RESUMEN

To be CMOS-compatible, a low preparation temperature (<500 °C) for ferroelectric films is required. In this study, BiFeO3 films were successfully fabricated at a low annealing temperature (<450 °C) on aluminum foils by a metal-organic decomposition process. The effect of the annealing atmosphere on the performance of BiFeO3 films was assessed at 440 ± 5 °C. By using a N2-rich atmosphere, a large remnant polarization (Pr~78.1 µC/cm2 @ 1165.2 kV/cm), and a high rectangularity (~91.3% @ 1165.2 kV/cm) of the P-E loop, excellent charge-retaining ability of up to 1.0 × 103 s and outstanding fatigue resistance after 1.0 × 109 switching cycles could be observed. By adopting a N2-rich atmosphere and aluminum foil substrates, acceptable electrical properties (Pr~70 µC/cm2 @ 1118.1 kV/cm) of the BiFeO3 films were achieved at the very low annealing temperature of 365 ± 5 °C. These results offer a new approach for lowering the annealing temperature for integrated ferroelectrics in high-density FeRAM applications.

RESUMEN

Organic molecular electrode materials are promising candidates in batteries. However, direct application of small molecule materials usually suffers from drastic capacity decay and inefficient utilization of active materials because of their high solubility in organic electrolytes and low electrical conductivity. Herein, a simple strategy is found to address the above issues through coating the small-molecule organic materials on a commercialized carbon-coated aluminum foil (CCAF) as the enhanced electrode. Both the experimental and calculation results confirm that the relatively rough carbon coating on the aluminum foil not only exhibits superior adsorption capacity of small-molecule organic electrode materials with a tight contact interface but also provides continuous electronic conduction channels for the facilitated charge transfer and accelerated reaction kinetics. In addition, the carbon coating also inhibits Al corrosion in electrochemical process. As a result, by using the tetrahydroxy quinone-fused aza-phenazine (THQAP) molecule as an example, the THQAP-CCAF electrode exhibits an excellent rate performance with a high capacity of 220 and 180 mAh g-1 at 0.1 and 2 A/g, respectively, and also a remarkable cyclability with a capacity retention of 77.3% even after 1700 cycles in sodium-ion batteries. These performances are much more superior than that of batteries with the THQAP on bare aluminum foil (THQAP-AF). This work provides a substantial step in the practical application of the small-molecule organic electrode materials for future sustainable batteries.

RESUMEN

Direct mass spectrometry (MS) is an exciting strategy in bioanalysis, enabling rapid decision-making in different scenarios. Its application is usually hindered by matrix effects and the typically low concentration of the target compounds in the biofluids. In this sense, combining a previous sample preparation step minimizes or removes these shortcomings. This article describes sorptive tape-spray tandem mass spectrometry (STS-MS/MS) based on mixed-mode particles as a strategy to combine sample preparation and MS analysis in a single device. The technique uses a sorptive tape (ST) consisting of mixed-mode polymeric microparticles (combining ionic exchange and hydrophobic interactions) coated over aluminum foil in a spatial controlled way. The tapes act as the sorptive phases to isolate the analytes from the sample matrix and substrates for STS-MS/MS. The performance of the technique has been evaluated by developing a method to determine codeine in saliva as proof of concept. The affordability of the STs elements allows the preparation of many individual phases at low cost so that several samples can be extracted simultaneously, thus increasing the sample throughput. The extraction variables were optimized following a multivariate approach. Working under the optimum conditions, the limit of detection was 0.3 µg L-1, while the intraday precision, calculated as relative standard deviation (RSD) at three concentration levels, was better than 9.4 %. The accuracy, expressed as relative recovery, was in the range of 78-98 %. The method was also applied to the analysis of real samples. Despite being a powerful strategy, the direct combination of microextraction to MS is not always affordable in all laboratories. For this reason, the STs were also combined with commercial liquid chromatography-MS working under the direct infusion mode to demonstrate the usefulness of the ST in classical extraction workflows.

Asunto(s)

RESUMEN

The cold spot forge-welding method, recently developed to achieve high-productivity and high-strength dissimilar material joining, was applied to multiple solid-phase joining of aluminum (Al) foils simulating tab-lead electrodes. Fifty Al foils of 12-µm thickness were sandwiched between 0.5 and 0.8 mm A1050 Al alloy plates and pressurized with 6-mm diameter punch for 1 s. The effect of bonding temperature (330-420 °C) and the reduction ratio (R, 1.4-3) on the tensile shear load of the joint was investigated. A lower R value at a higher bonding temperature resulted in base metal fracture (i.e., plug fracture) of the Al alloy plate. The maximum load reached 410 N using a reduction ratio of higher than 2.1 and bonding temperature of 420 °C. The processed foils were properly stretched in the plane without breakage, and a total of 51 sound layered bonded interfaces were formed. The results also confirmed that the oxide film became more rarefied with increasing R. These results are expected to be applicable to high-throughput, high-reliability bonding of secondary battery electrodes.

RESUMEN

Each year, the phosphate industries in Morocco discard over 20 million tons of phosphogypsum into the Atlantic Ocean, posing a significant threat to aquatic life and causing potential long-term damage to ecosystems due to the accumulation of harmful substances. Hence, developing eco-friendly and cost-effective strategies to valorize phosphogypsum is vital to protect ecosystems and human health. This study aims to provide a concrete and efficient strategy for exploiting phosphogypsum and aluminum wastes in the preparation of hydrocalumite using the co-precipitation method. The synthesis strategy's effectiveness was assessed through a comprehensive analysis of the phosphogypsum-based hydrocalumite using various techniques, including FT-IR spectroscopy, X-ray powder diffraction, scanning electron microscopy (SEM), Energy-Dispersive X-Ray (EDX) analysis, X-ray fluorescence (XRF), and inductively coupled plasma optical emission spectrometry (ICP-OES). In addition, the structure was refined to discuss the arrangement of the polyhedrons occupied by the different ions in the hydrocalumite framework. It was found that the phosphogypsum-based hydrocalumite exhibited chemical and structural properties comparable to those of conventionally synthesized hydrocalumite, suggesting its potential applicability in diverse fields, including catalysis, cement and concrete production, polymer additives, medicine, and environmental remediation. Overall, in this work, the Moroccan phosphogypsum and aluminum wastes proved to be effective precursors of hydrocalumite, with structural and chemical properties presumably close to the conventional hydrocalumite.

RESUMEN

A novel annealing process of controlled heating rate is used to produce severe cold-formed aluminum plates, which are processed into aluminum foil and mainly used for high-voltage electrolytic capacitor anodes. The experiment in this study focused on various aspects such as microstructure, recrystallization behavior, grain size, and grain boundary characteristics. The results revealed a comprehensive influence of cold-rolled reduction rate, annealing temperature, and heating rate on recrystallization behavior and grain boundary characteristics during the annealing process. The heating rate applied plays a crucial role in controlling the recrystallization process and the subsequent grain growth, which ultimately determines whether or not the grains will become larger. In addition, as the annealing temperature rises, the recrystallized fraction increases and the grains size decreases; conversely, the recrystallized fraction decreases as the heating rate increases. When the annealing temperature remains constant, the recrystallization fraction increases with a greater deformation degree. Once complete recrystallization occurs, the grain will undergo secondary growth and may even subsequently become coarser. If the deformation degree and annealing temperature remain constant, the increased heating rate will result in a lower recrystallization fraction. This is due to the inhibition of recrystallization, and most of the aluminum sheet even remains in a deformed state before recrystallization. This kind of microstructure evolution, grain characteristic revelation, and recrystallization behavior regulation can provide effective help for enterprise engineers and technicians to guide the production of capacitor aluminum foil to a certain extent, so as to improve the quality of aluminum foil and increase the electric storage performance.

RESUMEN

Metal-based aerogels have attracted numerous studies due to their unique physical, structural, thermal, and chemical properties. Utilizing aluminum waste, a novel, facile, environmentally friendly approach to aluminum-based aerogels is proposed. In this work, the aluminum-based aerogels produced do not use toxic chemicals unlike conventional aerogel production. Aluminum powder, with poly(acrylic acid) and carboxymethyl cellulose as binders, is converted into aluminum-based aerogels using the freeze-drying method. The aluminum-based aerogels have low density (0.08-0.12 g/cm3) and high porosity (93.83-95.68%). The thermal conductivity of the aerogels obtained is very low (0.038-0.045 W/m·K), comparable to other types of aerogels and commercial heat insulation materials. Additionally, the aerogels can withstand temperatures up to 1000 °C with less than 40% decomposition. The aerogels exhibited promising oil absorption properties with their absorption capacity of 9.8 g/g and 0.784 g/cm3. The Young's modulus of the aerogels ranged from 70.6 kPa to 330.2 kPa. This study suggests that aluminum-based aerogels have potential in thermal insulation and oil absorption applications.

RESUMEN

The first application of aluminum foil (Al F) as a low-cost/high-availability substrate for sandwich immunoassay using surface-enhanced Raman spectroscopy (SERS) is reported. Untreated and unmodified Al F and gold film are used as substrates for sandwich SERS immunoassay to detect tuberculosis biomarker MPT64 and human immunoglobulin (hIgG) in less than 24 h. The limits of detection (LODs) for tuberculosis (TB) biomarker MPT64 on Al foil, obtained with commercial antibodies, are about 1.8-1.9 ng/mL, which is comparable to the best LOD (2.1 ng/mL) reported in the literature for sandwich ELISA, made with fresh in-house antibodies. Not only is Al foil competitive with traditional SERS substrate gold for the sandwich SERS immunoassay in terms of LOD, which is in the range 18-30 pM or less than 1 pmol of human IgG, but it also has a large cost/availability advantage over gold film. Moreover, human IgG assays on Al foil and Si showed better selectivity (by about 30-70% on Al foil and at least eightfold on Si) and a nonspecific response to rat or rabbit IgG, in comparison to the selectivity in assays using gold film.

Asunto(s)

RESUMEN

Recently, significant progress has been made in the performance of supercapacitors through the development of composite electrodes that combine various charge storage mechanisms. A new method for preparing composite binder-free MnO2/MWCNT/Al electrodes for supercapacitors is proposed. The method is based on the original technique of direct growth of layers of multi-walled carbon nanotubes (MWCNTs) on aluminum foil by the catalytic pyrolysis of ethanol vapor. Binder-free MnO2/MWCNT/Al electrodes for electrochemical supercapacitors were obtained by simply treating MWCNT/Al samples with an aqueous solution of KMnO4 under mild conditions. The optimal conditions for the preparation of MnO2/MWCNT/Al electrodes were found. The treatment of MWCNT/Al samples in a 1% KMnO4 aqueous solution for 40 min increased the specific capacitance of the active material of the samples by a factor of 3, up to 100-120 F/g. At the same time, excellent adhesion and electrical contact of the working material to the aluminum substrate were maintained. The properties of the MnO2/MWCNT/Al samples were studied by electron probe microanalysis (EPMA), Raman spectroscopy, cyclic voltammetry (CV), and impedance spectroscopy. Excellent charge/discharge characteristics of composite electrodes were demonstrated. The obtained MnO2/MWCNT/Al electrodes maintained excellent stability to multiple charge-discharge cycles. After 60,000 CVs, the capacitance loss was less than 20%. Thus, this work opens up new possibilities for using the MWCNT/Al material obtained by direct deposition of carbon nanotubes on aluminum foil for the fabrication of composite binder-free electrodes of supercapacitors.

RESUMEN

Bigeye tuna (Thunnus obesus) is an economically valuable ocean fish species. It is susceptible to contamination during storage and transportation. Having proper transportation packaging and stable temperature during transportation are critical to prevent quality deterioration. However, the influence of packaging on retaining freshness in transit remains unknown. Here, the impact of different transportation packaging on the quality and microbiological variation of bigeye tuna during the logistics process was investigated by measuring physical-chemical indexes and microbial diversity. It turned out that aluminum foil paper (AFP) group had minimum temperature fluctuation, exhibited preferable water retaining capacity and color protection effect. AFP packaging could efficiently prevent TVB-N increase and microbial growth. After 40 h, the TVB-N value was 21.28 mg/100 g and microbial total plate count was 3.53 lg CFU/g, which was within the acceptable range. Temperature fluctuations and packaging materials had a major effect on the microbial community structure of bigeye tuna. Chitinophagaceae, Acinetobacter, and Knoellia were dominant in the AFP group, while Pseudomonas, Acinetobacter, and Macrococcus were dominant in the expanded polystyrene foam (EPSF) and European logistics (EUL) groups. AFP packaging could effectively slow down the growth and reproduction of Pseudomonas, restraining the growth of microorganisms and preserve the quality of bigeye tuna. This study provides insights into understanding the effects of packaging material on maintaining quality during logistics transportation.

RESUMEN

Vertical van der Waals heterostructures (vdWhs), which are made by layer-by-layer stacking of two-dimensional (2D) materials, offer great opportunities for the development of extraordinary physics and devices such as topological superconductivity, robust quantum Hall phenomenon, electron-hole pair condensation, Coulomb drag, and tunneling devices. However, the size of vdWhs is still limited to the order of a few micrometers, which restricts the large-scale roll-to-roll processes for industrial applications. Herein, we report the sequential growth of a 14 in. vertical vdWhs on a rollable Al foil via chemical vapor deposition. By supplying chalcogen precursors to liquid transition-metal precursor-coated Al foils, we grew a wide range of individual 2D transition-metal dichalcogenide (TMD) films, including MoS2, VS2, ReS2, WS2, SnS2, WSe2, and vanadium-doped MoS2. Additionally, by repeating the growth process, we successfully achieved the layer-by-layer growth of ReS2/MoS2 and SnS2/ReS2/MoS2 vdWhs. The chemically inert Al native oxide layer inhibits the diffusion of chalcogen and metal atoms into Al foils, allowing for the growth of diverse TMDs and their vdWhs. The conductive Al substrate enables the effective use of vdWhs/Al as a hydrogen evolution reaction electrocatalyst with a transfer-free process. This work provides a robust route for the commercialization of 2D TMDs and their vdWhs at a low cost.

RESUMEN

Measurement networks for ultrafine particulate matter (PM0.1) have been limited by the high costs for equipment, supplies, and labor associated with the need to collect PM0.1 samples on multiple substrates for full chemical analysis. Here we explore whether a single cascade impactor loaded with aluminum foil substrates is sufficient for PM0.1 source apportionment calculations in order to reduce those costs. An extraction method previously designed to measure elements on Teflon substrates was modified to accommodate features of aluminum foil substrates. Regression analysis between co-located aluminum foil and Teflon substrates in the particle diameter range 0.1-1.8 µm showed good agreement (R > 0.7) for 18 elements. Regression in the diameter range 0.1-0.18 µm (quasi-ultrafine particulate matter) was used to characterize the uncertainty introduced by the aluminum foil extraction method for the elements Li, K, V, Br, Rb, Mo, Cd, Sn, Sb, and Ba. This uncertainty was used to generate 30 simulated aluminum foil PM0.1 datasets at each of three sites, followed by source apportionment analysis using Positive Matrix Factorization (PMF). At two of the three sites, the PM0.1 source contributions calculated using aluminum foil substrates alone were almost identical to the PMF results from combined aluminum foil and Teflon substrates. The PM0.1 source contributions calculated using aluminum foil substrates at the third site were closer to the results from a previous Chemical Mass Balance (CMB) study than to the PMF results from the combined aluminum foil and Teflon substrates, possibly because the CMB study also relied exclusively on samples collected using aluminum foil substrates. The success of the PM0.1 source apportionment approach using aluminum foil substrates in a single cascade impactor provides a viable method for reducing costs in PM0.1 sampling networks by 40-47%. Similar results may be achievable at locations outside of California.

Asunto(s)

RESUMEN

Potassium (K)-metal batteries have emerged as a promising energy-storage device owing to abundant K resources. An anode-free architecture that bypasses the need for anode host materials can deliver an elevated energy density. However, the poor efficiency of K plating/stripping on potassiophobic anode current collectors results in rapid K inventory loss and a short cycle life. Herein, commercial Al foils are decorated with an ultrathin graphene-modified layer (Al@G) through roll-to-roll plasma-enhanced chemical vapor deposition. By harnessing strong adhesion (10.52 N m-1 ) and a high surface energy (66.6 mJ m-2 ), the designed Al@G structure ensures a highly smooth and ordered K plating/stripping process. Consequently, during K-metal plating/stripping, Al@G can operate at a current density of up to 4.0 mA cm-2 and cyclic capacity of up to 4.0 mAh cm-2 , with an ultralong lifespan of up to 1000 h at 0.5 mA cm-2 and stable cycling of up to 750 h under periodic current fluctuations of 0.1-2.0 mA cm-2 . In addition, a novel anode-free K-metal full-cell prototype enabled by Al@G anode current collectors is constructed, demonstrating ameliorative cyclic stability.

RESUMEN

Various scientists are looking for effective and easy solutions for the augmentation of yield from the hemispherical solar still (HSS). In this study, aluminum foil sheet was used to reflect the intensity, hence augmenting the evaporation rate and daily yield. Experimentations were conducted on two SS: the first SS is HSS; the second SS is HSS with reflective aluminum foil sheet walls (HSS-RAFW). The highest distilled water production from the HSS and HSS-RAFW is 3.36 and 4.1 kg/m2, respectively. Compared to the HSS, the yield of distilled water was augmented by 22.21% when using the HSS-RAFW. The daily energy and exergy efficiencies (EnE and ExE) of the HSS are 26.27 and 1.04%, respectively, and the daily EnE and ExE of the HSS-RAFW are 32.75 and 1.71%, respectively.

Asunto(s)

RESUMEN

Even though acoustic cavitation has been widely investigated, only few researchers focused on the relationship between sonochemical and sonophysical activities and on the enhancement of sonophysical activity. In this study, sonochemical and sonophysical activities were investigated in a heterogeneous system to understand the relationship between these two activities and to suggest optimal conditions for ultrasonic desorption/extraction processes comprising milli-sized glass beads. The sonochemical activity was quantitatively analyzed using potassium iodide dosimetry in homogeneous and heterogeneous systems. Sonophysical activity was quantitatively and qualitatively analyzed using paint-coated bead desorption tests and aluminum foil erosion tests under three probe positions of "T" (1 cm below the liquid surface), "B" (1 cm above the vessel bottom), and "M" (midpoint between "T" and "B"). Three different sizes of glass beads (diameter: 0.2, 1.0, and 4.0 mm) were used in this study. The highest sonochemical activity was obtained at "B" in both homogeneous and heterogeneous systems. However, three times lower sonochemical activity was observed in the heterogeneous system than in the homogeneous system because significant attenuation and unstable reflection of ultrasound occurred in the bead layer and suspension. Higher sonophysical activity was observed, when the bead size decreased and the probe approached the bottom. However, no significant sonophysical activity was detected when the beads were attached to the bottom. Therefore, the sonophysically active region was the zone around the probe body, opposite to the ultrasound irradiation tip, and only suspended beads could undergo severe cavitational actions. This was confirmed via aluminum foil tests. Several erosion marks on the foil were observed in the area around the probe body, whereas no severe damage was observed at the bottom. Moreover, the degree of sonophysical activity did not change for various saturating gases. This might be due to the different thresholds of sonochemical and sonophysical activities.

RESUMEN

An original technique of chemical deposition (CVD) by catalytic pyrolysis of ethanol vapor was used to directly grow multiwall carbon nanotubes (MWCNTs) layers on aluminum foil. The grown nanotubes had excellent adhesion and direct electrical contact to the aluminum substrate. This material was perfect for use in electrochemical supercapacitors. In this work, the possibility of a significant increase in the specific capacity of MWCNTs by simple electrochemical oxidation was investigated. The optimal conditions for improving the characteristics of the MWCNT/Al electrodes were found. Electrochemical treatment of MWCNT/Al electrodes in a 0.005 M Na2SO4 solution at a potential of 4-5 V for 20-30 min increased the specific capacity of MWCNTs from 30 F/g to 140 F/g. The properties of modified nanotubes were investigated by X-ray photoelectron spectroscopy, cyclic voltammetry (CV), and impedance spectroscopy. A significant increase in the concentration of oxygen-containing functional groups on the surface of MWCNTs was found as a result of electrochemical oxidation. The modified MWCNT/Al electrodes maintained excellent stability to multiple charge-discharge cycles. After 20,000 CVs, the capacity loss was less than 5%. Thus, the results obtained significantly expanded the possibilities of using MWCNT/Al composite materials obtained by the method of direct deposition of carbon nanotubes on aluminum foil as electrodes for supercapacitors.

RESUMEN

We report a robust technique to fabricate a cost-efficient Raman substrate which is composed of polyvinylpyrrolidone (PVP) coated gold nanoparticles layer on commercial aluminum foil. The layer of metal nanoparticles on the aluminum foil, i.e., the nanoparticle-on-mirror (NPoM) structure was fabricated by spraying nanoparticle colloidal solution directly on the foil. The detection limit (LOD) of NPoM substrate is investigated by performing the SERS for Rhodamine 6G (R6G) with the concentration ranging from mM to nM without any post treatment of the substrate. The findings show that the LOD of 1 nM and maximum intensity enhancement factor of ~ 24 is accomplished. Field enhancement owing to reflection from the metallic mirror is the reason behind the signal enhancement and it would be beneficial for routine clinical applications, trace chemical detection, and disease diagnostics.

Asunto(s)

RESUMEN

The volumetric growth, composition, and morphology of porous alumina films fabricated by reduced temperature 280 K galvanostatic anodizing of aluminum foil in 0.4, 1.0, and 2.0 M aqueous sulfuric acid with 0.5-10 mA·cm-2 current densities were investigated. It appeared that an increase in the solution concentration from 0.4 to 2 M has no significant effect on the anodizing rate, but leads to an increase in the porous alumina film growth. The volumetric growth coefficient increases from 1.26 to 1.67 with increasing current density from 0.5 to 10 mA·cm-2 and decreases with increasing solution concentration from 0.4 to 2.0 M. In addition, in the anodized samples, metallic aluminum phases are identified, and a tendency towards a decrease in the aluminum content with an increase in solution concentration is observed. Anodizing at 0.5 mA·cm-2 in 2.0 M sulfuric acid leads to formation of a non-typical nanostructured porous alumina film, consisting of ordered hemispheres containing radially diverging pores.

RESUMEN

Surface enhanced fluorescence (SEF) is observed with very high contrast (100-200) from single E. coli bacteria cells labeled with Carbon nanodots (CDs), on aluminum foil and aluminum film. Likely, it is the first application of organic CDs in SEF. SEF with 633 nm excitation delivered a much higher contrast than SEF with 532 nm excitation. Contrast is the ratio of the fluorescent intensities of labeled CDs to unlabeled (control) cells. High contrast with CDs is also observed on the gold film, silicon, and glass. Enhancement factor (EF) is the ratio of the signal on the metal substrate to the signal on the glass. Single E. coli cells, labeled with commercial graphene quantum dots (GCDs), demonstrated higher EFs (44 on gold, 35 on Al film), but at least one order of magnitude lower contrast (7-10 on aluminum and gold) than cells labeled with organic CDs. Therefore, organic CDs can be a good choice for cell imaging/labeling, capable of achieving a signal to noise (standard deviation of the control) as high as 700 on Al film. Overall, aluminum foil and film are highlighted as inexpensive but efficient substrates for Metal Enhanced Fluorescence, particularly MEF of bacterial cells stained with CDs.

Asunto(s)

RESUMEN

Aluminum (Al) foil serving as the most widely used cathode current collector for lithium-ion batteries (LIBs) is still not flawless to fulfill the increasing demand of rechargeable energy storage systems. The limited contact area and weak adhesion to cathode material as well as local corrosion during long-term operations could deteriorate the performance of LIBs with a higher working voltage. Herein, a reduced graphene oxide (RGO)-modified Al foil (RGO/Al) is developed via electrospraying to increase interfacial adhesion and inhibit anodic corrosion as a functional current collector. Valid corrosion resistance to electrolyte and strengthened adhesion of electrode particles to current collectors are beneficial to improve the interfacial reaction dynamics. The RGO/Al-based LiNi0.5Mn1.5O4 cells (LNMO-RGO/Al) exhibit better electrochemical performances in terms of long-term cycling discharge capacity retention (90% after 840 cycles at 1 C), rate capability (101.8 mAh g-1 at 5 C), and interfacial resistance, prominently superior to bare Al-based cells (LNMO-Al). This work not only contributes to long-term stable operation of high-voltage LIBs but also brings new opportunities for the development of next-generation 5 V LIBs.