Simultaneous electro

Scientific Reports volume 13, Article number: 1201 (2023) Cite this article

717 Accesses

2 Citations

3 Altmetric

Metrics details

Cu nanoparticles (NPs) have been shown to be excellent electrocatalysts, particularly for CO2 reduction – a critical reaction for sequestering anthropogenic, atmospheric carbon. Herein, the micro interface between two immiscible electrolyte solutions (ITIES) is exploited for the simultaneous electropolymerization of 2,2′:5′,2′′-terthiophene (TT) and reduction of Cu2+ to Cu nanoparticles (NPs) generating a flexible electrocatalytic composite electrode material. TT acts as an electron donor in 1,2-dichloroethane (DCE) through heterogeneous electron transfer across the water|DCE (w|DCE) interface to CuSO4 dissolved in water. The nanocomposite formation process was probed using cyclic voltammetry as well as electrochemical impedance spectroscopy (EIS). CV and EIS data show that the film forms quickly; however, the interfacial reaction is not spontaneous and does not proceed without an applied potential. At high [TT] the heterogeneous electron transfer wave was recorded voltammetrically but not at low [TT]. However, probing the edge of the polarizable potential window was found to be sufficient to initiate electrogeneration/electropolymerization. SEM and TEM were used to image and analyze the final Cu NP/poly-TT composites and it was discovered that there is a concomitant decrease in NP size with increasing [TT]. Preliminary electrocatalysis results at a nanocomposite modified large glassy carbon electrode saw a > 2 × increase in CO2 reduction currents versus an unmodified electrode. These data suggest that this strategy is a promising means of generating electrocatalytic materials for carbon capture. However, films electrosynthesized at a micro and ~ 1 mm ITIES demonstrated poor reusability.

Owing to their flexibility1,2,3 and biocompatibility4, conductive polymeric thin films have seen a significant rise in usage and interest. Motivated to reduce production cost, less expensive and involved preparation methods are being sought. For example, many polymerization methods generate relatively high average molecular weight materials that are robust; however, require electrodeposition onto an anode5, often binding the polymer to the electrode surface, or uses specialized bulky methods such as electrospinning6. In the case of the former, this likely eliminates the possibility of obtaining a free-standing film/conductive polymer electrode as the polymer is difficult to liberate from the anode and thus can limit the type of applications.

Meanwhile, metal nanoparticles (NPs) form the basis of numerous analytical and electrocatalytic platforms7,8,9; particularly copper (Cu) based NPs which are effective in catalyzing CO2 reduction10,11,12,13. Many metal NP preparation methods have emerged; however, the Brust-Schiffrin method, first described in 199414,15, reproducibly generated low dispersity Au NPs by exploiting the interface between two immiscible electrolyte solutions (ITIES), i.e., the liquid|liquid interface. Indeed, the ITIES has recently come under increasing activity in the electrodeless synthesis of both metal NPs15,16,17,18,19,20,21,22,23,24,25,26,27 and conductive polymer films4,28,29,30,31,32,33,34,35,36. Initially, efforts were focused on the immiscible water|oil (w|o) interface4,27,28,29,30,31,32,33,34,35,36; however, these have recently expanded to the water|ionic liquid (w|IL)21,22,23,24,25,26 and oil|ionic liquid (o|IL)20 ones. In a simple 2-electrode configuration with one electrode immersed in either phase, the Galvani potential difference can be controlled externally via a potentiostat with the potential drop spanning 1–4 nm across the ITIES, ϕw – ϕo = \(\Delta_{o}^{w} \phi\)8,37.

Johans et al.38 were the first to describe an analytical solution for nucleation of metal NPs at the liquid|liquid interface. In their work, they emphasized the absence of defect sites that are common at a solid/solution interface; thus, there is a large thermodynamic barrier to particle formation at ITIES. Nevertheless, they38 and others8,15,16,17,18,20,23,24,27,28,39,40 were able to experimentally demonstrate electrochemically controlled metal NP nucleation at w|o interfaces. Interestingly, Nishi's group has suggested that the molecular structure of the liquid|liquid interface is transcribed onto the NP framework22. They recently demonstrated that the w|IL interface played an important role mechanistically in the formation of nanostructures. Their IL was modified with a ferrocene (Fc) functional group making it redox active, and was exploited in the formation of Pd nanofiber arrays22.

Meanwhile, electropolymerization at liquid|liquid interfaces was initially investigated by Cunnane's group36, and more recently by Scanlon's group4 and ourselves28. In these later reports, large, free-standing polymer films were formed. In the case of Lehane et al.4 who generated PEDOT (poly(3,4-ethylenedioxythiophene)) using Ce4+ in aqueous and EDOT in α,α,α-trifluorotoluene (TFT), the films were shown to be highly stable and biocompatible. Our work showcased the simultaneous electropolymerization of 2,2′:5′,2′′-terthiophene (TT) and electrogeneration of Au NPs at a micro-ITIES (25 µm in diameter)26, building on Cunnane's study at a large ITIES29,30,32. We demonstrated that miniaturization of the ITIES could be used to provide another layer of mechanistic and thermodynamic control towards smaller, low dispersity NPs.

Herein, this is expanded to the simultaneous electrogeneration and electropolymerization of Cu nanocluster incorporated poly-TT films. Electrochemical impedance spectroscopy was used to monitor film growth, while SEM and TEM imaging were used to compare film/NP morphology at different TT concentrations between the large and micro-ITIES. Two large ITIES platforms were investigated, including a 1.16 and 10 mm diameter interface. Initial testing of glassy carbon (GC) electrodes modified with the nanocomposite demonstrate excellent electrocatalytic activity towards CO2 reduction; however, films electrosynthesized at the 25 µm and 1.16 mm interfaces demonstrated poor stability and surface coverage.

Copper sulphate (CuSO4, > 98%), lithium sulphate (Li2SO4, > 98%), 1,2-dichloroethane (DCE, ≥ 99.0%), 1-bromooctane (99%), trioctylphosphine (97%), and 2,2′:5′,2′′-terthiophene (TT, 99%) were acquired from Sigma-Aldrich. All reagents were used without additional purification. Ultrapure water from a MilliQ filtration system (> 18.2 MΩ cm) was used throughout to generate aqueous solutions. The tetraoctylphosphonium tetrakis(pentafluorophenyl)borate (P8888TB) ionic liquid used as an oil phase supporting electrolyte was prepared as detailed previously41.

Liquid|liquid electrochemical experiments were performed using a PG-618-USB potentiostat (HEKA Electroniks) in four-, three-, and two-electrode configurations at the large and micro-ITIES. In the 4-electrode mode a specialized 10 mm inner diameter cell with two Pt wires annealed into the side of the glass cell were connected to the working (WE) and counter electrode (CE) leads of the potentiostat as shown in Fig. 1B. The WE was positioned in the aqueous phase, while the CE was in the organic phase. Two references electrodes (RE) were also employed, one in either phase and inserted into Luggin capillaries built into the specialized cell with their tips facing each other ~ 5 mm apart with the liquid|liquid interface positioned in between them, see Fig. 1B.

Diagram of the specialized (A) micro and (B) large ITIES (interface between two immiscible electrolyte solutions) cell. WE, CE, and RE refer to the working, counter and reference electrode leads, respectively.

When using the micro-ITIES in two-electrode mode, one Ag wire (Goodfellow Inc.) was integrated into the specialized pipette holder containing the aqueous phase and connected to the WE port of the head-stage, and another Ag wire immersed in the organic phase was connected to the CE/RE port, see Fig. 1A. The body of the holder was fabricated from poly(ether ether ketone) (PEEK). The pipette was backfilled with the aqueous phase through a syringe attached to a 3-way valve incorporated into the side of the specialized holder, then the tip of the pipette was immersed in the organic phase. The 25 µm diameter ITIES was maintained at the pipette tip using the syringe and monitored using an 18-megapixel CCD camera (AmScope) equipped with a 12 × magnifying lens assembly (Navitar). Micropipette fabrication has been described elsewhere42. Scheme 1 details the electrolytic cells employed. The experimental potential scale was referenced to the Galvani scale by simple SO42– transfer, whose formal ion transfer potential \(\left( {\Delta_{o}^{w} \phi_{{{\text{SO}}_{4}^{2 - } }}^{o^{\prime}} } \right)\) was taken to be –0.540 V16.

Electrolytic cells used where x mM of CuSO4 was added to the aqueous phase and y mM the electron donor, 2,2′:5′,2′′-terthiophene (TT), was added to the DCE phase in Cells 1 and 2, while 5 mM of the ionic liquid P8888TB (tetraoctylphosphonium tetrakis(pentafluorophenyl)borate) was employed as supporting electrolyte in the organic phase. The double bars indicate the polarizable potential w|DCE interface, with diameters of 25 µm in the case of the ITIES maintained at the tip of the micropipette (Cell 1), as well as 1.16 (Cell 1) or 10 mm (Cell 2) for the two large electrolytic cells, see Fig. 1.

A second large ITIES electrolytic cell (Cell 1, general configuration) was created by using the modified holder shown in Fig. 1A; however, an unmodified borosilicate capillary (2.0/1.16 mm outer/inner diameter, Sutter Instruments) was used in place of a micropipette. Additionally, a Pt wire counter and Ag wire reference electrodes were used, coupled to the integrated Ag wire as WE in the aqueous phase, in a 3-electrode configuration.

Electrochemical impedance spectroscopy (EIS) measurements were performed with a frequency range between 10 and 20 kHz, as well as a 20 mV peak-to-peak perturbation. EIS was only measured using Cell 1 at a 25 µm ITIES in a 2-electrode configuration.

Before or in-between experiments, electrolytic cells/capillaries were cleaned using the procedure outlined in the Supplementary Information (SI).

Electrocatalysis studies were performed using a 3-electrode cell connected to a CH Instruments potentiostat (model# CHI602E) with a glassy carbon (GC, Pine Research) WE (~ 4 mm in diameter) coupled with Ag/AgCl reference (Dek Research) and Pt wire counter electrodes.

All transmission electron microscopy (TEM) images were taken using the Tecnai Spirit transmission electron microscope with samples prepared on 200 Mesh Cu ultrathin/lacey carbon or 2 µm holey Au grids (Electron Microscopy Sciences).

SEM imaging was performed using a JEOL JSM 7100 F equipped with energy dispersive x-ray (EDX) which were analyzed via DTSA II software provided by the National Institute of Standards and Technology (NIST) in the US, see https://www.nist.gov/services-resources/software/nist-dtsa-ii.

The black, dashed curves shown in Fig. 2A-C illustrate cyclic voltammograms (CVs) recorded using Cells 1 and 2 at the micro (25 µm diameter), 1.16 mm, and ~ 10 mm diameter ITIES, respectively, without TT added, but with 5 mM of CuSO4 in the aqueous phase. In each case, the polarizable potential window (PPW) is limited by the transfer of the supporting electrolyte ions. The large positive current increase at positive potentials is owing to the transfer of Li+/Cu2+ from water to oil (w → o) or TB– from o → w, while the sharp negative increase in current towards negative potentials is owing to the transfer of SO42– from w → o and P8888+ from o → w8,43.

i-V curves recorded at 0.020 V s–1 using Cell 1 (A,B) and 2 (C), or the 25 µm, 1.16 mm, and 10 mm ITIES, respectively, with [TT] = 20 mM and [CuSO4] = 5 mM, while the black, dashed traces show the system without TT added, i.e., blank curves. DCE was used as the organic solvent in all cases. Cyclic voltammograms have been scanned consecutively 25 times and overlaid such that the red and dark purple traces are the first and last scans, respectively; dashed, purple arrows indicate the evolution of the current signals with successive scans. Black arrows indicate scan direction.

The red, solid trace shows the initial i-V cycle at the micro-ITIES (Fig. 2A), after addition of 20 mM of TT to DCE. A positive peak-shaped wave was observed during the forward scan, towards positive potentials, with a peak potential (Ep) at roughly 0.52 V. During the reverse scan, towards negative potentials, a sigmoidal wave was observed with a half-wave potential \(\left( {\Delta_{o}^{w} \phi_{1/2} } \right)\) at ~ 0.515 V. Since the interface was maintained at the tip of a pulled micropipette, the diffusion regime inside and outside the pipette is asymmetric. The former behaves under linear diffusion owing to geometric confinement within the micropipette, while the latter is hemispherical with responses similar to an inlaid disc ultramicroelectrode (UME)44. Thus, this signal is consistent with the transfer of negative charge from o → w during the forward scan, such that the process is diffusion limited by a species in the aqueous phase. Therefore, it was hypothesized that this signal is owing to electron transfer from TT in DCE across the ITIES to Cu2+ in water; whereby, Cu2+ is reduced to Cu0 and forms nanoparticles, while TT is oxidized and electropolymerized.

To investigate this, the system was cycled a total of 25 times with these i-V curves overlaid in Fig. 2A; the dashed, purple arrow indicates how the peak current (ip) signal evolves with each consecutive scan. There is only a small change in ip that may be owing to a localized consumption at the interface, or the formation of a nanoparticle incorporated polymer film at the ITIES. The latter would fundamentally alter the effective surface area of the interface as well as its charge transfer characteristics; both would impact the magnitude of ip. Cell 1 was also tested using [CuSO4] = 0 mM and [TT] = 20 mM; however, no peak-shaped signal was recorded (data not shown). Thus, it is likely that Li+ does not interact with TT and is a good electro-inactive supporting electrolyte. However, when [TT] was decreased to 10 and 5 mM in DCE, no electron transfer wave was recorded voltammetrically (data not shown).

In all cases at the micro-ITIES, an aqueous droplet was ejected onto a TEM grid for imaging using the syringe equipped on the back of the modified holder. Even at 5 and 10 mM TT, a film-like deposit was visible on the substrate under an optical microscope. Therefore, despite no observable electron transfer wave, cycling at the PPW edge-of-scan can induce electrogeneration of the nanocomposite film. These results agree well with our recent work at the w|DCE micro-interface using KAuCl4(aq) and TT(org)28; whereby, a thin conductive polymer film, with embedded Au NPs was formed. Lehane et al.4 also recently employed a large w|DCE interface in the electropolymerization of PEDOT with Ce4+ as oxidant/electron acceptor in the aqueous phase. Moreover, electrodeposition of Cu, Au, Pd, and Pt NPs at large16,30,38,40,45 and micro27,39 interfaces have been demonstrated previously using metallocenes as electron donors dissolved in oil.

An ITIES with a diameter of 1.16 mm using a 3-electrode configuration was also tested voltammetrically, see Fig. 2B. The overall CV profile is similar to the one at a ~ 10 mm ITIES (see below) with a signal at ~ 0.7 V which is likely the electron transfer wave; however, two negative current peaks were recorded at roughly 0.4 and 0.15 V during the scan from positive to negative potentials. These may be the re-oxidation of Cu0 or anion adsorption waves. Future work will focus on in situ spectroscopic methods to evaluate these two curve features.

Next, film generation was investigated at a 10 mm diameter ITIES using Cell 2 (see Fig. 2C). When scanning from negative to positive potentials, two peak-shaped waves were observed at – 0.22 and 0.66 V, while on the reverse scan towards negative potentials, two peak signals were recorded at 0.09 and – 0.26 V. The two peaks towards the negative end of the PPW form a reversible signal with a \(\Delta_{o}^{w} \phi_{1/2}\) of – 0.240 V which may be the result of the adsorption of anions at the surface of the growing composite film. Indeed, this agrees well with the results of Lehane et al.4 The two signals at the positive end of the PPW are irreversible electron transfer similar to the result observed at the micro-ITIES in this potential region. With repeated sweeps of the potential, the irreversible electron transfer wave shifts to more negative potentials indicating a reduction in the required overpotential. As mentioned above, the liquid|liquid interface is initially free of nucleation sites which increases the amount of applied driving force necessary to achieve NP nucleation/polymerization38 versus at a solid/electrolyte one. However, once the film begins forming, the population of viable sites increases which is reflected in the concomitant decrease in peak potential of the electron transfer wave. Simultaneously, the signal decreases in current intensity which is likely owing to the consumption of material in the vicinity of the ITIES. The nanocomposite film formed in the large ITIES cell was thick, brittle, and difficult to extract from the cell. However, pieces were deposited onto glass substrates for SEM imaging and onto a GC electrode for electrocatalytic testing (see below).

The voltammetric negative peak during the reverse scan in Fig. 2C with a \(\Delta_{o}^{w} \phi_{1/2}\) at – 0.240 V may be owing to the reorganization of the electric double layer (EDL) and adsorption of supporting electrolyte anions on either side of the forming liquid|solid|liquid interface4. As shown by Scanlon's group4, supporting electrolyte anions from both phases stabilize film growth through adsorption; however, due to the size and shielded negative charge on B(C6F5)4–, it is likely a minor contributor and most anion adsorption comes from SO42– on the aqueous side. Moreover, SO42– is molecularly smaller with exposed dense negative charge on the oxygens, doping the film with sulphate is more efficient in stabilizing and neutralizing the film as it forms. However, during the later stages of film growth, diffusion of anions through the film is inhibited making doping/de-doping a slow process and causing voltammetric peak broadening46. Regardless, the film will likely be p-doped.

Both micro and large ITIES experiments were also performed at open circuit potential (OCP), i.e., without an applied external potential. In both cases, no film or NPs were observed. Thus, an applied potential is required to induce nanocomposite film formation.

Using the syringe affixed to the back of the pipette holder, a droplet of the aqueous phase was ejected from the tip of the micropipette after 25 consecutive CV scans using Cell 1 with 5 mM of CuSO4 paired with 5 or 20 mM of TT in DCE and deposited on a holey-Au TEM grid. Next, the TEM grids were imaged using both TEM and SEM (see Fig. 3). TEM micrographs in Fig. 3A and B show the low dispersity spherical Cu NPs electrogenerated and embedded within the poly-TT film with average sizes of 5.3 and 1.7 nm at [TT] equal to 5 and 20 mM, respectively. NP sizes were measured using ImageJ software and collated into histograms plotted inset in Fig. 3; average NP sizes were determined by curve fitting the histograms with a Gaussian distribution. Fig. S1 of the SI shows the histogram of Cu NP sizes with the poly-TT film formed using Cell 1 with 10 mM of TT in DCE. With increasing [TT] the NP size decreased such that at TT = 10 or 20 mM, Cu particles are in the range of nanoclusters, i.e., 1.3 or 1.7 nm in diameter, respectively47,48. In this case, with higher [TT] the thermodynamics and kinetics of the heterogeneous electron transfer reaction are enhanced facilitating faster electropolymerization, which in turn likely limits the size of the Cu nanoclusters.

TEM micrographs were also obtained for films electrogenerated at the 1.16 and 10 mm interfaces and deposited onto 200 mesh Cu lacey carbon TEM grids. Fig. S3 of the SI shows the TEM micrographs along with histograms for the analysis of the Cu NP sizes performed using ImageJ software. Cu NPs at 1.16 and 10 mm ITIES demonstrate a high dispersity despite Gaussian curve fitting showing peaks at 2.2 and 4.1 nm. Errors shown inset in Fig. S3 are for the Gaussian peak position/fitting. Fig. S4 shows a photograph of the aqueous droplet suspended from the unmodified capillary (1.16 mm in diameter) post Cu NP/poly-TT electrogeneration and after removal from the oil phase. A thin-film can be observed spread across the droplet surface.

Figure 3C depicts the SEM micrograph of the nanocomposite Cu NP/poly-TT film deposited on a holey-Au TEM grid. The film was dense, compact, and smooth; however, it was also quite fragile and broke apart easily. Relatively large sections can be seen covering the TEM grid and occluding several of the 2 µm holes. These images agree well with the reported morphology for electropolymerized terthiophene in low current densities49,50 and are similar to the PEDOT film electropolymerized at a large ITIES reported by Scanlon's group4. Cu NPs were confirmed by energy dispersive x-ray (EDX) spectroscopy performed during SEM imaging (data not shown). 24-h shake-flask experiments performed in a 2 mL vial (large ITIES) using the same electrolyte compositions and TT concentrations as Cell 2 revealed no observable thin film or Cu NPs. Therefore, while not strictly observable voltammetrically at [TT] = 5 mM, by probing the positive edge of the PPW one can initiate Cu NP/poly-TT electrodeposition at relatively low [TT]. Moreover, this can be achieved without the use of extreme overpotentials that risk over-oxidizing the film31,51.

Figure 3D shows the film generated at the large ITIES with [CuSO4] = 5 mM and [TT] = 20 mM after 1000 CV cycles. The film is smooth; however, the Cu NPs cannot be resolved with SEM. Fig. S2A in the SI shows the CVs recorded during Cu NP/poly-TT electrosynthesis with [CuSO4] = 1 mM and [TT] = 5 mM. The first and every subsequent fifth scan was plotted. The Cu2+/TT reduction/oxidation and Cu re-oxidation waves are visible at roughly 0.85 and 0.55 V, respectively. The Cu NP/poly-TT film was extracted from the cell and deposited on a glass slide, then imaged in the SEM. Fig. S2B shows the SEM micrograph, while Fig. S2C and D contain plots of the EDX spectra obtained at the two points indicated in Fig. S2B. In Fig. S2B, the EDX spectra show that point C is rich in Cu and likely an agglomeration of Cu NPs, while point D is the polymer film itself containing sulphur and carbon.

The stepwise nucleation, oligomerization, and elongation of complex polymer/composite materials at liquid|liquid interfaces has been described by Vignali et al.31, Robayo-Molina et al.52, and recently by us28. The early stages of TT electropolymerization via heterogeneous electron transfer and electrodeposition can be described generally by the following,

where H-TT is the terthiophene molecule emphasizing the proton at the α- or β-carbon position on one of the terminal thiophene units, TT+• is the radical cation, and TT2 is the dimer. This initial stage is likely thermodynamically prohibitive at the liquid|liquid interface since it lacks nucleation sites38. However, once seeded with Cu0 nuclei and the positively doped TT oligomers as capping agents, the thermodynamics likely greatly improve, as mentioned above. It should be emphasized that the glass walls of the micropipette likely behave as nucleation sites; this would also apply to the walls of large glass ITIES electrolytic cells. Using Eqs. (1–4) as a basis, an overall reaction can be composed,

The overall electron transfer potential \(\left( {\Delta_{o}^{w} \phi_{{{\text{ET}}}} } \right)\) for Eq. (5) can be written as27,28,38,

where \(E_{{{\text{TT}}^{{ +\cdot }} {\text{/TT}}}}^{{o^{\prime},{\text{DCE}}}}\) and \(E_{{\text{Cu(II)/Cu}}}^{{o^{\prime},{\text{H}}_{{2}} {\text{O}}}}\) are the standard redox potentials for TT+•/TT and Cu2+/Cu0 and were taken to be 1.2028 and 0.342 V53, respectively. In this way, \(\Delta_{o}^{w} \phi_{{{\text{ET}}}}\) was calculated to be 1.57, 1.36, and 1.18 V for pH's 2, 5.5–6, and 8.5, respectively; since ΔG = \(nF\Delta_{o}^{w} \phi_{{{\text{ET}}}}\)54, this leads to ΔG >  > 0 that nevertheless decreases with increasing pH. These values are much higher than the experimentally determined values at pH ~ 5.5–6; thus, the difference is likely the thermodynamic contribution of the glass walls. However, silanization of the inside of the micropipette resulted in no observable change in the film produced (data not shown).

Next, electrochemical impedance spectroscopy (EIS) was employed during electrosynthesis at the micro-ITIES to elucidate the underlying physical and electrochemical dynamics of film formation. The sinusoidal applied potential waveform (VAC) can be described by55,

where VDC and V0 are the applied DC voltage and AC voltage amplitude (0.020 V peak-to-peak), respectively, while ω (= 2πf) is the angular frequency and t is time. In each case, VDC of roughly 0.7 V was applied (vs. \(\Delta_{o}^{w} \phi_{{{\text{SO}}_{4}^{2 - } }}^{o^{\prime}}\)) and a CV was performed between each impedance measurement at a scan rate of 0.020 V s–1. In this way, the Nyquist diagrams in Fig. 4A–C were recorded using Cell 1 at a 25 µm diameter interface with [TT] equal to 0, 5, and 20 mM in DCE, respectively. The semi-circle at high-frequency and partial semi-circle at low-frequencies describe the two typical branches of impedance spectra that are associated with electrical and electrochemical dynamics (i.e., mass transport), respectively55. In the case of the liquid|liquid interface, the high-frequency region is often associated with the capacitance of the back-to-back EDLs found in either phase, while the low frequency region is influenced by ion diffusion and electron transfer reactions55,56,57. These two features give rise to two "time constants" 55, so called since they are often modelled in equivalent circuits using a resistor and capacitor (C╧) in parallel.

TEM micrographs obtained for aqueous phase samples after 25 consecutive CV scans using Cell 1 at a w|DCE interface with [CuSO4] = 5 mM, as well as 5 (A) and 20 mM (B) of TT in DCE and deposited on a 2 µm diameter holey Au TEM grid; inset are histograms of Cu NP/nanocluster sizes. (C) SEM micrograph of the sample shown in B. (D) SEM image of the film generated at a large ITIES using Cell 2 with 5 mM of CuSO4(aq) and 20 mM of TT(org).

Equivalent electric circuits (EECs) used to model the impedance data have been drawn in Fig. 4D, which include constant phase elements (CPEs) in place of simple capacitors, in parallel with resistors added to model charge transfer reactions (RCT) and kinetic resistance (RC). As is common, a resistor was added in series to account for the total solution resistance (Rs). EEC1, a Randles-like equivalent circuit, and EEC2 feature the two terminals at either end for the WE and CE/RE employed experimentally. The 2-electrode configuration limits parasitic impedance artifacts from cabling and/or the CE and RE that are often observed at 3- and 4-electrode cells57,58. Operating at the micro-ITIES has added benefits and is able to resolve the charge transfer resistance over the solution electrolyte resistance; moreover, by repeatedly using the same micropipette, one can greatly enhance reproducibility.

EIS offers avenues to valuable physical insight into charge transfer processes at the liquid|liquid interface. The geometric capacitance (Cgeo), recently modeled by von Hauff and Klotz55 in the context of perovskite solar cells, may be considered analogous to the structural parasitic coupling elements proposed and modelled by Trojánek et al.57 for a 4-electrode cell, which they modelled using a 4-terminal EEC. In either case, Cgeo is normally modelled in parallel with all the other circuit elements. If it exceeded the individual capacitive circuit elements, i.e., CPE1 and CPE2 in Fig. 4D, then the high-frequency semi-circle would become enlarged and dominate the impedance spectrum. However, by operating in the 2-electrode mode, and ensuring that the overall impedance of the micropipette was < 1 MΩ during single phase experiments, then individual circuit elements can be resolved59. Thus, Cgeo/parasitic coupling elements can be ignored, greatly simplifying EEC modelling57,60,61. The faradaic impedance (Zf) is described by57,

where kf is the apparent rate of charge transfer, A is the surface area of the interface, F is Faraday's constant (96,485.33 C mol–1), R is the gas constant (8.314 J mol–1 K–1), T is the absolute temperature (298.15 K), z is the number of electrons transferred, and ZW is a Warburg impedance, within which, j2 = –1, and σ is defined as57,

Here, Di,o and \(c_{i,o}^{*}\) are the diffusion coefficient and bulk concentration of species i in the oil (o) phase, while subscript w indicates their values in the water phase. CPEs were used to account for the dynamic nature of the interface and facilitate the evolving properties of the growing polymer-NP network. CPE impedance can be written generally as62,

In which Q (F s1–n) is a constant and when n = 1 the element is a perfect capacitor, while n = 0.5 is in line with a typical Warburg element for semi-infinite diffusion.

At a freshly cleaned micro-ITIES, a CV was performed followed by impedance measurement using a VDC = 0.7 V; whereby, the CV-EIS pulse sequence was performed a total of 11 times. Figure 4A shows the impedance spectra using Cell 1 with [TT] = 0 and [CuSO4] = 5 mM, i.e., a blank spectrum. The pronounced low-frequency tail is likely owing to the relatively high VDC close to the edge of the PPW where supporting electrolyte ions will undergo transfer, e.g., Li+ w → o. This spectrum agrees well with one shown recently by Mareček's group59 which was associated with simple tetraethylammonium ion transfer at a micro-ITIES.

At low [TT] (Fig. 4B) the impedance profile does not undergo significant change; however, the tail in the low-frequency region is greatly suppressed relative to the blank spectra performed in the absence of TT (Fig. 4A). This may indicate that the film has formed after the first CV-EIS sequence and is blocking, or at least inhibiting simple ion transfer of the supporting electrolyte.

Figure 4C shows the response at high [TT] in which the high frequency region of the EIS increases by 50% between the first and second CV-EIS pulse sequence. There is then a small decrease in the high frequency branch, which stabilizes across the 3rd to 11th iteration. Meanwhile, the low-frequency branch at high [TT] becomes more pronounced with each iteration. Based on the CV results (Fig. 2A), the film forms immediately generating a liquid|solid|liquid interface and, thus, the low-frequency branch is then associated with mediated electron transfer between Cu2+(aq) and TT(org) rather than simple ion transfer. Thus, as the film grows the electron transfer properties change (see below).

Nevertheless, these data indicate a change in the nature of the interface brought about by the development of a liquid|solid|liquid system that occurs immediately upon application of the first CV-EIS. It has been shown that forming a barrier at the interface mainly affects the low-frequency region28. However, as the film develops, and likely due to the build up of local micro-convections in this domain63, it was found that by pushing the impedance measurement to lower and lower frequencies the interface becomes unstable. This either lead to a higher noise level or the interface itself physically broke down, erupting into the organic phase as an electrophoretically induced droplet. Thus, it was not possible to carry out EIS measurements below 10 Hz.

EEC2 (Fig. 4D) was employed during thin film growth in the presence of CuSO4(aq) and TT(org), while EEC1 was used in the absence of TT, see the blue, solid curves in Fig. 5. Figure 5 shows the changes in the six EEC parameters after each CV-EIS iteration. With 5 mM of TT in the system, orange filled circle curves, CPE1 shows little deviation from the initial value of ~ 12.0 pF with only a slight decrease over the 11 CV-EIS pulse sequences before finally stabilizing at ~ 11.7 pF. As mentioned above, this circuit element is typically associated with the liquid|liquid back-to-back EDLs and these small changes in capacitance may be owing to ion rearrangement on either side of the interface during thin film electrogeneration or changes in the surface morphology at either side of the liquid|solid|liquid junction. At [TT] = 20 mM, yellow filled square traces in Fig. 5, there is a sudden decrease in CPE1 until the 4th CV-EIS pulse sequence, after which the element recovers and increases to a final value of 12.1 pF. In both cases, n varies between roughly 0.96 and 0.98, indicative of a conventional capacitor with likely an inhomogeneity in ion distribution at the interface.

The measured (markers) and the fitted (solid line) Nyquist diagrams acquired using Cell 1 with 0 (A), 5 (B), and 20 mM (C) of TT added to the DCE phase as well as 5 mM of CuSO4(aq). Spectra were obtained with a direct applied potential (VDC) of ~ 0.7 V after performing one CV cycle using the potential range shown in Fig. 2 with v = 0.020 V s–1; similarly, in-between each spectrum in B and C a CV pulse was applied. (D) equivalent electric circuits (EEC) for a simple ion transfer (EEC1) or coupled electron and ion transfer during electro-generation (EEC2) of the thin film at an ITIES, such that Rs, RCT, and RC, are the solution, charge transfer, and kinetic resistance, while CPE1 and CPE2 are constant phase elements.

The n value for CPE2, RCT, and RC increase slightly with [TT] = 5 mM and each CV-EIS pulse iteration, while all three parameters show a much larger increase at [TT] = 20 mM. RCT and RC are ½ and 2 × as high, respectively, when [TT] = 20 mM versus 5 mM. This agrees well with impeded electron transfer or ion diffusion through the growing polymer/NP network. The limited diffusion within the nanocomposite structure likely results in limited anion exchange to neutralize individual TT units contributing to its p-doped nature and accumulation of negative charge on the surface of the Cu NP/poly-TT composite. These values agree with those recently reported by us for Au NP/poly-TT nanocomposites electrogenerated at a micro-ITIES28 after multiple CV-EIS pulses were performed. Herein, the interface was monitored in situ using a CCD camera equipped with a 12 × zoom lens assembly with a 10–12 cm working distance; however, unlike the Au NP/poly-TT film grown previously28, the Cu NP/poly-TT nanocomposite film was clear/colourless and, therefore, no observable change was observed optically.

Preliminary electrocatalysis results were obtained by modifying the surface of a glassy carbon (GC) electrode with a layer of Cu NP/poly-TT film and using 0.1 M NaHCO3(aq) as supporting electrolyte. Figure 6 shows CVs recorded at a bare and modified electrode; whereby, the solution was purged with either N2 or CO2 gas for ~ 15 min prior to polarization.

Equivalent electric circuit (EEC) parameter values obtained from fitting experimental impedance spectra from Fig. 4A–C using EEC2 depicted in Fig. 4D, with the orange filled circle and yellow filled square, curves derived from curve fitting impedance data obtained from Cell 1 with [TT] = 5 and 20 mM, respectively. The blue trace was determined using Cell 1 with [TT] = 0 mM.

At a bare GC electrode, and in the N2 saturated case, the cathodic peak at roughly – 0.45 V (vs. Ag/AgCl) is likely H+ reduction. However, this cathodic signal experiences a shift in the onset potential to – 0.57 V when purged with CO2 but maintains the same current intensity. The GC electrode modified with the Cu NP/poly-TT film electrosynthesized at a 1.16 mm ITIES shows a greater than 2 × CO2 reduction current at 0.75 V (vs. Ag/AgCl). To modify the GC electrode with a Cu NP/poly-TT composite at a 10 mm ITIES, the GC plug was dipped into the electrolytic cell after the 25 CV cycles were performed. Afterwards, the i-V response shown in Fig. 6, yellow trace, demonstrated a further shift in the overpotential towards more negative potentials with no increase in the peak current; thus, electrocatalysis is likely suppressed in this instance. Modification of the interface with a single deposit from the 25 µm diameter interface resulted in no significant change relative to the bare GC electrode (data not shown).

Figure 7 depicts SEM images of the GC electrode surface modified with films generated at the 25 µm (A, D), 1.16 mm (B, E), and 10 mm (C, F) diameter interfaces before (left-hand side) and after (right-hand side) one CV cycle; additionally, using ImageJ software the GC surface coverage was estimated to be 0.3, 9.9, and 62.5%, respectively. The film electrosynthesized at the 25 µm ITIES is smooth and shows evidence of folding with Cu NPs distributed along creases in the film. It is hypothesized that the film quickly occludes the ITIES and new polymeric growth pushes the film into the aqueous side of the interface generating these folds. The Cu NP are likely concentrated towards the bottom of these folds, adjacent to the ITIES. Advanced, high-resolution optical methods will be needed to monitor film growth at the micro-ITIES in situ; however, this will be the focus of future work.

CVs recorded at a ~ 4 mm glassy carbon (GC) electrode immersed in a 0.1 M NaHCO3 aqueous solution without (bare) and with (modified) a layer of Cu NP/poly-TT film deposited on the surface. Films were electrogenerated at the 1.16 or 10 mm ITIES using Cells 1 or 2, as indicated inset, with [TT] = 20 mM and [CuSO4] = 5 mM, after 25 CV cycles at v = 0.020 V s–1. CVs were recorded in 3-electrode mode using a Ag/AgCl reference (Dek Research) and Pt wire counter electrode at 0.050 V s–1.

SEM micrographs of Cu NP/poly-TT film deposited on a glassy carbon (GC) electrode before (left-hand side) and after (right-hand side) CV electrocatalysis as shown in Fig. 6. The top (A,D), middle (B,E), and bottom (C,F) rows were films generated at a 25 µm, 1.16 mm, and 10 mm diameter ITIES, respectively. Scale is indicated inset.

Films developed at the two large ITIES were smooth with a relatively even distribution of Cu NPs and no evidence of folding. Therefore, this phenomenon is likely owing to geometric confinement of the growing polymer film within the micropipette tip.

After electrocatalysis, the Cu NPs in the films generated at the 25 µm and 1.16 mm interfaces showed large changes in NP morphology which have grown by orders of magnitude; therefore, the thin, polymer network in these cases is insufficient to protect them against aggregation/agglomeration. The film created at the 10 mm ITIES showed little change; however, further experimentation is required.

While preliminary, these results are promising. Future work will focus on controlling Cu NP and polymer film morphology while tracking any changes the nanocomposite experiences during electrocatalysis, as well as detailed product analysis.

The successful application of a micro-ITIES towards electrodeless synthesis of Cu NP/poly-TT has been demonstrated and compared to films generated at a large (mm scale) ITIES. At [TT] = 20 mM a well resolved electron transfer wave was observed at the micro-ITIES. However, the large interfaces showed a more complex CV profile with an irreversible electron transfer wave at high, positive potentials and a reversible signal towards the negative end. The latter is likely anion adsorption/exchange at the liquid|solid|liquid interfaces and agrees well with recent results by Scanlon's group4. Impedance data confirm that the nanocomposite film forms early through large changes in RCT and RC; moreover, increasing [TT] improves film formation while decreasing the median Cu NP size to < 2 nm.

Interestingly, while no electron transfer signal was observed at the micro-ITIES a low [TT], a film was electrogenerated and imaged using SEM. These data show that simply by probing the edge of the PPW one can facilitate electrodeless synthesis of the nanocomposite and avoid overoxidation of the polymer network.

Preliminary voltammetric results at a GC electrode modified with the Cu NP/poly-TT film electrogenerated at a 1.16 mm diameter interface elicited a > 2 × enhancement in the electrocatalytic CO2 reduction current versus an unmodified electrode. However, this film underwent large changes in NP morphology. While a tentative first step, these results are indicators that these films are promising alternative electrode materials for carbon capture; however, more optimization of nanocomposite electrosynthesis is necessary.

All data is available upon request to T.J.S., [email protected].

Cheng, H.-W. et al. Realizing intrinsically stretchable semiconducting polymer films by nontoxic additives. ACS Mater. Lett. https://doi.org/10.1021/acsmaterialslett.2c00749 (2022).

Article Google Scholar

Zhang, Q. et al. An elastic autonomous self-healing capacitive sensor based on a dynamic dual crosslinked chemical system. Adv. Mater. 30, 1801435. https://doi.org/10.1002/adma.201801435 (2018).

Article CAS Google Scholar

Wang, S., Oh, J. Y., Xu, J., Tran, H. & Bao, Z. Skin-inspired electronics: An emerging paradigm. Acc. Chem. Res. 51, 1033–1045. https://doi.org/10.1021/acs.accounts.8b00015 (2018).

Article CAS Google Scholar

Lehane, R. A. et al. Electrosynthesis of biocompatible free-standing PEDOT thin films at a polarized liquid|liquid interface. J. Am. Chem. Soc. 144, 4853–4862. https://doi.org/10.1021/jacs.1c12373 (2022).

Article CAS Google Scholar

Nezakati, T., Seifalian, A., Tan, A. & Seifalian, A. M. Conductive polymers: Opportunities and challenges in biomedical applications. Chem. Rev. 118, 6766–6843. https://doi.org/10.1021/acs.chemrev.6b00275 (2018).

Article CAS Google Scholar

Guo, Y. & Thérien-Aubin, H. Nanofibrous photocatalytic membranes based on tailored anisotropic gold/ceria nanoparticles. ACS Appl. Mater. Interfaces 13, 37578–37588. https://doi.org/10.1021/acsami.1c11954 (2021).

Article CAS Google Scholar

Roy, D., Pal, A. & Pal, T. Electrochemical aspects of coinage metal nanoparticles for catalysis and spectroscopy. RSC Adv. 12, 12116–12135. https://doi.org/10.1039/D2RA00403H (2022).

Article CAS Google Scholar

Scanlon, M. D., Smirnov, E., Stockmann, T. J. & Peljo, P. Gold nanofilms at liquid-liquid interfaces: An emerging platform for redox electrocatalysis, nanoplasmonic sensors, and electrovariable optics. Chem. Rev. 118, 3722–3751. https://doi.org/10.1021/acs.chemrev.7b00595 (2018).

Article CAS Google Scholar

Ben Aissa, M. A. et al. Copper nanoparticles of well-controlled size and shape: A new advance in synthesis and self-organization. Nanoscale 7, 3189–3195. https://doi.org/10.1039/C4NR06893A (2015).

Article ADS CAS Google Scholar

Kim, D., Kley, C. S., Li, Y. & Yang, P. Copper nanoparticle ensembles for selective electroreduction of CO2 to C2–C3 products. Proc. Natl. Acad. Sci. https://doi.org/10.1073/pnas.1711493114%JProceedingsoftheNationalAcademyofSciences (2017).

Article Google Scholar

Song, Y. et al. High-selectivity electrochemical conversion of CO2 to ethanol using a copper nanoparticle/N-doped graphene electrode. ChemistrySelect 1, 6055–6061. https://doi.org/10.1002/slct.201601169 (2016).

Article CAS Google Scholar

Nguyen, T. N. et al. Catalyst regeneration via chemical oxidation enables long-term electrochemical carbon dioxide reduction. J. Am. Chem. Soc. 144, 13254–13265. https://doi.org/10.1021/jacs.2c04081 (2022).

Article CAS Google Scholar

Anum, Z., Shah, A. & Shah, I. Oxide derived copper for electrochemical reduction of CO2 to C2+ products. Nanomaterials 12, 1380. https://doi.org/10.3390/nano12081380 (2022).

Article CAS Google Scholar

Brust, M., Walker, M., Bethell, D., Schiffrin, D. J. & Whyman, R. Synthesis of thiol-derivatised gold nanoparticles in a two-phase liquid-liquid system. J. Chem. Soc. Chem. Commun. https://doi.org/10.1039/C39940000801 (1994).

Article Google Scholar

Uehara, A. et al. Electrochemical insight into the Brust-Schiffrin synthesis of Au nanoparticles. J. Am. Chem. Soc. 137, 15135–15144. https://doi.org/10.1021/jacs.5b07825 (2015).

Article CAS Google Scholar

Aslan, E., Patir, I. H. & Ersoz, M. Cu nanoparticles electrodeposited at liquid-liquid interfaces: A highly efficient catalyst for the hydrogen evolution reaction. Chem. Eur. J. 21, 4585–4589. https://doi.org/10.1002/chem.201406615 (2015).

Article CAS Google Scholar

Uehara, A., Hashimoto, T. & Dryfe, R. A. W. Au electrodeposition at the liquid-liquid interface: Mechanistic aspects. Electrochim. Acta 118, 26–32. https://doi.org/10.1016/j.electacta.2013.11.162 (2014).

Article CAS Google Scholar

Dryfe, R. A. W., Uehara, A. & Booth, S. G. Metal deposition at the liquid-liquid interface. Chem. Rec. 14, 1013–1023. https://doi.org/10.1002/tcr.201402027 (2014).

Article CAS Google Scholar

Booth, S. G. et al. The significance of bromide in the Brust-Schiffrin synthesis of thiol protected gold nanoparticles. Chem. Sci. 8, 7954–7962. https://doi.org/10.1039/C7SC03266H (2017).

Article CAS Google Scholar

Kuroyama, Y., Nishi, N. & Sakka, T. Electrochemical liquid-liquid interface between oil and ionic liquid for reductive deposition of metal nanostructures. J. Electroanal. Chem. 881, 114959. https://doi.org/10.1016/j.jelechem.2020.114959 (2021).

Article CAS Google Scholar

Katakura, S. et al. Evolution and reversible polarity of multilayering at the ionic liquid/water interface. J. Phys. Chem. B 124, 6412–6419. https://doi.org/10.1021/acs.jpcb.0c03711 (2020).

Article CAS Google Scholar

Zhang, Y., Nishi, N. & Sakka, T. Template-free and spontaneous formation of vertically aligned Pd nanofiber arrays at the liquid-liquid interface between redox-active ionic liquid and water. ACS Appl. Mater. Interfaces 11, 23731–23740. https://doi.org/10.1021/acsami.9b05255 (2019).

Article CAS Google Scholar

Zhang, Y., Nishi, N., Amano, K.-I. & Sakka, T. One-dimensional Pt nanofibers formed by the redox reaction at the ionic liquid|water interface. Electrochim. Acta 282, 886–891. https://doi.org/10.1016/j.electacta.2018.06.024 (2018).

Article CAS Google Scholar

Nishi, N., Yajima, I., Amano, K.-I. & Sakka, T. Janus-type gold/polythiophene composites formed via redox reaction at the ionic liquid|water interface. Langmuir 34, 2441–2447. https://doi.org/10.1021/acs.langmuir.7b03792 (2018).

Article CAS Google Scholar

Nishi, N., Kakinami, T. & Sakka, T. Dendritic nanofibers of gold formed by the electron transfer at the interface between water and a highly hydrophobic ionic liquid. Chem. Commun. 51, 13638–13641. https://doi.org/10.1039/C5CC05476A (2015).

Article CAS Google Scholar

Moshrefi, R. & Stockmann, T. J. Electrodeless synthesis of low dispersity Au nanoparticles and nanoclusters at an immiscible micro water/ionic liquid interface. Nanomaterials 12, 2748. https://doi.org/10.3390/nano12162748 (2022).

Article CAS Google Scholar

Moshrefi, R., Suryawanshi, A. & Stockmann, T. J. Electrochemically controlled Au nanoparticle nucleation at a micro liquid/liquid interface using ferrocene as reducing agent. Electrochem. Commun. 122, 106894. https://doi.org/10.1016/j.elecom.2020.106894 (2021).

Article CAS Google Scholar

Moshrefi, R., Connors, E. P., Merschrod, E. & Stockmann, T. J. Simultaneous electropolymerization/Au nanoparticle generation at an electrified liquid/liquid micro-interface. Electrochim. Acta 426, 140749. https://doi.org/10.1016/j.electacta.2022.140749 (2022).

Article CAS Google Scholar

Lepková, K., Clohessy, J. & Cunnane, V. J. Electrodeposition of metal-based nanocomposites at a liquid–liquid interface controlled via the interfacial Galvani potential difference. Electrochim. Acta 53, 6273–6277. https://doi.org/10.1016/j.electacta.2008.04.025 (2008).

Article CAS Google Scholar

Lepková, K., Clohessy, J. & Cunnane, V. J. The pH-controlled synthesis of a gold nanoparticle/polymer matrix via electrodeposition at a liquid–liquid interface. J. Phys. 19, 375106. https://doi.org/10.1088/0953-8984/19/37/375106 (2007).

Article CAS Google Scholar

Vignali, M., Edwards, R. & Cunnane, V. J. Characterization of doping and electropolymerization of free standing films of polyterthiophene. J. Electroanal. Chem. 592, 37–45. https://doi.org/10.1016/j.jelechem.2006.04.020 (2006).

Article CAS Google Scholar

Knake, R. et al. Electrochemical nucleation of gold nanoparticles in a polymer film at a liquid−liquid interface. Langmuir 21, 1001–1008. https://doi.org/10.1021/la048277q (2005).

Article CAS Google Scholar

Sezai Sarac, A., Evans, U., Serantoni, M., Clohessy, J. & Cunnane, V. J. Electrochemical and morphological study of the effect of polymerization conditions on poly(terthiophene). Surf. Coat. Technol. 182, 7–13. https://doi.org/10.1016/j.surfcoat.2003.08.002 (2004).

Article CAS Google Scholar

Evans-Kennedy, U., Clohessy, J. & Cunnane, V. J. Spectroelectrochemical study of 2,2‘:5‘,2‘ ‘-terthiophene polymerization at a liquid/liquid interface controlled by potential-determining ions. Macromolecules 37, 3630–3634. https://doi.org/10.1021/ma0348223 (2004).

Article ADS CAS Google Scholar

Johans, C., Clohessy, J., Fantini, S., Kontturi, K. & Cunnane, V. J. Electrosynthesis of polyphenylpyrrole coated silver particles at a liquid–liquid interface. Electrochem. Commun. 4, 227–230. https://doi.org/10.1016/S1388-2481(02)00256-4 (2002).

Article CAS Google Scholar

Gorgy, K., Fusalba, F., Evans, U., Kontturi, K. & Cunnane, V. J. Electropolymerization of 2,2′:5′,2″ terthiophene at an electrified liquid–liquid interface. Synth. Met. 125, 365–373. https://doi.org/10.1016/S0379-6779(01)00474-X (2001).

Article Google Scholar

Samec, Z., Langmaier, J. & Kakiuchi, T. Charge-transfer processes at the interface between hydrophobic ionic liquid and water. Pure Appl. Chem. 81, 1473–1488. https://doi.org/10.1351/pac-con-08-08-36 (2009).

Article CAS Google Scholar

Johans, C., Lahtinen, R., Kontturi, K. & Schiffrin, D. J. Nucleation at liquid∣liquid interfaces: Electrodeposition without electrodes. J. Electroanal. Chem. 488, 99–109. https://doi.org/10.1016/S0022-0728(00)00185-6 (2000).

Article CAS Google Scholar

Nieminen, E. & Murtomäki, L. Kinetics of Cu2+ reduction and nanoparticle nucleation at micro-scale 1,2-dichlorobenzene-water interface studied by cyclic voltammetry and square-wave voltammetry. Electroanalysis 33, 2087–2095. https://doi.org/10.1002/elan.202100172 (2021).

Article CAS Google Scholar

Cheng, Y. & Schiffrin, D. J. Electrodeposition of metallic gold clusters at the water/1,2-dichloroethane interface. J. Chem. Soc. Faraday Trans. 92, 3865–3871. https://doi.org/10.1039/FT9969203865 (1996).

Article CAS Google Scholar

Stockmann, T. J., Boyle, P. D. & Ding, Z. Preparation and crystal structure of tetraoctylphosphonium tetrakis(pentafluorophenyl)borate ionic liquid for electrochemistry at its interface with water. Catal. Today 295, 89–94. https://doi.org/10.1016/j.cattod.2017.05.030 (2017).

Article CAS Google Scholar

Stockmann, T. J., Lu, Y., Zhang, J., Girault, H. H. & Ding, Z. Interfacial complexation reactions of Sr2+ with octyl(phenyl)-N, N-diisobutylcarbamoylmethylphosphine oxide for understanding its extraction in reprocessing spent nuclear fuels. Chem. Eur. J. 17, 13206–13216. https://doi.org/10.1002/chem.201102491 (2011).

Article CAS Google Scholar

Stockmann, T. J., Guterman, R., Ragogna, P. J. & Ding, Z. Trends in hydrophilicity/lipophilicity of phosphonium ionic liquids as determined by ion-transfer electrochemistry. Langmuir 32, 12966–12974. https://doi.org/10.1021/acs.langmuir.6b03031 (2016).

Article CAS Google Scholar

Liu, S., Li, Q. & Shao, Y. Electrochemistry at micro- and nanoscopic liquid/liquid interfaces. Chem. Soc. Rev. 40, 2236–2253. https://doi.org/10.1039/c0cs00168f (2011).

Article CAS Google Scholar

Nieminen, J. J. et al. Hydrogen evolution catalyzed by electrodeposited nanoparticles at the liquid/liquid interface. Chem. Commun. 47, 5548–5550. https://doi.org/10.1039/c1cc10637f (2011).

Article CAS Google Scholar

Wei, Y., Chan, C. C., Tian, J., Jang, G. W. & Hsueh, K. F. Electrochemical polymerization of thiophenes in the presence of bithiophene or terthiophene: Kinetics and mechanism of the polymerization. Chem. Mater. 3, 888–897. https://doi.org/10.1021/cm00017a026 (1991).

Article CAS Google Scholar

Jorabchi, M. N., Abbaspour, M., Goharshadi, E. K. & Wohlrab, S. Ag, Au, Pt and Au-Pt nanoclusters in [N1114][C1SO3] ionic liquid: A molecular dynamics study. J. Mol. Liq. 360, 119447. https://doi.org/10.1016/j.molliq.2022.119447 (2022).

Article CAS Google Scholar

Baletto, F. & Ferrando, R. Structural properties of nanoclusters: Energetic, thermodynamic and kinetic effects. Rev. Mod. Phys. 77, 371–423. https://doi.org/10.1103/RevModPhys.77.371 (2005).

Article ADS CAS Google Scholar

Wakeham, D. L., Donne, S. W., Belcher, W. J. & Dastoor, P. C. Electrochemical and morphological characterization of electrodeposited poly(2,2′:5′,2″-terthiophene) for photovoltaic applications. Synth. Met. 158, 661–669. https://doi.org/10.1016/j.synthmet.2008.04.022 (2008).

Article CAS Google Scholar

Harris, C. J., Belcher, W. J. & Dastoor, P. C. Effect of film thickness and morphology on the performance of photoelectrochemical cells based on poly(terthiophene). Sol. Energy Mater. Sol. Cells 91, 1127–1136. https://doi.org/10.1016/j.solmat.2007.03.018 (2007).

Article CAS Google Scholar

Barsch, U. & Beck, F. Anodic overoxidation of polythiophenes in wet acetonitrile electrolytes. Electrochim. Acta 41, 1761–1771. https://doi.org/10.1016/0013-4686(95)00493-9 (1996).

Article CAS Google Scholar

Robayo-Molina, I., Molina-Osorio, A. F., Guinane, L., Tofail, S. A. M. & Scanlon, M. D. Pathway complexity in supramolecular porphyrin self-assembly at an immiscible liquid-liquid interface. J. Am. Chem. Soc. 143, 9060–9069. https://doi.org/10.1021/jacs.1c02481 (2021).

Article CAS Google Scholar

Vanýsek, P. CRC Handbook of Chemistry and Physics 8.20-28.29 (CRC Press/Taylor, 2021).

Google Scholar

Méndez, M. A. et al. Molecular electrocatalysis at soft interfaces. Phys. Chem. Chem. Phys. 12, 15163–15171. https://doi.org/10.1039/c0cp00590h (2010).

Article CAS Google Scholar

von Hauff, E. & Klotz, D. Impedance spectroscopy for perovskite solar cells: Characterisation, analysis and diagnosis. J. Mater. Chem. C 10, 742–761. https://doi.org/10.1039/D1TC04727B (2022).

Article Google Scholar

Suárez-Herrera, M. F., Cazade, P.-A., Thompson, D. & Scanlon, M. D. Monitoring transient changes in the structure of water at a polarised liquid-liquid interface using electrocapillary curves. Electrochem. Commun. 109, 106564. https://doi.org/10.1016/j.elecom.2019.106564 (2019).

Article CAS Google Scholar

Trojánek, A., Mareček, V. & Samec, Z. Some aspects of impedance measurements at the interface between two immiscible electrolyte solutions in the four-electrode cell. Electrochim. Acta 179, 3–8. https://doi.org/10.1016/j.electacta.2014.12.013 (2015).

Article CAS Google Scholar

Tran, A. T., Huet, F., Ngo, K. & Rousseau, P. Artefacts in electrochemical impedance measurement in electrolytic solutions due to the reference electrode. Electrochim. Acta 56, 8034–8039. https://doi.org/10.1016/j.electacta.2010.12.088 (2011).

Article CAS Google Scholar

Silver, B. R., Holub, K. & Mareček, V. Ion transfer kinetics at the micro-interface between two immiscible electrolyte solutions investigated by electrochemical impedance spectroscopy and steady-state voltammetry. J. Electroanal. Chem. 731, 107–111. https://doi.org/10.1016/j.jelechem.2014.08.017 (2014).

Article CAS Google Scholar

Trojánek, A., Mareček, V. & Samec, Z. Temperature effect in the ion transfer kinetics at the micro-interface between two immiscible electrolyte solutions. Electrochim. Acta 180, 366–372. https://doi.org/10.1016/j.electacta.2015.08.110 (2015).

Article CAS Google Scholar

Josypčuk, O., Holub, K. & Mareček, V. Noise and ac impedance analysis of ion transfer kinetics at the micro liquid/liquid interface. Electrochem. Commun. 56, 43–45. https://doi.org/10.1016/j.elecom.2015.04.006 (2015).

Article CAS Google Scholar

Bisquert, J., Garcia-Belmonte, G., Bueno, P., Longo, E. & Bulhões, L. O. S. Impedance of constant phase element (CPE)-blocked diffusion in film electrodes. J. Electroanal. Chem. 452, 229–234. https://doi.org/10.1016/S0022-0728(98)00115-6 (1998).

Article CAS Google Scholar

Lhotský, A., Holub, K., Neužil, P. & Mareček, V. Ac impedance analysis of tetraethylammonium ion transfer at liquid/liquid microinterfaces. J. Chem. Soc. Faraday Trans. 92, 3851–3857. https://doi.org/10.1039/FT9969203851 (1996).

Article Google Scholar

Download references

TJS would like to thank the Natural Sciences and Engineering Research Council (NSERC) for a Discovery Grant (#006074-2019) as well as Memorial University of Newfoundland for start-up funding.

Chemistry Department, Core Science Facility, Memorial University of Newfoundland, 45 Artic Ave., St. John's, NL, A1C 5S7, Canada

Reza Moshrefi, Hanna Przybyła & Talia Jane Stockmann

You can also search for this author in PubMed Google Scholar

You can also search for this author in PubMed Google Scholar

You can also search for this author in PubMed Google Scholar

R.M.: Formal analysis, Investigation, Writing—review & editing, Validation. H.P.: Formal analysis, Investigation. T.J.S.: Conceptualization, Methodology, Writing—original draft, Writing—review & editing, Validation, Supervision, Project administration, Funding acquisition. All authors have read and agreed to the published version of the manuscript.

Correspondence to Talia Jane Stockmann.

The authors declare no competing interests.

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and Permissions

Moshrefi, R., Przybyła, H. & Stockmann, T.J. Simultaneous electro-generation/polymerization of Cu nanocluster embedded conductive poly(2,2′:5′,2′′-terthiophene) films at micro and macro liquid/liquid interfaces. Sci Rep 13, 1201 (2023). https://doi.org/10.1038/s41598-023-28391-9

Download citation

Received: 08 November 2022

Accepted: 18 January 2023

Published: 21 January 2023

DOI: https://doi.org/10.1038/s41598-023-28391-9

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.