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

• were submitted to carbonization under a N2 atmosphere at 1100 °C. The influence of the ordering and porosity of CGCNFs on their electrochemical performance was studied. The results showed that by adding deionized water to the spinning solution one could increase the number of mesopores and the specific

• improvement of the current supercapacitor electrochemical performance, the capacitance and cycle stability of supercapacitors are still subjects of research interest. Electrospinning is one of the most convenient methods to synthesize nanofibers in a continuous manner. Electrospinning has many advantages over

• conductivity impedes their use in high-power-density supercapacitors. Therefore, by adding high-performance conductive materials one can enhance the electrochemical performance of carbon nanofibers. Experiments have shown that by introducing graphene into the carbon matrix, various mechanical and

Role of redox-active axial ligands of metal porphyrins adsorbed at solid–liquid interfaces in a liquid-STM setup

• Thomas Habets,
• Sylvia Speller and
• Johannes A. A. W. Elemans

Beilstein J. Nanotechnol. 2020, 11, 1264–1271, doi:10.3762/bjnano.11.110

• of these complications may be eliminated by adding a third, reference electrode to the setup and by using a conducting electrolyte (so that it turns into a so-called electrochemical (EC) STM [20][21]). At the same time, the absence of an electrolyte, which typically contains a high concentration of

• added salts, allows us to pinpoint the behavior of the axial ligand of our catalyst in the non-polar liquid in which also our catalysis studies were carried out. Still, our system shows several of the characteristics of a conventional electrochemical cell. Apart from the bias dependency of the reaction

Ultrasensitive detection of cadmium ions using a microcantilever-based piezoresistive sensor for groundwater

• Dinesh Rotake,
• Anand Darji and
• Nitin Kale

Beilstein J. Nanotechnol. 2020, 11, 1242–1253, doi:10.3762/bjnano.11.108

• , expensive, and not suitable for on-site determination. The calorimetric approach proposed by [34][35][36][37] is free from these problems but not capable of differentiating between two nearby ranges and the LOD is also on the higher side. The electrochemical sensor described in [38] is a good approach, but

Gas sorption porosimetry for the evaluation of hard carbons as anodes for Li- and Na-ion batteries

• Yuko Matsukawa,
• Fabian Linsenmann,
• Maximilian A. Plass,
• George Hasegawa,
• Katsuro Hayashi and
• Tim-Patrick Fellinger

Beilstein J. Nanotechnol. 2020, 11, 1217–1229, doi:10.3762/bjnano.11.106

• pores is nontrivial, we herein employ Kr, N2 and CO2 gas sorption porosimetry, as well as H2O vapor sorption porosimetry, to investigate eight hard carbons. Electrochemical lithium as well as sodium storage tests are compared to the obtained apparent surface areas and pore volumes. H2O, and more

• decomposition at potentials below the stability window of the electrolyte (for LIBs typically around 0.8 VLi) [21]. Since the dielectric SEI passivates the electrode, an irreversible capacity proportional to the electrochemical active surface area is expected. Accordingly, the reduction of the specific surface

• –electrolyte interphase, HCs can act as molecular sieves. Here, Na ions are adsorbed in the pores in a metal-plating-like mechanism and separated from bigger solvent molecules that suffer from electrochemical reductive decomposition at potentials below ca. 0.8 VLi or towards the alkali metal, respectively

Excitonic and electronic transitions in Me–Sb₂Se₃ structures

• Nicolae N. Syrbu,
• Victor V. Zalamai,
• Ivan G. Stamov and
• Stepan I. Beril

Beilstein J. Nanotechnol. 2020, 11, 1045–1053, doi:10.3762/bjnano.11.89

• (In–Sb2Se3) contacts, the structures were obtained by either thermal sputtering under vacuum or electrochemical deposition onto the cleaved faces of single crystals (Figure 3A). Current–voltage characteristics suggest that the contacts have an ohmic behavior. The impedance has a frequency dependence

• . The increase in intensity with the applied voltage confirms the excitonic character of the maximum, which is consistent with the fact that the binding energy of these excitons is 130–136 meV. The In–Sb2Se3 structures, in which the contacts were deposited by electrochemical methods, show

• structures and the excitonic band symmetries in the Brillouin zone center for crystals with an orthorhombic symmetry (Pnma). The In–Sb2Se3 structures were generated either by thermal sputtering under vacuum or by electrochemical deposition. The photoconductivity spectra at different applied voltages were

Gas-sensing features of nanostructured tellurium thin films

• Dumitru Tsiulyanu

Beilstein J. Nanotechnol. 2020, 11, 1010–1018, doi:10.3762/bjnano.11.85

• given to growing, studying and applying nanostructured Te. To achieve these goals, different and sometimes quite sophisticated chemical, electrochemical and physical methods have been developed. In line with this, Wang and collaborators [12] used thermal decomposition of Te dietyldithiocarbamato film to

Electrochemical nanostructuring of (111) oriented GaAs crystals: from porous structures to nanowires

• Elena I. Monaico,
• Eduard V. Monaico,
• Veaceslav V. Ursaki,
• Shashank Honnali,
• Vitalie Postolache,
• Karin Leistner,
• Kornelius Nielsch and
• Ion M. Tiginyanu

Beilstein J. Nanotechnol. 2020, 11, 966–975, doi:10.3762/bjnano.11.81

• , Chisinau MD-2001, Republic of Moldova Leibniz IFW Dresden, Helmholtzstr. 20, 01069 Dresden, Germany 10.3762/bjnano.11.81 Abstract A comparative study of the anodization processes occurring at the GaAs(111)A and GaAs(111)B surfaces exposed to electrochemical etching in neutral NaCl and acidic HNO3 aqueous

• Electrochemical technology became an established and cost-effective approach for the preparation of porous semiconductor matrices and arrays of nanowires with tailored architecture at the submicrometer scale [1][2][3]. Semiconductor nanotemplates provide many possibilities for nanofabrication through

• templating, anisotropic chemical etching, localized anodic etching, and isotropic anodic oxidation [15][16]. However, this is a complex multistep technology. A more simple and cost-effective technology was applied for obtaining triangular GaAs nanowires through electrochemical etching of GaAs(100) surfaces

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

• well documented in the literature, and this paper provides a direct comparison under identical experimental conditions of electrochemical measurements and in identical units. In the first method, based on classical engineering, the bimetallic catalyst is deposited by dip-coating in a precursor solution

• ); Introduction Reversible electrochemical energy storage devices such as rechargeable batteries, redox flow batteries (RFBs) and regenerative fuel cells (bifunctional devices able to work as electrolyzers and fuel cells) are at the forefront of a renewable energy economy as they allow one to overcome the

• methods [12] as well as particles of various sizes [13] and shapes [14]. However, each study is presented as a self-sufficient piece of work with limited critical comparison to the state of the art. The conditions under which electrochemical performance is quantified (electrode substrate, electrolyte

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

• method. CTF-1-600 and Ni/CTF-1-600 show high catalytic activity towards OER and a clear activity for the electrochemical oxygen reduction reaction (ORR). Ni/CTF-1-600 requires 374 mV overpotential in OER to reach 10 mA/cm2, which outperforms the benchmark RuO2 catalyst, which requires 403 mV under the

• OER catalysts or catalyst support and the activities were far lower than that of benchmark OER catalysts [38][39]. At present, there are no reports about nickel/CTF catalysts for electrochemical OER studies, to the best of our knowledge. Although various carbon materials or nitrogen-doped carbon

• nanoparticles supported on CTF-1 in the ionic liquid (IL) [BMIm][NTf2] using a microwave-assisted synthesis. The obtained material Ni/CTF-1 was investigated as a catalyst for electrochemical OER and ORR for the first time and showed a superior OER performance compared to commercial RuO2 under alkaline

Hexagonal boron nitride: a review of the emerging material platform for single-photon sources and the spin–photon interface

• Stefania Castelletto,
• Faraz A. Inam,
• Shin-ichiro Sato and
• Alberto Boretti

Beilstein J. Nanotechnol. 2020, 11, 740–769, doi:10.3762/bjnano.11.61

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

• (SCE) as reference electrode were used for the electrochemical testing of the exfoliated MoO3 dispersions and its composites. In brief, the GCE was cleaned with a polishing cloth using fine alumina abrasive powders and washed thoroughly in deionized water. The required amount of the dispersion of known

• were then dripped on the GCE. All electrochemical measurements were performed in 1 M H2SO4 electrolyte. Two-electrode system: The optimized ratio obtained from measurements of the three-electrode configuration were used to fabricate two-electrode devices. The respective amounts of MoO3 and carbon black

Preparation, characterization and photocatalytic performance of heterostructured CuO–ZnO-loaded composite nanofiber membranes

• Wei Fang,
• Liang Yu and
• Lan Xu

Beilstein J. Nanotechnol. 2020, 11, 631–650, doi:10.3762/bjnano.11.50

• protection. Water pollution with organic dyes (such as congo red, methylene blue, and methyl orange) is becoming a major environmental problem. Therefore, water purification technologies, such as photocatalytic purification, electrochemical oxidation, membrane filtration, ozonation, and chlorination

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

• producing biocompatible CDs from biomass and biowaste and manipulating their PL characteristics. It is worth mentioning that we [33] previously studied the electrochemical performance of carbon particles of micrometer size, which were synthesized from the soybean residuals via hydrothermal carbonization and

• high-temperature annealing in nitrogen. In contrast to the analysis of the electrochemical performance of large carbon particles of micrometer size [33], this work is focused on the optical characteristics of nanometer-sized CDs, which are synthesized by two different approaches. One is similar to the

• one used for the electrochemical study and the other uses multiple processes including annealing in argon. Note that filtration is needed to obtain carbon nanoparticles from the carbonized soybean residual. Experimental Hydrothermal carbonization Following the approach in Wang et al. [33], we

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

• , Institute of Building Energetics, Thermal Engineering and Energy Storage (IGTE), Pfaffenwaldring 31, 70569 Stuttgart, Germany 10.3762/bjnano.11.46 Abstract Electrochemical strain microscopy (ESM) is a powerful atomic force microscopy (AFM) mode for the investigation of ion dynamics and activities in energy

• ionic concentration in the material volume under the AFM tip. The ageing of the cathode is found to be governed by a decrease of the electrochemical activity and the loss of available lithium for cycling, which can be stored in the cathode. Keywords: activity; ageing; cathode; electrochemical strain

• additional mechanical (stiffness, elasticity), electrical (conductivity, surface potential), electrochemical (reactivity, mobility and activity), mechanoelectrical (piezoelectricity) and chemical (chemical bonding) material properties. In situ AFM imaging of the sample topography is often used to study the

Nanoarchitectonics: bottom-up creation of functional materials and systems

• Katsuhiko Ariga

Beilstein J. Nanotechnol. 2020, 11, 450–452, doi:10.3762/bjnano.11.36

• spectroscopy [37], bio-nanocomposites with clay nanoarchitectures for electrochemical devices [38], a biomimetic nanofluidic diode with polymeric carbon nitride nanotubes [39], and a unique Janus-micromotor applied as a luminescence sensor for sensitive TNT detection [40]. The variety of nanoarchitectonics

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

• Munaiah Yeddala Pallavi Thakur Anugraha A Tharangattu N. Narayanan Tata Institute of Fundamental Research - Hyderabad, Sy. No. 36/P, Gopanapally Village, Serilingampally Mandal, Hyderabad 500107, India 10.3762/bjnano.11.34 Abstract On-site peroxide generation via electrochemical reduction is

• gaining tremendous attention due to its importance in many fields, including water treatment technologies. Oxidized graphitic carbon-based materials have been recently proposed as an alternative to metal-based catalysts in the electrochemical oxygen reduction reaction (ORR), and in this work we unravel

• the role of C=O groups in graphene towards sustainable peroxide formation. We demonstrate a versatile single-step electrochemical exfoliation of graphite to graphene with a controllable degree of oxygen functionalities and thickness, leading to the formation of large quantities of functionalized

Synthesis and enhanced photocatalytic performance of 0D/2D CuO/tourmaline composite photocatalysts

• Changqiang Yu,
• Min Wen,
• Zhen Tong,
• Shuhua Li,
• Yanhong Yin,
• Xianbin Liu,
• Yesheng Li,
• Tongxiang Liang,
• Ziping Wu and
• Dionysios D. Dionysiou

Beilstein J. Nanotechnol. 2020, 11, 407–416, doi:10.3762/bjnano.11.31

• . The transient photocurrent was measured with two Interface 1010E electrochemical workstations (Gamry, USA) using Na2SO3 (0.2 M) and Na2S (0.2 M) solutions with a volume ratio of 1:1 as electrolyte under LED lamp (λ = 470 nm) irradiation for 20 min. The samples were prepared as follows: Firstly, 10 mg

• Information File 1, Figure S1). Generally speaking, the higher the transient photocurrent density, the smaller the electrochemical impedance spectra (EIS) [33][34]. According to the time-resolved PL spectra in Figure 5d, the average fluorescence lifetime of the CuO/tourmaline composite (2.94 ns) was shortened

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

• can provide a much higher specific capacitance as a result of rapid reversible redox reactions [9][10]. Recently, advanced electrode materials based on transition metal molybdates such as NiMoO4 [11], CoMoO4 [12], MnMoO4 [13] and FeMoO4 [14] with suitable oxidation states and unique electrochemical

• properties are regarded as very promising materials for pseudocapacitors [15][16]. Particularly, NiMoO4 has been widely applied in high-performance pseudocapacitors due to its enhanced electrochemical properties resulting from the high electrochemical activity of the Ni ion and the superb electrical

• construction of an integrated hierarchical porous nanoarchitecture by combining two metal oxides is a brilliant way to greatly enhance the overall electrochemical performance owing to synergistic effects [20]. For example, Li et al. synthesized 3D hybrid Co3O4/NiMoO4 nanowire/nanosheet arrays on a carbon cloth

Rational design of block copolymer self-assemblies in photodynamic therapy

• Maxime Demazeau,
• Laure Gibot,
• Anne-Françoise Mingotaud,
• Patricia Vicendo,
• Clément Roux and
• Barbara Lonetti

Beilstein J. Nanotechnol. 2020, 11, 180–212, doi:10.3762/bjnano.11.15

Molecular architectonics of DNA for functional nanoarchitectures

• Debasis Ghosh,
• Lakshmi P. Datta and
• Thimmaiah Govindaraju

Beilstein J. Nanotechnol. 2020, 11, 124–140, doi:10.3762/bjnano.11.11

• vector and provided efficient sensing of changes in the intracellular acidic pH value. In recent years, DNA thin film-based biosensors received significant interest for the detection of biologically relevant analytes, such has forensic samples [61][62]. The design of active electrochemical DNA sensors

• involves critical optimization of the sensor platforms. The length of the target oligonucleotide sequence and the selective use of dopants significantly dominate the sensing efficacy [63]. In this context, electrochemical DNA sensors were developed by noncovalent layer-by-layer assemblies of phenothiazine

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

• temperature naturally. The resulting product was collected and used for the electrochemical supercapacitor measurements. The obtained results were compared with the as-synthesized rGO nanosheets. Materials characterization The samples were characterized using transmission electron microscopy (TEM), atomic

• °C·min−1 using a Mettler-Toledo-TG-850 apparatus. AFM measurements were performed using a CP2 atomic force microscope. Electrode preparation and electrochemical characterization The catalyst inks of as-synthesized rGO and reduced graphene oxide H-rGO were prepared by ultrasonication separately. A mixture

• 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

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

• decomposition of the carbon framework and a decrease of the N content [29][30]. The availability of active sites (for a certain electrochemical reaction) correlates with the electrochemically active surface area for this reaction. For most conventional porous carbon materials micropores contribute significantly

• to the surface area, but their small pore size is considered to only allow a limited mass transport, which might result in a low accessibility of the active sites therein for electrochemical processes. Investigations of N-doped 3D ordered porous carbon materials showed, e.g., that a high content of

• correlations between structural properties and electrochemical performance. In the following we will first give a detailed structural and chemical analysis of the resulting materials (section 1 in “Results and Discussion”), followed by a discussion of their performance as ORR catalyst in electrocatalytic

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

• insertion material, because magnesium can form intermetallic compounds with antimony. In addition, Sb has a rhombohedral crystal structure, which can form an alloy over a wide composition range [6][7]. The high initial capacity of 298 mAh/g at 1C rate has been reported for electrochemical magnetization at

• 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

• deposition on a Au electrode was carried out by Jung [8], who found that antimony deposition on Au(100) and Au(111) in acid electrolyte undergoes two electrochemical processes involving an irreversible adsorption and underpotential deposition. This irreversible adsorption was attributed to oxygenous Sb(III

Label-free highly sensitive probe detection with novel hierarchical SERS substrates fabricated by nanoindentation and chemical reaction methods

• Jingran Zhang,
• Tianqi Jia,
• Yongda Yan,
• Li Wang,
• Peng Miao,
• Yimin Han,
• Xinming Zhang,
• Guangfeng Shi,
• Yanquan Geng,
• Zhankun Weng,
• Daniel Laipple and
• Zuobin Wang

Beilstein J. Nanotechnol. 2019, 10, 2483–2496, doi:10.3762/bjnano.10.239

• nanoparticles or micro/nanostructures can be applied as a SERS sensor to detect adsorbed markers. Generally, nanoparticles can be fabricated as SERS substrates at low cost and high production via chemical synthesis methods [8][9][10][11][12][13], including chemical/electrochemical deposition and electrochemical

• etching. For instance, Chen et al. [8] employed an electrochemical etching method to fabricate nanocube structures on a Cu30Mn70 surface by controlling the voltage. In addition, Zhang et al. [10] showed that gold nanoparticles can be fabricated by a gold etchant on a silicon surface as SERS substrates

Semitransparent Sb₂S₃ thin film solar cells by ultrasonic spray pyrolysis for use in solar windows

• Jako S. Eensalu,
• Atanas Katerski,
• Erki Kärber,
• Lothar Weinhardt,
• Monika Blum,
• Clemens Heske,
• Wanli Yang,
• Ilona Oja Acik and
• Malle Krunks

Beilstein J. Nanotechnol. 2019, 10, 2396–2409, doi:10.3762/bjnano.10.230

• in photo-electrochemical cells, thin film cells, extremely thin absorber (ETA) cells, and hybrid solar cells based on a planar underlay or on nano- or mesostructured scaffolds [15][16][17][18][19][20][21][22]. Studies on ETA Sb2S3 cells, which became the basis for respective hybrid solar cells, were