AC Impedance Spectroscopy of a-nc-Si:H Thin Films

The AC impedance of amorphous-nano-crystalline silicon composite thin films (a-nc-Si:H) from mHz to MHz at different temperatures has been studied. The samples were prepared by Plasma Enhanced Chemical Vapor Deposition technique. The X-ray diffraction and high resolution electron microscopy showed that films consist of isolated nano-crystals embedded in amorphous matrix. In analysis of impedance data, two approaches were tested: the ideal Deby type equivalent circuit and modified one, with CPE (constant phase elements). It was found that the later better fits to results. The amorphous matrix showed larger resistance and lower capacity than nano-crystals. By heat treatment in vacuum, the capacity for both phases changes, according to expected change in size of ordered domains.

Reducing active layer thickness of polyamide composite membranes using a covalent organic framework interlayer in interfacial polymerization

Polyamide(PA)-based thin-film composite membranes exhibit enormous potential in water purification,owing to their facile fabrication,decent performance and desirable stability.However,the thick PA active layer with high transport resistance from the conventional interfacial polymerization hampers their applications.The controllable fabrication of a thin PA active layer is essential for high separation efficiency but still challenging.Herein,a covalent organic framework TpPa-1 interlayer was firstly deposited on a polyethersulfone(PES)substrate to reduce the thickness of PA active layer in interfacial polymerization.The abundant pores of TpPa-1 increase the local concentration of amine monomers by adsorbing piperazine molecules,while hydrogen bonds between hydrophilic groups of TpPa-1 and piperazine molecules slow down their diffusion rate.Arising from those synergetic effects,the PA active layer is effectively reduced from 200 nm to 120 nm.By optimizing TpPa-1 interlayer and PA active layer,the water flux of resultant membranes can reach 171.35 L·m^-2·h^-1·MPa^-1,which increased by 125.4%compared with PA/PES membranes,while the rejection rates of sodium sulfate and dyes solution remained more than 90%and 99%,respectively.Our strategy may stimulate rational design of ultrathin PA-based nanofiltration membranes with high performances.

Surface-tailoring chlorine resistant materials and strategies for polyamide thin film composite reverse osmosis membranes

Polyamide thin film composite membranes have dominated current reverse osmosis market on account of their excellent separation performances compared to the integrally skinned counterparts.Despite their very promising separation performance,chlorine-induced degradation resulted from the susceptibility of polyamide toward chlorine attack has been regarded as the Achilles’s heel of polyamide thin film composite.The free chlorine species present during chlorine treatment can impair membrane performance through chlorination and depolymerization of the polyamide selective layer.From material point of view,a chemically stable membrane is crucial for the sustainable application of membrane separation process as it warrants a longer membrane lifespan and reduces the cost involved in membrane replacement.Various strategies,particularly those involved membrane material optimization and surface modifications,have been established to address this issue.This review discusses membrane degradation by free chlorine attack and its correlation with the surface chemistry of polyamide.The advancement in the development of chlorine resistant polyamide thin film composite membranes is reviewed based on the state-of-the-art surface modifications and tailoring approaches which include the in situ and postfabrication membrane modifications using a broad range of functional materials.The challenges and future directions in this field are also highlighted.

Preparation and characterization of La_(0.8)Sr_(0.04)Ca_(0.16)Co_(0.6)Fe_(0.4)O_(3-δ)-La_(0.9)Sr_(0.1)Ga_(0.8)Mg_(0.2)O_3 composite cathode thin film for SOFC by slurry spin coating

The La0.8Sr0.04Ca0.16Co0.6Fe0.4O3-δ (LSCCoF) and La0.9Sr0.1Ga0.8Mg0.2O3 (LSGM) powders were synthesized by glycine-nitrate combustion process and conventional solid-state reaction method, respectively. The LSCCoF-LSGM composite cathode material was successfully elaborated and deposited on dense pellets of the LSGM electrolyte by means of slurry spin-coating process. The cathode films with the best surface morphology and microstructure were obtained when the operating parameters fixed as follows: the content of ethyl cellulose which acted as pore former and binder is 10 wt.%, the content of terpineol which acted as modifier is 5 wt.%, the speed of rotation rate is 3200 r/min and the best post-deposition sintering temperature is 1000°C.

Polydopamine/Imogolite Nanotubes(PDA/INTs)Interlayer Modulated Thin Film Composite Forward Osmosis Membrane for Minimizing Internal Concentration Polarization

Forward osmosis(FO)as an energy-saving membrane process has attracted much attention in food concentration,water treatment,and desalination.Thin film composite(TFC)membrane is the most popular FO membrane,but it suffers from the internal concentration polarization(ICP),which significantly limits the water flux and FO efficiency.In this report,we demonstrate a novel and high-performing thin film nanocomposite(TFN)membrane that employs a hydrophilic interlayer composed of imogolite nanotubes(INTs)and polydopamine(PDA).The INTs can be adhered to the porous substrate by the self-polymerization of PDA,and the as-prepared PDA/INTs interlayer displays a nanostructured network with outstanding hydrophilicity.The detailed investigation was conducted to understand the relationship between the structure and property of the PDA/INTs interlayer and the morphology and performance of the TFN membrane.The TFN membrane with the PDA/INTs interlayer performs a thinner and smoother polyamide selective layer.Correspondingly,the TFN membrane shows a water flux of 18.38 L·m^(-2)·h^(-1),which is 2.18 times of the pristine TFC membrane.Moreover,the TFN membrane has a minimized structural parameter(577μm),almost a half of that of the pristine one(949μm).It reveals that the ICP effect of TFC membrane can be effectively alleviated by using a hydrophilic PDA/INTs interlayer.This TFN membrane with a satisfactory water permeability is promising in terms of future applications.

The effect of altering crosslinker chemistry during interfacial polymerization on the performance of nanofiltration membranes for desalination, organic, and micropollutants removal

Chemistry of the polyamide active layer of a desalination membrane is critical in determining both its physical and chemical properties.In this study,we designed and fabricated three novel membranes with different active layers using the crosslinkers:terephthaloyl chloride,isophthaloyl chloride,and trimesoyl chloride.The crosslinkers were reacted with an aqueous solution of an aliphatic tetra-amine.Because these crosslinkers differ in their structures and crosslinking mechanisms during interfacial polymerization,the resultant membranes also possess different structural properties.The water contact angle of the fabricated membranes also varies;the water contact angles of 4A-3P-TPC@PSF/PET,4A-3P-TMC@PSF/PET,and 4A-3P-IPC@PSF/PET,are 68.9°,65.6°,and 53.9°,respectively.Similarly,the desalination performance of resultant membranes also showed variations,with 4A-3P-TPC@PSF/PET,4A-3P-IPC@PSF/PET,and 4A-3P-TMC@PSF/PET having a permeate flux of 17.14,25.70,and 30.90 L·m^(−2)·h^(−1),respectively,at 2.5 MPa.The 4A-3P-TPC@PSF/PET membrane exhibited extensive crosslinking with aliphatic linear amine,and cationic dye rhodamine B,MgCl_(2),and amitriptyline rejection rates of 98.6%,92.7%and 80.9%,respectively.The 4A-3P-TMC@PSF/PET membrane showed mediocre performance,while 4A-3P-IPC@PSF/PET membrane showed even lower performance,with a 35%rejection of methyl orange dye.