Adsorption of CO_(2) on MgAl layered double hydroxides: Effect of intercalated anion and alkaline etching time

The adsorption of CO_(2) on MgAl layered double hydroxides(MgAl-LDHs) based adsorbents has been an effective way to capture CO_(2),however the adsorption capacity was hampered due to the pore structure and the dispersibility of adsorption active sites.To address the problem,we investigate the effect of intercalated anion and alkaline etching time on the structure,morphology and CO_(2) uptake performances of MgAl-LDHs.MgAl-LDHs are synthesized by the onepot hydrothermal method,followed by alkaline etching of NaOH,and characterized by x-ray diffraction,N_(2) adsorption,scanning electron microscopy and Fourier transform infrared spectroscopy.The CO_(2) adsorption tests of the samples are performed on a thermogravimetric analyzer,and the adsorption data are fitted by the first-order,pseudo-second-order and Elovich models,respectively.The results demonstrate that among the three intercalated samples,MgAl(Cl) using chloride salts as precursors possesses the highest adsorption capacity of CO_(2),owing to high crystallinity and porous structure,while MgAl(Ac) employing acetate salts as precursors displays the lowest CO_(2) uptake because of poor crystallinity,disorderly stacked structure and unsatisfactory pore structure.With regard to alkaline etching,the surface of the treated MgAl(Cl) is partly corroded,thus the specific surface area and pore volume increase,which is conducive to the exposure of adsorption active sites.Correspondingly,the adsorption performance of the alkaline-etched adsorbents is significantly improved,and MgAl(Cl)-6 has the highest CO_(2) uptake.With the alkaline etching time further increasing,the CO_(2) adsorption capacity of MgAl(Cl)-9 sharply decreases,mainly due to the collapse of pore structure and the fragmentized sheet-structure.Hence,the CO_(2) adsorption performance is greatly influenced by alkaline etching time,and appropriate alkaline etching time can facilitate the contact between CO_(2) molecules and the adsorbent.

Maskless fabrication of quasi-omnidirectional V-groove solar cells using an alkaline solution-based method

Silicon passivated emitter and rear contact(PERC) solar cells with V-groove texture were fabricated using maskless alkaline solution etching with in-house developed additive. Compared with the traditional pyramid texture, the V-groove texture possesses superior effective minority carrier lifetime, enhanced p–n junction quality and better applied filling factor(FF). In addition, a V-groove texture can greatly reduce the shading area and edge damage of front Ag electrodes when the V-groove direction is parallel to the gridline electrodes. Due to these factors, the V-groove solar cells have a higher efficiency(21.78%) than pyramid solar cells(21.62%). Interestingly, external quantum efficiency(EQE) and reflectance of the V-groove solar cells exhibit a slight decrease when the incident light angle(θ) is increased from 0° to 75°, which confirms the excellent quasi omnidirectionality of the V-groove solar cells. The proposed V-groove solar cell design shows a 2.84% relative enhancement of energy output over traditional pyramid solar cells.

Puffing quaternary FexCoyNi1-x-yP nanoarray via kinetically controlled alkaline etching for robust overall water splitting

Designing and constructing bifunctional electrocatalysts with high efficiency,high stability and low cost for overall water splitting to produce clean hydrogen fuel is attractive but highly challenging.Here we constructed puffed quaternary FexCoyNi1-x-yP nanoarrays as bifunctional electrodes for robust overall water splitting.The iron was used as the modulator to manipulate the electron density of NiCoP nanoarray,which could increase the positive charges of metal(Ni and Co)and P sites.The resultant electronic structure of FexCoyNi1-x-yP was supposed to balance the adsorption and desorption of H and accelerate the oxygen evolution reaction(OER)kinetics.Moreover,the morphological structure of FexCoyNi1-x-yP was modulated through the kinetically controlled alkaline etching by using the amphoteric features of initial FeCoNi hydroxide nanowires.The resultant puffed structure has rich porosity,cavity and defects,which benefit the exposure of more active sites and the transport of mass/charge.As a result,the cell integrated with the puffed quaternary FexCoyNi1-x-yP nanoarrays as both the cathode and anode only requires the overpotentials of 25 and 230 mV for hydrogen evolution reaction(HER)and OER at the current density of 10 mA cm^-2 in alkaline media and a cell voltage of 1.48 V to drive the overall water splitting.Moreover,the puffed FexCoyNi1-x-yP demonstrates remarkable durability for continuous electrolysis even at a large current density of 240 mA cm^-2.

Construction of monodispersed single-crystalline hierarchical ZSM-5 nanosheets via anisotropic etching

Hierarchical zeolites and single-crystalline zeolite nanosheets(NSs)have been recognized as two separate types of targeting porous materials to overcome the diffusion limitations of traditional bulk zeolites.The synthesis of uniform single-crystalline hierarchical zeolite NSs featured with NS morphology and interconnected mesoporosity,remains rarely reported.In this work,we prepared ZSM-5 zeolites with the above microstructural features via simple alkaline etching.Moreover,both their microstructure and acid strength could be accurately tuned with this approach,resulting in not only higher conversion rate and BTX selectivity but also superior anti-coking performance in the subsequent methanol aromatization reaction.

Effect of Surface Pretreatment on Adhesive Properties of Aluminum Alloys

The lap-shear strength and durability of adhesive bonded AI alloy joints with different pretreatments were studied by the lap-shear test and wedge test. The results indicate that the maximum lap-shear strength and durability of the bonding joints pretreated by different processes are influenced by the grade of abrasive papers and can be obviously improved by phosphoric acid anodizing. Alkali etching can obviously improve the durability of bonding joints although it slightly influences the maximum lap-shear strength. The process which is composed of grit-finishing, acetone degreasing, alkali etching and phosphoric acid anodizing, provides a better adhesive bonding property of Al alloy.

Defects-rich MgFe LDH:A high-capacity adsorbent for methyl orange wastewater

Dye pollution is a common pollutant in wastewater that poses a serious threat to human health.Layered double hydroxide(LDH)is a commonly used adsorbent for dye removal.However,its adsorption efficiency is significantly limited by the limited adsorption active sites of the adsorbent.In this paper,a defects-rich MgFe LDH adsorbent for anionic dye wastewater was synthesized by a simple hydrothermal method and alkaline etching.Different analytical techniques,such as XRD,FT-IR,SEM,TEM,XPS,and N2 adsorption-desorption isotherm,were used to verify the chemical composition and surface characteristics of the materials,and the effects of pH,temperature,and contact time on the adsorption effect of methyl orange and the adsorption mechanism were analyzed.Alkaline etching of Al and Zn in the laminate generated defects that expose unsaturated coordination centers and create abundant adsorption sites,which can electrostatically attract and coordinate with dye ions.At 25℃,the adsorption capacity of MgFe LDH with Al etched and MgFe LDH with Zn etched for methyl orange dye reached 1722 mg·g^(-1 ) and 1685 mg·g^(-1 ),respectively,much higher than that of MgFe LDH(544 mg·g^(-1 )).This work provides a promising method for the removal of dye wastewater by adsorption and a new idea for the design and development of high-performance dye wastewater adsorbents.