MXene-derived TiO₂/RGO composite was designed and synthesized by the hydrothermal process as a universal anode for Li-ion and K-ion batteries.

Urea electrolysis offers the prospect of cost-effective and energy-saving hydrogen production together with mitigating urea-rich wastewater pollution instead of overall water splitting. Hence, here, high-efficiency bifunctional electrocatalysts were developed for both the urea oxidation reaction (UOR) and hydrogen evolution reaction (HER) via the in situ vertical growth of thorny leaf-like (2D nanosheets supporting 1D nanowires) NiCoP on a carbon cloth (NiCoP/CC). After integrating the advantages of the synergistic effect between Ni and Co as well as the unique hierarchical structure combined with 1D nanowires, 2D nanosheets and a 3D conductive carbon cloth substrate, the electrode exhibited excellent electrocatalytic activity toward HER and UOR. The electrolytic cell assembled using NiCoP/CC as the anode and the cathode could provide current density of 10 mA cm⁻² at a cell voltage of 1.42 V (160 mV less than that for its urea-free counterpart) as well as remarkable durability over 30 h. Thus, the cost-effectiveness and high activity of the NiCoP/CC electrode pave the way to explore transition metal-based electrocatalysts for urea electrolysis.

In our work, we successfully design boron (B) and nitrogen (N) co-doped porous carbon tube bundle (B/N-PCTB) electrode materials which are directly derived from the biomass of dandelion fluff. The low-tortuosity, and open and porous structures contribute to electron transport along the tube wall and unimpeded ion diffusion inside the carbon tubes. The incorporation of heteroatoms into PCTBs can bring extra pseudocapacitance and double layer capacitance to enhance the overall capacitance. Benefiting from the hollow and open microstructure and heteroatom doping, the optimized B/N-PCTB electrode (active materials: 2.6 mg cm⁻²) possesses an impressive specific capacitance of 355 F g⁻¹ at 1 A g⁻¹. Even with an ultrahigh loading mass of 40 mg cm⁻², the electrode still has a relatively high specific capacity of 216 F g⁻¹ at 1 A g⁻¹. The assembled symmetric cell with an active material loading of 80 mg cm⁻² (cathode: 40 mg cm⁻²; anode: 40 mg cm⁻²) shows a superior volumetric energy density of 12.15 W h L⁻¹ at the power density of 699.84 W L⁻¹. The facile yet high-performance porous carbon tube bundle is a promising material which can be applied in many other fields such as lithium ion batteries, hydrogen evolution reaction, and heavy metal ion adsorption.