A high-efficiency and long-cycling aqueous indium metal battery enabled by synergistic In/K interactions.

Aqueous trivalent metal batteries are promising options for energy storage, owing to their ability to transfer three electrons during redox reactions. However, advances in this field have been limited by challenges such as incompatible M/M electrode potentials and salt hydrolysis. Herein, we identify the trivalent indium metal as a viable candidate and demonstrate a high-performance indium-Prussian blue hybrid battery using a K/In mixture electrolyte.

Building a High-Potential Silver-Sulfur Redox Reaction Based on the Hard-Soft Acid-Base Theory.

Sulfur holds immense promise for battery applications owing to its abundant availability, low cost, and high capacity. Currently, sulfur is commonly combined with alkali or alkaline earth metals in metal-sulfur batteries. However, these batteries universally face challenges in cycling stability due to the inevitable issue of polysulfide dissolution and shuttling.

Building a Rechargeable Voltaic Battery via Reversible Oxide Anion Insertion in Copper Electrodes.

Voltaic pile, the very first battery built by humanity in 1800, plays a seminal role in battery development history. However, the premature design leads to the inevitable copper ion dissolution issue, which dictates its primary battery nature. To address this issue, solid-state electrolytes, ion exchange membranes, and/or sophisticated electrolytes are widely utilized, leading to high costs and complicated cell configuration.

Trivalent Indium Metal as a High-Capacity, High-Efficiency, Low-Polarization, and Long-Cycling Anode for Aqueous Batteries.

Aqueous batteries using multivalent metals hold great promise for energy storage due to their low cost, high energy, and high safety. Presently, divalent metals (zinc, iron, nickel, and manganese) prevail as the leading choice, which, however, suffer from low Coulombic efficiency or dendrite growth. In stark contrast, trivalent metals have received rare attention despite their capability to unlock unique redox reactions.

Construction of 3D CrN@nitrogen-doped carbon nanosheet arrays by reactive magnetron sputtering for the free-standing electrode of supercapacitor.

Owing to their favorable chemical stabilities and electronic conductivities, transition metal nitrides (TMNs) have been targeted as the potential electrode materials for the supercapacitors. Herein, 3D CrN@nitrogen-doped carbon nanosheet arrays (NCs) were successfully deposited on carbon paper (CP) by reactive magnetron sputtering method. The CrN@NCs@CP electrode exhibited satisfactory electrochemical properties: initially, the electrode showed a 132.