Walnut shell (WS), as an economic and environmental-friendly adsorbent, was utilized to remove methylene blue (MB) from aqueous solutions. The effects of WS particle size, solution pH, adsorbent dosage and contact time, and concentration of NaCl on MB removal were systematically investigated. Under the optimized conditions (i.e., contact time ∼ 2 h, pH ∼ 6, particle size ∼ 80 mesh, dye concentration 20 mg/L, and 1.25 g/L adsorbent), the removal percentages can achieve ∼97.1%, indicating WS was a promising absorbent to remove MB. Other supplementary experiments, such as Fourier transform infrared spectroscopy (FTIR), dynamic light scattering (DLS), and Brunauer-Emmett-Teller (BET) method, were also employed to understand the adsorption mechanisms. FTIR confirmed that the successful adsorption of MB on WS particles was through functional groups of WS. Using DLS method, the interactions between WS particles and dyes under various pH were investigated, which can be ascribed to the electrostatic forces. Kinetic data can be well fitted by the pseudo-second-order model, indicating a chemical adsorption. The adsorption isotherms were well described by both Langmuir and Freundlich models. Dubinin-Radushkevich model also showed that the adsorption process was a chemical adsorption. Thermodynamic data indicated that the adsorption was spontaneous, exothermic, and favorable at room temperature.

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The alkaline hydrogen evolution reaction (HER) of MoS2 is hampered by its sluggish water dissociation kinetics as well as limited edge sites. Herein, Ni3S2/MoS2 is fabricated as a model catalyst to highlight interfacial structural and electronic modulations of MoS2 for realizing its high performance in the alkaline HER. Experiments and density functional theory results demonstrate that the coupled Ni3S2 species can not only promote the adsorption and dissociation of H2O to boost the alkaline HER kinetics but also tailor the inert plane of MoS2 to create abundant unsaturated edge-like active sites, while the interfacial electron interaction can regulate the band gaps and Gibbs free energy of hydrogen adsorption of MoS2 to improve the electron conductivity as well as HER activity. Moreover, field emission scanning electron microscopy, transmission electron microscopy, Raman, ex situ synchrotron radiation X-ray absorption, and X-ray photoelectron spectroscopy results reveal the excellent structural stability of Ni3S2/MoS2 during the HER. As expected, the target Ni3S2/MoS2 achieves an ultralow overpotential of 68 mV at 10 mA cm–2, a fast alkaline HER kinetics, and remarkable durability. The proposed concept of interfacial structural and electronic reorganization could be extended to develop other functional materials.