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Vasily Artemov

Publications and source records attributed to Vasily Artemov.

4 recordsLinked to original sources

All-water supercapacitor enabled by 1-nm clay channels

Water confined to channels one nanometer thick exhibits electrochemical behavior distinct from bulk water, including enhanced protonic conductivity and large dielectric anisotropy. Here, we exploit these characteristics to design a scalable electrochemical energy-storage system ("blue capacitor") constructed entirely from naturally abundant materials. By assembling layered clays and conductive graphene, we produce 1-nm-thick channels in which confined water acts as the sole electrolyte. We systematically study different clay types, the electrode composition, and separator thickness using complementary physicochemical and electrochemical techniques. The device operates stably up to 1.6 V, achieves specific capacitances of up to 40 F/g, nearly 100% coulombic efficiency, and stable performance over more than 60,000 charge-discharge cycles. Structural and dynamic analyses validate the device architecture, water purity, and proton transport in the nanopores. These results demonstrate that nanoconfined water can function as an electrolyte in a macroscopic electrochemical device, providing a platform for exploring sustainable aqueous energy-storage systems.

cond-mat.soft↗

Isotopic Fingerprints of Proton-mediated Dielectric Relaxation in Solid and Liquid Water

We report cross-validated measurements of the isotope effect on dielectric relaxation for four isotopologues of ice and water, including the 1-10^5 Hz region, in which only sporadic and inconsistent measurements were previously available. In ice, the relaxation rates exhibit an activated temperature dependence with an isotope-independent activation energy. Across 248-273 K, the H_2O/D_2O relaxation rate ratio remains constant at 2.0 \pm 0.1. This scaling agrees with Kramers' theory in the high-friction limit if the moving mass is the proton or deuteron, indicating that dielectric relaxation is governed by a classic proton transfer over an energy barrier rather than molecular reorientation.

physics.chem-ph↗

Nanofluidic logic with mechano-ionic memristive switches

While most neuromorphic systems are based on nanoscale electronic devices, nature relies on ions for energy-efficient information processing. Therefore, finding memristive nanofluidic devices is a milestone toward realizing electrolytic computers mimicking the brain down to its basic principles of operation. Here, we present a nanofluidic device designed for circuit scale in-memory processing that combines single-digit nanometric confinement and large entrance asymmetry. Our fabrication process is scalable while the device operates at the second timescale with a conductance ratio in the range 10-60. In-operando optical microscopy unveils the origin of memory, arising from the reversible formation of liquid blisters modulating the device conductance. The combination of features of these mechano-ionic memristive switches permits assembling logic circuits composed of two interactive devices and an ohmic resistor. These results open the way to design multi-component ionic machinery, such as nanofluidic neural networks, and implementing brain-inspired ionic computations.

cond-mat.soft↗

Elucidating contact electrification mechanism of water

The open water surface is known to be charged. Yet, the magnitude of the charge and the physical mechanism of the charging remain unclear, causing heated debates across the scientific community. Here we directly measure the charge Q of microdrops ejected from hydrophilic and hydrophobic capillaries and show that the water surface can take both positive or negative charge values depending on pH and the capillary type. Our experiments, theory, and simulations provide evidence that a junction of two aqueous interfaces with a different ion adsorption energy (e.g., liquid-solid and liquid-air interfaces) develops a pH-dependent contact potential difference Δϕ up to 52 mV. The longitudinal charge transfer between the interfaces stimulated by Δϕ determines the charge of the open water surface. The suggested static electrification mechanism provides far-reaching insights into the origin of electrical potentials in biological and electrochemical energy systems.

cond-mat.soft↗