Acid-in-clay electrolyte for wide-temperature-range and long-cycle proton batteries

Proton conduction underlies many important electrochemical technologies. We report a series of new proton electrolytes: acid-in-clay electrolyte termed AiCE, prepared by integrating fast proton carriers in a natural phyllosilicate clay network, that can be made into thin-film (tens of microns) fluid-impervious membranes. The chosen example systems (sepiolite-phosphoric acid) rank top among the solid proton conductors in consideration of proton conductivities (15 mS cm−1 at 25 °C, 0.023 mS cm−1 at −82 °C), the stability window (3.35 V), and reduced chemical activity. A solid-state proton battery was assembled using AiCE as the electrolyte to demonstrate the performance of these electrolytes. Benefitting from the wider electrochemical stability window, reduced corrosivity, and excellent ionic selectivity of AiCE, the two main problems (gasification and cyclability) of proton batteries have been successfully solved. This work also draws the attention of elemental cross-over in proton batteries and illustrates a simple “acid-in-clay” approach to synthesize a series of solid proton electrolytes with a superfast proton permeability, outstanding selectivity, and improved stability for many potential applications associated with protons.

Controllable preparation and electrocatalytic hydrogen evolution characteristics of Fe3S4 nanocrystals

In order to obtain better electrocatalytic hydrogen evolution performance, Fe3S4 with different morphologies was synthesized by controlling the reaction conditions. During that progress, the ferric oleate as an iron source, and the sulfur powder dissolved in oleylamine as a sulfur source. Fe3S4 with particle morphology proved to have the best electrochemical catalytic activity after adding 40% carbon black. In dehydrogenation, the overpotential was 234 mV and the Tafel slope was 213 mV/dec at a current density of 10 mA/cm2. Meanwhile, Fe3S4 with a particle morphology exhibited superior electrochemical stability. Therefore, the controllably fabricated Fe3S4 with a particle morphology is a promising electrocatalyst for dehydrogenation.

Doped Polythiophene Chiral Electrodes as Electrochemical Biosensors

π-conducting materials such as chiral polythiophenes exhibit excellent electrochemical stability in doped and undoped states on electrode surfaces (chiral electrodes), which help tune their physical and electronic properties for a wide range of uses. To overcome the limitations of traditional surface immobilization methods, an alternative pathway for the detection of organic and bioorganic targets using chiral electrodes has been developed. Moreover, chiral electrodes have the ability to carry functionalities, which helps the immobilization and recognition of bioorganic molecules. In this review, we describe the use of polythiophenes for the design of chiral electrodes and their applications as electrochemical biosensors.