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

• that the carbon support is wettable by water. Making macroscopic carbon surfaces hydrophilic necessitates carbon surface oxygenates that are thermodynamically stable only at graphitic edges spaced closely enough to retain adsorbed water [22]. This precludes glassy carbon and basal-plane highly ordered

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

• numbers in parentheses stand for the volume ratio of peroxo titanium complex to GQDs solutions. Electrochemical studies Voltammetric measurements were performed at room temperature using a CPA-HH5 electrochemical workstation, Vietnam. A conventional three-electrode cell with a glassy carbon working

• solution, and acetic acid solution in appropriate ratios. To prepare a TiO2/GQDs-modified glassy carbon electrode (TiO2/GQDs-GCE), 5 mL of TiO2/GQDs suspension in water (0.1 mg/mL) was cast onto the surface of the bare GCE. The modified electrode was allowed to dry naturally for some hours at ambient

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

• 0.01 Hz – 10 kHz and at an amplitude of 10 mV. The data was analysed by the ZView software. Electrode preparation and electrochemical measurements For the electrochemical analysis, 5 µL of the hydrogel precursor solution was dropped on a rotating glassy carbon (GC) electrode with a working area of

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

• -cell configuration, were assembled in an argon-filled glovebox (MB 20 G, MBRAUN), with oxygen content and moisture below 1.0 ppm. A disc-shaped lithium metal foil was used as counter electrode, and a glassy carbon fiber pad soaked in 1 M electrolyte of LiPF6 in ethylene carbonate/dimethyl carbonate

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

• diffraction were used to characterize the morphological and structural properties of GQDs. An electrochemical sensor was developed by drop casting GQDs on a glassy carbon electrode (GCE). The sensor detects the organophosphate pesticide malathion in a selective and sensitive manner. Using cyclic voltammetry

• -functionalized nickel/silver/graphene quantum dot/graphene hybrid for the colorimetric detection of malathion [28]. This paper describes the development of an electrochemical sensor based on a graphene quantum dot-modified glassy carbon electrode (GQDs/GCE) for the determination and quantification of the

• organophosphate pesticide malathion. Graphene quantum dots were synthesized hydrothermally using glucose as precursor. The glassy carbon electrode that served as working electrode in the electrochemical cell was modified with graphene quantum dots by drop casting. To evaluate the modified electrode’s oxidation

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

• electrochemical sensor for the detection of tetracycline based on a glassy carbon electrode modified with MIL-53 (Fe) was published by Chen and co-workers [71]. The authors claim that the electrochemical sensor has a good linear relationship for tetracycline detection in the range of 0.0643–1.53 mol L−1 and that

Evaluation of electrosynthesized reduced graphene oxide–Ni/Fe/Co-based (oxy)hydroxide catalysts towards the oxygen evolution reaction

• Karolina Cysewska,
• Marcin Łapiński,
• Marcin Zając,
• Jakub Karczewski,
• Piotr Jasiński and
• Sebastian Molin

Beilstein J. Nanotechnol. 2023, 14, 420–433, doi:10.3762/bjnano.14.34

• and/or GO. For example, Wu et al. [13] chemically fabricated metal alloys and their oxides (NiCo, CoFe) with nitrogen-doped graphene (N-rGO/NiCo-NiO-CoO, N-rGO/CoFe-Co2FeO4) on a glassy carbon electrode (GCE). The N-rGO/NiCo-NiO-CoO and N-rGO/CoFe-Co2FeO4 catalysts revealed an OER overpotential (η) of

A novel approach to pulsed laser deposition of platinum catalyst on carbon particles for use in polymer electrolyte membrane fuel cells

• Bogusław Budner,
• Wojciech Tokarz,
• Sławomir Dyjak,
• Andrzej Czerwiński,
• Bartosz Bartosewicz and
• Bartłomiej Jankiewicz

Beilstein J. Nanotechnol. 2023, 14, 190–204, doi:10.3762/bjnano.14.19

• ) with a glassy carbon (GC) disc electrode of 0.1642 cm2 surface, driven by a CHI 700C bipotentiostat (CH Instruments, United States). A solution of 0.5 M H2SO4 was used as the base electrolyte. A mercury sulfate electrode Hg/HgSO4/1 M H2SO4 (potential 600 mV), and a gold metal sheet were used as

A nonenzymatic reduced graphene oxide-based nanosensor for parathion

• Sarani Sen,
• Anurag Roy,
• Ambarish Sanyal and
• Parukuttyamma Sujatha Devi

Beilstein J. Nanotechnol. 2022, 13, 730–744, doi:10.3762/bjnano.13.65

• nanoribbons doped with silver nanoparticles, rGO doped with ZrO2, and CuO–TiO2 hybrid nanocomposites were proposed to detect methyl parathion [19][20][21][22]. Rajaji et al. (2019) modified glassy carbon electrodes with graphene oxide encapsulated 3D porous chalcopyrite (CuFeS2) nanocomposites to detect

• methyl paraoxon in vegetables [23]. Recently, Jangid et al. (2021) also described the electrocatalytic activity of fenitrothion on glassy carbon electrodes modified with nitrogen and sulfur co-doped activated carbon-coated multiwalled carbon nanotubes [24]. Nevertheless, the fabrication process of the

• at 3000 rpm for 15 min. The product (GO) was collected and dried at room temperature for further studies. Fabrication of electrochemically reduced graphene oxide modified electrodes Before surface modification of GO, a bare glassy carbon electrode (GCE, φ = 3 mm) was polished in 1.0, 0.3, and 0.05

Tubular glassy carbon microneedles with fullerene-like tips for biomedical applications

• Sharali Malik and
• George E. Kostakis

Beilstein J. Nanotechnol. 2022, 13, 455–461, doi:10.3762/bjnano.13.38

• /bjnano.13.38 Abstract Glassy carbon, in general, is made by the pyrolysis of polymeric materials and has been the subject of research for at least fifty years. However, as understanding its microstructure is far from straightforward, it continues to be an area of active research. Glassy carbon adopts

• the nanoarchitectonics concept of bottom-up creation of functional materials, we use methane rather than a polymer to form glassy carbon. Here we show that tubular glassy carbon microneedles with fullerene-like tips form when methane undergoes pyrolysis on a curved alumina surface. X-ray diffraction

• of these glassy carbon tubules shows long-range order with a d-spacing of 4.89 Å, which is indicative of glassy carbon. Raman spectroscopy shows the material to be graphitic in nature, and SEM shows the fullerene-like structure of the material. This work provides new insights into the structure of

Sputtering onto liquids: a critical review

• Anastasiya Sergievskaya,
• Adrien Chauvin and
• Stephanos Konstantinidis

Beilstein J. Nanotechnol. 2022, 13, 10–53, doi:10.3762/bjnano.13.2

Morphology-driven gas sensing by fabricated fractals: A review

• Vishal Kamathe and
• Rupali Nagar

Beilstein J. Nanotechnol. 2021, 12, 1187–1208, doi:10.3762/bjnano.12.88

Stability and activity of platinum nanoparticles in the oxygen electroreduction reaction: is size or uniformity of primary importance?

• Kirill O. Paperzh,
• Anastasia A. Alekseenko,
• Vadim A. Volochaev,
• Ilya V. Pankov,
• Olga A. Safronenko and
• Vladimir E. Guterman

Beilstein J. Nanotechnol. 2021, 12, 593–606, doi:10.3762/bjnano.12.49

• taken with a microdispenser and applied to the end of a polished and degreased glassy carbon disk with an area of 0.196 cm2, the exact weight of the drop was recorded. The electrode was dried in air for 20 min while rotating at 700 rpm. Prior to measuring the ESA of the catalyst, the electrolyte was

One-step synthesis of carbon-supported electrocatalysts

• Sebastian Tigges,
• Nicolas Wöhrl,
• Ivan Radev,
• Ulrich Hagemann,
• Markus Heidelmann,
• Thai Binh Nguyen,
• Stanislav Gorelkov,
• Stephan Schulz and
• Axel Lorke

Beilstein J. Nanotechnol. 2020, 11, 1419–1431, doi:10.3762/bjnano.11.126

• (including preheating), and M is the molar mass of the precursor (393.302 g/mol). The material deposition was mainly done on 1 × 1 cm2 silicon substrates. In preparation for the cyclic voltammetry measurements, glassy carbon electrodes (GCEs; diameter 4 mm, Catalog No. 013338, ALS Co., Ltd.) were used as

Nickel nanoparticles supported on a covalent triazine framework as electrocatalyst for oxygen evolution reaction and oxygen reduction reactions

• Secil Öztürk,
• Yu-Xuan Xiao,
• Dennis Dietrich,
• Beatriz Giesen,
• Juri Barthel,
• Jie Ying,
• Xiao-Yu Yang and
• Christoph Janiak

Beilstein J. Nanotechnol. 2020, 11, 770–781, doi:10.3762/bjnano.11.62

• Autolab working station from Metrohm, Switzerland. Typically, a Ag/AgCl electrode (with saturated KCl solution) was used as a reference electrode, a carbon rod was used as a counter electrode, and a glassy-carbon rotating disk electrode (RDE, diameter: 5 mm, area: 0.196 cm2) was used as the working

• electrode. The loading amount of all catalysts was 0.255 mg/cm2. The OER measurements were carried out in 1 mol/L KOH using the glassy-carbon RDE at a rotation rate of 1600 rpm with a 5 mV/s sweep rate. The accelerated durability tests (ADTs) for OER were performed in 1 mol/L KOH solution with cyclic

• potential sweeps between 1.23 and 1.53 V vs reversible hydrogen electrode (RHE) at a 100 mV/s sweep rate for 2000 cycles. The ORR measurements were carried out in 1 mol/L O2-saturated KOH solution under O2 flow using the glassy-carbon RDE at a rotation rate of 1600 rpm with a 10 mV/s sweep rate. The ADTs

Exfoliation in a low boiling point solvent and electrochemical applications of MoO₃

• Matangi Sricharan,
• Bikesh Gupta,
• Sreejesh Moolayadukkam and
• H. S. S. Ramakrishna Matte

Beilstein J. Nanotechnol. 2020, 11, 662–670, doi:10.3762/bjnano.11.52

• Zetasizer NanoZS. All electrochemical measurements were carried out using Autolab PGSTAT302N. Electrode preparation and electrochemical testing Three-electrode system: A glassy carbon electrode (GCE, 0.3 cm diameter) as the working electrode, Pt wire as counter electrode and a saturated calomel electrode

Soybean-derived blue photoluminescent carbon dots

• Shanshan Wang,
• Wei Sun,
• Dong-sheng Yang and
• Fuqian Yang

Beilstein J. Nanotechnol. 2020, 11, 606–619, doi:10.3762/bjnano.11.48

• synthesized from glassy carbon [16], graphite [26], polymethyl methacrylate (PMMA) [27], and a graphite–cement mixture [6] via LAL in various liquids. In general, there are three major mechanisms contributing to the photoluminescence (PL) of CDs: 1) size-dependent bandgap (quantum confinement), 2) surface

Electrochemically derived functionalized graphene for bulk production of hydrogen peroxide

• Munaiah Yeddala,
• Pallavi Thakur,
• Anugraha A and
• Tharangattu N. Narayanan

Beilstein J. Nanotechnol. 2020, 11, 432–442, doi:10.3762/bjnano.11.34

• electrolyte concentration also determines the extent of functionalization of graphene. The presence of the C=O groups is further confirmed by cyclic voltammetry (CV) measurements in alkaline and acidic electrolyte. The CV profiles of the EEG samples (EEG-modified glassy carbon electrode (GCE) as the working

An advanced structural characterization of templated meso-macroporous carbon monoliths by small- and wide-angle scattering techniques

• Felix M. Badaczewski,
• Marc O. Loeh,
• Torben Pfaff,
• Dirk Wallacher,
• Daniel Clemens and
• Bernd M. Smarsly

Beilstein J. Nanotechnol. 2020, 11, 310–322, doi:10.3762/bjnano.11.23

• the carbon microstructure, on the nanopore structure, and on the template process. A graphitizable pitch and a non-graphitizable resin, which carbonization turns into a glassy carbon, is used for comparison. Glassy carbon materials are derived from thermally processed phenolic formaldehyde resins

• treatment, the PF resin is gradually transformed into a non-graphitizing glassy carbon [49][50] consisting of highly cross-linked graphene stacks, which once were thought to be ribbon-like, but are now acknowledged as being of made of highly curved graphene sheets with a high content of fullerene-like

• structures [51][52][53][54]. Key properties of glassy carbon materials, such as thermal conductivity, chemical resistance, hardness, density, and coefficient of thermal expansion are closely related to the carbon microstructure and the porosity. Resin-based carbon materials are known to possess a substantial

Simple synthesis of nanosheets of rGO and nitrogenated rGO

• Pallellappa Chithaiah,
• Madhan Mohan Raju,
• Giridhar U. Kulkarni and
• C. N. R. Rao

Beilstein J. Nanotechnol. 2020, 11, 68–75, doi:10.3762/bjnano.11.7

• of 4.0 mg rGO and 0.025 wt % (5 μL) of Nafion in 0.4 mL of dimethylformamide (DMF) was sonicated until a homogeneous dispersion was obtained. 3 μL catalyst ink was taken and drop-cast onto a glassy carbon electrode, which was allowed to dry at room temperature. A similar procedure was followed to

• glassy carbon working electrode (3 mM), a platinum wire counter electrode and a Hg/Hg2SO4 reference electrode with 1 M H2SO4 electrolyte. The specific capacitance (SC) of rGO and H-rGO was calculated from CV curves, according to Equation 1: where ∫IdV is the area under the CV curve, m is the mass of the

Synthesis of amorphous and graphitized porous nitrogen-doped carbon spheres as oxygen reduction reaction catalysts

• Maximilian Wassner,
• Markus Eckardt,
• Andreas Reyer,
• Thomas Diemant,
• Michael S. Elsaesser,
• R. Jürgen Behm and
• Nicola Hüsing

Beilstein J. Nanotechnol. 2020, 11, 1–15, doi:10.3762/bjnano.11.1

• -Tek reference catalyst) was prepared by pipetting an aqueous suspension of the synthesized materials (20 µL of a 4 mg·mL−1 suspension; Millipore MilliQ, 18.2 MΩ·cm) onto a mirror-polished glassy carbon (GC) disc (Sigradur G from Hochtemperatur Werkstoffe, d = 6 mm), followed by subsequent drying under

• a N2 stream. With these loadings we could form homogeneous, thin and stable catalyst layers on the electrode. The resulting film was covered with the same volume of a 1 wt % aqueous Nafion solution and dried again to ensure the mechanical stability of the catalyst layer on the glassy carbon without

• were performed by pipetting and drying 80 µL of the catalysts suspension on a glassy carbon disk, similar to preparation of the catalyst film for the electrochemical measurements. The dried catalyst film is than covered by another glassy carbon disk, and the two disks were tightly pressed together. The

Abrupt elastic-to-plastic transition in pentagonal nanowires under bending

• Sergei Vlassov,
• Magnus Mets,
• Boris Polyakov,
• Jianjun Bian,
• Leonid Dorogin and
• Vahur Zadin

Beilstein J. Nanotechnol. 2019, 10, 2468–2476, doi:10.3762/bjnano.10.237

• obtained with a high-resolution scanning electron microscope (HR-SEM, Helios Nanolab 600, FEI) and transmission electron microscope (TEM, Tecnai GF20, FEI). The NWs were drop-cast on either TEM grids with lacey carbon (Agar, UK) for TEM characterization, or on glassy carbon and silicon wafers (100, n

Tuning the performance of vanadium redox flow batteries by modifying the structural defects of the carbon felt electrode

• Ditty Dixon,
• Deepu Joseph Babu,
• Aiswarya Bhaskar,
• Hans-Michael Bruns,
• Joerg J. Schneider,
• Frieder Scheiba and
• Helmut Ehrenberg

Beilstein J. Nanotechnol. 2019, 10, 1698–1706, doi:10.3762/bjnano.10.165

• attached to a glassy carbon rod were used as the WE. To achieve a better electrical contact, the punched-out felt was pierced through the middle by 5 cm long glassy carbon rod with a diameter of 1 mm. The positive half-cell reaction was measured in 0.1 molar vanadyl sulphate (Alfa Aeser) dissolved in 2

Synthesis of P- and N-doped carbon catalysts for the oxygen reduction reaction via controlled phosphoric acid treatment of folic acid

• Rieko Kobayashi,
• Takafumi Ishii,
• Yasuo Imashiro and
• Jun-ichi Ozaki

Beilstein J. Nanotechnol. 2019, 10, 1497–1510, doi:10.3762/bjnano.10.148

• voltammetry. The working electrode was prepared by loading the catalyst (200 μg·cm−2) on a glassy carbon disk electrode. The carbon ink was prepared in the following manner: 2.5 mg of the prepared sample was mixed with 25 μL of Nafion solution (5% solution of lower aliphatic alcohols, Aldrich), 75 μL of

• 200 μg·cm−2). A reversible hydrogen electrode (RHE) and a glassy carbon plate were employed as reference and counter electrodes, respectively. The electrolyte was a 0.5 M solution of H2SO4 in deionized water. Prior to the measurements, dissolved oxygen in the acid solution was purged by bubbling

Hierarchically structured 3D carbon nanotube electrodes for electrocatalytic applications

• Pei Wang,
• Katarzyna Kulp and
• Michael Bron

Beilstein J. Nanotechnol. 2019, 10, 1475–1487, doi:10.3762/bjnano.10.146

• a glassy carbon (GC) substrate in a sequence of electrodeposition and chemical vapor deposition (CVD) steps as follows: Primary CNTs are grown over electrodeposited iron by CVD followed by a second Fe deposition and finally the CVD growth of secondary CNTs. The prepared 3-dimensional CNT structures

• the preparation of hierarchically structured CNTs on glassy carbon (GC) based on a sequential CNT growth over electrodeposited Fe nanoparticles via chemical vapor deposition (CVD) with cyclohexane as the carbon precursor. Pt electrodeposition onto these hierarchical structures leads to active

• above results demonstrate that by choosing the appropriate experimental conditions, it is possible to tune the thickness and length of the primary CNTs grown on glassy carbon. Growth of secondary CNTs and Pt deposition After the growth of the primary CNTs, a subsequent Fe electrodeposition and growth of