Considering the intrinsic activity of non-precious metal oxygen reduction reaction (ORR) catalysts is typically lower than that of precious metal catalysts, it is crucial to focus on the rational design of their micro-morphology and active site. This paper employed a simple molten salt-mediated template method to fabricate a Fe3C composite N-doped C catalyst with a layered porous framework ( Fe3C@NC). Tannic acid was utilized to form a strong coordination with iron to limit the grain size of Fe3C nanocrystals generated by high-temperature pyrolysis. Moreover, urea achieved nitrogen doping in tannic acidderived porous carbon, while the graphite phase nitrogen-doped carbon (g-C3N4) formed by its pyrolysis, together with the molten salt-mediated environment, jointly controlled the two-dimensional sheet-like structure of the material. The optimized Fe3C@ NC-800 demonstrated efficient ORR performance, with an ORR half-wave potential of 0.883 V. Its application as a cathode catalyst in a liquid zinc-air battery (ZABs) exhibits a maximum power density of 211.5 mW cm− 2, surpassing that of a Pt/C-based ZAB and indicating the potential practical utility of this material.

Biomass carbon materials with high rate capacity have great potential to boost supercapacitors with cost effective, fast charging– discharging performance and high safety requirements, yet currently suffers from a lack of targeted preparation methods. Here we propose a facile FeCl3 assisted hydrothermal carbonization strategy to prepare ultra-high rate biomass carbon from apple residues (ARs). In the preparation process, ARs were first hydrothermally carbonized into a porous precursor which embedded by Fe species, and then synchronously graphitized and activated to form biocarbon with a large special surface area (2159.3 m2 g− 1) and high degree of graphitization. The material exhibited a considerable specific capacitance of 297.5 F g− 1 at 0.5 A g− 1 and outstanding capacitance retention of 85.7% at 10 A g− 1 in 6 M KOH, and moreover, achieved an energy density of 16.2 Wh kg− 1 with the power density of 350.3 W kg− 1. After 8000 cycles, an initial capacitance of 95.2% was maintained. Our findings provide a new idea for boosting the rate capacity of carbon-based electrode materials.

The present work introduces a new method for the recycling of waste flocculation sludge to prepare electrode materials for supercapacitor. Hazardous azo dye was removal from textile dying wastewater by a new chitosan-based flocculant, and the generated dye sludge flocs was used as a nitrogen-containing precursor for the fabrication of N-doped carbon materials. The influence of azo dye on specific surface areas, nitrogen content, pore evolution of the resulting products and their electrochemical performance were investigated in detail. The results demonstrated a dual role of azo dye worked as both a nitrogen resource and pore-forming agent. The resulting N-doped carbon nanosheets derived from azo dye flocs demonstrated high electrochemical capacitance and good stability for supercapacitor electrode, which is attributed to the unique nitrogen doping, higher specific surface area and efficient charge transfer ability.