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Lucie Navratilova

Publications and source records attributed to Lucie Navratilova.

2 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

Thin-wall Single-crystal Gold Nanoelectrodes towards Advanced Chemical Probing and Imaging

Thin-wall metal ultramicro- and nanoelectrodes (UMEs/NEs), especially gold NEs, are indispensable for high-resolution electrochemical microscopy, biosensing, and fundamental research. However, their damage susceptibility and the lack of scalable fabrication methods hinder broader adoption. We present a versatile wet-chemical approach for high-throughput fabrication of thin-wall Au NEs/UMEs and multifunctional NEs with ~80% reproducibility. This method is based on a unique template-assisted 1D growth of single-crystalline Au in borosilicate nanopipettes followed by electrochemical contacting with tungsten microwires, and focused ion beam milling, ensuring precise control over NEs dimensions. Adaptable to various metals and integrable in multifunctional probes, the method facilitates batch production of high-quality NEs with standardized electrical connections. Structural and electrochemical characterization reveals a twinned single-crystalline Au core, a seamless Au/glass interface, and highly stable electrochemical performance. Notably, smaller electrodes exhibit higher current densities, enhancing chemical detection sensitivity. Specifically, we demonstrate outstanding spatial (< 200 nm) and current (< 1 pA) resolutions, low limit of detection (~11.0 μM) and high stability (7 h) in scanning photoelectrochemical microscopy (photo-SECM), by detecting photo-oxidation reaction on atomically smooth Au micro-flakes. We also demonstrate growth in double-barrel pipettes for SECM/SICM probes as well as Pt NEs. Overall, this scalable method addresses longstanding challenges in NEs, paving the way for advanced electrochemical and spectro-electrochemical microscopy, including SERS/TERS integration. With single-crystalline surfaces, these electrodes open new frontiers in catalysis, interfacial electrochemistry, biosensing, and molecular-scale investigations.

physics.chem-ph