Conductive Substrate Research Articles

Three-dimensional ordered CdS/ZnO porous nanostructures for high-performance photoelectrochemical water splitting

Three-dimensional ordered porous nanostructures have been considered as a key factor in developing high-performance photoelectrodes for photoelectrochemical (PEC) water splitting applications due to their high light absorption capacity and large surface area. In this study, the authors design and fabricate the three-dimensional ordered CdS/ZnO porous structures by the hard mould method. Firstly, polystyrene (PS) spheres were deposited on the indium tin oxide (ITO) conductive substrate; secondly, the gaps among the spheres were filled with ZnO material using electrochemical deposition; then the PS spheres were burned and formed the ordered porous structure of ZnO; finally, CdS nanoparticles were deposited on the surface of ZnO by wet chemical method to form a three-dimensional ordered CdS/ZnO porous structure.The photoelectrochemical water-splitting properties of the fabricated structures were studied and compared systematically. The results show that, under the irradiation of solar simulation, the efficiency of the optimised three-dimensional ordered CdS/ZnO porous structure is 3.4%, nearly 1.9 times higher than that of with 1.8% efficiency of thin-film CdS/ZnO structure at the same fabrication conditions.

MeNPs-PEDOT Composite-Based Detection Platforms for Epinephrine and Quercetin.

The development of low-cost, sensitive, and simple analytical tools for biomolecule detection in health status monitoring is nowadays a growing research topic. Sensing platforms integrating nanocomposite materials as recognition elements in the monitoring of various biomolecules and biomarkers are addressing this challenging objective. Herein, we have developed electrochemical sensing platforms by means of a novel fabrication procedure for biomolecule detection. The platforms are based on commercially available low-cost conductive substrates like glassy carbon and/or screen-printed carbon electrodes selectively functionalized with nanocomposite materials composed of Ag and Au metallic nanoparticles and an organic polymer, poly(3,4-ethylenedioxythiophene). The novel fabrication method made use of alternating currents with controlled amplitude and frequency. The frequency of the applied alternating current was 100 mHz for the polymer deposition, while a frequency value of 50 mHz was used for the in situ electrodeposition of Ag and Au nanoparticles. The selected frequency values ensured the successful preparation of the composite materials. The use of readily available composite materials is intended to produce cost-effective analytical tools. The judicious modification of the organic conductive matrix by various metallic nanoparticles, such as Ag and Au, extends the potential applications of the sensing platform toward a range of biomolecules like quercetin and epinephrine, chosen as benchmark analytes for proof-of-concept antioxidant and neurotransmitter detection. The sensing platforms were tested successfully for quercetin and epinephrine determination on synthetic and real samples. Wide linear response ranges and low limit-of-detection values were obtained for epinephrine and quercetin detection.

Cu-doped NiCo2S4/Kochia biomass porous carbon electrode material with high performance for hybrid supercapacitors

The suitable strategy combining metal doping and the introduction of porous carbon as a conductive substrate is proposed to address the shortcomings of the nickel‑cobalt sulfide (NiCo2S4) electrode material under development for supercapacitor energy storage. The multiplicative performance and cycle stability of NiCo2S4 have been significantly enhanced by the low cost and outstanding conductivity of copper (Cu) as a dopant. As well, the incorporation of Kochia biomass porous carbon (KAC-5), which has made it feasible to recycle waste biomass, into Cu-doped NiCo2S4 has effectively addressed the structural stability and electrochemical performance issues of NiCo2S4 electrode. The results showed that the introduction of Cu effectively optimizes the electrochemical properties by modifying the electronic state of the NiCo2S4 electrode to achieve the desired outcome. A composite material (Cu-NCS-10) was produced by adding KAC-5, due to the effects of KAC-5 on its geometry and electronic state, as well as its unique surface and structural characteristics, Cu-NCS-10 exhibits highly desirable energy storage. In comparison to the NiCo2S4 electrode, the Cu-NCS-10 electrode enhances specific capacity at 1 A·g−1 from 627C·g−1 to 754C·g−1, rate capability increased from 78.2 % to 88.1 % (1 A·g−1 to 10 A·g−1), and capacity retention after 5000 cycles from 75.9 % to 83.7 %. The electrochemical performance of the hybrid supercapacitor Cu-NCS-10||KAC-5 showed a wider voltage window, an energy density of up to 46.3 Wh·kg−1 at a power density of 775 W·kg−1, and maintenance of 80.9 % after 5000 cycles.

One-Step synthesis of nanosized Cu-Ag films using atmospheric pressure plasma jet

Thin films of copper-silver (Cu-Ag) composed of nanosized particles were successfully synthesised and deposited on glass and carbon substrates under various metal ratios in a single step using an atmospheric pressure plasma jet (APPJ) system. This rapid synthesis and deposition technique only requires very low power input (20 W) and rudimentary solutions of metal salt precursors and DI water without additives, pretreatment, or post-treatment process. Successful Cu-Ag alloying was observed, with excellent compositional and deposition area control. Strongly adherent films can be formed on conductive and non-conductive substrate, making APPJ an ideal and sustainable approach for large-scale deposition of multi-component thin metallic films. A comprehensive characterisation of Cu-Ag alloys deposited using APPJ and their potential use as electrocatalytic CO2 reduction catalysts is discussed.

Plasma-induced, N-doped, and reduced graphene oxide–incorporated NiCo–layered double hydroxide nanowires as a high-capacity redox mediator for sustainable decoupled water electrolysis

Although the recent emergence of decoupled water electrolysis prevents typical H2/O2 mixing, the further development of decoupled water electrolysis has been confined by the lack of reliable redox mediator (RM) electrodes to support sustainable H2 production. As energy storage electrodes, layered double hydroxides (LDHs) possess inherently poor conductivity/stability, which can be improved by growing LDHs on graphene substrates in situ. The proper modification of the graphene surface structure can improve the electron transport and energy storage capacity of composite electrodes, while current methods are usually cumbersome and require high temperatures/chemical reagents. Therefore, in this study, dip coating was adopted to grow graphene oxide (GO) on nickel foam (NF). Then, the GO was reduced using nonthermal plasma (NTP) to reduced GO (rGO) in situ while simultaneously implementing N doping to obtain plasma-assisted N-doped rGO on NF (PNrGO/NF). The uniform conductive substrate ensured the subsequent growth of less-aggregated NiCo-LDH nanowires, which improved the conductivity and energy storage capacity (5.93 C/cm2 at 5 mA/cm2) of the NiCo-LDH@PNrGO/NF. For the decoupled system, the composite RM electrode exhibited a high buffering capacity for 1300 s during the decoupled H2/O2 evolution, and in the conventional coupled system, the necessary input voltage of 1.67 V was separated into two lower ones, 1.42/0.33 V for H2/O2 evolutions, respectively. Simultaneously, the RM possessed outstanding redox reversibility and structural stability during long-term cycling. This work could offer a feasible strategy for using NTP to synthesize excellent RM electrodes for application to decoupled water electrolysis.

Out-of-plane preferential growth of 2D molybdenum diselenide nanosheets on laser-induced periodic surface structures

In this study, we explore the morphology and orientation of molybdenum diselenide, a Van der Waals 2D material, through isothermal closed space vapor deposition on both pristine and laser-structured substrates. Laser structuring is conducted on dielectric (sapphire), semiconductor (silicon), and conductive (titanium nitride) substrates using ultrashort laser pulses, resulting in smooth topographic changes such as laser-induced periodic surface structures (LIPSS) or selective ablation. Scanning electron microscopy (SEM) reveals the pivotal role of surface structuring in the growth of out-of-plane MoSe2 nanosheets. This effect is particularly pronounced on monocrystalline substrates like sapphire and silicon, exhibiting in-plane growth on pristine substrates. Additionally, Raman spectroscopy confirms the vertical orientation of flakes on structured substrates and highlights the presence of active edge sites by demonstrating an increased abundance of deposited material. Overall, our findings emphasize the controllability of directing the growth of MoSe2 flakes through appropriate pre-treatment of the substrate, with potential applications in various fields, including Surface-Enhanced Raman Scattering (SERS). Furthermore, the scalability, reproducibility, and applicability to any substrate make ultrashort laser structuration a promising general strategy for orienting 2D materials.

Highly Thermally Conductive Super-Aligned Boron Nitride Nanotube Films for Flexible Electronics Thermal Management.

Flexible electronics toward high integration, miniaturization, and multifunctionality, leading to a dramatic increase in power density. However, the low thermal conductivity of flexible substrates impedes efficient heat dissipation and device performance improvement. In this work, we propose a template-assisted chemical conversion strategy for obtaining boron nitride nanotube (BNNT) films with high thermal conductivity and great flexibility. Aligned carbon nanotube (CNT) films have been adopted as templates; a low-temperature chemical conversion followed by a high-temperature annealing has been carried out to produce a highly ordered BNNT film. Benefiting from the high orientation order, the BNNT film exhibits an exceptional thermal conductivity of 45.5 W m-1 K-1 and presents excellent heat dissipation capability, much superior to the commonly used polyimide film. Furthermore, the BNNT film demonstrated excellent flexibility and high insulation resistance. The test of integration with film resistors demonstrated its potential as a thermally conductive substrate for electronics cooling. This work provides a solution for the effective thermal management of flexible electronics.

UV–Vis photodetector based on electrospun MgFe2O4 microfibers

Photodetector is an essential component in the effort to develop optoelectronic information system. Magnesium ferrite (MgFe2O4) with a band gap around 1.9 eV is expected to serve as a good photosensitive semiconductor for UV–Vis photodetectors. Here, the first MgFe2O4 microfibers based photodetector was demonstrated by combining the unique one-dimensional morphology of microfibers and the photoelectric conversion performance of MgFe2O4 semiconductor. The uniform MgFe2O4 microfibers were prepared by electrospinning method and then transferred to the FTO (fluorine-doped tin oxide) conductive substrate to obtain the simple photodetector. The device exhibited nearly linear response to 360 nm UV light with a maximum responsivity of 63.1 μA/W. It also showed a significant response to 450 nm blue light. Our findings not only provide a feasible path for constructing MgFe2O4 based photodetector but also open up a brand new application field of MgFe2O4 semiconductor.

Cerium-doped Nickel SulfideNanospheres as EfficientCatalysts for Overall Water Splitting.

The development of non-precious metal electrocatalysts with excellent activity and durability for electrochemical water splitting has always been a goal. Transition metal sulfides are attractive electrocatalysts for both hydrogen evolution reaction (HER) and oxygen evolution reaction(OER). In this article, we designed and constructed efficient catalysts with multiple synergistic interactions and synthesized Ce-NiS2@NFnanosphere using a solvothermal method. Ce-NiS2@NF exhibits excellent HER performance, OER performance, and overall water splitting capability in alkaline electrolytes, demonstrating good stability. The addition of Ce influences the activity of the catalysts, attributed to the synergistic interactions creating more active sites and higher intrinsic activity through the introduction of Ce heteroatoms. Additionally, the self-supported conductive substrate promotes electron transfer, enhancing the intrinsic activity and active site density of the catalyst.This study provides an in-depth investigation into structural design and performance enhancement, offering ideas for designing efficient catalysts for overall water electrolysis. This work provides an in-depth study in terms of structural design performance enhancement and provides ideas for designing efficient alkaline bifunctional catalysts. Valuable insights have been provided in elucidating the intrinsic mechanism of the catalytic activity of cerium-doped nickel sulfidenanospheres,thus providing new guidance in the field of energy conversion technology.

Reduced graphene oxide nanosheets as electron sink for MnFe2O4 nanoparticles: A synergistically boosted supercapacitance

Spinel ferrite structures have shown promise for energy storage. However, they are insulators and need a conductive substrate for better charge transfer. Here, we utilized a simple hydrothermal technique to in-situ coat a nickel foam with few-layer nanosheets of reduced graphene oxide (rGO) decorated with manganese ferrite (MnFe2O4) nanoparticles. We then studied the supercapacitance/pseudocapacitance properties of the rGO/MnFe2O4 composite. X-ray diffraction patterns, energy-dispersive X-ray maps, and X-ray photoelectron spectra of the composite were investigated to confirm its structural, elemental, and surface chemical composition, respectively. Scanning electron microscopy and transmission electron microscopy images demonstrated the decoration of rGO nanosheets with MnFe2O4 nanoparticles. In a three-electrode setup, the rGO/MnFe2O4 nanocomposite exhibits a specific capacitance per loaded material mass (2446 F/g at 1 A/g) which is higher than the sum of rGO (304 F/g) and MnFe2O4 (1084 F/g) electrodes, suggesting a synergistic effect between rGO and MnFe2O4. The energy density and power density of the rGO/MnFe2O4 electrode were also calculated 58.24 Wh/kg and 260.82 W/kg (at 1 A/g), respectively. We found that the resistance of the rGO/MnFe2O4 electrode (2.53 Ω) is much lower than the MnFe2O4 electrode (6.15 Ω), and the interfacial resistance of the rGO/MnFe2O4 electrode with electrolyte was found low, confirming the rGO role as a conductive substrate for insulating MnFe2O4 nanoparticles. We also showed that surface-related capacitance, rather than pseudocapacitance, is more dominant in the rGO/MnFe2O4 composite electrode than in the separate rGO and MnFe2O4 electrodes. We also demonstrated the practical performance of the rGO/MnFe2O4 electrode in a two-electrode setup. Finally, density functional theory calculations showed the considerable potential drop (16.5 eV) between MnFe2O4 and graphene that leads to a strong built-in electric field from graphene towards MnFe2O4. This indicates the role of graphene as a wide electron sink for MnFe2O4 nanoparticles that results in better charge distribution and storage.

Persulphate assisted photoelectrochemical degradation of organic pollutants in water on a silver nanoparticle modified Cu2O photoanode

This work presents the photoelectrochemical production of sulphate radicals using fluorine-doped tine oxide – silver nanoparticles – copper(I) oxide (FTO-AgNPs-Cu2O) photoanode in the presence of peroxydisulphate salt for the enhanced degradation of selected organic pollutants in water. Firstly, Cu2O was prepared via a facile and template-free one-pot method, then AgNPs were photo-reduced on the surface of the Cu2O, and the resultant product was immobilised on an FTO conductive substrate to form FTO-AgNPs-Cu2O photoanode. When the electrode was applied for the abatement of tetracycline in the presence of 3 mM peroxydisulphate salt and 1.5 V external potential, the degree of tetracycline degradation and mineralisation after 90 min was 82 % and 78 % respectively. Furthermore, the same system was able to achieve degradation of 81 % sulfamethoxazole degradation within 90 min and 100 % orange II dye degradation within 30 min. The photoanode was efficient in the treatment of real wastewater containing tetracycline. Scavenger studies reveal that holes, hydroxyl, and sulphate radicals significantly participated in the degradation process. The electrode is stable and therefore applicable for the abatement of other organic pollutants in a persulphate-assisted photoelectrochemical degradation system.

Analyze photocatalytic degradation of methylene blue using TiO2 deposited onto conductive and non-conductive substrates under UV-C light

Abstract Degradation of methylene blue has been extensively studied by using TiO2 thin film as photocatalyst deposited onto non-conductive substrates. In this research, we proposed to utilize TiO2 thin film deposited onto conductive substrate, i.e., PCB. We compared concentration degradation between TiO2 thin film deposited onto conductive and non-conductive substrates. In this study, a photocatalysis process was carried out to decompose methylene blue pollutants. This research aims to obtain the performance of TiO2 photocatalyst coated with spray coating method on conductive and non-conductive substrates using UV-C light. This research begins with the manufacture of photocatalysis reactor, manufacture and coating of substrate, manufacture of methylene blue solution, concentration calculation. In this study, two types of thin layer substrates were made using the spray coating method. The first substrate is made using acrylic material as a non-conductive substrate, the second material uses a conductive substrate, PCB. The results shows that concentration of conductive and non-conductive substrates decreases 51% and 33,3 %, respectively. Therefore, conductive substrate may increase photocatalytic process. The use of substrates that are conductors can conduct electrons well, so that when interacting with TiO2, electrons generated by the photocatalysis process can move more easily. Acrylic and PCB materials are distinguished based on the ability to conduct electricity. Acrylic as an insulator and PCB acts as a conductor substrate.

Core-shell NiCo2S4@C with three dimensional carbon frameworks for enhanced asymmetrical supercapacitor and lithium storage performance

Transition-metal sulfides have been considered as promising candidates for electrochemical supercapacitor and lithium ion batteries. Unfortunately, the shortcomings including large volume change, low conductivity as well as severe structural exfoliation from conductive substrate or current collector inhibit their practical application. Herein, the hydrothermal and solvothermal approach are developed for the controllable synthesis of core-shell NiCo2S4@C with three dimensional carbon frameworks. As an asymmetric supercapacitor, the NiCo2S4@C/YP-50 F displays a high energy density of 46.7 Wh kg−1 at a power density of 0.8 kW kg−1 and the good cycling stability (∼110 % of the initial capacitance retention at 16 kW kg−1 over 2000 cycles). Furthermore, the NiCo2S4@C exhibits the specific capacity of 414 mAh g−1 after 500 cycles at 2000 mA g−1 when evaluated as anode for lithium ion batteries. The excellent performance can be ascribed to the core-shell structure and the three dimensional carbon frameworks. The synthetic approach can be extended to fabricate other high performance metal sulfides for energy storage.

Influence of precursor aging and condensation progression on silica thin films grown by electrochemically induced sol-gel deposition

Electrochemically induced sol-gel enables the fast synthesis of functional oxide coatings. In the case of silica, the condensation reaction can be catalysed by electrogenerated hydroxides. Using this technique, highly organized nanostructured thin films can be deposited onto conductive substrates by combining structure-directing templates with the electrochemically induced silica sol-gel process that occurs locally at the electrode surface. This specific template-directed process, called electrochemically assisted self-assembly (EASA), utilizes a sol-gel precursor solution optimized for a minimal spontaneous condensation (and gelation) rate in the absence of an electrochemical trigger. Despite the slow kinetics of the condensation reaction, the solution remains unstable and some incipient condensation reactions will still occur over time, continuously modifying the Si(IV) precursor solution. In this work, we discuss how precursor's aging affects the deposition rate and the properties of the deposited coatings. Two distinct aging effects are observed: an aging effect which occurs over time and an aging effect which occurs through electrochemical activation during preceding depositions. Both these aging effects result in accelerated film growth rates, up to 200 × faster than the deposition rate from a fresh precursor solution. Additionally, it was observed that time aging yields less resistive, weaker films, while electrochemical aging leads to films which retain similar properties as films grown using fresh precursor solutions. The time aging effect could be inhibited by storing the precursor solution at -35 °C. These observations are explained based on the different condensation pathways during acidic and alkaline condensation, which is known to yield inherently different silica oligomer products. The results and insights described here contribute to upscaling the electrochemical sol-gel process for mesoporous silica films and provides further fundamental insights into the underlying silica condensation reactions.

From Bulk to one-dimensional MoS2 nanochains: evolution of electronic, mechanical, and optical properties

We theoretically investigate the stability of a MoS2 nanochain, reporting its electronic, mechanical, and optical properties. The nanochain presents a semiconductor structure with a minute band gap of 67m eV compared to the larger gap bulk and monolayer structures. It is more malleable, enduring a maximum compressive (tensile) strain of 6% (6.5%). It is dynamically stable, showing no negative frequencies along its Brillouin zone (BZ) path. The nanochain is thermally stable at 300K, making it possible to synthesize as a freestanding structure. The optical properties of the bulk, monolayer, and 1D MoS2 materials are evaluated using the time-dependent density functional perturbation theory (TDDFPT) and compared to those determined via the independent particle approximation (IPA). Along the nanochain’s periodic x direction, the reflectivity retains a maximum value of ∼68% in the infrared (IR) region. Furthermore, its optical conductivity also exhibits a peak within the IR regime. These two features make such nanochains suitable as coating materials in applications involving infrared radiation or can even be exploited as conductive substrates in near-IR devices.

Synthesis by design and application to desalination of VO2/CTAB-Ti3C2 capacitive deionization electrode

As an emerging technology in capacitive deionization (CDI), flow-electrode capacitive deionization (FCDI) has attracted much attention due to its unlimited electrosorption capacity and continuous operation. Like CDI, carbon is generally chosen as the electrode material for FCDI at this stage, but conventional carbon materials have limited desalination capacity due to the double electric layer. The two-dimensional layered material MXene has been gradually applied to CDI due to its unique structure and physicochemical properties. However, the van der Waals forces exist between the MXene layers, and the layered structure of MXene is susceptible to stacking, while exhibiting an obvious swelling behavior in aqueous solution, thus affecting its desalination performance. Herein, we report a designed VO2/CTAB-Ti3C2 heterostructure synthesised by a simple hydrothermal method. The addition of VO2 can alleviate the lamellar structure buildup of Ti3C2 and improve the desalination performance of Ti3C2. On the other hand, Ti3C2 can be used as a conductive substrate for VO2, which improves the charge transfer rate of VO2, prevents VO2 agglomeration, and provides more contact surfaces for ion intercalation. Compared with the pure VO2 and Ti3C2 electrodes, the composite electrode has a good desalination performance, and its desalination reaches 1041.5 mg g−1 at 1.2 V. Therefore, this VO2/CTAB-Ti3C2 hybrid material is expected to be used as an electrode material for flow capacitive deionization.

Photoelectrochemical properties of doped TiO2 nanowires grown by seed-assisted thermal oxidation

Titanium dioxide Nanowires (NWs) are particularly interesting because of their very high surface/volume ratio and their photocatalytic activity allows them to be used in a myriad of applications. This manuscript presents a study of nanowires grown on a conductive substrate making use of a seed-assisted thermal oxidation process. To obtain doped NWs, before the oxidation, metallic titanium was doped with Fe (or Cr) by ion implantation technology. Analyses showed good quality Rutile phase and light absorption in the visible range. Transport properties of the NWs/electrolyte junction were investigated by using linear sweep voltammetry and electrochemical impedance spectroscopy. They allowed us to measure the photovoltage and the barrier height of the junction. We also evaluated the density of hole trap states at the interface during illumination. Electrical results indicate that the formation of deep levels, induced by doping, influences the electron concentration in the TiO2 and the transport properties.Graphical abstract

Bisphosphonate-Anchored Self-Assembled Molecules with Larger Dipole Moments for Efficient Inverted Perovskite Solar Cells with Excellent Stability.

In the fabrication of inverted perovskite solar cells (PSCs), the wettability, adsorbability, and compactness of self-assembled monolayers (SAMs) on conductive substrates have critical impacts on the quality of the perovskite films and the defects at the buried perovskite-substrate interface, which control the efficiency and stability of the devices. Herein, three bisphosphonate-anchored indolocarbazole (IDCz)-derived SAMs, IDCz-1, IDCz-2, and IDCz-3, are designed and synthesized by modulating the position of the two nitrogen atoms of the IDCz unit to improve the molecular dipole moments and strengthen the π-π interactions. Regulating the work functions (WF) of FTO electrodes through molecular dipole moments and energy levels, the perovskite band bends upwards with a small offset for ITO/IDCz-3/perovskite, thereby promoting hole extraction and blocking electrons. As a result, the inverted PSC employing IDCz-3 as hole-collecting layer exhibits a champion PCE of 25.15%, which is a record efficiency for the multipodal SAMs-based PSCs. Moreover, the unencapsulated device with IDCz-3 can be stored for at least 1800 h with little degradation in performance.

Exploration of Controllable Poring and Oscillation Phenomenon on FTO Conductive Substrates with Electrochemical Cathodization

Exploration of Controllable Poring and Oscillation Phenomenon on FTO Conductive Substrates with Electrochemical Cathodization

Organic Mixed Ionic-Electronic Conductors Based on Tunable and Functional Poly(3,4-ethylenedioxythiophene) Copolymers.

Organic mixed ionic-electronic conductors (OMIECs) are being explored in applications such as bioelectronics, biosensors, energy conversion and storage, and optoelectronics. OMIECs are largely composed of conjugated polymers that couple ionic and electronic transport in their structure as well as synthetic flexibility. Despite extensive research, previous studies have mainly focused on either enhancing ion conduction or enabling synthetic modification. This limited the number of OMIECs that excel in both domains. Here, a series of OMIECs based on functionalized poly(3,4-ethylenedioxythiophene) (PEDOT) copolymers that combine efficient ion/electron transport with the versatility of post-functionalization were developed. EDOT monomers bearing sulfonic (EDOTS) and carboxylic acid (EDOTCOOH) groups were electrochemically copolymerized in different ratios on oxygen plasma-treated conductive substrates. The plasma treatment enabled the synthesis of copolymers containing high ratios of EDOTS (up to 68%), otherwise not possible with untreated substrates. This flexibility in synthesis resulted in the fabrication of copolymers with tunable properties in terms of conductivity (2-0.0019 S/cm) and ion/electron transport, for example, as revealed by their volumetric capacitances (122-11 F/cm3). The importance of the organic nature of the OMIECs that are amenable to synthetic modification was also demonstrated. EDOTCOOH was successfully post-functionalized without influencing the ionic and electronic transport of the copolymers. This opens a new way to tailor the properties of the OMIECs to specific applications, especially in the field of bioelectronics.