Charged Nanochannels Research Articles

Asymmetric thermo-electro-osmotic responses in charged conical nanochannels

Nanofluidic thermo-electric and thermo-osmotic responses have attracted increasing attention for their potential in low-grade heat energy recovery. However, the synergistic influence of geometric asymmetry and electrolyte physical properties on these responses is often overlooked. This study investigates asymmetric thermo-electro-osmotic responses by systematically varying parameters such as conicity, Debye length, and surface charge density within conical nanochannels. We employ the numerical model coupling extended Poisson-Nernst-Planck-Navier-Stokes and energy equations to simulate ion transport, fluid flow, and heat transfer. Results demonstrate pronounced asymmetries in thermo-electric and thermo-osmotic responses between forward and backward nanochannel configurations. The short-circuit current strongly depends on conicity, Debye length, and surface charge density, while the Seebeck coefficient is primarily influenced by Debye length, and surface charge density. Thermo-osmotic flow is significantly affected by all parameters, with flow direction reversals observed under specific conditions. The study highlights that Debye length and surface charge density significantly influence both thermo-electric and -osmotic responses, whereas geometric asymmetry predominantly affects thermo-osmotic response. This study provides a valuable framework for understanding fundamental thermal-driven transport phenomena at the nanoscale. The observed synergistic effects between various parameters offer insights for optimizing thermo-electric energy conversion and fluidic control within conical nanochannels, paving the way for innovative applications in nanofluidic technology and energy recovery systems.

Self-adhesive ionic cable derived from natural bark as osmotic energy generator

Osmotic energy conversion technology plays an increasingly important role as clean energy alternatives. However, the excessive use of non-renewable materials in osmotic energy harvesting can lead to serious environmental pollution. Herein, we design a low-cost, eco-friendly, and high-ion-conductance ionic cable directly from natural Eucommia ulmoides bark owing to its unique sandwich structure and abundant charged nanochannels within the well-aligned lignocellulose nanofibers. In the cable, the natural biopolymer E. ulmoides gum (EUG) acts as a bio-adhesive tightly holding cellulose fibers together, rendering it with high morphological stability. The as-prepared ionic cable shows excellent ion conductance of 3.36 × 10−3 S cm−1, far surpassing the performance of natural bark (2.58 × 10−4 S cm−1). This work utilizes the natural E. ulmoides bark components and its unique lignocellulose-EUG sandwich structure to construct fully biomass-based cable with high-ion-conductance and water-stable, providing a sustainable strategy to accelerate the implementation of clean osmotic energy harvesting and forest waste utilization.

Mechanically activated and deactivated ion transport across nanopores with heterogeneous surface charge distributions

To mimic the intricate and adaptive functionalities of biological ion channels, electrohydrodynamic ion transport has been studied extensively, albeit mostly, across uniformly charged nanochannels. Here, we analyze the ion transport under coupled electric field and pressure across heterogeneously charged nanopores with oppositely charged sections on their lateral surface. We only consider such pores with symmetric hourglass-like and cylindrical shapes to focus on the effects of the non-uniform surface charge distribution. Finite-element simulations of a continuum model demonstrate that a pressure applied in either direction of the pore-axis equally suppresses or amplifies the ionic conductance, depending on the electric field polarity, by distorting the quasi-static distribution of ions in the pore. The resulting anomalous mechanical deactivation and activation of ionic current under opposite voltage biases exhibit the functional modularity of our setup, while their intensities are highly tunable, substantially greater than those of analogous behaviors in other nanochannels, and fundamentally correlated to ionic current rectification (ICR) in our pores. A detailed study of ICR subsequently reveals its counterintuitive non-monotonous variations, in the pores, with the magnitude of applied voltage and the pore length, that can help optimize their diode-like behavior. We further illustrate that while the hourglass-shaped nanopores yield the more efficient mechanical suppressors of ion transport, their cylindrical analogs are the superior rectifiers and mechanical amplifiers of ion conduction. Therefore, this article provides a blueprint for the strategic design of nanofluidic circuits to attain a robust, modular, and tunable control of ion transport under external electrical and mechanical stimuli.

Harvesting Enhanced Blue Energy in Charged Nanochannels Using Semidiluted Polyelectrolyte Solution.

Blue energy generation in nanochannels based on salinity gradients is currently the most promising method in the area of nonconventional energy production. We used a semidiluted pure sodium carboxymethylcellulose (NaCMC)-KCl aqueous solution to study the characteristics of blue energy generation within a charged nanochannel. We solve the corresponding equations for ionic transport using a numerical technique based on the finite element method. Our analysis focused on the electric double layer (EDL) potential field, open circuit current, diffuse potential, electric conductance, maximum generated pore power, and maximum energy conversion efficiency by varying concentrations of the salt in the left-side reservoir and the bulk polyelectrolyte. The results indicate that as the polyelectrolyte concentration increases, the extent of EDL overlap considerably reduces. With an increase in polyelectrolyte concentration, the open circuit current increases, while the diffuse potential reduces. It was observed that both electrical conductance and maximal pore power improve considerably with higher polyelectrolyte concentrations. Interestingly, our modeling framework demonstrates a power density substantially higher (up to 16.31 W/m2) than earlier configurations and surpasses the established commercial limit (5 W/m2). Furthermore, our findings reveal that the reservoir salt concentration significantly affects the rate of decline in the maximum energy conversion efficiency as the polyelectrolyte concentration increases. The research paves the way for the development of high-power-density devices with several practical applications.

Wood Ion Pumps Enabled by Light-Responsive MoS2-Decorated Nanocellulosic Channels.

Light-driven active ion transport discovered in nanomaterials (e.g., graphene, metal-organic framework, and MXene) implicates crucial applications in membrane-based technology and energy conversion systems. However, it remains a challenge to achieve bulk assembly. Herein, we employ the scalable wood as a framework for in situ growth of MoS2 nanosheets to facilitate light-responsive ion transport. Owing to the aligned and negatively charged wood nanochannels, the MoS2-decorated wood exhibits an excellent nanofluidic conductivity of 8.3 × 10-5 S cm-1 in 1 × 10-6 M KCl. Asymmetric light illumination creates the separation of electrons and holes in MoS2 nanosheets, enabling ions to move uphill against a wide range of concentration gradients. As a result, the MoS2-decorated wood can pump ions uphill against a 20-fold concentration gradient at a light intensity of 300 mW cm-2. When the illumination is applied to the opposite side, the osmotic current along the 20-fold concentration gradient can be enhanced to 75.1 nA, and the corresponding osmotic energy conversion power density increases to more than 12.6 times that of the nonilluminated state. Based on the light-responsive behaviors, we are extending the use of MoS2-decorated wood as the ionic elements for nanofluidic circuits, such as ion switches, ion diodes, and ion transistors. This work provides a facile and scalable strategy for fabricating light-controlled nanofluidic devices from biomass materials.

Advanced ion-selective wood membranes: Leveraging aligned cellulose nanofibers for enhanced osmotic energy conversion

Nanofluidic reverse electrodialysis (RED) is widely recognized as an exceptionally effective method for harvesting osmotic energy. Nevertheless, its progress has been impeded by the high costs and intricate fabrication processes associated with the required ion exchange membranes. The ion-selective wood membranes (ISWM) are derived directly from natural wood through a meticulously designed two-step chemical modification and densification process. The obtained ISWM with a highly charged surface effectively preserves the alignment of nanochannels from the cellulose fibers sourced in natural wood. Moreover, the laminated structure consisting of oriented nanofibers enhances ion conductivity by a factor of 4 compared to natural wood birch under low KCl concentrations. The charged and aligned nanochannels serve as nanofluidic conduits, facilitating selective ion transport. This, in turn, engenders efficient charge separation and the generation of an electrochemical potential difference. In energy harvesting systems such as ISWM-RED, the synergistic interplay between the electrochemical potential difference and ionic flux manifests in a remarkable output power density, reaching up to 658 mW m−2 to a salinity gradient of KCl at a magnitude of 50-fold. ISWM is an outstanding nanofluidic material that provides a cost-effective and easy-to-prepare solution for producing natural nanofluidic materials. Our investigation delineates a promising trajectory for developing high-performance nanofluidic RED devices tailored for efficient osmotic energy harvesting from renewable and abundant natural resources.

Memristive Characteristics in an Asymmetrically Charged Nanochannel.

The emergent nanofluidic memristor provides a promising way of emulating neuromorphic functions in the brain. The conical-shaped nanopore showed promising features for a nanofluidic memristor, inspiring us to investigate the memory effects in asymmetrically charged nanochannels due to their high current rectification, which may result in good memory effects. Here, the memory effects of an asymmetrically charged nanofluidic channel were numerically simulated by Poisson-Nernst-Planck equations. Our results showed that the I-V curves represented a diode in low scanning frequency and then became a memristor and finally a resistor as frequency increased. We successfully replicated the learning behavior in our system with history-dependent ion redistribution in the nanochannel. Some critical factors were quantitatively analyzed for the memory effects including voltage amplitude, optimal frequency, and Dukhin number. Experimental characterizations were also carried out. Our findings are useful for the design of nanofluidic memristors by the principle of enrichment and depletion as well as the determination of the best memory settings.

Effect of cation species on pressure-driven electrokinetic energy conversion in charged conical nanochannels

Electrokinetic energy conversion (EEC) offers a promising avenue for transforming elusive natural energy into electric power, showing a wide application spectrum. Unlike prevalent studies that chiefly utilize symmetrical electrolyte solution (e.g., KCl) and uniformly structured negatively charged nanochannels for EEC, this paper delves into a thorough examination of EEC characteristics—streaming current, streaming potential, and output power—in both positively and negatively charged conical nanochannels with symmetrical and asymmetric (CaCl2 and LaCl3) electrolytes solutions. Operating under the assumption that the electrolyte solutions (KCl, CaCl2, and LaCl3) possess equivalent ionic strength and, thereby, a common Debye length, our findings reveal a significant dependency of EEC characteristics and their regulation parameters on the electrolyte type, nanochannel charge polarity, and ionic strength. As the ionic strength increases, both the streaming current and output power initially rise to a peak before subsequently declining, with the ionic strength at the peak being influenced by the cation valence: lower valence leads to lower ionic strength. In asymmetric electrolyte scenarios, optimal EEC characteristic is observed in positively charged conical nanochannels under a reverse pressure difference, attributed to the ion-selective and ionic concentration distribution in the charged conical nanochannels. Moreover, the complex behaviors of the regulation parameters of EEC characteristics are unveiled. Notably, a tri-valent electrolyte's regulation parameters exceed those of a bi-valent electrolyte, indicating that ionic valence asymmetry enhances the regulation effects on EEC in conical nanochannels.

Impacts of multi-foulings on salinity gradient energy conversion process in negatively charged conical nanochannels

Impacts of multi-foulings on salinity gradient energy conversion process in negatively charged conical nanochannels

Eliminating lithium dendrites via dependable ion regulation of charged nanochannels

Reviving lithium metal anode is of great significance to developing high-energy-density batteries after addressing the lithium dendrite. Constructing functional separator with charged nanochannel configuration has been proven to be an effective way to inhibit nucleation of lithium dendrites due to the achievement of a fast and selective lithium ion transport. While the ion regulation capability of existing functional separators cannot be maximized because their nanochannels are much larger than the electric double layer (EDL) regions that dominate ion transport. Considering the tiny EDL thickness (∼1 nm) formed in the electrolyte, the sulfonate-rich covalent organic framework (COF) is developed as functional separator to achieve a dependable ion regulation based on the nano-confined channel (∼1.55 nm) and surface negative charges. Consequently, a high Li+ transference number tLi+ (0.85) and sufficient ionic conductivity (0.53 mS cm−1) are obtained simultaneously, which effectively alleviates dendrite nucleation and growth of lithium metal anode for over 1000 h. Moreover, the principle for fast and selective lithium-ion transport is revealed from a new perspective of EDL region embedded in the nanochannel. Overall, this work demonstrates a strategy to eliminate lithium dendrites via ion regulation of charged nanochannels, which is anticipated to promote the practical application of lithium metal batteries.

In Situ Grown Coordination-Supramolecular Layer Holding 3D Charged Channels for Highly Reversible Zn Anodes.

Dynamic reversible noncovalent interactions make supramolecular framework (SF) structures flexible and designable. A three-dimensional (3D) growth of such frameworks is beneficial to improve the structure stability while maintaining unique properties. Here, through the ionic interaction of the polyoxometalate cluster, coordination of zinc ions with cationic terpyridine, and hydrogen bonding of grafted carboxyl groups, the construction of a 3D SF at a well-crystallized state is realized. The framework can grow in situ on the Zn surface, further extending laterally into a full covering without defects. Relying on the dissolution and the postcoordination effects, the 3D SF layer is used as an artificial solid electrolyte interphase to improve the Zn-anode performance. The uniformly distributed clusters within nanosized pores create a negatively charged nanochannel, accelerating zinc ion transfer and homogenizing zinc deposition. The 3D SF/Zn symmetric cells demonstrate high stability for over 3000 h at a current density of 5 mA cm-2.

High-aligned oppositely-charged nanocellulose/MXene aerogel membranes through synergy of directional freeze-casting and structural densification for osmotic-energy harvesting

Optimization of ion-transport paths can considerably improve ion-transport capabilities in charged nanochannels. Thus, the assembly of high-charge-density one- and two-dimensional nanomaterials into aligned nanochannels is necessary for high-performance osmotic-energy harvesting. Herein, we prepared cellulose/MXene aerogel membranes with opposite charges and aligned nanochannels via chemical modification on algal cellulose nanofibers and MXene nanosheets, unidirectional freeze casting, and structural densification to considerably enhance the ionic conductivity in low-concentration solutions (maximum conductivity of 2.88 × 10−3 S cm−1). In particular, the aligned membrane had an output power density of 2.97 and 4.89 times higher than membranes used for suction filtration and isotropic nanochannels, respectively, demonstrating the necessity for nanostructure control. In addition, due to the photothermal effect of MXene, the positively–negatively (P–N) charged unit produced a maximum output power density of 8.87 W m−2 under a concentration gradient of artificial seawater and river water and simulated sunlight. Moreover, the unit maintained 90.4% of its original output capacity after 168 h of operation. As a proof of concept, we created nine series of P–N units and successfully powered an electronic calculator with an output voltage of 1.85 V. This study reveals improvements in developing renewable materials with an aligned nanostructure for high-performance osmotic-energy conversion.

Asymmetrically charged polyamide nanofilm of intrinsic microporosity containing quaternary ammonium groups for heavy metal removal

High-performance nanofiltration (NF) is a highly hopeful approach for removing heavy metals from water, which can effectively solve the hazards of heavy metals to the public health and environment security. In this study, a polyamide (PA) nanofilm of intrinsic microporosity was fabricated through interfacial polymerization of the novel spirocyclic diamine monomer (SBI) with trimesoyl chloride (TMC). The PA nanofilm demonstrated high microporosity due to the porous structure formed by the covalent cross-linking of SBI with TMC and the stacking of the SBI monomers due to its rigidly-contorted structure. Consequently, its free volume was high with the water permeance of 19.3 L m−2 h−1·bar−1. Meanwhile, the PA nanofilm exhibited asymmetrical charges on both sides with a positively charged bottom and a negatively charged top. The quaternary ammonium moieties in SBI produced positively charged nanochannels in the PA nanofilm, reinforcing the Donnan exclusion against multivalent cations. The proposed SBI-TMC membrane was able to effectively remove heavy metals from water, with rejections of Cu2+, Ni2+, Zn2+, and Pb2+ at 93.3%, 93.0%, 91.8%, and 88.3%, respectively. This study confirmed that the fit-for-purpose design of monomer with rigidly-contorted structure is a feasible approach to fabricate NF membrane with enhanced separation performance.

Maximizing blue energy: the role of ion partitioning in nanochannel systems.

This study describes a numerical analysis on blue energy generation using a charged nanochannel with an integrated pH-sensitive polyelectrolyte layer (PEL), considering ion partitioning effects due to permittivity differences. The mathematical model for ionic and fluidic transport is solved using the finite element method, and the model validation is performed against existing theoretical and experimental results. The study investigates the influence of electrolyte concentration, permittivity ratio, and salt types (KCl, BeCl2, AlCl3) on the energy conversion process. The findings illustrate the substantial role of ion partitioning in modulating ionic concentration and potential fields, thereby affecting current profiles and energy conversion efficiencies. Remarkably, overlooking ion partitioning leads to significant overestimations of power density, highlighting the necessity of this consideration for accurate device performance predictions. This work introduces a promising configuration that achieves higher power densities, paving the way for the next generation of efficient energy-harvesting devices. The findings offer valuable insights into the development of state-of-the-art blue energy harvesting nanofluidic devices, advancing sustainable energy production.

Ionic Hyperbranched Poly(amido-amine)-Incorporated Nanofiltration Membranes for High-Efficiency Dye Desalination.

High-efficiency dye desalination is crucial in the textile industry, considering its importance for human health, safe aquatic ecological systems, and resource recovery. In order to solve the problem of effective separation of univalent salt and ionic dye under the condition of high salt, ionic hyperbranched poly(amido-amine) (HBPs) were synthesized based on a simple and scalable one-step polycondensation method and then incorporated into the polyamide (PA) selective layers to construct charged nanochannels through interfacial polymerization (IP) on the surface of a polyvinyl chloride ultrafiltration (PVC-UF) hollow fiber membrane. Both the internal nanopores of HBPs (internal nanochannels) and the interfacial voids between HBPs and the PA matrix (external nanochannels) can be regarded as a fast water molecule transport pathway, while the terminal ionic groups of ionic HBPs endow the nanochannels with charge characteristics for improving ionic dye/salt selectivities. The permeate fluxes and dye/salt selectivities of HBP-TAC/PIP (57.3 L m-2 h-1 and rhodamine B (RB)/NaCl selectivity of 224.0) and HBP-PS/PIP (63.7 L m-2 h-1 and lemon yellow (LY)/NaCl selectivity of 664.0) membranes under 0.4 MPa operation pressure are much higher than PIP-only and HBP-NH2/PIP membranes. At the same time, this project also studied the membrane desalination process in a simulated high-salinity dye/salt mixture system to provide a theoretical basis and technical support for the actual dye desalination process.

Conformal Electrodeposition of Mesoporous Silica over High Aspect Ratio (AR>100) Nanomesh Electrodes

The high surface area provided by the nanopores of ordered mesoporous silica thin films enables a wide range of electrochemical applications such as sensors, catalysis, energy storage and ion-selective membranes. Further improvements are possible by coating such thin films on large surface area electrodes with high aspect ratios (> 100) to increase the active surface area. Atomic layer deposition (ALD) is often preferred to deposit conformal thin film oxides on high aspect ratio structures. Such vapor-phase depositions are limited by the available surface reactive sites to deposit thin films of thickness ranging from sub-nanometer to few tens of nanometer. However, there is a tradeoff in terms of deposition time/cycles to achieve quality films especially when high aspect ratios (>100) substrates are introduced. Electrochemistry offers an alternative, versatile method to conformally coat layers on 3D electrode surfaces. The electrochemically assisted self-assembly (EASA) of mesoporous silica, utilizes electrochemical reactions to locally increase the pH near the electrode surface, which in turn catalyzes the silica gelation and surfactant self-assembly, thus causing the controlled growth of mesoporous silica thin films [1]. Recently, our group has shown that good quality mesoporous silica films with thickness between 20-2000 nm could be achieved by controlling the hydrodynamic layer in a rotating disc electrode setup [2]. Moreover, EASA of mesoporous silica offers meso-channels that are aligned perpendicular to the underlaying conductive substrate which is optimal for mass-transport.In this follow-up work, we demonstrate a reliable, electrochemically controlled, conformal deposition of mesoporous silica onto large surface area nanomesh electrodes with an aspect ratio close to 100. Nanomesh electrodes developed in our group at imec, is built up of a regularly spaced (50 nm), inter-connected network of vertical and horizontal nanowires of diameter ~40 nm. These electrodes offer an 80x area enhancement (80 cm2 per geometric cm2) while maintaining a porosity close to 75%. We show that, the extent of silica deposition over these nanomesh electrodes can be electrochemically controlled from conformal coatings (~10 nm thick) uniformly coating the whole nanomesh architecture to complete fill and overfill of the nanomesh electrodes (~4 µm thick). Furthermore, excellent mass-transport properties of various silica coated nanomesh electrodes has been demonstrated using a ruthenium hexaammine redox probe. Finally, the area enhancement offered by the silica coated Ni nanomesh is demonstrated using the characteristic accumulation of a positively charged [Ru(NH3)6]3+ probe within the negatively charged silica nanochannels, which shows 55x increase for the amount of charge from the probe stored in the coated nanomesh, compared to a planar silica layer, consistent with the expected surface area enhancement of the 4 µm thick nanomesh electrodes.

Ion Transport in Intelligent Nanochannels: A Comparative Analysis of the Role of Electric Field.

This research delves into investigating ion transport behavior within nanochannels, enhanced through modification with a negatively charged polyelectrolyte layer (PEL), aimed at achieving superior control. The study examines two types of electric fields─direct current and alternating current with square, sinusoidal, triangular, and sawtooth waveforms─to understand their impact on ion transport. Furthermore, the study compares symmetric (cylindrical) and asymmetric (conical) nanochannel geometries to assess the influence of overlapping electrical double layers (EDLs) in generating specific electrokinetic behaviors such as ionic current rectification (ICR) and ion selectivity. The research employs the finite element method to solve the coupled Poisson-Nernst-Planck and Navier-Stokes equations under unsteady-state conditions. By considering factors such as electrolyte concentration, soft layer charge density, and electric field type, the study evaluates ion transport performance in charged nanochannels, investigating effects on concentration polarization, electroosmotic flow (EOF), ion current, rectification, and ion selectivity. Notably, the study accounts for ion partitioning between the PEL and electrolyte to simulate real conditions. Findings reveal that conical nanochannels, due to improved EDL overlap, significantly enhance ion transport and related characteristics compared to cylindrical ones. For instance, under ηε = ηD = 0.8, ημ = 2, C0 = 20 mM, and NPEL/NA = 80 mol m-3 conditions, the average EOF for conical and cylindrical geometries is 0.1 and 0.008 m/s, respectively. Additionally, the study explores ion selectivity and rectification based on the electric field type, unveiling the potential of nanochannels as ion gates or diodes. In cylindrical nanochannels, the ICR remains at unity, with lower ion selectivity across waveforms compared to conical channels. Furthermore, rectification and ion selectivity trends are identified as Rf,square > Rf,DC > Rf,triangular > Rf,sinusoidal > Rf,sawtooth and Ssawtooth > Ssinusoidal > Striangular > SDC > Ssquare for conical nanochannels. Our study of ion transport control in nanochannels, guided by tailored electric fields and unique geometries, offers versatile applications in the field of Analytical Chemistry. This includes enhanced sample separation, controlled drug delivery, optimized pharmaceutical analysis, and the development of advanced biosensing technologies for precise chemical analysis and detection. These applications highlight the diverse analytical contributions of our methodology, providing innovative solutions to challenges in chemical analysis and biosensing.

Electrochemiluminescence Aptasensor with Dual Signal Amplification by Silica Nanochannel-Based Confinement Effect on Nanocatalyst and Efficient Emitter Enrichment for Highly Sensitive Detection of C-Reactive Protein.

The rapid and sensitive detection of the important biomarker C-reactive protein (CRP) is of great significance for monitoring inflammation and tissue damage. In this work, an electrochemiluminescence (ECL) aptasensor was fabricated based on dual signal amplification for the sensitive detection of CRP in serum samples. The sensor was constructed by modifying a silica nanochannel array film (SNF) on a cost-effective indium tin oxide (ITO) electrode using the Stöber solution growth method. Gold nanoparticles (AuNPs) were grown in situ within the nanochannels using a simple electrodeposition method as a nanocatalyst to enhance the active electrode area as well as the ECL signal. The negatively charged nanochannels also significantly enriched the positively charged ECL emitters, further amplifying the signal. The recognition aptamer was covalently immobilized on the outer surface of SNF after modification with epoxy groups, constructing the aptasensor. In the presence of CRP, the formation of complexes on the recognitive interface led to a decrease in the diffusion of ECL emitters and co-reactants to the supporting electrode, resulting in a reduction in the ECL signal. Based on this mechanism, ECL detection of CRP was achieved with a linear range of 10 pg/mL to 1 μg/mL and a low limit of detection (7.4 pg/mL). The ECL aptasensor developed in this study offers advantages such as simple fabrication and high sensitivity, making promising applications in biomarker detection.

Viscoelectric effect on the chemiosmotic flow in charged soft nanochannels

The charged nanochannel surface and pH-sensitive grafted polyelectrolyte layer (PEL) play a critical role in the design of devices aimed at controlling nanofludic flow. They enable the manipulation of ionic transport by influencing the electric-double (EDL) layers that overlap. Additionally, the viscoelectric effect, amplified by a strong EDL electric field, may enhance the activation energy and viscosity of liquids. Motivated by this, we conducted a numerical investigation using a finite element method-based solver, COMSOL, to examine the effects of the viscoelectric effect on concentration-gradient-driven chemiosmotic flow in a charged soft nanochannel with grafted pH-sensitive polyelectrolyte layer on the inner wall surfaces. It is important to note that the nanochannel is positioned between two reservoirs with different pH values and bulk-ionic concentrations. The PEL is sensitive to protonic association–dissociation due to the presence of carboxylic and amine groups in monomeric units. In our study, we comprehensively demonstrate variations in key variables characterizing the underlying flow. These variations include changing the solute concentration in the left side reservoir within the range of 0.1–5 mol m−3, adjusting the pH of the right-side reservoir (pHR) within the range of 3–10, and varying the viscoelectric coefficient. The viscoelectric effect significantly raises viscosity near the wall due to the stronger EDL electric field generated at the left-side reservoir resulting from the higher solute concentration. On the other hand, viscosity tends to decrease with lower pHR values and remains unaffected by changes at higher pHR values. The average flow velocity shows an increasing–decreasing pattern as the concentration of the right-side reservoir is enhanced. Additionally, the decrease in flow velocity becomes noticeably more pronounced with higher solute concentrations in the right-side reservoir when accounting for the viscoelectric effect. The findings of the present study have practical implications for novel nanofluidic devices, frequently employed in various engineering applications to control flow.

Layer-by-Layer Nanofluidic Membranes for Promoting Blue Energy Conversion.

Access to and use of energy resources are now crucial components of modern human existence thanks to the exponential growth of technology. Traditional energy sources provide significant challenges, such as pollution, scarcity, and excessive prices. As a result, there is more need than ever before to replace depleting resources with brand-new, reliable, and environmentally friendly ones. With the aid of reverse electrodialysis, the salinity gradient between rivers and seawater as a clean supply with easy and infinite availability is a viable choice for energy generation. The development of nanofluidic-based reverse electrodialysis (NRED) as a novel high-efficiency technology is attributable to the progress of nanoscience. However, understanding the predominant mechanisms of this process at the nanoscale is necessary to develop and disseminate this technology. One viable option to gain insight into these systems while saving expenses is to employ simulation tools. In this study, we looked at how a layer-by-layer (LBL) soft layer influences ion transport and energy production in charged nanochannels. We solved the steady-state Poisson-Nernst-Planck (PNP) and Navier-Stokes (NS) equations for three different types of nanochannels with a trumpet geometry, where the narrow part is covered with a built-up LbL soft layer and the rest is a hard wall with a surface charge density of σ = -10, 0, or +10 mC/m2. The findings show that in type (I) nanochannels, at NPEL/NA = 100 mol/m3 and pH = 7, the maximum power output rises 675-fold as the concentration ratio rises from 10 to 1000. The results of this study can aid in a better understanding of energy harvesting processes using nanofluidic-based reverse electrodialysis in order to identify optimal conditions for the design of an intelligent route with great controllability and minimal pollution.