Two-dimensional (2D) nanomaterials show great potential for electrocatalysis or other applications that require large surface area. In this work, we developed porous zinc–cobalt layered double hydroxide (Zn–Co-LDH) nanosheets by using a one-step microwave-assisted approach, and examine their oxygen evolution reaction (OER) performance. The Zn–Co-LDH nanosheets with a high specific surface area of 116.4 m² g⁻¹ exhibit good OER activity, expressed as low onset overpotential, small Tafel slope and large exchange current density. At the overpotential of 0.54 V, the current density of Zn–Co-LDH nanosheets is about 15.06 mA cm⁻², which is much higher than that of Zn–Co-LDH nanoparticles. The comparable electrocatalytic performance may be attributed to the porous 2D structure generating more active sites and higher electronic conductivity. Furthermore, the obtained Zn–Co-LDH nanosheets show good stability during long time running at 1.55 V vs. RHE. Accordingly, an effective OER catalyst is exploited by using a simple microwave-assisted synthesis. Such an effective method could be extended to large-scale synthesis of uniform and stable 2D LDH nanomaterials.

Single-crystalline ZnO nanowires were synthesized, and further modified with Pd nanoparticles through self-assemblies. The self-assembly strategy shows advantages of tailoring the surface modification of ZnO nanowires with monodispersed Pd nanoparticles and further tuning of the functionalities of nano-architectures. It was found that poly(vinylpyrrolidone) (PVP) plays a key role in loading Pd nanoparticles onto the surfaces of ZnO nanowires. Having been turned into chemical sensors, the nano-architectures constructed from ZnO nanowires and Pd nanoparticles exhibit a highly enhanced response to H₂S gas, compared to the devices from pure ZnO nanowires.

Pt nanoparticles were introduced on the surface of ZnO nanowires using a chemically driven self-assembly method. Through this controllable method, Pt-nanoparticle-functionalized ZnO nanowires (Pt NPs-ZnO NWs) with uniform particle dispersion, tunable Pt particle sizes, and narrow particle size distribution were obtained. Changes in the morphology of the decorative preparation were observed as the amount of linker reagent and the concentration of Pt nanoparticle solution were altered. The as-prepared Pt NPs-ZnO NWs with optimal morphology showed excellent gas sensing and photocatalytic performance. Tuning of the functionalities of photocatalytic and gas sensors can be obtained by tailoring the morphology of Pt NP-ZnO NW composite materials.