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

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

• nitrogen gas. Cyclic voltammetry measurements were performed by sweeping the potential between 0.0 V and 1.0 V vs RHE at 50 mV/s for five cycles with a potentiostat (ALS 2323, BAS Inc.). Net ORR voltammograms were obtained as the difference between linear sweep voltammograms recorded at 1500 rpm in O2

Flexible freestanding MoS₂-based composite paper for energy conversion and storage

• Florian Zoller,
• Jan Luxa,
• Thomas Bein,
• Dina Fattakhova-Rohlfing,
• Daniel Bouša and
• Zdeněk Sofer

Beilstein J. Nanotechnol. 2019, 10, 1488–1496, doi:10.3762/bjnano.10.147

• paper for applications in supercapacitors (SCs). The capacitance was measured by a chronoamperometry technique in KCl solution (1 M) using different charging–discharging current densities (1–5 mA·cm−2) in a potential range determined by cyclic voltammetry (CV) shown in Supporting Information File 1

• -based composite paper was also tested as an anode material for LIBs. Hence, the MoS2-based composite paper was used directly as an anode without any binder, carbon additive or a Cu-foil current collector. Figure 5a shows the first four cycles of the cyclic voltammetry (CV) curves of the MoS2-based

• capacities at different current densities ranging from 0.1 to 2.0 A·g−1 and (d) cycling performance and coulombic efficiency at 0.2 A·g−1. Linear sweep voltammetry curves for the hydrogen evolution reaction measurements in 0.5 M H2SO4, 2 mV·s−1. Capacitance of MoS2-based composite paper measured using

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

• nanoparticles were electrochemically deposited onto CNT/CNT/GC and CNT/GC using linear-sweep voltammetry from 0 to −0.9 V vs Ag|AgCl|KClsat.. For comparison, Pt deposition onto oxidized GC was carried out in the same manner (compare Supporting Information File 1, Figure S7 for the resulting deposition curves

• , Figure S8). Electrochemical Investigations Cyclic voltammetry A basic electrochemical characterization of the prepared electrodes was carried out using cyclic voltammetry (CV). CVs of GC before and after oxidation in HNO3 as well as after growth of the primary CNTs and additional secondary CNTs are

• source to yield N-CNT/N-CNT/GC. Finally, Pt nanoparticles were electrochemically deposited onto CNT/GC and CNT/CNT/GC in an aqueous 0.005 M Pt(NO3)2 and 0.1 M NaNO3 solution via linear-sweep voltammetry from 0 to −0.9 V vs Ag|AgCl|KClsat at a scan rate of 5 mV s−1 to form Pt-CNT/GC and Pt-CNT/CNT/GC. For

Warped graphitic layers generated by oxidation of fullerene extraction residue and its oxygen reduction catalytic activity

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

Beilstein J. Nanotechnol. 2019, 10, 1391–1400, doi:10.3762/bjnano.10.137

• the amount of surface functional groups. The details of this technique are described elsewhere [45][46]. Electrochemical techniques Cyclic voltammetry was used to evaluate the heterogeneous electron transfer rate of the carbons in an aqueous solution consisting of 6 × 10−3 mol/L K3[Fe(CN)6] and 1 mol

• cyclic voltammograms in a potential range of 0.6 to −0.1 V vs Ag/AgCl at different sweep rates (1 to 50 mV/s). Linear sweep voltammetry with a rotating disk electrode was used to evaluate the ORR activity of the prepared carbons. The carbons were used to form a working electrode by using a Nafion (Nafion

Multicomponent bionanocomposites based on clay nanoarchitectures for electrochemical devices

• Giulia Lo Dico,
• Bernd Wicklein,
• Lorenzo Lisuzzo,
• Giuseppe Lazzara,
• Pilar Aranda and
• Eduardo Ruiz-Hitzky

Beilstein J. Nanotechnol. 2019, 10, 1303–1315, doi:10.3762/bjnano.10.129

• operational stability of EBCs [37][41]. Herein, the performance of the biosensor was evaluated by cyclic voltammetry exploiting the mediated electron transfer (MET) mechanism and the power density of the assembled biofuel cell is examined through polarization curves obtained with linear sweep voltammetry in

• tested as biosensor for the detection of glucose (Figure 5A). The performance of the biosensor was studied by cyclic voltammetry (CV) in the presence of potassium ferricyanide as mediator, relying on the mediated electron transfer (MET) mechanism. Figure 5B shows the CV curve of the biosensor in response

• [71]: The reaction occurring on the anode surface is: while the Pt cathode catalyses the reaction: Linear sweep voltammetry (LSV) experiments were carried out to evaluate the electrocatalytic properties of the bionanocomposite Foam-GOx as 3D bio-anode. Figure 5D displays the catalytic behaviour during

Alloyed Pt₃M (M = Co, Ni) nanoparticles supported on S- and N-doped carbon nanotubes for the oxygen reduction reaction

• Stéphane Louisia,
• Yohann R. J. Thomas,
• Pierre Lecante,
• Marie Heitzmann,
• M. Rosa Axet,
• Pierre-André Jacques and
• Philippe Serp

Beilstein J. Nanotechnol. 2019, 10, 1251–1269, doi:10.3762/bjnano.10.125

• with a commercial Pt3Co/Vulcan XC-72 (Pt3Co/CB) catalyst. This commercial reference has shown excellent activity in RRDE and during single cell tests [5]. Figure 4a,b shows the cyclic voltammetry (CV) curves obtained in N2-purged 0.5 M H2SO4 for Pt3Co/N-CNT, Pt3Co/N-CNTHT, Pt3Co/S-CNT, Pt3Ni/N-CNT

Porous N- and S-doped carbon–carbon composite electrodes by soft-templating for redox flow batteries

• Maike Schnucklake,
• László Eifert,
• Jonathan Schneider,
• Roswitha Zeis and
• Christina Roth

Beilstein J. Nanotechnol. 2019, 10, 1131–1139, doi:10.3762/bjnano.10.113

• obtained inside the macroporous carbon felt. For the investigation of electrode structure and porosity X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and nitrogen sorption (BET) were used. The electrochemical performance of the carbon felts was evaluated by cyclic voltammetry

• felt (a,b) and the co-doped composite electrode (1000 / N+S; c,d): spectra of C 1s (left) and O 1s region (right). Comparison between the cyclic voltammetry curves of the N-doped (purple) and co-doped (blue, green) composite electrode as well as the carbonized (orange, red) and the pristine (black

Glucose-derived carbon materials with tailored properties as electrocatalysts for the oxygen reduction reaction

• Rafael Gomes Morais,
• Natalia Rey-Raap,
• José Luís Figueiredo and
• Manuel Fernando Ribeiro Pereira

Beilstein J. Nanotechnol. 2019, 10, 1089–1102, doi:10.3762/bjnano.10.109

• basic electrolyte at 1600 rpm and the Nyquist plot obtained from electrochemical impedance spectroscopy measurements are shown in Figure 2a and 2b, respectively. To evaluate the performance of the prepared electrocatalysts, cyclic voltammetry (CV) and linear sweep voltammetry (LSV) were performed. LSV

• speed controller allowed the rotation of the working electrode to be adjusted according to the assessments being done. The experiments were carried out at room temperature in a 0.1 mol L−1 KOH solution saturated with N2 or O2 for 30 min before the cyclic voltammetry (CV) and linear sweep voltammetry

• ) of the activated carbons. Linear sweep voltammetry recorded in an O2-saturated 0.1 mol L−1 KOH electrolyte at 1600 rpm (a) and Nyquist plot obtained from electrochemical impedance spectroscopy (b). Relationship between BET surface area and the limiting current density of the activated samples