Ionic Rectification Research Articles

On the Origin of Ionic Rectification in DNA-Stuffed Nanopores: The Breaking and Retrieving Symmetry.

The discovery of ionic current rectification (ICR) phenomena in synthetic nanofluidic systems elicits broad interest from interdisciplinary fields of chemistry, physics, materials science, and nanotechnology; and thus, boosts their applications in, for example, chemical sensing, fluidic pumping, and energy related aspects. So far, it is generally accepted that the ICR effect stems from the broken symmetry either in the nanofluidic structures, or in the environmental conditions. Although this empirical regularity is supported by numerous experimental and theoretical results, great challenge still remains to precisely figure out the correlation between the asymmetric ion transport properties and the degree of symmetry breaking. An appropriate and quantified measure is therefore highly demanded. Herein, taking DNA-stuffed nanopores as a model system, we systematically investigate the evolution of dynamic ICR in between two symmetric states. The fully stuffed and fully opened nanopores are symmetric; therefore, they exhibit linear ion transport behaviors. Once the stuffed DNA superstructures are asymmetrically removed from one end of the nanopore via aptamer-target interaction, the nanofluidic system becomes asymmetric and starts to rectify ionic current. The peak of ICR is found right before the breakthrough of the stuffed DNA forest. After that, the nanofluidic system gradually retrieves symmetry, and becomes non-rectified. Theoretical results by both the coarse-grained Poisson-Nernst-Planck model and the 1D statistic model excellently support the experimental observations, and further establish a quantified correlation between the ICR effect and the degree of asymmetry for different molecular filling configurations. Based on the ICR properties, we develop a proof-of-concept demonstration for sensing ATP, termed the ATP balance. These findings help to clarify the origin of ICR, and show implications to other asymmetric transport phenomena for future innovative nanofluidic devices and materials.

3D Porous Hydrogel/Conducting Polymer Heterogeneous Membranes with Electro-/pH-Modulated Ionic Rectification.

Heterogeneous membranes composed of asymmetric structures or compositions have enormous potential in sensors, molecular sieves, and energy devices due to their unique ion transport properties such as ionic current rectification and ion selectivity. So far, heterogeneous membranes with 1D nanopores have been extensively studied. However, asymmetric structures with 3D micro-/nanoscale pore networks have never been investigated. Here, a simple and versatile approach to low-costly fabricate hydrogel/conducting polymer asymmetric heterogeneous membranes with electro-/pH-responsive 3D micro-/nanoscale ion channels is introduced. Due to the asymmetric heterojunctions between positively charged nanoporous polypyrrole (PPy) and negatively charged microscale porous hydrogel poly (acrylamide-co-acrylic acid) (P(AAm-co-AA)), the membrane can rectify ion transmembrane transport in response to both electro- and pH-stimuli. Numerical simulations based on coupled Poisson and Nernst-Plank equations are carried out to explain the ionic rectification mechanisms for the membranes. The membranes are not dependent on elaborately fabricated 1D ion channel substrates and hence can be facilely prepared in a low-cost and large-area way. The hybridization of hydrogel and conducting polymer offers a novel strategy for constructing low-cost, large-area and multifunctional membranes, expanding the tunable ionic rectification properties into macroscopic membranes with micro-/nanoscale pores, which would stimulate practical applications of the membranes.

Viscosity and Conductivity Tunable Diode-like Behavior for Meso- and Micropores.

Rectifying pores, which transport ions mainly in one direction blocking the ionic flow in the other, were shown to be important in the preparation of chemical sensors, components of ionic circuits, and mimics of biological channels. Ionic rectification has been shown with various engineered systems, but pores with similar opening diameters often rectify to a various uncontrolled extent. In this Letter we present a system of single meso-pores, whose current-voltage curves and rectification can be tuned with great precision via viscosity and conductivity gradients of solutions placed on both sides of the membrane. The mechanism of rectification is based on electroosmotically induced flow, which fills the entire volume of the pore with a single solution from either side of the membrane. The highly predictable rectifying system can find various applications, including measuring viscosity of unknown media and tuning electrokinetic passage of particles.

Redox switch of ionic transport in conductive polypyrrole-engineered unipolar nanofluidic diodes

Controlling ion transport in nanoconfined spaces is a key task for the creation of smart nanofluidic devices. In this work, redox-active polypyrrole (PPy) polymers are introduced into anodic aluminum oxide (AAO) nanochannels to form smart unipolar nanofluidic diodes (UNDs) for the first time. The ionic transport behavior of the present polypyrrole-engineered UNDs can be controlled through the redox reactions of PPy. Under an applied oxidation potential, conductive PPy exhibits several redox states carrying different charges, following the formation of polarons and bipolarons with different oxidation states. Combined with the asymmetric distribution of PPy in the AAO nanochannels, the UNDs investigated here exhibit redox-switchable ion rectification and ion-gating properties. The influence of the charge asymmetry of the UNDs on their ionic transport behavior is assessed by precisely controlling the length of oxidized PPy segments in the AAO nanochannels and by carrying out theoretical simulations based on the Poisson and Nernst–Planck (PNP) equations.

Large Rectification Effect of Single Graphene Nanopore Supported by PET Membrane.

Graphene is an ideal candidate for the development of solid state nanopores due to its thickness at the atomic scale and its high chemical and mechanical stabilities. A facile method was adopted to prepare single graphene nanopore supported by PET membrane (G/PET nanopore) within the three steps assisted by the swift heavy ion irradiation and asymmetric etching technology. The inversion of the ion rectification effect was confirmed in G/PET nanopore while comparing with bare PET nanopore in KCl electrolyte solution. By modifying the wall charge state of PET conical nanopore with hydrochloric acid from negative to positive, the ion rectification effect of G/PET nanopore was found to be greatly enhanced and the large rectification ratio up to 190 was obtained during this work. Moreover, the high ionic flux and high ion separation efficiency was also observed in the G/PET nanopore system. By comparing the "on" and "off" state conductance of G/PET nanopore while immersed in the solution with pH value lower than the isoelectric point of the etched PET (IEP, pH = 3.8), the voltage dependence of the off conductance was established and it was confirmed that the large rectification effect was strongly dependent on the particularly low off conductance at higher applied voltage.

Manipulating electrokinetic conductance of nanofluidic channel by varying inlet pH of solution

The electrokinetic conductivity of micro-/nanofluidic systems, which strongly depends on the local solution properties (e.g., pH and ionic strength), has wide applications in nanosystems to control the system performance and ion rectification. Accurate and active manipulation of this parameter is proven to be very challenging since, in nanoscale, the ion transport is particularly dominated by the acquired surface charge on the solid–liquid interfaces. In this study, we propose an approach to manipulate the nanochannel electrokinetic conductivity by changing the pH value of the solution at the inlet in order to impose asymmetrical conditions inside nanochannel. The variable surface charge of walls is determined by considering the chemical adsorption on the solid–liquid interface and the electrical double layer interaction. The presented numerical model, which couples Poisson–Nernst–Planck and Navier–Stokes equations, can fully consider the electro-chemo-mechanical transport phenomena and predict the electrokinetic conductivity of nanofluidic channels with good accuracy. Modeling results show that the electrokinetic conductivity of the nanofluidic systems can be regulated by varying the solution pH at the inlet. It is revealed that the stronger electric double layers interaction can enhance the sensitivity of the nanochannel electrokinetic conductance to the inlet pH. This unique behavior of the nanochannel electrokinetic conductivity could broaden potential applications in biomedical, energy, and environmental systems using nanofluidic devices.

Nanoporous Hybrid Electrolytes for High‐Energy Batteries Based on Reactive Metal Anodes

Successful strategies for stabilizing electrodeposition of reactive metals, including lithium, sodium, and aluminum are a requirement for safe, high‐energy electrochemical storage technologies that utilize these metals as anodes. Unstable deposition produces high‐surface area dendritic structures at the anode/electrolyte interface, which causes premature cell failure by complex physical and chemical processes that have presented formidable barriers to progress. Here, it is reported that hybrid electrolytes created by infusing conventional liquid electrolytes into nanoporous membranes provide exceptional ability to stabilize Li. Electrochemical cells based on γ‐Al2O3 ceramics with pore diameters below a cut‐off value above 200 nm exhibit long‐term stability even at a current density of 3 mA cm−2. The effect is not limited to ceramics; similar large enhancements in stability are observed for polypropylene membranes with less monodisperse pores below 450 nm. These findings are critically assessed using theories for ion rectification and electrodeposition reactions in porous solids and show that the source of stable electrodeposition in nanoporous electrolytes is fundamental.

Correlated Rectification Transport in Ultranarrow Charged Nanocones.

Using molecular dynamics simulations, we reveal ion rectification in charged nanocones with exit diameters of 1-2 nm. The simulations exhibit an opposite rectification current direction than experiments performed in conical channels with exit diameters larger than 5 nm. This can be understood by the fact that in ultranarrow charged cones screening ions are trapped close to the cone tip at both field directions, which necessitates them to be released from the cone in a correlated multi-ion fashion. Electroosmosis induced by a unidirectional ion flow is also observed.

Photo-switchable two-dimensional nanofluidic ionic diodes.

The bottom-up assembly of ion-channel-mimetic nanofluidic devices and materials with two-dimensional (2D) nano-building blocks paves a straightforward way towards the real-world applications of the novel transport phenomena on a nano- or sub-nanoscale. One immediate challenge is to provide the 2D nanofluidic systems with adaptive responsibilities and asymmetric ion transport characteristics. Herein, we introduce a facile and general strategy to provide a graphene-oxide-based 2D nanofluidic system with photo-switchable ionic current rectification (ICR). The degree of ICR can be prominently enhanced upon UV irradiation and it can be perfectly retrieved under irradiation with visible light. A maximum ICR ratio of about 48 was achieved. The smart and functional nanofluidic devices have applications in energy conversion, chemical sensing, water treatment, etc.

Asymmetric Multifunctional Heterogeneous Membranes for pH- and Temperature-Cooperative Smart Ion Transport Modulation.

Asymmetric multifunctional heterogeneous membranes are demonstrated by combing a block copolymer polystyrene-block-poly(N,N-dimethylaminoethylmethacrylate) membrane with a track-etched porous poly(ethylene terephthalate) membrane. This hybrid membrane is capable of integrating pH- and temperature-cooperative high-performance ionic rectification, highly efficient cation gating, and excellent stability and controllability, which allows broad application in biosensing, energy conversion, and filtration.

A redox-sensitive nanofluidic diode based on nicotinamide-modified asymmetric nanopores

We demonstrate a redox-sensitive nanofluidic diode whose ion rectification is modulated by the oxidation and reduction of chemical moieties incorporated on its surface. To achieve this goal, we have first synthesized the chemical compounds 1-(4-aminobutyl)-3-carbamoylpyridin-1-ium (Nic-BuNH2) and 3-carbamoyl-1-(2,4-dinitrophenyl)pyridinium (Nic-DNP). Then, the surface of track-etched single asymmetric nanopores is decorated with the redox-sensitive Nic-BuNH2 and Nic-DNP molecules using carbodiimide coupling chemistry and Zincke reaction, respectively. The success of the modification reactions is monitored through the changes in the current–voltage (I–V) curves prior to and after pore functionalization. Upon exposing the modified pore to solutions of hydrogen peroxide (oxidizing agent) and sodium dithionite (reducing agent) the surface charge is reversibly modulated from positive to neutral, leading to measurable changes in the electronic readout of ion current passing through the nanopore. On oxidation, the quaternary nicotinamide units impart positive charge to the pore surface, resulting in the ion current rectification (anion-selective pore). On the contrary, the complementary reduced dihydronicotinamide moieties resulted in the loss of surface charge and ohmic behaviour (non-selective pore). The experimental results are further theoretically described by using Poisson-Nernst-Planck equations.

Biomimetic Solid-State Nanochannels: From Fundamental Research to Practical Applications.

In recent years, solid-state smart nanopores/nanochannels for intelligent control of the transportation of ions and molecules as organisms have been extensively studied, because they hold great potential applications in molecular sieves, nanofluidics, energy conversion, and biosensors. To keep up with the fast development of this field, it is necessary to summarize the construction, characterization, and application of biomimetic smart nanopores/nanochannels. These can be classified into four sections: the fabrication of solid-state nanopores/nanochannels, the functionalization methods and materials, the mechanism explanation about the ion rectification, and the practical applications. A brief conclusion and outlook for the biomimetic nanochannels is provided, highlighting those that could be developed and integrated into devices for use in tackling current and the future problems including resources, energy, environment, and health.

Biomimetic heterogeneous multiple ion channels: a honeycomb structure composite film generated by breath figures.

We design a novel type of artificial multiple nanochannel system with remarkable ion rectification behavior via a facile breath figure (BF) method. Notably, even though the charge polarity in the channel wall reverses under different pH values, this nanofluidic device displays the same ionic rectification direction. Compared with traditional nanochannels, this composite multiple ion channel device can be more easily obtained and has directional ionic rectification advantages, which can be applied in many fields.

Fluoride-induced modulation of ionic transport in asymmetric nanopores functionalized with "caged" fluorescein moieties.

We demonstrate experimentally and theoretically a nanofluidic fluoride sensing device based on a single conical pore functionalized with "caged" fluorescein moieties. The nanopore functionalization is based on an amine-terminated fluorescein whose phenolic hydroxyl groups are protected with tert-butyldiphenylsilyl (TBDPS) moieties. The protected fluorescein (Fcn-TBDPS-NH2) molecules are then immobilized on the nanopore surface via carbodiimide coupling chemistry. Exposure to fluoride ions removes the uncharged TBDPS moieties due to the fluoride-promoted cleavage of the silicon-oxygen bond, leading to the generation of negatively charged groups on the fluorescein moieties immobilized onto the pore surface. The asymmetrical distribution of these groups along the conical nanopore leads to the electrical rectification observed in the current-voltage (I-V) curve. On the contrary, other halides and anions are not able to induce any significant ionic rectification in the asymmetric pore. In each case, the success of the chemical functionalization and deprotection reactions is monitored through the changes observed in the I-V curves before and after the specified reaction step. The theoretical results based on the Nernst-Planck and Poisson equations further demonstrate the validity of an experimental approach to fluoride-induced modulation of nanopore current rectification behaviour.

PH and Calcium Cooperative Regulation Nanofluidic Gating Device

In living body, Ca 2 + -responsive ion channels play crucial roles in many biological activities. Inspired by nature, the design and fabrication of artificial smart nanochannels system become a very significant research subject, mimicking the biological Ca 2 + -responsive signals in ion channels. In this article, by using track-etched artificial polyethylene terephthalate (PET) multiporous membrane materials and modifying intelligent molecules O-Phospho-L-tyrosine (OPLT) through chemical modification method, we demonstrate a new biomimetic artificial smart responsive ion channel system, which presents the cooperative response to pH and calcium. The nanosystem shows ion selective transport, ion gating and ion rectification prop- erty, which is similar to the property of biological Ca 2 + -responsive ion channels. And the cooperative responsive property of pH and calcium in OPLT modified nanochannels was also investigated by measuring the current-voltage (I-V) curves. At a low pH value, the surface charge of the nanochannels walls is positive as a result of the amino group ( 3 NH +

PH- and light-regulated ion transport in hourglass shaped Al2O3 nanochannels patterned with N719 and APTES

An investigation of the pH- and light-regulated ion rectification properties of symmetric and asymmetric Al2O3 nanochannels patterned with N719 and APTES at designated positions.

Ionic Current Rectification in a pH-Tunable Polyelectrolyte Brushes Functionalized Conical Nanopore: Effect of Salt Gradient.

The behavior of ionic current rectification (ICR) in a conical nanopore with its surface modified by pH-tunable polyelectrolyte (PE) brushes connecting two large reservoirs subject to an applied electric field and a salt gradient is investigated. Parameters including the solution pH, types of ionic species, strength of applied salt gradient, and applied potential bias are examined for their influences on the ionic current and rectification factor, and the mechanisms involved are investigated comprehensively. The ICR behavior depends highly on the charged conditions of the PE layer, the level of pH, the geometry of nanopore, and the thickness of the double layer. In particular, the distribution of ionic species and the local electric field near the nanopore openings play a key role, yielding profound and interesting results that are informative to device design as well as experimental data interpretation.

Nanofluidic Diodes with Dynamic Rectification Properties Stemming from Reversible Electrochemical Conversions in Conducting Polymers.

The use of solid state nanochannels as nanofluidic diodes is currently a topic of large interest in nanotechnology. Particularly, there is a focus in the development of nanochannels with surface functionalities that make them responsive to multiple environmental variables. Here, we present for the first time the construction of electrochemical potential- and pH-responsive nanofluidic diodes using a novel approach based on a controlled electrochemical polymerization of aniline on gold-coated polycarbonate asymmetric nanochannels. The polyaniline-modified nanochannels showed three different levels of reversible ionic rectification corresponding to the degrees of oxidation of the conducting polymer. Our results demonstrate that this strategy enables an accurate and reversible control of the rectification properties due to the well-defined and predictable electrochemical conversion of charged species generated on the pore walls. We envision that these results will create novel avenues to fabricate electrochemically modulated nanofluidic diodes using conducting polymers integrated into single conical nanopores.

Polymers of intrinsic microporosity in electrochemistry: Anion uptake and transport effects in thin film electrodes and in free-standing ionic diode membranes

Anion uptake and charge transport in a polymer of intrinsic microporosity (here PIM-EA-TB) is investigated for three cases: (i) the oxidation of ferrocene embedded into a thin film of PIM-EA-TB on a glassy carbon electrode, (ii) the reduction of protons absorbed into a thin film of PIM-EA-TB on a platinum electrode, and (iii) the potential-driven transport of anions and protons in an asymmetrically deposited free-standing PIM-EA-TB membrane working as a current rectifier or “ionic diode”. In all three cases the competing effects of the diameter and hydrophobicity (size and hydration energy) of the anion are important. For free-standing membranes very high ionic diode rectification ratios (>103 at ±1V) are observed in particular for thicker deposits of PIM-EA-TB and for chloride or perchlorate containing electrolyte.

Engineered Asymmetric Heterogeneous Membrane: A Concentration-Gradient-Driven Energy Harvesting Device.

Engineered asymmetric membranes for intelligent molecular and ionic transport control at the nanoscale have gained significant attention and offer prospects for broad application in nanofluidics, energy conversion, and biosensors. Therefore, it is desirable to construct a high-performance heterogeneous membrane capable of coordinating highly selective and rectified ionic transport with a simple, versatile, engineered method to mimic the delicate functionality of biological channels. Here, we demonstrate an engineered asymmetric heterogeneous membrane by combining a porous block copolymer (BCP) membrane, polystyrene-b-poly(4-vinylpyridine) (PS48400-b-P4VP21300), with a track-etched asymmetric porous polyethylene terephthalate membrane. The introduction of chemical, geometrical, and electrostatic heterostructures provides our heterogeneous membrane with excellent anion selectivity and ultrahigh ionic rectification with a ratio of ca. 1075, which is considerably higher than that of existing ionic rectifying systems. This anion-selective heterogeneous membrane was further developed into an energy conversion device to harvest the energy stored in an electrochemical concentration gradient. The concentration polarization phenomenon that commonly exists in traditional reverse electrodialysis can be eliminated with an asymmetric bipolar structure, which considerably increases the output power density. This work presents an important paradigm for the use of versatile BCPs in nanofluidic systems and opens new and promising routes to various breakthroughs in the fields of chemistry, materials science, bioscience, and nanotechnology.