Aqueous zinc-ion batteries offer sustainable large-scale storage potential with inherent safety and low cost, yet suffer from limited energy density and cycle life due to aqueous electrolyte constraints. Here, we introduce affordable, stable electrolyte (0.33 $·kg⁻¹) incorporating minimal multi-halogen anions (Cl⁻, Br⁻, and I⁻) to create a high-entropy solvation structure enabling high-performance zinc batteries. Despite the small amount, the diversified mono-halogenated contact ion pair and multi-halogenated aggregate solvation structures create the unique high-entropy solvation structure, to form the lean-water halogenated interfacial environment, suppressing the hydrogen evolution reaction, while facilitating cascade desolvation. Multi-halogen additives generate diverse contact ion pairs (Zn-X, X = Cl/Br/I) with compact solvation shells accelerating ion transport. In this way, the high-entropy solvation structure breaks the trade-off between plating overpotential (energy efficiency) and plating/stripping reversibility (Coulombic efficiency). As a result, the high-entropy solvation-based electrolyte enables practical zinc metal battery with 152.2 Wh kg⁻¹_electrode for 120 cycles at lean electrolyte of 2.4 μL mg⁻¹ and an Ah-level pouch cell is validated with high Coulombic efficiency of over 99.90% for over 250 cycles. Our findings emphasize the importance of electrolyte design for the precise control of anion-cation interactions for stable Zn/electrolyte interface and enable practical zinc metal battery with high energy and low cost.

Mesoporous NiAl ₂ O ₄ /MO _x (M = La, Ce, Ca, Mg)–γ-Al ₂ O ₃ composites through a one-pot partial hydrolysis method showed excellent catalytic performance for dry reforming of methane.

The preparation of one-dimensional carbon materials with complex dual-scale nanostructures for supercapacitor applications still remains a challenge. Herein we report a simple strategy for electrosynthesis of silicon carbide nanowire (SiC NW)-derived carbon with dual-scale nanostructures for high performance supercapacitors. This method is highlighted by using solid oxide membrane technology to directly convert powdered silicon dioxide/carbon precursors into SiC NWs, and then the synthesized SiC NWs are further transformed into mesoporous silicon carbide-derived carbon nanowires (SiC-CDC NWs) via a subsequent in situ molten salt electrochemical etching process. Benefitting from their dual-scale nanostructures, these SiC-CDC NWs exhibit highly reversible specific capacitance of 260 F g⁻¹ at 1 A g⁻¹ and good cyclability (97.9% after 5000 cycles) in 6 M KOH aqueous solution without the need for doping the SiC-CDC NWs. It is suggested that this process is a promising general approach for synthesizing CDC materials with dual-scale nanostructures for energy storage applications.