Humidity-dependent electrical performance of CuO nanowire networks studied by electrochemical impedance spectroscopy

• Jelena Kosmaca,
• Juris Katkevics,
• Jana Andzane,
• Raitis Sondors,
• Liga Jasulaneca,
• Raimonds Meija,
• Kiryl Niherysh,
• Yelyzaveta Rublova and
• Donats Erts

Beilstein J. Nanotechnol. 2023, 14, 683–691, doi:10.3762/bjnano.14.54

• chemisorption and physisorption at the nanowire interface, which suppress electronic transport inside the p-type semiconductor nanowire but enhance ionic transport in the water layers adsorbed on the nanowire surface. Possible physicochemical processes at the nanowire surface are discussed in line with

• explained by parallel contributions to the net electrical signal from different conduction paths, for example, electronic and ionic transport inside the material and on the surface [29]. First, the conduction at very low RH is presumed to be primarily due to electronic transport inside the material. The CuO

• surface (Figure 3c), H+ hopping between neighbouring OH− sites on the nanowire surface can be activated, which is an alternative conduction mechanism [29]. This ionic transport on the surface can compensate for the decrease of electronic transport conductivity inside the material. Since water

Electrical, electrochemical and structural studies of a chlorine-derived ionic liquid-based polymer gel electrolyte

• Ashish Gupta,
• Amrita Jain,
• Manju Kumari and
• Santosh K. Tripathi

Beilstein J. Nanotechnol. 2021, 12, 1252–1261, doi:10.3762/bjnano.12.92

• . Thereafter, the resultant current as a function of time is monitored. In order to calculate the values of the ionic transport number, Equation 2 was used and this value was found to be 0.91. This means that the total conductivity in the present electrolyte films is primarily due to ions, and the electron

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

• multiple chemical processes. Because the number of active sites is increased, a faster ionic transport is observed. Also, a specific capacitance of 260 F·g−1 was measured [21]. Jiang et al. developed a layered Co(OH)2/Ti3C2Tx composite material via growing Co(OH)2 nanosheets onto Ti3C2Tx MXene. The total

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

• CGCNF electrochemical performance. By improving fiber alignment, increasing the number of mesopores and enhancing the electrode specific surface area, one can effectively improve the electrochemical performance of an electrode. These improvements can significantly contribute to the electronic and ionic

• transport by decreasing the transfer resistance of electrodes. When compared to DCGCNFs and OCGCNFs, OPCGCNFs have a highly ordered structure and a larger number of mesopores. These features were achieved by simply using MPEM and adding DIW in the spinning solution. In addition, OPCGCNFs had a better

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

• porosity, stable structure, and the continuous conductive networks provide the electrodes with fast electronic and ionic transport paths [22][23][34][35]. This design and fabrication of all-fiber-based batteries provides a novel strategy for the development of advanced flexible lithium-ion batteries

Trapping polysulfide on two-dimensional molybdenum disulfide for Li–S batteries through phase selection with optimized binding

• Sha Dong,
• Xiaoli Sun and
• Zhiguo Wang

Beilstein J. Nanotechnol. 2019, 10, 774–780, doi:10.3762/bjnano.10.77

• nanotubes and porous materials, has been a common strategy to minimize the leakage of LPSs. However, the function of physical confinement is limited, and it slows down diffusion for ionic transport [9]. The addition of anchoring materials into the cathodes with a strong binding affinity to LPSs was thought

Review of time-resolved non-contact electrostatic force microscopy techniques with applications to ionic transport measurements

• Aaron Mascaro,
• Yoichi Miyahara,
• Tyler Enright,
• Omur E. Dagdeviren and
• Peter Grütter

Beilstein J. Nanotechnol. 2019, 10, 617–633, doi:10.3762/bjnano.10.62

• period of the cantilever and compare and contrast it with those previously established. Keywords: atomic force microscopy; electrostatic force microscopy; ionic transport; lithium ion batteries; nanotechnology; Introduction Since the inception of the atomic force microscope (AFM) a variety of

• difference (which can be used to extract the local work function) [1] and local piezoelectric response [2], and dynamic properties such as the charging and decay times of photoexcited carriers [3][4][5][6], and local activation energies for ionic transport [7][8]. These measurements play a crucial role in

• -domain EFM to measure ionic transport [7][12], time-resolved electrochemical strain microscopy (ESM) to measure ionic transport [8][13], various time-resolved Kelvin probe force microscopy (KPFM) techniques that utilize either optical pump-probe or advanced signal processing to measure time-resolved

Nanoscale electrochemical response of lithium-ion cathodes: a combined study using C-AFM and SIMS

• Jonathan Op de Beeck,
• Nouha Labyedh,
• Alfonso Sepúlveda,
• Valentina Spampinato,
• Alexis Franquet,
• Thierry Conard,
• Philippe M. Vereecken,
• Wilfried Vandervorst and
• Umberto Celano

Beilstein J. Nanotechnol. 2018, 9, 1623–1628, doi:10.3762/bjnano.9.154

• processes in the thin films, at their interfaces and the combined electronic–ionic transport. It goes without saying that in sub-micrometer films thickness, the nanoionic properties of the system become more dominant and, similarly, the interfaces between layers represent a higher (compared to bulk) volume

Nanoporous silicon nitride-based membranes of controlled pore size, shape and areal density: Fabrication as well as electrophoretic and molecular filtering characterization

• Axel Seidenstücker,
• Stefan Beirle,
• Fabian Enderle,
• Paul Ziemann,
• Othmar Marti and
• Alfred Plettl

Beilstein J. Nanotechnol. 2018, 9, 1390–1398, doi:10.3762/bjnano.9.131

• an array of millions of nanopores were characterized first by ionic transport measurements. The tests were performed on the three types, A, B and C, of membranes introduced above. The membranes were mounted between a cis- and trans-chamber made of Teflon, each equipped with an Ag/AgCl electrode

• such as pore shape and size (ranging between 14 and 50 nm) as well as inter-pore distance. By electrophoretic experiments and comparison to theory, the usability of the porous membranes for ionic transport has been proven. Additionally, size-selective filtering has been demonstrated by experimental

• . Diameter distributions for the Au NP etch mask (green) and the resulting nanopores of membrane C on the front side (black) and on the back side (red). Vertical bars represent experimental data to which the shaded Gaussians were fitted. Ionic transport measured through the three membranes A, B and C for KCl

First examples of organosilica-based ionogels: synthesis and electrochemical behavior

• Andreas Taubert,
• Ruben Löbbicke,
• Barbara Kirchner and
• Fabrice Leroux

Beilstein J. Nanotechnol. 2017, 8, 736–751, doi:10.3762/bjnano.8.77

• the zwitterionic nature of the [BmimSO3H][PTS] IL will lead to very strong interactions within the IL rather than between the IL and the silica pore wall. The main advantage of this behavior is that the IL is “self-sufficient” as far as the ionic transport is concerned and transport properties will

A facile synthesis of a carbon-encapsulated Fe₃O₄ nanocomposite and its performance as anode in lithium-ion batteries

• Raju Prakash,
• Katharina Fanselau,
• Shuhua Ren,
• Tapan Kumar Mandal,
• Christian Kübel,
• Horst Hahn and
• Maximilian Fichtner

Beilstein J. Nanotechnol. 2013, 4, 699–704, doi:10.3762/bjnano.4.79

• attributed to its special morphology, porosity and also the synergistic effect by combining metal oxide and carbon nanotubes, which provides better electronic and ionic transport, as well as a tolerance toward the volume change during the reaction. In summary, a new carbon encapsulated Fe3O4 nanocomposite

Large-scale atomistic and quantum-mechanical simulations of a Nafion membrane: Morphology, proton solvation and charge transport

• Pavel V. Komarov,
• Pavel G. Khalatur and
• Alexei R. Khokhlov

Beilstein J. Nanotechnol. 2013, 4, 567–587, doi:10.3762/bjnano.4.65

• water content in the system. In fact, these channels represent conductive nano-wires which should be responsible for the ionic transport during the operation of a fuel cell. From a global point of view, the channels can be considered as a spatial continuous network organized in an irregular ordered

Parallel- and serial-contact electrochemical metallization of monolayer nanopatterns: A versatile synthetic tool en route to bottom-up assembly of electric nanocircuits

• Jonathan Berson,
• Assaf Zeira,
• Rivka Maoz and
• Jacob Sagiv

Beilstein J. Nanotechnol. 2012, 3, 134–143, doi:10.3762/bjnano.3.14

• electrochemical rather than adhesion-promoted [32][33][34][35], involving dissolution of stamp-metal grains (anode), ionic transport through an ultrathin water film adsorbed on the metal grains, and subsequent nucleation and growth of new metal grains at the target monolayer (cathode); (ii) metal grains can