Polyaniline/Tungsten Trioxide Organic-Inorganic Hybrid Anode for Aqueous Proton Batteries.

Aqueous proton batteries have received increasing attention due to their outstanding rate performance, stability and high capacity. However, the selection of anode materials in strongly acidic electrolytes poses a challenge in achieving high-performance aqueous proton batteries. This study optimized the proton reaction kinetics of layered metal oxide WO3 by introducing interlayer structural water and coating polyaniline (PANI) on its surface to prepare organic-inorganic hybrid material (WO3 ⋅ 2H2O@PANI). We constructed an aqueous proton battery with WO3 ⋅ 2H2O@PANI anode and MnO2@GF cathode. After 1500 cycles at a current density of 10 A g-1, the capacity retention rate can still reach 80.2 %. These results can inspire the development of new aqueous proton batteries.

Organic Electrode Materials for Dual-Ion Batteries.

Organic materials are widely used in various energy storage devices due to their renewable, environmental friendliness and adjustable structure. Dual-ion batteries (DIBs), which use organic materials as the electrodes, are an attractive alternative to conventional lithium-ion batteries for sustainable energy storage devices owing to the advantages of low cost, environmental friendliness, and high operating voltage. To date, various organic electrode materials have been applied in DIBs. In this review, we present the development of DIBs with a following brief introduction of characteristics and mechanisms of organic materials. The latest progress in the application of organic materials as anode and cathode materials for DIBs is mainly reviewed. Finally, we also discussed the challenges and prospects of organic electrode materials for DIBs.

Proton Intercalation/De-intercalation Chemistry in Phenazine-based Anode for Hydronium-ion Batteries.

Hydronium-ion batteries have received significant attention owing to the merits of extraordinary sustainability and excellent rate abilities. However, achieving high-performance hydronium-ion batteries remains a challenge due to the inferior properties of anode materials in strong acid electrolyte. Herein, a hydronium-ion battery is constructed which is based on a diquinoxalino [2,3-a:2',3'-c] phenazine (HATN) anode and a MnO2 @graphite felt cathode in a hybrid acidic electrolyte. The fast kinetics of hydronium-ion insertion/extraction into HATN electrode endows the HATN//MnO2 @GF battery with enhanced electrochemical performance. This battery exhibits an excellent rate performance (266 mAh g-1 at 0.5 A g-1 , 97 mAh g-1 at 50 A g-1 ), attractive energy density (182.1 Wh kg-1 ) and power density (31.2 kW kg-1 ), along with long-term cycle stability. These results shed light on the development of advanced hydronium-ion batteries.

Charge-Storage Nickel Substrate-Boosted CuP2 Nanosheet for the Electrochemical Oxygen Evolution Reaction.

The electrochemical oxygen evolution reaction (OER) is an essential anodic reaction that converts sustainable energy into chemical fuels, as it can provide protons and electrons. One of the most challenging research directions for the practical application of the OER is the elevation of the activity of noble-metal-free electrocatalysts. Here, we report that the nickel foam can be used as an electron-deficient substrate to tune the surface oxidation state of catalytic electrodes and thus boost the OER activity of CuP2 nanosheets via a charge-storage mechanism. The as-obtained self-standing CuP2/Ni electrodes delivered a current density of 220 mA cm-2 at 370 mV overpotential, which is approximately 5.5 times higher than the benchmarked IrO2 on nickel foam. This work sheds some new light on the design of low-cost electrocatalysts or electrodes with high activity for the electrochemical OER.