Nanoporous Anodic Alumina Membranes Research Articles

Harnessing the Intrinsic Ionic Rectification Properties of Blind‐Hole Nanoporous Anodic Alumina for Osmotic Energy Generation

AbstractThe full potential of blue energy as a sustainable technology for high‐performance energy generation remains elusive. Nanoporous anodic alumina (NAA) is extensively used as a passive structural support to develop a broad variety of ion exchange membranes based on other materials for osmosis‐driven energy generation. However, the intrinsic ionic current rectification (ICR) properties of the inherited hemispherical barrier oxide layer (BOL) closing the bottom tips of NAA's nanopores are overlooked. As‐produced NAA provides new avenues to control ionic transport through its BOL, acting as an ICR model system to study electric current associated with the selective flow of ions across anodic oxides. This study explores the intrinsic capability of NAA membranes for osmotic energy generation. NAA membranes with a working area of 13.4 mm2 can generate a power density yield of ≈2.8×10−4 W m−2 when subjected to a 105‐fold salinity ratio at a pH 3 in CaCl2 electrolyte, achieving a high efficiency of 7%. With better understanding of the mechanism of ion transport on osmotic generation, the intrinsic properties of NAA membranes can be tailor‐engineered to maximize blue energy yield, paving the way for future developments in a scalable technology suited for real‐life applications.

Fabrication of ZnO/ZnAl2O4/Au Nanoarrays through DC Electrodeposition Utilizing Nanoporous Anodic Alumina Membranes for Environmental Application.

In this study, anodic aluminum oxide membranes (AAOMs) and Au-coated AAOMs (AAOM/Au) with pore diameters of 55 nm and inter-pore spacing of 100 nm are used to develop ZnO/AAOM and ZnO/ZnAl2O4/Au nanoarrays of different morphologies. The effects of the electrodeposition current, time, barrier layer, and Au coating on the morphology of the resultant nanostructures were investigated using field emission scanning electron microscopy. Energy dispersive X-ray and X-ray diffraction were used to analyze the structural parameters and elemental composition of the ZnO/ZnAl2O4/Au nanoarray, and the Kirkendall effect was confirmed. The developed ZnO/ZnAl2O4/Au electrode was applied to remove organic dyes from aqueous solutions, including methylene blue (MB) and methyl orange (MO). Using a 3 cm2 ZnO/ZnAl2O4/Au sample, the 100% dye removal for 20 ppm MB and MO dyes at pH 7 and 25 °C was achieved after approximately 50 and 180 min, respectively. According to the kinetics analysis, the pseudo-second-order model controls the dye adsorption onto the sample surface. AAOM/Au and ZnO/ZnAl2O4/Au nanoarrays are also used as pH sensor electrodes. The sensing capability of AAOM/Au showed Nernstian behavior with a sensitivity of 65.1 mV/pH (R2 = 0.99) in a wide pH range of 2-9 and a detection limit of pH 12.6, whereas the ZnO/ZnAl2O4/Au electrode showed a slope of 40.1 ± 1.6 mV/pH (R2 = 0.996) in a pH range of 2-6. The electrode's behavior was more consistent with non-Nernstian behavior over the whole pH range under investigation. The sensitivity equation was given by V(mV) = 482.6 + 372.6 e-0.2095 pH at 25 °C with R2 = 1.0, which could be explained in terms of changes in the surface charge during protonation and deprotonation.

Understanding the Intrinsic Rectification Properties of Nanoporous Anodic Alumina by Selective Chemical Etching.

The distribution of oxygen and aluminum vacancies across the hemispherical barrier oxide layer (BOL) of nanoporous anodic alumina (NAA) relies intrinsically on the electric field-driven flow of electrolytic species and the incorporation of electrolyte impurities during the growth of anodic oxide through anodization. This phenomenon provides new opportunities to engineer BOL's inherited ionic current rectification (ICR) fingerprints. NAA's characteristic ICR signals are associated with the space charge density gradient across BOL and electric field-induced ion migration through hopping from vacancy to vacancy. In this study, we engineer the intrinsic space charge density gradient of the BOL of NAA under a range of anodizing potentials in hard and mild anodization regimes. Real-time characterization of the ICR fingerprints of NAA during selective etching of the BOL makes it possible to unravel the distribution pattern of vacancies through rectification signals as a function of etching direction and time. Our analysis demonstrates that the space charge density gradient varies across the BOL of NAA, where the magnitude and distribution of the space charge density gradient are revealed to be critically determined by anodizing the electrolyte, regime, and potential. This study provides a comprehensive understanding of the engineering of ion transport behavior across blind-hole NAA membranes by tuning the distribution of defects across BOL through anodization conditions. This method has the potential to be harnessed for developing nanofluidic devices with tailored ionic rectification properties for energy generation and storage and sensing applications.

Guard Cell-Inspired Ion Channels: Harnessing the Photomechanical Effect via Supramolecular Assembly of Cross-Linked Azobenzene/Polymers.

Stimuli-responsive ion nanochannels have attracted considerable attention in various fields because of their remote controllability of ionic transportation. For photoresponsive ion nanochannels, however, achieving precise regulation of ion conductivity is still challenging, primarily due to the difficulty of programmable structural changes in confined environments. Moreover, the relationship between noncontact photo-stimulation in nanoscale and light-induced ion conductivity has not been well understood. In this work, a versatile design for fabricating guard cell-inspired photoswitchable ion channels is presented by infiltrating azobenzene-cross-linked polymer (AAZO-PDAC) into nanoporous anodic aluminum oxide (AAO) membranes. The azobenzene-cross-linked polymer is formed by azobenzene chromophore (AAZO)-cross-linked poly(diallyldimethylammonium chloride) (PDAC) with electrostatic interactions. Under UV irradiation, the trans-AAZO isomerizes to the cis-AAZO, causing the volume compression of the polymer network, whereas, in darkness, the cis-AAZO reverts to the trans-AAZO, leading to the recovery of the structure. Consequently, the resultant nanopore sizes can be manipulated by the photomechanical effect of the AAZO-PDAC polymers. By adding ionic liquids, the ion conductivity of the light-driven ion nanochannels can be controlled with good repeatability and fast responses (within seconds) in multiple cycles. The ion channels have promising potential in the applications of biomimetic materials, sensors, and biomedical sciences.

(Invited) harnessing the Barrier Oxide Layer of Nanoporous Anodic Alumina for Iontronic Sensing

The hemispherical barrier oxide layer (BOL) closing the tips of hexagonally distributed arrays of cylindrical nanochannels in nanoporous anodic alumina (NAA) membranes is structurally engineered by anodizing aluminum substrates in three distinct acid electrolytes at their corresponding self-ordering anodizing potentials. These nanochannels display a characteristic ionic current rectification (ICR) signal between high and low ionic conduction states, which is determined by the thickness and chemical composition of the BOL, and the pH of the ionic electrolyte solution. Rectification efficiency of ionic current associated with the flow of ions across the anodic BOL increases with its thickness, under optimal pH conditions. The inner surface of nanopores in NAA membranes was chemically modified with thiol-terminated functional molecules. The resultant NAA-based iontronic system provides a model platform to selectively detect gold metal ions (Au3+) by harnessing dynamic ICR signal shifts as the core sensing principle. The sensitivity of the system is proportional to the thickness of the barrier oxide layer, where NAA membranes produced in phosphoric acid at 195 V with a BOL thickness of 232 ± 6 nm achieve the highest sensitivity and low limit of detection in the sub-picomolar range. This study provides exciting opportunities to engineer NAA structures with tailorable ICR signals for specific applications across iontronic sensing and other nanofluidic disciplines. Figure 1

A Free-Standing Chitosan Membrane Prepared by the Vibration-Assisted Solvent Casting Method.

Much attention has been paid to the surface modification of artificial skin barriers for the treatment of skin tissue damage. Chitosan is one of the natural materials that could be characterized by its biocompatibility. A number of methods for the preparation of chitosan membranes have been described in scientific articles, including solvent casting methods. This study investigates an improved technology to produce chitosan membranes. Thus, chitosan membranes were prepared using a vibration-assisted solvent casting method. First, aqueous acetic acid was used to pretreat chitosan. Then, free-standing chitosan membranes were prepared by solvent casting on nanoporous anodized aluminum oxide (AAO) membrane templates, allowing for the solvent to evaporate. Using finite element methods, a study was obtained showing the influence of chitosan solutions of different concentrations on the fluid flow into nanopores using high-frequency excitation. The height of the nanopillars and the surface area of the chitosan membrane were also evaluated. In this study, the surface area of the chitosan membrane was found to increase by 15, 10 and 6 times compared to the original flat surface area. The newly produced nanopillared chitosan membranes will be applicable in the fabrication of skin barriers due to the longer nanopillars on their surface and the larger surface area.

Electrochemical and photocatalytic properties of ZnO nanostructures deposited on nanoporous anodized aluminum oxide membrane and its application for degradation of reactive blue 19 in textile wastewater

The current study's objective was to develop a ZnO photocatalyst for the treatment of reactive blue 19 (RB19) from textile wastewater by depositing ZnO nanostructures over nanoporous anodized aluminum oxide (ZnO-AAO). The ZnO-AAO membrane was created using the atomic layer deposition (ALD) technique. SEM, XRD, and EDS morphological and structural characterizations demonstrated that ZnO nanostructures were successfully deposited on the AAO membrane. Studying the optical properties revealed that the band gap energies for ZnO, AAO, and ZnO-AAO membranes were found to be 3.19, 2.85, and 2.92 eV, respectively. This resulted in an improvement in the separation efficiency of photo-excited electrons and holes as well as an increase in the photocatalytic activity of the ZnO-AAO sample in the visible light region. Studying the electrochemical parameters revealed that ZnO-AAO had the lowest charge transfer resistance, which indicates that photoinduced electrons and holes in ZnO-AAO contacts effectively transfer charge and have slower recombination rates. According to research on photocatalytic performance, ZnO-AAO and ZnO photocatalysts required 70 and 90 min of visible light exposure to completely decolorize RB19, respectively. The photocatalytic decolorization of RB19 in an actual sample of textile wastewater showed that the dye could be effectively removed by photocatalytic means when ZnO-AAO membrane photocatalyst was present.

A reusable electrochemiluminescence biosensor controlled by a nanochannel gating system for T-2 toxin detection

A reusable electrochemiluminescence (ECL) biosensor based on the switchable gating property of nanochannels has been successfully developed and applied in the detection of T-2 toxin. The sensing interface was achieved by modifying nanoporous anodic aluminum oxide membrane with gold nanoparticles and T-2 aptamers, which has a switchable gating property triggered by the target. Once triggered by the target, the gating system could be switched from the "OFF" state to the "ON" state allowing diffusion of ascorbic acid (AA) and H2O2. Due to the consumption of reactive oxygen species by AA, ECL signals of luminol/Au NPs was significantly inhibited. Through the treatment of heating and washing, captured T-2 toxin can be fully released and the gating system can be switched to the “OFF” state and applied in the following detection. Due to the spatial separation, reactivation of the sensing interface by repeated heating and washing will not affect the ECL emitters after repeated tests. This biosensor was applied in the analysis of actual samples. There’s a good linear relationship between ECL intensity and the logarithm value of the concentration in the range of 10 pg mL−1 to 100 μg mL−1 with a limit of detection of 3.2 pg mL−1.

Electrophoretic Deposition of Rochelle Salt Nanocrystals on Aluminum Plate

A straightforward and inexpensive electrophoretic method for obtaining environment-friendly nanocrystalline piezo layers from Rochelle salt (RS) is presented here. The electrophoretic deposition process includes the formation of nanocrystals by precipitation of Rochelle salt/water solutions in ethanol (anti-solvent method) under the influence of a high electric field. A nanoporous anodic aluminum oxide membrane is used to separate the electrochemical cell into two chambers. The composition of the RS:H2O:EtOH mixture and the spatial separation of the process of precipitation from electrophoretic deposition allow control of the nanocrystal size and the uniformity of the layer. The reaction kinetics, the morphology, and the piezo response to the resulting layers are all investigated. The best samples were obtained at RS:H2O:EtOH ratio 1:22.5:37.5. Under these conditions, the nanocrystals are preferentially oriented on the aluminum substrate and form a dense and homogeneous layer. Although the obtained structure is polycrystalline, the resulting piezo effect is 1120 pC/N, which is comparable to inorganic monocrystals and piezoceramics. This allows the use of electrophoretically deposited polycrystalline piezo layers in applications such as energy harvesting.

Influence of heat transfer and wetting angle on condensable fluid flow through nanoporous anodic alumina membranes.

The flow of isobutane and of freon 142b (1-chloro-1,1-difluoro-ethane) through anodic alumina membranes with pore diameters between 18 and 60 nm in a capillary condensation regime is experimentally and theoretically explored. The capillary condensation effect increases the membrane permeance for condensable gases from 25 to 150 m3(STP) m-2 bar-1 h-1 at certain conditions. To describe the experimental results, a model is suggested accounting for heat transfer from the condensing to the evaporating meniscus, different boundary conditions for the heat transfer between the environment and the membrane, and wettability of the pore wall. The proposed model indicates a large influence of heat supply from the environment to the membrane on the permeance in the capillary condensation regime and a moderate influence of condensate contact angle in the range of 0-60°. Measuring the temperature of the permeate side of the membrane allows to find a suitable boundary condition to describe heat transfer. The obtained boundary condition yields an excellent fit of experimental results of condensate flow through membranes with different pore diameters for the two utilized fluids. Also, confocal Raman spectroscopy gave evidence on the fraction of pores filled with condensate.

Random Walks and Sticky Surfaces: Single-Molecule Measurements of Solute Diffusion in Ethanol/Water-Filled Anodic Alumina Nanopores

Nanoporous anodic aluminum oxide (AAO) membranes are now being explored for use in advanced chemical separations, including in the dehydration of biofuels such as ethanol. Optimization of membrane performance requires an in-depth understanding of how solvent mixtures and solutes behave under nanoconfinement. In this work, the diffusion of rhodamine B (RhB) dye through 10 and 20 nm AAO nanopores filled with a series of ethanol/water mixtures (0–33% water) is explored by fluorescence correlation spectroscopy (FCS). RhB was found to diffuse through the pores by two distinct mechanisms with mean diffusion coefficients, Df and Ds, reflecting fast and slow diffusive motions, respectively, with values that differ by nearly 2 orders of magnitude. Both Df and Ds increased with pore size and were significantly smaller than Db, the RhB diffusion coefficient in bulk liquid. Mean Df values follow a composition-dependent trend that closely mimics the viscosity dependence of Db. Additional slowing of fast RhB diffusion is attributed to both hydrodynamic drag and electrostatic interactions with the nanopore surface. The mean Ds values exhibit a different trend with increasing water content, revealing an increase in Ds and a decrease in the contributions of slow diffusion to the observed dynamics. The fluorescence time transient data used in the analysis show that the slow diffusion process is strongly hindered and likely involves frequent adsorption of RhB to the pore surfaces. These results provide new insights into the detailed molecular-level mechanisms of mass transport in nanoporous AAO membranes.

Vibration-Assisted Synthesis of Nanoporous Anodic Aluminum Oxide (AAO) Membranes.

In recent years, many research achievements in the field of anodic aluminum oxide (AAO) membranes can be observed. Nevertheless, it is still an interesting research topic due to its high versatility and applications in various fields, such as template-assisted methods, filtration, sensors, etc. Nowadays, miniaturization is an integral part of different technologies; therefore, research on micro- and nanosized elements is relevant in areas such as LEDs and OLEDs, solar cells, etc. To achieve an efficient mixing process of fluid flow in straight nanopores, acoustofluidic physics has attracted great interest in recent decades. Unfortunately, the renewal of the electrolyte concentration at the bottom of a pore is limited. Thus, excitation is used to improve fluid mixing along nanosized diameters. The effect of excitation by high-frequency vibrations on pore geometry is also investigated. In this study, theoretical simulations were performed. Using theoretical calculations, the acoustic pressure, acoustic velocity, and velocity magnitude were obtained at frequencies of 2, 20, and 40 kHz. Moreover, nanoporous AAO membranes were synthesized, and the influence of high-frequency vibrations on the geometry of the pores was determined. Using a high-frequency excitation of 20 kHz, the thickness of the AAO membrane increased by 17.8%. In addition, the thickness increased by 31.1% at 40 kHz and 33.3% at the resonant frequency of 40 kHz. Using high-frequency vibrations during the anodization process, the electrolyte inside the pores is mixed, and as a result, a higher oxide growth rate and a deeper structure can be achieved. On the other hand, to obtain pores of the same depth, the reaction can be performed in a shorter time.

Development and Analysis of Electrochemical Reactor with Vibrating Functional Element for AAO Nanoporous Membranes Fabrication.

Nanoporous anodic aluminum oxide (AAO) is needed for a variety of purposes due to its unique properties, including high hardness, thermal stability, large surface area, and light weight. Nevertheless, the use of AAO in different applications is limited because of its brittleness. A new design of an electrochemical reactor with a vibrating element for AAO nanoporous membranes fabrication is proposed. The vibrating element in the form of a piezoceramic ring was installed inside the developed reactor, which allows to create a high-frequency excitation. Furthermore, mixing and vibration simulations in the novel reactor were carried out using ANSYS 17 and COMSOL Multiphysics 5.4 software, respectively. By theoretical calculations, the possibility to excite the vibrations of five resonant modes at different frequencies in the AAO membrane was shown. The theoretical results were experimentally confirmed. Five vibration modes at close to the theoretical frequencies were obtained in the novel reactor. Moreover, nanoporous AAO membranes were synthesized. The novel aluminum anodization technology results in AAO membranes with 82.6 ± 10 nm pore diameters and 43% porosity at 3.1 kHz frequency excitation and AAO membranes with 86.1 ± 10 nm pore diameters and 46% porosity at 4.1 kHz frequency excitation. Furthermore, the chemical composition of the membrane remained unchanged, and the hardness decreased. Nanoporous AAO has become less brittle but hard enough to be used for template synthesis.

Impact of Nanostructurization of the Pore Walls on the Dynamics of a Series of Phenyl Alcohols Incorporated within Nanoporous Aluminum Oxide Templates

Herein, we studied the impact of surface roughness on the molecular dynamics of a series of phenyl-terminated monohydroxyalcohols under spatial confinement provided by nanoporous anodic aluminum oxide (AAO) membranes of constant (const-AAO) and modulated (modul-AAO) pore diameter using Broadband Dielectric Spectroscopy and Differential Scanning Calorimetry. Interestingly, we observed that both types of AAO membranes affect the behavior of examined associating materials in a different manner. Calorimetric measurements showed that the double glass transition phenomenon, commonly reported for many compounds infiltrated into const-AAO membranes, is not observed in the case of modul-AAO templates, where a single glass transition temperature was detected. Consequently, the dynamics of the dominant process was bulk-like in the whole range of studied temperatures for the samples infiltrated into the latter templates. Moreover, the Debye character of the dominant relaxation process characteristic for bulk samples was lost for the confined samples. Interestingly, the width of the dominant mode was the greatest in the alcohols infiltrated into modulated pores. It was assigned to the higher heterogeneity in the mobility introduced by the nanostructurization of the interface. The presented data emphasize the crucial impact of modulated-induced surface roughness of an applied constrained medium on the dynamics and phase transition of the liquids infiltrated into pores.

Continuous Ion Separations Using Non-Faradaic Capacitive AC Ratcheting

Traditional electrochemical separations processes require Faradaic reactions for sustained currents. We discovered that this limitation can be overcome by oscillating the applied potential across an ion-permeable material that has an asymmetric electric potential profile. We demonstrated this phenomenon for the first time using a flashing ratchet consisting of a nanoporous anodized aluminum oxide membrane infiltrated with salt water and containing metallic contacts on either side. When a symmetric +/-300 mV square-wave potential was applied to the metallic contacts at a frequency of ~100 Hz, an open-circuit potential as large as ~50 mV was observed between Ag/AgCl electrodes immersed in the chloride-containing electrolyte and positioned across the membrane. While this open-circuit potential was determined to be a consequence of net ionic polarization, additional electrochemical data were also consistent with transport of neutral salt across the membrane via a proposed ambipolar transport mechanism. In comparison, application of a DC potential bias resulted in non-Faradaic charging, and a near-zero long-time open-circuit potential. Moreover, high ionic strengths and large pore sizes diminished ratcheting behavior, consistent will more complete screening of surface charges in the nanopores. Collectively, this work represents a new paradigm for direct ion pumping and salt separations that requires no Faradaic reactions or additional transport pathway for ions or electrons.

Structural Engineering of the Barrier Oxide Layer of Nanoporous Anodic Alumina for Iontronic Sensing.

The hemispherical barrier oxide layer (BOL) closing the bottom tips of hexagonally distributed arrays of cylindrical nanochannels in nanoporous anodic alumina (NAA) membranes is structurally engineered by anodizing aluminum substrates in three distinct acid electrolytes at their corresponding self-ordering anodizing potentials. These nanochannels display a characteristic ionic current rectification (ICR) signal between high and low ionic conduction states, which is determined by the thickness and chemical composition of the BOL and the pH of the ionic electrolyte solution. The rectification efficiency of the ionic current associated with the flow of ions across the anodic BOL increases with its thickness, under optimal pH conditions. The inner surface of the nanopores in NAA membranes was chemically modified with thiol-terminated functional molecules. The resultant NAA-based iontronic system provides a model platform to selectively detect gold metal ions (Au3+) by harnessing dynamic ICR signal shifts as the core sensing principle. The sensitivity of the system is proportional to the thickness of the barrier oxide layer, where NAA membranes produced in phosphoric acid at 195 V with a BOL thickness of 232 ± 6 nm achieve the highest sensitivity and low limit of detection in the sub-picomolar range. This study provides exciting opportunities to engineer NAA structures with tailorable ICR signals for specific applications across iontronic sensing and other nanofluidic disciplines.

Development of Carbon Nanotubes (CNTs) Membrane from Waste Plastic: Towards Waste to Wealth for Water Treatment

Plastic, a non-biodegradable material has always been a concern to the environment and people. This single-use item generates waste to landfills and it persists for centuries once disposed. The urge of transforming such material into a highly valuable product has sought attention from many researchers. This study emphasizes on a nanotechnological approach to synthesize vertically-aligned carbon nanotubes (CNTs) on a substrate template using commercially available plastic bags as carbon precursor. CNTs are grown inside a hexagonally arranged nanoporous anodic alumina membranes (NAAMs). CNTs are liberated by wet chemical etching to dissolve the alumina matrix. The resulting CNTs are used as adsorption media filters for water treatment purpose. The high adsorption affinity towards heavy metals, organic matters and microbes, ability to antifouling and self-cleaning function have made CNTs a better choice over others. This article briefly discusses the catalyst-free synthesis, growth mechanism, characterization and functionalization of CNTs for water treatment application.

Fabrication of nanostructured Pt electrodes templated by nanoporous anodic alumina for electrochemical sensors

Although platinum electrodes are widely used in electrochemical sensors their functionality can be affected by formed components of complex biological fluids. We demonstrated a simple approach to the formation of Pt nanopillars sandwiched between W metal layers and nanoporous anodic alumina membranes, by anodization of W/Al bilayers and substitution of WO3 nanopillars formed by the local anodization of W under the nanopores with Pt. By exploiting the Pourbaix corrosion diagram of W, we could find conditions that allow the selective dissolution of WO3 in pH = 7.4 buffer solution and formation of Pt nanopillars inside the nanoporous aluminum membrane via electroless deposition.

Electrochemical sensing at nanoporous film‐coated electrodes

AbstractIn this paper, we highlight the uniqueness of nanoporous film‐coated electrodes as electrochemical sensing platforms. Specifically, we focus on discussing electrodes coated with insulator‐based monolithic films comprising vertically‐oriented, rigid cylindrical nanopores of uniform diameters (2–200 nm). The electrode coating results in the formation of an array of recessed nanodisk electrodes, and thus we named them recessed nanodisk‐array electrodes (RNEs). We first summarize the properties of nanoporous films commonly used for RNE fabrication, including nanoporous anodic alumina membranes, track‐etched polymer membranes, block copolymer‐derived nanoporous films, and mesoporous silica films. Subsequently, we discuss representative works that take advantage of the uniform size/shape of the nanopores for enhancing electrochemical detection selectivity and sensitivity. RNE‐based sensors measure faradaic currents from redox‐active analytes or exogenously‐added electroactive species that penetrate through the nanopores, or those from redox‐active moieties tethered to the surface of the nanopores or underlying electrodes. The enhanced detection selectivity of these sensors is attributed to the preferential partitioning of analytes into the nanopores or steric/electrostatic exclusion of interfering species. In particular, the uniform sizes/shapes of RNE nanopores play key roles in their higher molecular sieving selectivity and also in the better control of the detection selectivity based on electrostatic/chemical interactions. The detection sensitivity of RNE‐based sensors can be improved by tailoring the chemical environments of the nanopores for analyte preconcentration or for steric/electrostatic manipulation of the dynamics of redox‐tagged binding moieties. These unique characteristics of RNEs, in addition to the mitigation of electrode fouling by the nanoporous films, will enable the development of pretreatment‐free electrochemical sensors for complex matrix solutions.

Surface Functionalized Anodic Aluminum Oxide Membrane for Opto-Nanofluidic SARS-CoV-2 Genomic Target Detection.

An ultra-thin and highly sensitive SARS-CoV-2 detection platform was demonstrated using a nano-porous anodic aluminum oxide (AAO) membrane. The membrane surface was functionalized to enable efficient trapping and identification of SARS-CoV-2 genomic targets through DNA-DNA and DNA-RNA hybridization. To immobilize the probe oligonucleotides on the AAO membrane, the pore surface was first coated with the linking reagents, 3-aminopropyltrimethoxysilane (APTMS) and glutaraldehyde (GA), by a compact vacuum infiltration module. After that, complementary target oligos with fluorescent modifier was pulled and infiltrated into the nano-fluidic channels formed by the AAO pores. The fluorescent signal applying the AAO membrane sensors was two orders stronger than a flat glass template. In addition, the dependence between the nano-pore size and the fluorescent intensity was evaluated. The optimized pore diameter d is 200 nm, which can accommodate the assembled oligonucleotide and aminosilane layers without blocking the AAO nano-fluidic channels. Our DNA functionalized membrane sensor is an accurate and high throughput platform supporting rapid virus tests, which is critical for population-wide diagnostic applications result in a page being rejected by search engines.