Ambient pressure XPS at MAX IV

• Mattia Scardamaglia,
• Ulrike Küst,
• Alexander Klyushin,
• Rosemary Jones,
• Jan Knudsen,
• Robert Temperton,
• Andrey Shavorskiy and
• Esko Kokkonen

Beilstein J. Nanotechnol. 2025, 16, 1677–1694, doi:10.3762/bjnano.16.118

• electrochemical (EC) cell; a liquid microjet is also used to a smaller extent. In the EC setup, a three-electrode setup is immersed and retracted from a beaker of liquid electrolyte, forming a thin, electrochemically active meniscus on the working electrode that can be probed using APXPS or XAS, see Figure 1

• some case-studies that use the dip-and-pull method available at HIPPIE. The measurements can be performed in situ or operando. In the first, easier, case, the electrochemical reaction is performed with the sample immersed in the electrolyte, then all potentials are dropped, and the sample is pulled for

• APXPS measurements at the vapor pressure of the electrolyte. This method is used mostly for corrosion studies. In the second case, the potential is held during the XPS analysis, and a thin electrolyte film (meniscus) is maintained at the interface of the working electrode (WE) during measurement. This

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

• × 2 cm in size) was taken as working electrode, the Pt electrode as counter electrode (3 cm × 3 cm in size), and a saturated calomel electrode as reference electrode; the electrolyte is 0.5 mol/L aqueous Na2SO4 solution. No bias potential was applied for the photocurrent evaluations. Results and

• effective degradations of OFL with a high initial concentration, say, 100 ppm and 200 ppm. The photocurrent response in Figure 7b increases with increasing H2O2 concentrations in the 0.5 M Na2SO4 electrolyte, because H2O2 acts as an electron acceptor, facilitating charge separation and the generation of ROS

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

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

• electrochemical workstation (CHI650E, CH Instruments, USA). The three electrodes included a working electrode (BiVO4 photoelectrode, 1.0 × 1.0 cm2), counter electrode (Pt plate), and reference electrode (Ag/AgCl). The electrolyte used in the photoelectrochemical measurements was 0.50 M Na2SO4 (pH 5.6), and the

• electrolyte (Figure 6c). The photocurrent density initially peaked at approximately 1.6 mA·cm−2 and stabilized quickly at ≈1.2 mA·cm−2, maintaining this value consistently for 600 min (10 h) of operation. This stable behavior demonstrates the excellent PEC durability of the BiVO4(326) photoanode and confirms

Better together: biomimetic nanomedicines for high performance tumor therapy

• Imran Shair Mohammad,
• Gizem Kursunluoglu,
• Anup Kumar Patel,
• Hafiz Muhammad Ishaq,
• Cansu Umran Tunc,
• Dilek Kanarya,
• Mubashar Rehman,
• Omer Aydin and
• Yin Lifang

Beilstein J. Nanotechnol. 2025, 16, 1246–1276, doi:10.3762/bjnano.16.92

• essential to maintain hemostasis by binding various biomolecules circulating in blood. They not only maintain the electrolyte and osmotic pressure but also deliver a variety of molecules across the body [73][74]. Peptides possess different functional groups on their surface that can act as a template for

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

• . The following examples illustrate the potential of nanoarchitectonics based on plastic crystals. Solid electrolytes can be used safely in secondary magnesium batteries but show lower ionic conductivity compared to conventional liquid electrolytes. A class of solid electrolyte known as organic ionic

• crystals. The aim of this research was to create a new solid electrolyte made of organic ionic plastic crystals with magnesium salt incorporated for the use in next-generation secondary batteries (Figure 9) [248]. A series of organic ionic plastic crystal/Mg salt composites were prepared with varying

• as new organic solid electrolyte materials. However, their practical application remains elusive due to insufficient mechanical strength and ionic conductivity. Yoshizawa-Fujita and colleagues introduced a lithium salt, lithium bis(fluorosulfonyl)amide, and an inorganic solid electrolyte

Shape, membrane morphology, and morphodynamic response of metabolically active human mitochondria revealed by scanning ion conductance microscopy

• Eric Lieberwirth,
• Anja Schaeper,
• Regina Lange,
• Ingo Barke,
• Simone Baltrusch and
• Sylvia Speller

Beilstein J. Nanotechnol. 2025, 16, 951–967, doi:10.3762/bjnano.16.73

• nanopipette with a sub-micrometer aperture, which is brought near the sample surface via piezo actuators in an electrolyte bath. A voltage applied between two Ag/AgCl electrodes, one in the pipette and the other in the bath, generates an ion current. If the pipette approaches the sample, the ionic current

• as quantity to be measured by a feedback loop. This current is generated by applying a voltage between two Ag/AgCl electrodes, one located in an electrolyte bath containing the non-conductive sample and the other within the nanopipette (Supporting Information File 1, Section S7, Figure S20). When the

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

• energy demand. Therefore, a notable research focus has been given to advancements in renewable energy storage systems. Secondary batteries and supercapacitors are promising alternatives for energy storage applications [1][2]. Through the electrostatic polarization of electrolyte solutions, supercapacitor

• distribution of PG-CDs-AgNPs was responsible for the enhanced surface area [35]. The pore size distribution plot of PG-CDs-AgNPs suggests the mesoporous characteristics (Supporting Information File 1, Figure S1b), which, via the diffusion of electrolyte ions, is highly efficient for electrochemical charge

• . Electrochemical properties of the synthesized electrode Three-electrode analysis Firstly, utilizing a three-electrode configuration in an aqueous electrolyte (1 M aqueous KCl), the electrochemical properties (capacitive characteristics, charge transportation, and charging/discharging) of PG-CDs-AgNPs were

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

• heterostructures [32] demonstrated an advantage in studying the interaction of lithium with carbon and other elements of the materials. It should be noted that anode materials with alkali ions introduced during electrochemical reactions in SIBs are difficult to study because of the presence of electrolyte

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

• ohmic resistance of the phosphate-buffered saline (PBS) electrolyte solution. The circuit is connected in series to the parallel combination of a capacitor (Cdl) representing the double layer capacitance of the electrode–solution interphase and a resistor (Rct) accounting for the faradaic charge

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

• resistances (R) and capacitances at all interfaces and the electrolyte. In our EIS measurements, the most relevant circuit element is the charge transfer resistance (Rct) between the gold nanoparticles and the graphitic carbon support, measured at open circuit potential so that electrochemical reactions do

• not obfuscate the electrical characteristics [2]. The other circuit elements are the electrolyte resistance (Rel, the x-axis intercept), which was small because of the high ionic conductivity of the 1.0 M aqueous KHCO3 electrolyte, the Warburg impedance (Zw) due to mass transport limitations of the

• redox species to the electrode, and the ubiquitous capacitance at the interface between the electrode and the electrolyte. This capacitance is non-ideal at the porous, non-flat gold nanoparticle–carbon fiber paper electrode, necessitating incorporation of a constant phase element. In a Nyquist plot

Characterization of ZnO nanoparticles synthesized using probiotic Lactiplantibacillus plantarum GP258

• Prashantkumar Siddappa Chakra,
• Aishwarya Banakar,
• Shriram Narayan Puranik,
• Vishwas Kaveeshwar,
• C. R. Ravikumar and
• Devaraja Gayathri

Beilstein J. Nanotechnol. 2025, 16, 78–89, doi:10.3762/bjnano.16.8

• (CV) and electrochemical impedance spectroscopy (EIS) were carried out at room temperature using a three-electrode cell with 0.1 M KCl electrolyte. The ZnO NP electrode was measured at scan rates from 10 to 50 mV/s. The measurements revealed reversibility and electrode load efficiency along with

• reduction currents and increased peak oxidation, indicating rapid electron transport at the contacts between the electrolyte and electrode. Pseudo-capacitive behavior was observed in both electrolytes, where ionic conductivity influenced capacitance [17][18]. The addition of dextrose increased the redox

Electrochemical nanostructured CuBTC/FeBTC MOF composite sensor for enrofloxacin detection

• Thi Kim Ngan Nguyen,
• Tien Dat Doan,
• Huy Hieu Luu,
• Hoang Anh Nguyen,
• Thi Thu Ha Vu,
• Quang Hai Tran,
• Ha Tran Nguyen,
• Thanh Binh Dang,
• Thi Hai Yen Pham and
• Mai Ha Hoang

Beilstein J. Nanotechnol. 2024, 15, 1522–1535, doi:10.3762/bjnano.15.120

• current of approximately 6 µA. Therefore, the optimal weight percentages of 5% CuBTC and 5% FeBTC were chosen for electrode fabrication in the subsequent experiments. Effect of supporting electrolyte on the ENR signal The electrolyte plays a crucial role in the oxidation reaction of ENR. Four electrolytes

• peak in PBS is higher, sharper, and more symmetric compared to that in BR. Therefore, PBS was selected as the optimal electrolyte for subsequent experiments. Effect of pH of the electrolyte on the ENR signal The effect of pH on the ENR signal was investigated by performing SW-AdSV using the (Cu)(Fe)BTC

• K2HPO4 in double-distilled water. The pH of the solution used for the optimization of electrolyte solution was changed from 6.0 to 9.0 by controlling the amount of these phosphate salts. Enrofloxacin stock solution was prepared by dissolving ENR powder in double-distilled water. The ENR solutions with

Effect of wavelength and liquid on formation of Ag, Au, Ag/Au nanoparticles via picosecond laser ablation and SERS-based detection of DMMP

• Sree Satya Bharati Moram,
• Chandu Byram and
• Venugopal Rao Soma

Beilstein J. Nanotechnol. 2024, 15, 1054–1069, doi:10.3762/bjnano.15.86

• simulants was observed at a 325 nm Raman excitation. Our findings reveal that a higher ablation yield was observed at IR irradiation than those obtained at the other wavelengths. A size decrease of the NPs was noticed by changing the liquid environment to an electrolyte. These findings have significant

• . Stability tests revealed that NPs in the electrolyte (NaCl) solution displayed a quicker decline in SERS signal than those obtained in DW, despite satisfactory initial signal strengths. However, gold NPs in DW demonstrated optimal long-term stability, maintaining uniform SERS intensities over 60 days

• the generation of the NPs. The presence of electrostatic repulsion among charged NPs generated in an electrolyte solution reduces the average size of the NPs. Rehbock et al. [21] pointed out the size reduction in Au NPs from 30 nm at 3 µM to 7 nm at 500 µM in the presence of aqueous NaCl solution

Intermixing of MoS₂ and WS₂ photocatalysts toward methylene blue photodegradation

• Maryam Al Qaydi,
• Nitul S. Rajput,
• Michael Lejeune,
• Abdellatif Bouchalkha,
• Mimoun El Marssi,
• Steevy Cordette,
• Chaouki Kasmi and
• Mustapha Jouiad

Beilstein J. Nanotechnol. 2024, 15, 817–829, doi:10.3762/bjnano.15.68

• cost-effective technology. By harnessing impinging photons, the photocatalytic degradation of pollutants takes place at the interface between the photocatalyst surface and the MB-contaminated electrolyte. The photon energy is the driving force for breaking down the MB compound leading to its removal [9

Electrospun polysuccinimide scaffolds containing different salts as potential wound dressing material

• Veronika Pálos,
• Krisztina S. Nagy,
• Rita Pázmány,
• Krisztina Juriga-Tóth,
• Bálint Budavári,
• Judit Domokos,
• Dóra Szabó,
• Ákos Zsembery and
• Angela Jedlovszky-Hajdu

Beilstein J. Nanotechnol. 2024, 15, 781–796, doi:10.3762/bjnano.15.65

• increased, which was also observed by Sim and collaborators in the case of polymer electrolyte films containing LiCF3SO3 [51]. At 1634 cm−1, rising peaks also appeared as the concentration of salts increased. It was presumably the peak corresponding to bending vibration of water, H–O–H (Supporting

Simultaneous electrochemical determination of uric acid and hypoxanthine at a TiO₂/graphene quantum dot-modified electrode

• Vu Ngoc Hoang,
• Dang Thi Ngoc Hoa,
• Nguyen Quang Man,
• Le Vu Truong Son,
• Le Van Thanh Son,
• Vo Thang Nguyen,
• Le Thi Hong Phong,
• Ly Hoang Diem,
• Kieu Chan Ly,
• Ho Sy Thang and
• Dinh Quang Khieu

Beilstein J. Nanotechnol. 2024, 15, 719–732, doi:10.3762/bjnano.15.60

• electrode (GCE, 3 mm diameter), a platinum wire auxiliary electrode, and a Ag/AgCl reference electrode was used. Electrolyte solutions were prepared using doubly distilled water. Britton–Robinson (BR) buffer solutions with pH between 2 and 6 were prepared by mixing boric acid solution, phosphoric acid

Cholesterol nanoarchaeosomes for alendronate targeted delivery as an anti-endothelial dysfunction agent

• Horacio Emanuel Jerez,
• Yamila Roxana Simioni,
• Kajal Ghosal,
• Maria Jose Morilla and
• Eder Lilia Romero

Beilstein J. Nanotechnol. 2024, 15, 517–534, doi:10.3762/bjnano.15.46

• tract, osteonecrosis of the jaws (BRONJ), and serious musculoskeletal pain and cardiovascular risks [13][59][60]. Its intravenous delivery poses the risk of nephrotoxicity, fever, flu symptoms, and electrolyte imbalance [61]. Together, these disadvantages complicate its exploitation as an anti

In situ optical sub-wavelength thickness control of porous anodic aluminum oxide

• Aleksandrs Dutovs,
• Raimonds Popļausks,
• Oskars Putāns,
• Vladislavs Perkanuks,
• Aušrinė Jurkevičiūtė,
• Tomas Tamulevičius,
• Uldis Malinovskis,
• Iryna Olyshevets,
• Donats Erts and
• Juris Prikulis

Beilstein J. Nanotechnol. 2024, 15, 126–133, doi:10.3762/bjnano.15.12

• . Automation software was designed to terminate the anodization process at preset PAAO thickness values. While the concept was illustrated using the widely used method of anodization in a 0.3 M oxalic acid electrolyte with a 40 V potential, it can be readily customized for other protocols. PAAO layers with

• heating, electrolyte flow [19], arrangement of the electrodes, and crystallographic orientation of the aluminum substrate [20]. In this work, we continuously recorded the reflectance spectra from a PAAO-coated aluminum surface during anodization. In a similar reflective interference spectroscopy (RIfS

• -center distance, and ≈30 nm pore diameter corresponded well to the expected results of using anodization in 0.3 M oxalic acid electrolyte and 40 V voltage [24][25]. PAAO is not a homogeneous material; instead, it consists of a porous layer and the barrier layer on top of the Al substrate (Figure 1b). To

Influence of conductive carbon and MnCo₂O₄ on morphological and electrical properties of hydrogels for electrochemical energy conversion

• Sylwia Pawłowska,
• Karolina Cysewska,
• Yasamin Ziai,
• Jakub Karczewski,
• Piotr Jasiński and
• Sebastian Molin

Beilstein J. Nanotechnol. 2024, 15, 57–70, doi:10.3762/bjnano.15.6

• catalytic activity of the electrode in the oxygen evolution reaction. The use of a hydrogel as a matrix to suspend the catalyst particles, and thus increase their availability through the electrolyte, seems to be an interesting and promising application approach. Keywords: electrical properties; energy

• the morphology also facilitates the penetration by the electrolyte, the diffusion of ions to electroactive sites, and the rapid release of the reaction, thus promoting the kinetics of the reaction and achieving higher efficiency of the catalyst built into the 3D structure [19]. The hydrogel matrix

• porous structure is capable of swelling and thus accommodating large amounts of ionic liquids. Moreover, the swollen hydrogel structure provides constant access of electrolyte molecules/ions to the catalyst particles, increasing the speed and efficiency of the electrochemical reaction [20]. The swelling

In situ magnesiothermic reduction synthesis of a Ge@C composite for high-performance lithium-ion batterie anodes

• Ha Tran Huu,
• Ngoc Phi Nguyen,
• Vuong Hoang Ngo,
• Huy Hoang Luc,
• Minh Kha Le,
• Minh Thu Nguyen,
• My Loan Phung Le,
• Hye Rim Kim,
• In Young Kim,
• Sung Jin Kim,
• Van Man Tran and
• Vien Vo

Beilstein J. Nanotechnol. 2023, 14, 751–761, doi:10.3762/bjnano.14.62

• compositions such as Li7Ge2, Li9Ge4, and Li22Ge2 [53][54][55]. The remaining shoulder can be ascribed to the decomposition of the electrolyte and the formation of solid–electrolyte interface (SEI) layers [55][56]. In the following cycles, the signal of the SEI layer formation at a potentials of 0.3 V vs Li/Li

• + remains, demonstrating the continuous loss of lithium in this irreversible process. This is consistent with the fact that the alloying electrodes suffer from damages caused by the volume variation during lithiation/delithiation, leading to the continuous exposure of new active material and electrolyte [57

• conductivity of the additional carbon matrix, indicating the decrease in charge transfer resistance of the composite electrodes. The EIS results were fitted using an equivalent circuit model, including an internal or electrolyte resistance (Re), a charge transfer resistance (Rct), and two constant phase

A graphene quantum dots–glassy carbon electrode-based electrochemical sensor for monitoring malathion

• Sanju Tanwar,
• Aditi Sharma and
• Dhirendra Mathur

Beilstein J. Nanotechnol. 2023, 14, 701–710, doi:10.3762/bjnano.14.56

• on a SP Biologic 150 electrochemical workstation at room temperature. A solution of 0.1 M KCl containing 0.05 M K3[Fe(CN)6] was used as an electrolyte to analyze the oxidation–reduction behavior of the working electrode through cyclic voltammetry. For detection and quantification of pesticides

Metal-organic framework-based nanomaterials as opto-electrochemical sensors for the detection of antibiotics and hormones: A review

• Akeem Adeyemi Oladipo,
• Saba Derakhshan Oskouei and
• Mustafa Gazi

Beilstein J. Nanotechnol. 2023, 14, 631–673, doi:10.3762/bjnano.14.52

• 100 nm are the main choice for the design of electrochemical sensors. These characteristics all combine to improve the electrochemical process. A sensing or working electrode that acts as a transducer, an electrolyte, a diffusion barrier, and a reference counter electrode are the common components of

Molecular nanoarchitectonics: unification of nanotechnology and molecular/materials science

• Katsuhiko Ariga

Beilstein J. Nanotechnol. 2023, 14, 434–453, doi:10.3762/bjnano.14.35

• multistep electrochemical epitaxial polymerization technique [113]. This technique consists of combining two electrochemical polymerization processes using different monomer solutions. First, a voltage pulse was applied to an iodine-covered Au(111) substrate in an electrolyte solution containing the first

• thiophene monomer. This process produced the first polythiophene wires on the substrate. The substrate was then transferred to an electrolyte solution containing another thiophene monomer. The second process of applying voltage oxidized both the thiophene monomer in solution and the polythiophene on the

Polymer nanoparticles from low-energy nanoemulsions for biomedical applications

• Santiago Grijalvo and
• Carlos Rodriguez-Abreu

Beilstein J. Nanotechnol. 2023, 14, 339–350, doi:10.3762/bjnano.14.29

• [58]. The region for nanoemulsion formation in the phase diagram changes with the electrolyte (PBS) concentration (Figure 4a). There seems to be an optimum value for which this region is the largest, and the colloidal stability is maximum. Note that the presence of electrolyte is expected to reduce

• Ostwald ripening, especially considering that the solubility of ethyl acetate in water is relatively high (about 80 g/L at 20 °C). The hydrodynamic diameter of the particles decreases sharply (from 300–400 nm to ca. 40 nm) at a given electrolyte concentration (Figure 4b), with a concomitant decrease in