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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., Comment: 21 pages, 3 figures. The supplementary information includes Samples preparation and treatment, Measurement methods, Figures S1 to S10, and Table S1

The electrolysis of water is of global importance to store renewable energy and the methodical design of next-generation oxygen evolution catalysts requires a greater understanding of the structural and electronic contributions that give rise to increased activities. Herein, we report a series of Ruddlesden–Popper La[subscript 0.5]Sr[subscript 1.5]Ni[subscript 1−x]FexO[subscript 4±δ] oxides that promote charge transfer via cross-gap hybridization to enhance electrocatalytic water splitting. Using selective substitution of lanthanum with strontium and nickel with iron to tune the extent to which transition metal and oxygen valence bands hybridize, we demonstrate remarkable catalytic activity of 10 mA cm⁻² at a 360 mV overpotential and mass activity of 1930 mA mg⁻¹[subscript ox] at 1.63 V via a mechanism that utilizes lattice oxygen. This work demonstrates that Ruddlesden–Popper materials can be utilized as active catalysts for oxygen evolution through rational design of structural and electronic configurations that are unattainable in many other crystalline metal oxide phases., Robert A. Welch Foundation (Grant F-1529), Robert A. Welch Foundation (Grant F-1319)