Nickel/iron-layered double hydroxide (NiFe-LDH) tends to undergo an electrochemically induced surface reconstruction during the water oxidation in alkaline, which will consume excess electric energy to overcome the reconstruction thermodynamic barrier. In the present work, a novel ultrasonic wave-assisted Fenton reaction strategy is employed to synthesize the surface reconstructed NiFe-LDH nanosheets cultivated directly on Ni foam (NiFe-LDH/NF-W). Morphological and structural characterizations reveal that the low-spin states of Ni²⁺ (t_2g⁶e_g²) and Fe²⁺ (t_2g⁴e_g²) on the NiFe-LDH surface partially transform into high-spin states of Ni³⁺ (t_2g⁶e_g¹) and Fe³⁺ (t_2g³e_g²) and formation of the highly active species of NiFeOOH. A lower surface reconstruction thermodynamic barrier advantages the electrochemical process and enables the NiFe-LDH/NF-W electrode to exhibit superior electrocatalytic water oxidation activity, which delivers 10 mA cm^-2 merely needing an overpotential of 235 mV. Besides, surface reconstruction endows NiFe-LDH/NF-W with outstanding electrooxidation activities for organic molecules of methanol, ethanol, glycerol, ethylene glycol, glucose, and urea. Ultrasonic-assisted Fenton reaction inducing surface reconstruction strategy will further advance the utilization of NiFe-LDH catalyst in water and organics electrooxidation.

Multi-walled carbon nanotubes (MWCNTs) with one-dimensional nanostructure are an ideal support for oxygen reduction reaction (ORR) catalysts thanks to their intrinsic outstanding electrical conductivity and high specific surface area. Iron and nitrogen doping could alter the local electronic structure and therefore enhance the ORR activity of MWCNTs, but the preparation process always includes complicated growth conditions and post-treatment. Herein, an iron and nitrogen co-modified multi-walled carbon nanotubes (Fe–N-MWCNTs) with hierarchical nanostructure is engineered and synthesized via a simple two-step pyrolysis approach. Large specific surface area, low resistivity, and intensified charge density near the Fermi level synergistically endow the Fe–N-MWCNTs with outstanding ORR activity. The optimal Fe–N-MWCNTs exhibit a higher onset potential value of 0.92 V (versus RHE) and half-wave potential (E _1/2) of 0.85 V (versus RHE) in 0.1 M KOH medium, which exceeds the benchmark Pt/C electrocatalyst (E _1/2 = 0.84 V). This strategy of modifying MWCNTs support by a simple calcination process provides a feasible method to prepare cost-efficient ORR electrocatalysts.

Toxic acetone gas emissions and leakage are a potential threat to the environment and human health. Gas sensors founded on metal oxide semiconductors (MOS) have become an effective strategy for toxic gas detection with their mature process. In the present work, an efficient acetone gas sensor based on Au-modified ZnO porous nanofoam (Au/ZnO) is synthesized by polyvinylpyrrolidone-blowing followed by a calcination method. XRD and XPS spectra were utilized to investigate its structure, while SEM and TEM characterized its morphology. The gas sensitivity of the Au/ZnO sensors was investigated in a static test system. The results reveal that the gas-sensitive performance of porous ZnO toward the acetone can be enhanced by adjusting the loading ratio of noble Au nanoparticles. Specifically, the Au/ZnO sensor prepared by the Au loading ratio of 3.0% (Au/ZnO-3.0%) achieved a 100 ppm acetone gas response of 20.02 at the optimum working temperature of 275 °C. Additionally, a portable electronic device used a STM32 primary control chip to integrate the Au/ZnO-3.0% gas sensor with other modules to achieve the function of detecting and alarming toxic acetone gas. This work is of great significance for efficiently detecting and reducing acetone emissions.