Confinement-controlled Water Engenders High Energy Density Electrochemical-double-layer Capacitance
arXiv:2204.10127 · doi:10.1021/acs.jpclett.3c01498
Abstract
The renewable energy sector critically needs low-cost and environmentally neutral energy storage solutions throughout the entire device life cycle. However, the limited performance of standard water-based electrochemical systems prevents their use in specific applications. Meanwhile, recent fundamental studies revealed dielectric anomalies of water near solid-liquid interfaces of carbon-based nanomaterials. In contrast to the bulk water properties, these anomalies of water under nano-confinement and in the presence of electric fields have not yet been understood and used. Here, we experimentally study the ability of the interfacial water layer to engender and store charge in electrochemical double-layer capacitance. We demonstrate the prototype of a 'water only' membrane-electrode assembly. The prototype exhibits characteristics with a perspective of competing with existing batteries and supercapacitors without using electrolytes as ionic carriers. The results provide the impetus for developing high-energy-density electrochemical double-layer capacitors and open up other avenues for ecologically-neutral batteries, fuel cells, and nanofluidic devices.
arXiv comment21 pages, 3 figures. The supplementary information includes Samples preparation and treatment, Measurement methods, Figures S1 to S10, and Table S1
References in corpus (7)
- Anomalously low dielectric constant of confined water
- Proton transport through one atom thick crystals
- Friction of Water on Graphene and Hexagonal Boron Nitride from ab initio Methods: Very Different Slippage Despite Very Similar Interface Structures
- Fluctuation-induced quantum friction in nanoscale water flows
- Giant photo-effect in proton transport through graphene membranes
- Revealing excess protons in the infrared spectrum of liquid water
- Autoionization of water: does it really occur?