ABSTRACT
Charge engineering of carbon materials with many defects shows great potential in electrocatalysis, and molybdenum carbide (Mo2C) is one of the noble-metal-free electrocatalysts with the most potential. Herein, we study the Mo2C on pyridinic nitrogen-doped defective carbon sheets (MoNCs) as catalysts for the hydrogen evolution reaction. Theoretical calculations imply that the introduction of Mo2C produces a graphene wave structure, which in some senses behaves like N doping to form localized charges. Being an active electrocatalyst, MoNCs demonstrate a Tafel slope as low as 60.6 mV dec-1 and high durability of up to 10 h in acidic media. Besides charge engineering, plentiful defects and hierarchical morphology also contribute to good performance. This work underlines the importance of charge engineering to boost catalytic performance.
ABSTRACT
Hierarchically porous nickel-iron-layered double hydroxide (NiFe-LDH) with a Ni2+/Fe3+ molar ratio of 3 was successfully synthesised through a simple hydrothermal route. After calcination at 400°C, NiFe-LDH transformed into nickel-iron-layered double oxides (NiFe-LDO). The as-prepared samples were characterised through X-ray powder diffraction, field emission scanning electron microscopy, energy dispersive X-ray spectroscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy and nitrogen adsorption. The calcined and uncalcined NiFe-LDH was used as adsorbents to remove Congo red (CR) dye in an aqueous solution. The equilibrium adsorption data of NiFe-LDH and NiFe-LDO samples were well fitted to Langmuir model and were characterised by excellent adsorption capacities of 205 and 330mg/g, respectively. Pseudo-second-order kinetic and intra-particle diffusion models indicated that CR was well adsorbed on the adsorbent. The underlying adsorption mechanism was investigated and observed as anion exchange and reconstruction.
ABSTRACT
Hierarchical porous zinc oxide (ZnO) was successfully synthesized via a facile hydrothermal method followed by calcination, and characterized by X-ray diffraction, field-emission scanning electron microscopy, transmission electron microscopy, nitrogen adsorption-desorption, and Fourier transform infrared spectroscopy analyses. The as-prepared porous ZnO exhibits microsphere morphologies with diameters of 6-8µm, which are assembled from two-dimensional nanosheets. The as-prepared hierarchical porous ZnO microspheres possessed high specific surface areas (57m2/g), and were evaluated for adsorption of Congo red (CR) in aqueous solution. The adsorption kinetics data were described by the pseudo-second-order kinetics and intraparticle diffusion models, while the equilibrium adsorption data were well fitted to the Langmuir model, with a maximum adsorption amount of 334mg/g. The as-prepared hierarchical porous ZnO exhibited higher CR adsorption capacity than commercial ZnO and various other materials, and thus could be an effective adsorbent for removal of anionic organic dyes from wastewater.
ABSTRACT
The preparation of hierarchical porous materials as catalysts and sorbents has attracted much attention in the field of environmental pollution control. Herein, Ni/Mg/Al layered double hydroxides (NMA-LDHs) hierarchical flower-like hollow microspheres were synthesized by a hydrothermal method. After the NMA-LDHs was calcined at 600°C, NMA-LDHs transformed into Ni/Mg/Al layered double oxides (NMA-LDOs), which maintained the hierarchical flower-like hollow structure. The crystal phase, morphology, and microstructure of the as-prepared samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy elemental mapping, Fourier transform infrared spectroscopy, and nitrogen adsorption-desorption methods. Both the calcined and non-calcined NMA-LDHs were examined for their performance to remove Congo red (CR) and hexavalent chromium (Cr(VI)) ions in aqueous solution. The maximum monolayer adsorption capacities of CR and Cr(VI) ions over the NMA-LDOs sample were 1250 and 103.4mg/g at 30°C, respectively. Thermodynamic studies indicated that the adsorption process was endothermic in nature. In addition, the addition of coexisting anions negatively influenced the adsorption capacity of Cr(VI) ions, in the following order: CO32->SO42->H2PO4->Cl-. This work will provide new insight into the design and fabrication of advanced adsorption materials for water pollutant removal.
ABSTRACT
Hollow microspheres and hierarchical porous nanostructured materials with desired morphologies have gained remarkable attention for their potential applications in environmental technology. In this study, NiO-SiO2 hollow microspheres were prepared by co-precipitation with SiO2 and nickel salt as precursors, followed by dipping in alkaline solution and calcination. The samples were characterized by X-ray diffraction, field-emission scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, nitrogen adsorption, and X-ray photoelectron spectroscopy. The synthesized hollow spheres were composed of a SiO2 shell and hierarchical porous NiO nanosheets on the surface. Adsorption experiments suggested that NiO-SiO2 composite particles were powerful adsorbents for removal of Congo red from water, with a maximum adsorption capacity of 204.1 mg/g. The high specific surface areas, hollow structures, and hierarchical porous surfaces of the hollow composite particles are suitable for various applications, including adsorption of pollutants, chemical separation, and water purification.
