The effect of cobalt on morphology, structure, and ORR activity of electrospun carbon fibre mats in aqueous alkaline environments

• Markus Gehring,
• Tobias Kutsch,
• Osmane Camara,
• Alexandre Merlen,
• Hermann Tempel,
• Hans Kungl and
• Rüdiger-A. Eichel

Beilstein J. Nanotechnol. 2021, 12, 1173–1186, doi:10.3762/bjnano.12.87

• electrochemical activity using linear sweep voltammetry with a focus on the oxygen reduction reaction. Experimental Synthesis of carbon fibres and electrode preparation Polyacrylonitrile (PAN) (98%, MW = 150,000 g·mol−1; BOC sciences, USA) was dissolved in N,N-dimethyl formamide (DMF) to obtain 10 wt % solutions

• equilibrated for 1 h before each measurement. Subsequent linear sweep voltammetry measurements were performed with a scan rate of 1 mV·s−1 in a potential window of 1 V, from 0.5 V vs MMO to −0.5 V vs MMO. The stability tests were performed by applying discharge currents of 6, 12, 18, and 6 mA (2, 4, 6, and 2

• demonstrated by elemental analysis (Figure 7a) the significance of nitrogen doping in the cobalt-decorated carbon fibres is, however, substantially reduced, in favour of cobalt-based activity. Electrochemical ORR characterisation Linear sweep voltammetry using fibre-based electrodes The oxygen reduction

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

• ), which is due to the difference in their structural characteristics described above (Table 1). The commercial catalyst JM40 has the minimal ESA value (Table 2). The study of the ORR kinetics, carried out by linear voltammetry using RDE (Figure 5), showed that the ORR proceeds according to the four

Paper-based triboelectric nanogenerators and their applications: a review

• Jing Han,
• Nuo Xu,
• Yuchen Liang,
• Mei Ding,
• Junyi Zhai,
• Qijun Sun and
• Zhong Lin Wang

Beilstein J. Nanotechnol. 2021, 12, 151–171, doi:10.3762/bjnano.12.12

• spectra in Figure 10c. The electrochemical behavior of CNT and PANI–CNT electrodes were evaluated by using cyclic voltammetry (CV) and galvanostatic charge–discharge characterization (GCD). Compared with the pristine CNT, two pairs of redox peaks appeared in the CV curve of PANI–CNT electrodes at a scan

ZnO and MXenes as electrode materials for supercapacitor devices

• Ameen Uddin Ammar,
• Ipek Deniz Yildirim,
• Feray Bakan and
• Emre Erdem

Beilstein J. Nanotechnol. 2021, 12, 49–57, doi:10.3762/bjnano.12.4

• ) spectroscopy techniques among the most powerful techniques to extract detailed information on the defect structures of ZnO. Also, electrical impedance spectroscopy (EIS) and cyclic voltammetry (CV) are sensitive to electrical properties such as specific capacitance and impedance, which can be correlated with

Atomic layer deposited films of Al₂O₃ on fluorine-doped tin oxide electrodes: stability and barrier properties

• Hana Krýsová,
• Michael Neumann-Spallart,
• Hana Tarábková,
• Pavel Janda,
• Ladislav Kavan and
• Josef Krýsa

Beilstein J. Nanotechnol. 2021, 12, 24–34, doi:10.3762/bjnano.12.2

• M KCl) and a platinum rod was used as the counter electrode. The blocking properties of the deposited layers were evaluated by cyclic voltammetry (CV) in an aqueous electrolyte composed of 0.5 mM K3[Fe(CN)6] and 0.5 mM K4[Fe(CN)6] in 0.5 M KCl (pH 2.5, adjusted with HCl) or in phosphate buffer (pH

• FTO coated with a 17 nm Al2O3 layer were practically the same (i.e., 35 and 34 nm, respectively). This shows that Al2O3 was conformally deposited onto the FTO surface. Next, the blocking properties of the aluminium oxide layers were tested via cyclic voltammetry on ALD-deposited Al2O3 films of various

• (free of Prussian blue) was observed when the Al2O3-protected electrode was denuded by the dissolution of its coating, both in acidic (Figure 6) and alkaline (Figure 4) media. Exposure to phosphate buffer (pH 7.2) Cyclic voltammetry curves of 17 nm thick Al2O3 films on FTO substrates (in the presence of

Self-standing heterostructured NiC_x-NiFe-NC/biochar as a highly efficient cathode for lithium–oxygen batteries

• Shengyu Jing,
• Xu Gong,
• Shan Ji,
• Linhui Jia,
• Bruno G. Pollet,
• Sheng Yan and
• Huagen Liang

Beilstein J. Nanotechnol. 2020, 11, 1809–1821, doi:10.3762/bjnano.11.163

• impedance spectroscopy (EIS) in a frequency range from 100 kHz to 0.1 Hz and with a perturbation amplitude of 5 mV was used on the PARSTAT 4000 (AMETEK, USA) electrochemical workstation. Cyclic voltammetry (CV) was performed at a scan rate of 0.1 mV·s−1 and in a cell voltage range from 2.0 to 4.5 V vs Li

• electrocatalytic properties of NiFe-PBA/PP-T samples were initially evaluated by cyclic voltammetry. As shown in Figure 5a, the current response in N2 was very low, close to zero, during positive and negative scans. This suggests that the as-prepared cathode has no ability to catalyze N2 reduction. In contrast

• of NiFe-PBA (inset, black curve). (a–c) HR-TEM images and (d,e) element mappings of NiFe-PBA/PP-900. High-resolution XPS spectra of NiFe-PBA/PP-T calcined at 700 (top panels) and 900 °C (bottom panels) for (a) C 1s, (b) N 1s, (c) Ni 2p, and (d) Fe 2p. (a) In situ cyclic voltammetry curves of Li–O2

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

• by cyclic voltammetry (CV) measurements. Results and Discussion One-step synthesis and its product Platinum acetylacetonate was used as a single-source precursor for the deposition of Pt-NPs embedded in the supporting CNW matrix. CNWs are vertically aligned, graphitic, multilayer carbon sheets, which

• (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

Structure and electrochemical performance of electrospun-ordered porous carbon/graphene composite nanofibers

• Yi Wang,
• Yanhua Song,
• Chengwei Ye and
• Lan Xu

Beilstein J. Nanotechnol. 2020, 11, 1280–1290, doi:10.3762/bjnano.11.112

• station (CHI660E, Chenhua, Shanghai) by using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and constant current galvanostatic charge/discharge (GCD) techniques. A voltage range of 0–1.0 V was applied to the CV electrode at a scan rate of 25 mV·s−1. The impedance measurements of

• the electrochemical process [42]. Electrochemical characterization Cyclic voltammetry is a reliable method to analyze the capacitance of supercapacitor electrodes [43]. Capacitors made of CGCNFs were submitted to a CV experiment at a scan rate of 25 mV·s−1 and the obtained curves are shown in Figure 5

Atomic layer deposition for efficient oxygen evolution reaction at Pt/Ir catalyst layers

• Stefanie Schlicht,
• Korcan Percin,
• Stefanie Kriescher,
• André Hofer,
• Claudia Weidlich,
• Matthias Wessling and
• Julien Bachmann

Beilstein J. Nanotechnol. 2020, 11, 952–959, doi:10.3762/bjnano.11.79

• room temperature), one electrochemical characterization (linear voltammetry performed at room temperature), and we will quantify (a) current densities, (b) mass activites (given a certain noble-metal loading) and (c) stability (quantified as a change in current density after bulk electrolysis). We

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

• properties of the exfoliated MoO3 nanosheets were evaluated using a three-electrode configuration and are shown in Figure 3. Figure 3a shows the cyclic voltammetry (CV) measurement of the electrodes recorded between −0.8 and −0.1 V with a scan rate of 50 mV/s. Initially, pristine exfoliated MoO3 sheets were

• change in slope, which could be due to the electrochemically reversible hydrogen intercalation, which was also seen in the voltammetry curves. The charge and discharge times were found to be 15 and 13 s at a current density of 1 A·g−1. Cycling stability is a key factor for the commercialization of

• saturates at 5 wt % CB. This observation also supports the observation from voltammetry data where the composite with 5 wt % CB shows a better performance. Typically, electrode materials are tested for supercapacitor applications in a three-electrode configuration. But for practical applications, it is

Comparison of fresh and aged lithium iron phosphate cathodes using a tailored electrochemical strain microscopy technique

• Matthias Simolka,
• Hanno Kaess and
• Kaspar Andreas Friedrich

Beilstein J. Nanotechnol. 2020, 11, 583–596, doi:10.3762/bjnano.11.46

• cathode material due to ageing. A decrease of the electrochemical activity of the cathode could result in a smaller current peak intensity in a cyclic voltammetry (CV) experiment. However, performing CV with the fresh and an aged cathode in combination with a fresh graphite anode as counter electrode for

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

• samples in between these two samples. To understand the ORR reaction pathway, rotating ring and disk electrode (RRDE)-based hydrodynamic voltammetry is conducted. Figure 4a shows ORR linear sweep voltammetry (LSV) scans of different EEG samples on GCE disk (4 mm diameter) and the H2O2 oxidation over the

• -checked with graphite rod counter electrode, too) used as a reference and counter electrodes, respectively. The electrochemical performance of the materials was analyzed using cyclic voltammetry (CV), linear sweep voltammetry (LSV), and rotating ring and disk electrode (RRDE) measurements. A BioLogic SP

High-performance asymmetric supercapacitor made of NiMoO₄ nanorods@Co₃O₄ on a cellulose-based carbon aerogel

• Meixia Wang,
• Jing Zhang,
• Xibin Yi,
• Benxue Liu,
• Xinfu Zhao and
• Xiaochan Liu

Beilstein J. Nanotechnol. 2020, 11, 240–251, doi:10.3762/bjnano.11.18

• counter electrode were a saturated calomel electrode (SCE) and a platinum electrode, respectively. Figure 6a shows the cyclic voltammetry (CV) curves of the NiMoO4@Co3O4/CA electrode at voltage scan rates of 2.5–50 mV/s. All the CV curves shown in Figure 6a consist of a pair of strong redox current peaks

• (b) C 1s, (c) Co 2p, (d) Ni 2p, (e) Mo 3d and (f) O 1s. Nitrogen adsorption/desorption isotherms and pore size distribution curves of (a) CA, (b) NiMoO4/CA (b), and (c) NiMoO4@Co3O4/CA composite. (a) Cyclic voltammetry (CV) curves at scan rates of 2.5–50 mV/s and (b) galvanostatic charge/discharge

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

• voltammetry and CD experiments with three-electrode system using 1 M H2SO4 as electrolyte (Figure 8). CV curves of rGO and H-rGO at different scan rates from 5 to 200 mV·s−1 vs Hg/Hg2SO4 are shown in Figure 8a and Figure 8b, respectively. These curves show increase in current density with decreasing scan rate

• prepare the H-rGO electrode. The electrochemical studies, including cyclic voltammetry (CV) and chronopotentiometry charge–discharge (CD), were carried out at room temperature in 1 M H2SO4 solution in a standard three-electrode cell using an electrochemical workstation CHI 660E. This system consists of a

Antimony deposition onto Au(111) and insertion of Mg

• Lingxing Zan,
• Da Xing,
• Abdelaziz Ali Abd-El-Latif and
• Helmut Baltruschat

Beilstein J. Nanotechnol. 2019, 10, 2541–2552, doi:10.3762/bjnano.10.245

• processes are kinetically slow because of the large ionic radius and high charge density of Mg2+ compared with Li+. In this work, we prepared very thin films of Sb by electrodeposition on a Au(111) substrate. Monolayer and multilayer deposition (up to 20 monolayers) were characterized by cyclic voltammetry

• surface has never been reported. Using this layer for such an insertion study in fundamental research offers the advantage of a better defined structure of the insertion compound as compared to the use of small particles in battery research. The initial cyclic voltammetry study of antimony electrochemical

• counter electrode and another one as a reference electrode. All the magnesium electrochemical deposition measurements were carried out in a MBraun glovebox (H2O < 0.5 ppm, O2 < 0.5 ppm) in a similar manner as described in [19]. Cyclic voltammetry (CV) A polycrystalline Au electrode with a similar size was

Adsorption and desorption of self-assembled L-cysteine monolayers on nanoporous gold monitored by in situ resistometry

• Elisabeth Hengge,
• Eva-Maria Steyskal,
• Rupert Bachler,
• Alexander Dennig,
• Bernd Nidetzky and
• Roland Würschum

Beilstein J. Nanotechnol. 2019, 10, 2275–2279, doi:10.3762/bjnano.10.219

• accompanied by additional adsorption takes place. The successful binding of cysteine on the Au surface was confirmed by cyclic voltammetry, which showed a significant decrease of the double-layer capacitance. Also, the electrochemically controlled desorption of cysteine was monitored by concomitant in situ

• ); voltammetry; Findings Nanoporous gold, produced by selective etching of the less noble component of a AuAg master alloy (also known as dealloying), is a very promising material in many applications due to its three-dimensional nanoporous structure. Among many other technological applications as sensing [1][2

• with a Pt-wire counter electrode under chronoamperometric conditions at UAg/AgCl = 1100 mV until the current had fallen below 50 μA. For all following procedures, a carbon fabric served as the counter electrode. After dealloying, the sample was cleaned from the primary oxide [10] by cyclic voltammetry

Design and facile synthesis of defect-rich C-MoS₂/rGO nanosheets for enhanced lithium–sulfur battery performance

• Chengxiang Tian,
• Juwei Wu,
• Zheng Ma,
• Bo Li,
• Pengcheng Li,
• Xiaotao Zu and
• Xia Xiang

Beilstein J. Nanotechnol. 2019, 10, 2251–2260, doi:10.3762/bjnano.10.217

• voltammetry tests were carried out on a LAND battery cycler (CT2001A) in a voltage range of 1.7 to 2.9 V (vs Li/Li+). The specific capacity was calculated based on the mass of sulfur. Cyclic voltammetry (CV) tests were carried out between 1.6 and 2.9 V at a scan rate of 0.1 mV·s−1. The electrochemical

Nontoxic pyrite iron sulfide nanocrystals as second electron acceptor in PTB7:PC₇₁BM-based organic photovoltaic cells

• Olivia Amargós-Reyes,
• José-Luis Maldonado,
• Omar Martínez-Alvarez,
• María-Elena Nicho,
• José Santos-Cruz,
• Juan Nicasio-Collazo,
• Irving Caballero-Quintana and
• Concepción Arenas-Arrocena

Beilstein J. Nanotechnol. 2019, 10, 2238–2250, doi:10.3762/bjnano.10.216

• levels of the FeS2 NCs were characterized by cyclic voltammetry (CV), as shown in Figure 4a. The voltammograms show an oxidation peak, assigned to the ionization potential, at approximately +0.39 V and a reduction peak, assigned to the electron affinity, at about −0.40 V. In order to estimate the

• by drop casting. Mechanically cut Pt–Ir wires were used as STM tips. Before the deposition of each film, HOPG substrates were cleaved by using the adhesive tape technique to obtain an atomically clean surface. Cyclic voltammetry (CV) measurements were carried out using a PARSTAT 2273 potentiostat in

A novel all-fiber-based LiFePO₄/Li₄Ti₅O₁₂ battery with self-standing nanofiber membrane electrodes

• Li-li Chen,
• Hua Yang,
• Mao-xiang Jing,
• Chong Han,
• Fei Chen,
• Xin-yu Hu,
• Wei-yong Yuan,
• Shan-shan Yao and
• Xiang-qian Shen

Beilstein J. Nanotechnol. 2019, 10, 2229–2237, doi:10.3762/bjnano.10.215

• . Electrode performance The two fiber membranes were directly cut into free-standing electrodes, and coin-cell batteries were assembled for a series of performance tests. Figure 7 are the cyclic voltammetry curves (CV, the second cycle) of the two electrodes. It can be seen that the strong redox peaks of the

• assembled in an Ar-filled glovebox by using lithium foil as anode and 1 M LiPF6 electrolyte (ethylene carbonate/dimethyl carbonate/ethyl methyl carbonate = 1:1:1). A Celgard 2400 polypropylene membrane was used as separator. The cyclic voltammetry and electrochemical impedance spectroscopy measurements were

Ultrathin Ni_1−xCo_xS₂ nanoflakes as high energy density electrode materials for asymmetric supercapacitors

• Xiaoxiang Wang,
• Teng Wang,
• Rusen Zhou,
• Lijuan Fan,
• Shengli Zhang,
• Feng Yu,
• Tuquabo Tesfamichael,
• Liwei Su and
• Hongxia Wang

Beilstein J. Nanotechnol. 2019, 10, 2207–2216, doi:10.3762/bjnano.10.213

• and Hg/HgO electrode were used as a counter and a reference electrode, respectively. The electrolyte was a 2 M aqueous KOH solution. Cyclic voltammetry (CV) curves of Ni1−xCoxS2 at scan rates from 2 to 100 mV·s−1 are shown in Figure 3a. As expected, redox peaks observed within the potential window

Facile synthesis of carbon nanotube-supported NiO//Fe₂O₃ for all-solid-state supercapacitors

• Shengming Zhang,
• Xuhui Wang,
• Yan Li,
• Xuemei Mu,
• Yaxiong Zhang,
• Jingwei Du,
• Guo Liu,
• Xiaohui Hua,
• Yingzhuo Sheng,
• Erqing Xie and
• Zhenxing Zhang

Beilstein J. Nanotechnol. 2019, 10, 1923–1932, doi:10.3762/bjnano.10.188

• as a reference electrode, CC-CNT@Fe2O3 as the binder-free working electrode and 2 M KOH as the electrolyte. Figure 4a shows cyclic voltammetry (CV) curves of the CC-CNT@Fe2O3 electrode at scan rates of 2, 5, 10, 20, 50 and 100 mV·s−1, from which visible redox peaks can be seen. The reduction peak at

High-tolerance crystalline hydrogels formed from self-assembling cyclic dipeptide

• Yongcai You,
• Ruirui Xing,
• Qianli Zou,
• Feng Shi and
• Xuehai Yan

Beilstein J. Nanotechnol. 2019, 10, 1894–1901, doi:10.3762/bjnano.10.184

• voltammetry (CV) curves of the hydrogel at different scan rates ranging from 10 to 40 mV were studied (Figure 4A). Typical capacitor shapes were observed in the curves, indicating that the C-WY hydrogel can be applied for electrochemical supercapacitors. In addition, the capacitive charge–discharge curves

TiO₂/GO-coated functional separator to suppress polysulfide migration in lithium–sulfur batteries

• Ning Liu,
• Lu Wang,
• Taizhe Tan,
• Yan Zhao and
• Yongguang Zhang

Beilstein J. Nanotechnol. 2019, 10, 1726–1736, doi:10.3762/bjnano.10.168

• μm (Figure 4c). Furthermore, the interface does not contain any cracks, suggesting the excellent adhesion of the TiO2/GO composite layer with a pristine separator. Figure 5 compares the cycle voltammetry (CV) curves of the Li/S batteries with pristine, GO-coated and TiO2/GO-coated separators at a

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

• did not show any increase in surface area for oxygen-plasma-treated samples [7]. The SEM images of the pristine as well as the N2-plasma-treated samples are shown in Figure 4. In order to evaluate the electrochemical performance of the N2-plasma-treated sample, cyclic voltammetry (CV) measurements

• energies of 5 keV and 15 keV and an in-lens detector. Electrochemical measurements In this work, commercial carbon felts obtained from SGL Carbon in pristine form and after N2 plasma treatment were used as electrode materials. Cyclic voltammetry (CV) was performed in a three-electrode setup using a

• the charging current reached less than 10 mA cm−2. All the cyclic voltammetry measurements were carried out at a scan rate of 5 mV s−1. Single-cell measurements were performed using a modified direct methanol fuel cell from ElectroChem, having a pin-type flow field with an active area of 25 cm2

Upcycling of polyurethane waste by mechanochemistry: synthesis of N-doped porous carbon materials for supercapacitor applications

• Christina Schneidermann,
• Pascal Otto,
• Desirée Leistenschneider,
• Sven Grätz,
• Claudia Eßbach and
• Lars Borchardt

Beilstein J. Nanotechnol. 2019, 10, 1618–1627, doi:10.3762/bjnano.10.157

• for cyclic voltammetry (CV) and galvanostatic cycling with potential limitation (GCPL). CVs were recorded in full-cell mode at a scan rate 5 mV·s−1. In GCPL mode the specific current was increased from 0.1 to 10 A·g−1. In order to obtain information about the IR drop, a rest period of 10 s was