Processes associated with ionic current rectification at a 2D-titanate nanosheet deposit on a microhole poly(ethylene terephthalate) substrate
- 374 Downloads
Films of titanate nanosheets (approx. 1.8-nm layer thickness and 200-nm size) having a lamellar structure can form electrolyte-filled semi-permeable channels containing tetrabutylammonium cations. By evaporation of a colloidal solution, persistent deposits are readily formed with approx. 10-μm thickness on a 6-μm-thick poly(ethylene-terephthalate) (PET) substrate with a 20-μm diameter microhole. When immersed in aqueous solution, the titanate nanosheets exhibit a p.z.c. of − 37 mV, consistent with the formation of a cation conducting (semi-permeable) deposit. With a sufficiently low ionic strength in the aqueous electrolyte, ionic current rectification is observed (cationic diode behaviour). Currents can be dissected into (i) electrolyte cation transport, (ii) electrolyte anion transport and (iii) water heterolysis causing additional proton transport. For all types of electrolyte cations, a water heterolysis mechanism is observed. For Ca2+ and Mg2+ions, water heterolysis causes ion current blocking, presumably due to localised hydroxide-induced precipitation processes. Aqueous NBu4+ is shown to ‘invert’ the diode effect (from cationic to anionic diode). Potential for applications in desalination and/or ion sensing are discussed.
KeywordsVoltammetry Ion valve Ionic logic Sensing Nanostructure Iontronics
Ion binding and transport through microporous and mesoporous materials is of considerable importance in water purification and in membrane science [1, 2]. Recent interest has arisen in particular in the porosity of new types of lamellar nano-structures (in particular graphene oxide [3, 4]), which are linked to ion transport  and water transport  phenomena, and the desire to exploit new types of lamellar 2D-materials more widely . There are now ranges of novel materials available based, for example on 2D-nanosheets of modified carbons , phosphorous , oxides , chalcogenides  and mixed oxides such as BiVO4  and MXenes . 2D-titanates have been of considerable interest and lamellar titanate deposits have been shown to be electrochemically and photo-electrochemically active depending on the pH and intercalated guest species . In this report, we focus on titanate nanosheet materials that have been developed in pioneering work by Sasaki and coworkers [15, 16].
Titanate nanosheet materials are produced in two steps ; TiO2 reacts with caesium salts to give an intermediate solid lepidocrocite-type product, which is exfoliated into aqueous solution containing alkylammonium cations (here tetrabutylammonium, ) to give a stable colloidal solution of negatively charged titanate nanosheets. The surface charge of the colloid is associated with a point of zero charge (p.z.c.) at approximately pH 4 . The colloidal solutions contain single unit cell thick titanate layers, which are typically 200 nm in diameter . The deposits of this colloid when dried up (without heating) give a lamellar gel with typically 1.7 to 1.8 nm unit cell spacing (based on the X-ray diffraction pattern, ). This is consistent with an approximately 1.2- to 1.3-nm-thick titanate unit cell layer sandwiched between electrolyte layers of typically 0.5 nm. At elevated temperature, these types of gels can collapse back to the anatase crystal form but, at room temperature, these lamellar nano-structures persist.
Applications of titanate nanosheets have been proposed as component in batteries , in heterogeneous catalysis , in photocatalysis  and as functional filler in polymer blends . Recently, we have demonstrated that a film deposit of titanate nanosheet material on a glassy carbon electrode allows ferroceneboronic acid to be immobilised and binding of fructose within the nano-lamellar space to be detected . Further study has shown that the titanate deposits behave more similar to organic media (and not to hydrophilic oxides) with the ability to bind hydrophobic organic molecules (e.g. anthraquinone) from cyclopentanone and to allow redox conversion of these immobilised inter-lamellar redox systems . The ability to host hydrophobic guests has been attributed to the presence of tetrabutylammonium cations within the electrolyte layer.
In order to investigate ion transport through the lamellar titanate nanosheets, deposits of the titanate are studied here on a poly(ethylene-terephthalate) substrate (PET with 6-μm thickness) with a microhole (20-μm diameter). The experimental arrangement is very similar to that introduced by Girault et al.  for the study of liquid|liquid micro-interfaces. Recently, other types of ionomer systems (such as re-constituted cellulose , Nafion™ , the commercial ionomer Fumasep™ , graphene oxide  and a polymer of intrinsic microporosity ) have been investigated on this type of microhole substrate in order to reveal the mechanisms/characteristics for ionic current rectification (or ‘ionic diode’ phenomena). The ionic diode or ionic current rectification effect requires a semi-permeable material. This type of effect allows cation transport (cationic diodes for cation conductors) and anion transport (anionic diodes for anion conductors) to be distinguished. New ideas for ionic current rectifier applications have been proposed, for example for water purification  or for ionic diode sensing .
Ionic diode phenomena are associated with processes that occur at different length scales due to potential dependent compositional changes. There are different types of mechanisms, for example based on double-layer changes within nanopores, based on diffusion-migration layer compositional changes and due to interfacial precipitation or blocking. The diffusion-migration layer–based processes in microhole diodes (as described in Fig. 1) can be contrasted with processes reported in work on nanochannel diodes , nano-cones  and on electrolytic microfluidic/nanofluidic channel diodes [39, 40]. Other types of ionic diodes have been proposed based on gel-gel interfaces . Ionic circuits have been proposed based on polymer gels [42, 43]. Ionic diode switching effects have been demonstrated also due to interfacial precipitation  and due to pH gradients . The term ‘iontronics’ has been coined by Chun and Chung  to emphasise the excitement associated with developments functionality, such as that in ionic amplifiers , transistors  or flip-flops . More fundamentally, ionic rectifiers under AC-excitation can be considered as ‘ion pumps’. A device based on coupling cationic diodes and anionic diodes has been proposed for desalination applications . Selectivity in ionic diode behaviour is desirable in order to broaden the possible range of applications. In particular, selectivity for higher valent cations such as Mg2+ and Ca2+ could be very useful for water treatment applications.
In this report, ion transport in the inter-lamellar space of titanate nanosheets is investigated. The semi-permeable nature of titanate nanosheet deposits (immersed in electrolyte with not too high ionic strength) allows cation transport and therefore causes cationic diode effects. This is studied here for a wider range of electrolytes and conditions. Inversion to anionic diode behaviour is observed in the presence of tetrabutylammonium cations.
Titanate nanosheet material was synthesised as described previously by Sasaki et al.  and by Harito et al. [49, 50]. Hydrochloric acid, sodium chloride, potassium chloride, lithium chloride, ammonium chloride, tetrabutylammonium chloride, magnesium chloride, calcium chloride, sodium hydroxide, sodium nitrate, sodium perchlorate and sodium sulphate were obtained in analytical grade from Sigma-Aldrich or Fischer Scientific and used without further purification. Phosphate buffer saline (PBS) was prepared with NaH2PO4, Na2HPO4 and NaCl and adjusted to pH 7. Solutions were prepared under ambient condition in volumetric flasks with ultrapure water with resistivity of 18.2 MΩ cm (at 22 °C) from an ELGA Purelab Classic System.
The zeta potential for the colloidal titanate solution was measured on a Zetasizer Nano ZS (Malvern Instruments Ltd., Malvern, UK) confirmed an average of − 32.5 mV and an average size of 216 nm . In order to form films of titanate nanosheets on PET substrates (20-μm diameter hole in 6-μm-thick PET from Laser Micromaching Ltd., Birmingham, UK), 10 μL aqueous titanate nanosheet colloidal solution (2.56 g L−1) was applied to a PET film on a glass substrate (the glass was pre-coated with a thin layer of 1% agarose gel by solution casting to stop titanate nanosheet material penetrating through the PET microhole). A volume of 10 μL titanate nanosheet colloidal solution was applied to the surface over PET to give a 1-cm2 film coating, which after drying produced a thin uniform coating. For the formation of symmetric deposits on both sides of the PET film, the deposition was repeated on the back side of the PET. In order to image the TiO2 films, stacked fluorescence images were obtained for a symmetric (double-sided) and for the asymmetric (one-sided) deposits.
Titanate nanosheet film characterisation
Results and discussion
Ion transport through lamellar titanate nanosheet deposits: Na+ transport
Figure 4 b shows cyclic voltammetry data for asymmetrically deposited titanate nanosheets. Rectified currents flow with positive applied potentials and therefore cation conduction must be possible through the titanate deposit. With the increasing concentration of NaCl from 1 to 1000 mM, a well-defined steady-state voltammetric response is observed. For experiments at lower NaCl concentration, the current in the negative potential range is lower compared to the current in the positive potential range. This is consistent with cationic diode behaviour as seen in cases such as Nafion™  and Fumasep™ FKS-30 ionomer . The effect of NaCl electrolyte concentration on the currents and on the switching time for the cationic diode is shown more clearly in chronoamperometry data in Fig. 4 c. From these data, the rectification ratio can be calculated (obtained by dividing the absolute currents at + 1 V and at − 1 V; see inset in Fig. 4 b). An increase in NaCl concentration causes an increase in both the current in the open state and the current in the closed state. An optimum in rectification effect is observed in the range from 50 to 100 mM NaCl solution. The decrease in rectification ratio when going to higher ionic strength can be explained due to loss of semi-permeability and onset of anion transport through the titanate nanosheet film.
Ion transport through lamellar titanate nanosheet deposits: electrolyte cations versus anions
Next, the effects of electrolyte anions are investigated. Figures 5 c–d show a summary of data from cyclic voltammogram, chronoamperometry and a rectification ratio bar plot for aqueous 10 mM NaOH, NaNO3, NaCl, NaClO4, Na2SO4 and PBS pH 7. For all types of anions, similar levels of rectification are observed. Currents for the open diode (in the positive potential range) become significantly higher for higher valent anions (SO42− and PO43−), but effects of the type of anion on the rectification ratio data seem insignificant. Clearly, anions at a sufficiently high concentration can enter into the inter-lamellar space and significantly change the rate of transport. This suggests that there could be always an underlying contribution from anion transport, even when the cation transport appears dominant. Sulphate and phosphate are likely to more strongly collapse the internal double layer and thereby to open up the nanochannels to both cation and anion transport. This can give rise to a higher ion current and less semi-permeability. Chronoamperometry data show relatively complex transients (rising and falling) with transient features mainly taking place in the first 0.5 s of the data. It is likely that during this period, not only concentration gradients in the solution in the vicinity of the microhole develop, but also that concentration gradients within the nanosheet material change. The current traces measured during chronoamperometry may contain a component of ‘adsorption currents’ that are associated with compositional changes in the inter-lamellar space. Although electrolyte anion effects are clearly significant, it is currently difficult to disect these and to provide a more detailed assessment of the nature of these effects.
Ion transport through lamellar titanate nanosheet deposits: competing cation and proton transport
The observation of current through the titanate nanosheet deposit can be associated generally with three types of processes based on (i) flow of cations, (ii) flow of anions or (iii) the potential-driven water heterolysis process leading to the formation of mobile protons and mobile hydroxide (with a resulting net pH gradient). The latter process has been reported for biological  and for bipolar membrane processes . Catalysts for heterolytic water splitting such as graphene oxide  have been proposed to considerably enhance the potential-driven proton and hydroxide formation. In measurements as those reported in Fig. 5, it is not immediately clear whether water heterolysis can contribute to or even dominate the observed currents.
Figure 6 a shows both the generator current (WE1, membrane) and the collector current (WE2). The magnitude of the collector current approaches that of the generator current (with the opposite sign) in the case of a pure proton current. Therefore, the data for the proton transport for 10 mM HCl in Fig. 6 a provide proof for the methodology to work. Data in Fig. 6 b are shown for 10 mM LiCl. Perhaps surprisingly, again a significant proton transport is observed with the collector current almost mirroring the generator current. This suggests that water heterolysis at titanate nanosheets is important and that the transport of Li+ is likely to be accompanied by proton transport. Results for NaCl (Fig. 6c), KCl (Fig. 6d) and NH4Cl (Fig. 6e) are very similar, and also suggest proton formation by heterolysis and transport through the titanate film.
Data observed for MgCl2 (Fig. 6f) and for CaCl2 (Fig. 6g) are different not only with much lower proton fluxes, but also much lower generator currents. The shape of the voltammetric signal for Ca2+ is more complex and indicative of some blocking of the diode as the potential is scanned into the positive potential range. For both Mg2+ and Ca2+, small transient peaks are seen on the negative going potential scan, which could be associated with an ‘unblocking’ process. These observations are consistent with a blocking effect for Mg2+ and Ca2+ caused by a localised pH changes at the titanate film surface. Water heterolysis occurs at the titanate nanosheets, and this then causes locally the formation of hydroxide which then in combination with Mg2+ or Ca2+ causes blocking of the titanate nanochannels. However, the importance of this effect and the relative importance of proton versus electrolyte cation transport through the titanate film are difficult to quantify from these data. Further evidence for these processes comes from direct pH measurements.
The effect of protonic current flow through the diode can be estimated in terms of an upper limit for the pH changes in the right/left compartment when assuming a fixed volume V of ca. 0.01 dm3 (an estimated volume where pH changes occur close to the membrane surface). Eqs. (1) and (2) express the shift in pH (from the initial value pHinitial) in the right compartment (where protons are lost) and in the left compartment (where protons are gained).
Parameters in these equations are the time-average absolute current I, the time t = 600 s and the Faraday constant F = 96,487 C mol−1. For the case of a 1 mM NaCl electrolyte (see Fig. 7c), the average current at an applied voltage of 4 V was 10 μA over 600 s, which (with pHinitial = 6.39) translates to pHleft = 5.2 and pHright = 8.8. Comparison to the experimental results in Fig. 7 c shows that the predicted trend is indeed observed. For a concentration of 10 mM NaCl (Fig. 7d), the observed average current was 23 μA at 4 V applied voltage. This gives pHleft = 4.8 and pHright = 9.2. Experimental data suggest a less strong change in pH and therefore less competition between Na+ transport and water heterolysis at the higher NaCl concentration. Additional experiments for 100 mM NaCl (not shown) suggest even lower pH drift even at higher currents. Water heterolysis appears to be strongly electrolyte concentration dependent and probably insignificant at electrolyte concentrations of 10 mM or higher. Although conclusive in terms of providing direct evidence for the water heterolysis process, the data provide only qualitative insights and further work will be required to provide a quantitative measure of the water heterolysis process under these conditions.
Ion transport through lamellar titanate nanosheet deposits: interference of NBu4 + with proton transport
It is possible to envisage the processes responsible for the ion transport in the lamellar structure based on the equilibration of competing cation in the titanate double layer. Both protons and NBu4+ can be bound (Fig. 8c). In the absence of NBu4+ vacancies exist for protons (or other cations) to bind and to conduct through the titanate deposit. However, when adding NBu4+ cations these bind and block the transport of other cations (protons). For 10 mM NBu4+ cations both the current in the open state and the rectification ratio half. When adding more NBu4Cl, it is possible to ‘invert’ the diode behaviour. This can be explained by excess of NBu4Cl binding into the inter-lamellar space and a net anion transport mechanism (due to mobile chloride) being activated. More work will be needed to further exploit this switch from cationic to anionic current rectification.
Summary and conclusions
It has been shown that asymmetry in the deposition of a titanate nanosheet film can be used to induce current rectification phenomena or ionic diode effects, as long as the semi-permeable character due to cation transport is maintained. In this case, a ‘cationic diode’ has been produced with rectification effects observed for many types of cations. A cation vacancy model is proposed based on NBu4+ cations occupying part of the inter-lamellar space with vacancies for other types of cations to bind. The excess of negative charges on the titanate allow cation binding and transport.
The rectification ratio for NaCl electrolyte considerably decreased when concentration of aqueous NaCl (or the ionic strength) was increased on the side of titanate nanosheet film (consistent with anion uptake into the lamellar space and anion transport in addition to cation transport at higher ionic strength). Currents for the open diode are shown to be associated with additional water hydrolysis and proton transport rather than pure Li+, Na+, K+, NH4+, Mg2+ and Ca2+ transport. In the case of Mg2+ and Ca2+, this resulted in blocking of transport presumably due to precipitation effects in the presence of hydroxide. Water heterolysis requires catalytic sites for the potential-driven dissociation reaction. Sharp edges at the 2D-titanate surfaces (causing high local field gradients) with a pKA close to 4 (resulting in active sites for field-driven water dissociation) could provide well-suited reaction environments, but further study will be needed to confirm this. A more quantitative observation of the relative contributions of proton and electrolyte cation transport to the diode current will be required. NBu4+ cations have been shown to suppress cation conduction and ultimately ‘invert’ the diode to anion conduction due to an increase in positive charge in the lamellar space. In order to improve the understanding of these processes, in future, theory could be developed at both the atomic level and the meso-level to take in account localised field effects as well as interfacial concentration gradient/polarisation effects that are caused by the current flow.
Applications of titanate films could be possible (i) under low ionic strength conditions as a catalyst for water heterolysis  or (ii) under higher ionic strength conditions in desalination. However, the ability of the lamellar structures to maintain effective rectification at higher ionic strengths is currently poor. Therefore, the inter-lamellar space needs to be better designed to maintain a higher rectification effect (by maintaining semi-permeability). This could be achieved by tuning the concentration and structure of the tetraalkylammonium guest cations. Further work will be directed toward the effects of inter-lamellar guests on the mechanism and the use of nanosheet materials in desalination and sensing.
B.R.P. would like to thank the Indonesian Endowment (LPDP RI) for a PhD scholarship.
- 18.Maluangnont T, Matsuba K, Geng FX, Ma RZ, Yamauchi Y, Sasaki T (2013) Osmotic swelling of layered compounds as a route to producing high-quality two-dimensional materials. A comparative study of tetramethylammonium versus tetrabutylammonium cation in a Lepidocrocite-type titanate. Chem Mater 25:3137–3146CrossRefGoogle Scholar
- 23.Lee Y, Kwon KY (2017) Synthesis and oxidative catalytic property of ruthenium-doped titanate nanosheets. Appl Chem Engineer 28:593–596Google Scholar
- 25.Harito C, Bavykin DV, Walsh FC (2017) Incorporation of titanate nanosheets to enhance mechanical properties of water-soluble polyamic acid. In: Yudianti R, Azuma J (eds) Innovation in Polymer Science and Technology. IOP Conference Series-Materials Science and Engineering, vol 223, p 012054. https://doi.org/10.1088/1757-899X/223/1/012054
- 26.Wahyuni WT, Putra BR, Harito C, Bavykin DV, Walsh FC, Fletcher PJ, Marken F (2019) Extraction of hydrophobic analytes from organic solution into a titanate 2D-nanosheet host: Electroanalytical perspectives. Anal Chim Acta X. https://doi.org/10.1016/j.acax.2018.100001
- 28.Aaronson BDB, He DP, Madrid E, Johns MA, Scott JL, Fan L, Doughty J, Kadowaki MAS, Polikarpov I, McKeown NB, Marken F (2017) Ionic diodes based on regenerated alpha-cellulose films deposited asymmetrically onto a microhole. Chem Select 2:871–875Google Scholar
- 31.Putra BR, Aoki KJ, Chen JY, Marken F (2019) A cationic rectifier based on a graphene oxide covered microhole: Theory and experiment. Langmuir. https://doi.org/10.1021/acs.langmuir.8b03223
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.