General Capacitance Upper Limit and Its Manifestation for Aqueous Graphene Interfaces.

Double-layer capacitance (Cdl) is essential for chemical and biological sensors and capacitor applications. The correct formula for Cdl is a controversial subject for practically useful graphene interfaces with water, aqueous solutions, and other liquids. We have developed a model of Cdl, considering the capacitance of a charge accumulation layer (Cca) and capacitance (Ce) of a capacitance-limiting edge region with negligible electric susceptibility and conductivity between this layer and the capacitor electrode. These capacitances are connected in series, and Cdl can be obtained from 1/Cdl = 1/Cca + 1/Ce. In the case of aqueous graphene interfaces, this model predicts that Cdl is significantly affected by Ce. We have studied the graphene/water interface capacitance by low-frequency impedance spectroscopy. Comparison of the model predictions with the experimental results implies that the distance from charge carriers in graphene to the nearest molecular charges at the interface can be ~(0.05-0.1)nm and is about a typical length of the carbon-hydrogen bond. Generalization of this model, assuming that such an edge region between a conducting electrode and a charge accumulating region is intrinsic for a broad range of non-faradaic capacitors and cannot be thinner than an atomic size of ~0.05 nm, predicts a general capacitance upper limit of ~18 µF/cm2.

Ga-In Alloy Segregation within a Porous Glass as Studied by SANS.

Nanolattices can play the role of templates for metals and metallic alloys to produce functional nanocomposites with particular properties affected by nanoconfinement. To imitate the impact of nanoconfinement on the structure of solid eutectic alloys, we filled porous silica glasses with the Ga-In alloy, which is widely used in applications. Small-angle neutron scattering was observed for two nanocomposites, which comprised alloys of close compositions. The results obtained were treated using different approaches: the common Guinier and extended Guinier models, the recently suggested computer simulation method based on the initial formulae for neutron scattering, and ordinary estimates of the scattering hump positions. All of the approaches predicted a similar structure of the confined eutectic alloy. The formation of ellipsoid-like indium-rich segregates was demonstrated.

Magnetic Studies of Superconductivity in the Ga-Sn Alloy Regular Nanostructures.

For applications of nanolattices in low-temperature nanoelectronics, the inter-unit space can be filled with superconducting metallic alloys. However, superconductivity under nanoconfinement is expected to be strongly affected by size-effects and other factors. We studied the magnetic properties and structure of the Ga-Sn eutectic alloy within regular nanopores of an opal template, to understand the specifics of the alloy superconductivity. Two superconducting transitions were observed, in contrast to the bulk alloy. The transitions were ascribed to the segregates with the structures of tetragonal tin and a particular gallium polymorph. The superconducting-phase diagram was constructed, which demonstrated crossovers from the positive- to the common negative-curvature of the upper critical-field lines. Hysteresis was found between the susceptibilities obtained at cooling and warming in the applied magnetic field.

SANS Studies of the Gallium-Indium Alloy Structure within Regular Nanopores.

Potential applications of nanolattices often require filling their empty space with eutectic metallic alloys. Due to confinement to nanolattices, the structure of phase segregates in eutectic alloys can differ from that in bulk. These problems are poorly understood now. We have used small angle neutron scattering (SANS) to study the segregation in the Ga-In alloy confined to an opal template with the regular pore network, created by a strict regularity of opal constituents in close similarity with nanolattices. We showed that SANS is a powerful tool to reveal the configuration of segregated phases within nanotemplates. The In-rich segregates were found to have specific structural features as small sizes and ordered arrangement.

Influence of Substrate Microstructure on the Transport Properties of CVD-Graphene.

We report the study of electrical transport in few-layered CVD-graphene located on nanostructured surfaces in view of its potential application as a transparent contact to optoelectronic devices. Two specific surfaces with a different characteristic feature scale are analyzed: semiconductor micropyramids covered with SiO2 layer and opal structures composed of SiO2 nanospheres. Scanning tunneling microscopy (STM) and scanning electron microscopy (SEM), as well as Raman spectroscopy, have been used to determine graphene/substrate surface profile. The graphene transfer on the opal face centered cubic arrangement of spheres with a diameter of 230 nm leads to graphene corrugation (graphene partially reproduces the opal surface profile). This structure results in a reduction by more than 3 times of the graphene sheet conductivity compared to the conductivity of reference graphene located on a planar SiO2 surface but does not affect the contact resistance to graphene. The graphene transfer onto an organized array of micropyramids results in a graphene suspension. Unlike opal, the graphene suspension on pyramids leads to a reduction of both the contact resistance and the sheet resistance of graphene compared to resistance of the reference graphene/flat SiO2 sample. The sample annealing is favorable to improve the contact resistance to CVD-graphene; however, it leads to the increase of its sheet resistance.