regulatory proteins (IRPs) such as IRP1 and IRP2 regulate the expression of DMT1 and TfR1, ferritin, and FPN1 by binding to the mRNA of iron response elements (IREs). Under iron deficiency conditions

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

• renewable and sustainable energy sources has become a top priority in science and technology [1][2]. Photoelectrochemical (PEC) water-splitting systems hold significant promises for converting abundant solar energy into chemical fuels, such as hydrogen [3][4]. However, their widespread application is still

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

• matrix properties, including tensile strength, elasticity, and thermal stability, due to its high surface area, hydroxy groups forming hydrogen bonds, and excellent dispersion within the matrix [20][21]. This improvement is attributed to interaction between hydroxy groups in NC and PVA, effectively

• ), 2900 cm−1 (C–H stretching), and 1420 cm−1 (C–H bending), which align with the chemical structure of PVA [22][24]. When NC was added, the O–H stretching peak became broader and shifted slightly to 3315 cm−1, which can be attributed to the hydrogen bonding between PVA and NC [24]. For rCBP, additional

• characteristic peaks confirm the presence of functional groups associated with PE-CEO and polymer interactions. The broad absorption band around 3300 cm−1 corresponds to O–H stretching vibrations, indicating hydrogen bonding between the biopolymer and PE-CEO components [24]. The intensity of the peaks at 1730 cm

Hydrogels and nanogels: effectiveness in dermal applications

• Jéssica da Cruz Ludwig,
• Diana Fortkamp Grigoletto,
• Daniele Fernanda Renzi,
• Wolf-Rainer Abraham,
• Daniel de Paula and
• Najeh Maissar Khalil

Beilstein J. Nanotechnol. 2025, 16, 1216–1233, doi:10.3762/bjnano.16.90

• - or intermolecularly cross-linked by chemical bonding or physical interaction (Figure 1). Physical cross-linking is performed using interactions other than the covalent bond, such as hydrogen bonding or ionic interaction. Physical cross-links can be reversibly dissociated and recombined under specific

• through the oxidative coupling of catechol groups using a hydrogen peroxide/horseradish peroxidase (H2O2/HRP) catalytic system [41]. The addition of the antibiotic doxycycline provided the hydrogels with antimicrobial activity to treat infected full-thickness defect wounds. Flexible films composed of

Chitosan nanocomposite containing rotenoids: an alternative bioinsecticidal approach for the management of Aedes aegypti

• Maria A. A. Bertonceli,
• Vitor D. C. Cristo,
• Ivo J. Vieira,
• Francisco J. A. Lemos,
• Arnoldo R. Façanha,
• Raimundo Braz-Filho,
• Gustavo V. T. Batista,
• Luis G. M. Basso,
• Sérgio H. Seabra,
• Thalya S. R. Nogueira,
• Felipe F. Moreira,
• Arícia L. E. M. Assis,
• Antônia E. A. Oliveira and
• Kátia V. S. Fernandes

Beilstein J. Nanotechnol. 2025, 16, 1197–1208, doi:10.3762/bjnano.16.88

• with smaller size, improved polydispersity index, and enhanced stability, evidenced by a higher zeta potential. FTIR analysis confirmed rotenoid incorporation into the nanocomposite and suggested hydrogen bonding or potential covalent interaction with chitosan functional groups. Bioassays demonstrated

• nanocomposite. Additionally, a noticeable reduction in the intensity of the amide-related bands in CS/TPP-β-CD-rot suggests possible interactions – such as hydrogen bonding or covalent bonding – between rotenoids and the chitosan matrix. These spectral features confirm the successful incorporation of rotenoids

• suggest the occurrence of hydrogen bonding or potential covalent interaction with functional groups of chitosan, which may help explain the improved stability of the formulation. The high efficacy of the nanocomposite was demonstrated by bioassays which revealed an LC50 of 91.7 ppm, equivalent to a 23.6

Single-layer graphene oxide film grown on α-Al₂O₃(0001) for use as an adsorbent

• Shiro Entani,
• Mitsunori Honda,
• Masaru Takizawa and
• Makoto Kohda

Beilstein J. Nanotechnol. 2025, 16, 1082–1087, doi:10.3762/bjnano.16.79

• therefore be surmised that the ability of SLGO for the Cs adsorption is significantly decreased in strong acid aqueous solutions due to the suppression of hydrogen dissociation from oxygen functional groups in SLGO. It is claimed that the pH value of the aqueous solution should be maintained at neutrality

• groups. It was also indicated that SLGO shows the high Cs adsorption capacity of 650–850 mg·g−1 in the 1.0 mol/L-Cs aqueous solution. SLGO adsorbs Cs via hydrogen exchange, resulting in an accelerated adsorption rate and a higher weight adsorption capacity compared to existing adsorbents, including

Piezoelectricity of hexagonal boron nitrides improves bone tissue generation as tested on osteoblasts

• Sevin Adiguzel,
• Nilay Cicek,
• Zehra Cobandede,
• Feray B. Misirlioglu,
• Hulya Yilmaz and
• Mustafa Culha

Beilstein J. Nanotechnol. 2025, 16, 1068–1081, doi:10.3762/bjnano.16.78

• ’-dicfloroflurescin diacetate (DCFDA) (D6883-50MG; Mw: 487.29 g/mol) probe, chosen specifically for its ability to detect the presence of cellular hydrogen peroxide (H2O2) in HOb cells following treatment with NMs and US exposure. First, the cells were seeded in 96-well plates at 104 cells/well and incubated for 24 h

Soft materials nanoarchitectonics: liquid crystals, polymers, gels, biomaterials, and others

• Katsuhiko Ariga

Beilstein J. Nanotechnol. 2025, 16, 1025–1067, doi:10.3762/bjnano.16.77

• colleagues have reported the rapid and reversible microactuation of liquid crystals based on the surface catalysis of H₂ and O₂ at room temperature on a late transition metal alloy film (Figure 7) [242]. The reaction of gaseous hydrogen and oxygen, catalyzed by a Pd/Au surface, is employed to rapidly and

• reversibly alter the orientation of liquid crystals at room temperature. The dissociative adsorption of hydrogen on the palladium/gold film results in the reduction of pre-adsorbed oxygen and the generation of adsorbed hydrogen. This process causes the nitrile-containing liquid crystal to undergo a change in

• alignment, from vertical to planar. Subsequently, exposure to oxygen oxidizes the adsorbed hydrogen, reforming the adsorbed oxygen on the Pd/Au surface and restoring the liquid crystal to its initial alignment. The motion of the liquid crystal can be controlled by exposure to gas mixtures of H2 and O2 with

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

• first 2 ps after laser excitation, with the corresponding ΔPDF result presented in Figure 5D–F. After laser excitation, ΔPDF clearly shows pair density reductions at radial distances corresponding to O···H hydrogen bond and the first three O···O coordination shells of neutral water. For better

Tendency in tip polarity changes in non-contact atomic force microscopy imaging on a fluorite surface

• Bob Kyeyune,
• Philipp Rahe and
• Michael Reichling

Beilstein J. Nanotechnol. 2025, 16, 944–950, doi:10.3762/bjnano.16.72

• . This particularly concerns the transfer of surface species to the tip when the tip is subject to intentional or unintentional contact with the surface. Furthermore, ambient species like native oxides, hydrogen ions, or residual water can adsorb on the tip apex during scanning. Additionally, the

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

• applications. Experimental Materials Vanadium (V) oxide (V2O5) powder and ferrocene were purchased from Alfa Aesar. The other chemicals used for the synthesis of graphite oxide, such as conc. sulfuric acid (H2SO4), hydrogen peroxide (H2O2), conc. hydrochloric acid (HCl), potassium chlorate (KClO3), conc

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

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

• transformation of bare and nickel-coated polycrystalline diamond films under high-vacuum annealing The PCD film was produced by plasma-enhanced chemical vapor deposition (PE CVD) using acetone (CH3)2CO, hydrogen, and air as the precursor gases for the plasma [37]. The film consists of crystallites with

• 1150 °C [27] and for the (111) face of SCD annealed at 1250 °C [15]. Conclusion Polycrystalline diamond films with mixed grain orientations were synthesized by the PE CVD method from hydrogen/acetone/air plasma and coated with a 40 nm thick nickel layer. In situ XPS and NEXAFS data revealed the

• hydrogen/acetone/air mixture. The deposition parameters were typical of those previously employed for an “Astex” system (2.45 GHz, 4.5 kW): a pressure of 115 Torr, hydrogen, acetone, and air flow rates of 500, 18, and 0.3 sccm, respectively, and substrate temperature in the range of 940–980 °C [28][37

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

• soft X-ray range. Reaction cells with an ultrathin membrane that confines the gas in a narrow region extremely close to the sample surface were applied to the study of Cu- and Fe-doped cerium oxide films during thermal treatments in hydrogen at ambient pressure [58]. The combination of ambient pressure

• XANES and gas chromatography was employed to correlate in real time the changes of the chemical state of Cu, Fe, and Ce cations with oxygen vacancy and water formation during thermal treatments in hydrogen at ambient pressure [58]. The pure ceria film, in the Ce4+ oxidation state with a dominant Ce L3

• structure of CeO2 and in enabling a more efficient hydrogen production at lower temperatures, as compared to the pure oxide [59]. Dynamic studies of photoexcited states The advent of X-ray free electron lasers has opened entirely new research pathways in the field of oxides for energy applications. 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

• temperature of 873 K for 30 min. Heating the raw film in a hydrogen atmosphere at 1073 K removes excess sulfur and other contaminations from the film surface. In the final step, a thin PyC film synthesized by chemical vapor deposition (CVD) technique is placed on the surface of the cleaned MoS2 film using the

• . The scanning electron microscopy (SEM) images of the surface of raw MoS2 film, hydrogen-annealed film, and PyC film are compared in Figure 1b,c,e. The raw MoS2 film covers the entire area of the substrate and contains polysulfide nanoparticles on the surface (Figure 1b). These nanoparticles are absent

• on the surface of the MoS2 film annealed in a hydrogen atmosphere (Figure 1c). An attempt to measure the cross section of this film did not yield a contrast image because of the charging effect. Therefore, to estimate the thickness of the studied film, we used a thicker MoS2 film synthesized with a

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

• 700000, Vietnam 10.3762/bjnano.16.63 Abstract The advancement of affordable, ultrastable, and efficient electrode materials for basic hydrogen evolution reaction (HER) plays a crucial role in industrial hydrogen manufacture, resolving problems caused by carbon dioxide emissions. Ni-based

• electrocatalysts have been well accepted as potential candidates to replace Pt-based electrocatalysts for HER because of their suitable Gibbs free hydrogen adsorption energy, good intrinsic catalytic properties, and high stability. However, solution-based synthetic approaches can be highly harmful to human beings

• operation. The high efficiency is attributed to the collaborative work of the NiO and Ni metal components and the good electrical conductivity of SS, which is advantageous for dissociative adsorption of water molecules, recombination of hydrogen atoms, and improvement of electronic/ionic motion. This work

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

• deoxyribonucleic acid (DNA) [1]. Water molecules and their hydrogen bonding network function as lubricants for biomolecular dynamics. Recent scientific works have analyzed the important role of hydration shells on DNA, proteins, and phospholipid membranes [2][3][4]. The first hydration shell (about 3.5 Å) at the

• interface of biomolecules has considerably slower dynamics than water molecules in the bulk. Besides, the first water layer on the interface is responsible for hydration forces between biomolecular structures [5]. The rearrangement of water molecules through hydrogen bonding on hydrated surfaces generates

• interactions, a type of van der Waals force, for supramolecular attraction [9]. Particularly, graphene sheets with a large surface area and π-conjugated network are likely to stack together through hydrophobic agglomeration and π–π interaction. Although π–π interactions are generally weaker than hydrogen

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

• within the range of 3600–3200 cm−1, with weaker bands in the vicinity of 3000–2800 cm−1. The former bands originate from stretching vibrations of hydroxyl groups, encompassing both covalent (cb) and hydrogen bonds (hb), as well as aliphatic CHx groups, where x = 1,2 [48][49][50][51][52][53][54]. The

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

• , hydrogen bonding, and CH–π interactions, with surface complexation between Ca2+ and TCs being dominant. Batch adsorption experiments conducted to examine the factors influencing adsorption capacity revealed that PGC achieved up to 70% TC removal efficiency at an adsorbent dosage of 40 mg and an initial TC

• spectrum, the sample matrix, and the radiation intensity. Activated carbon is a conventional approach [10][11], however, a major drawback of activated carbon is its incomplete recovery after adsorption. Because adsorption primarily relies on physical interactions such as hydrogen bonding interactions

• + ions and TC for adsorption sites, along with the ionization of hydroxy groups and the subsequent formation of hydrogen bonds with TC molecules, results in a rapid increase in adsorption capacity. Beyond pH 7, adsorption capacity decreases sharply as TC transforms into negatively charged anions, causing

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

• with trimethylindium and phosphine precursors. Axial p–n junctions were created by switching from diethylzinc to hydrogen sulfide as dopant precursors halfway during nanowire growth. More growth details can be found in references [18][30]. After growth, nanowires were mechanically transferred onto

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

• include superoxide radicals, hydroxyl radicals, and hydrogen peroxide, are natural byproducts of the oxidative metabolism. Mammalian cells maintain balanced ROS levels for homeostasis and cellular proliferation. However, excess ROS creates an electron imbalance that triggers continuous electron transfer

• reactions, leading to oxidative stress [17]. Studies have shown that TA exhibits significant antioxidant properties by suppressing hydroxyl radical formation and neutralizing both superoxide anion radicals and hydrogen peroxide. However, its antioxidant efficacy is concentration-dependent. While it shows

• hydrogen bonds and coat various surfaces [23]. Our results are compatible with a model where adsorbed TA molecules create a partially active antioxidant layer on the FLG surface, maintaining bioactivity while enhancing graphene colloid stability. Unfortunately, the zeta potential of the FLG–TA material in

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

• exhibited less sharp peaks than APT because of a reduction of the polymer crystallinity. Also, the interaction of polymeric content with APT via hydrogen bonding converts the crystalline form of APT into an amorphous form [20]. TGA and DSC studies Thermogravimetric analysis showed that the thermal

A formulation containing Cymbopogon flexuosus essential oil: improvement of biochemical parameters and oxidative stress in diabetic rats

• Ailton Santos Sena-Júnior,
• Cleverton Nascimento Santana Andrade,
• Pedro Henrique Macedo Moura,
• Jocsã Hémany Cândido dos Santos,
• Cauãn Torres Trancoso,
• Eloia Emanuelly Dias Silva,
• Deise Maria Rego Rodrigues Silva,
• Ênio Pereira Telles,
• Luiz André Santos Silva,
• Isabella Lima Dantas Teles,
• Sara Fernanda Mota de Almeida,
• Daniel Alves de Souza,
• Jileno Ferreira Santos,
• Felipe José Aidar Martins,
• Ana Mara de Oliveira e Silva,
• Sandra Lauton-Santos,
• Guilherme Rodolfo Souza de Araujo,
• Cristiane Bani Correa,
• Rogéria De Souza Nunes,
• Lysandro Pinto Borges and
• Ana Amélia Moreira Lira

Beilstein J. Nanotechnol. 2025, 16, 617–636, doi:10.3762/bjnano.16.48

• difference between the DPPH method and the others can be explained by the different antioxidant mechanisms. DPPH is more useful in apolar surroundings and mainly involves hydrogen donation. ABTS is a method that includes electron and hydrogen donation, in addition to being useful for both nonpolar and polar

• surroundings, covering a wider spectrum of compounds [34]. Finally, FRAP evaluates the interaction of the compounds with a ferric complex (TPTZ-Fe3+), with hydrogen donation and reduction effects (TPTZ-Fe2+). Another point to be raised is the saturation of the system. In the DPPH test, the antioxidant activity