Electrochemical Polymerization Research Articles

An ambipolar PEDOT-perfluorinated porphyrin electropolymer: application as an active material in energy storage systems.

The development of functional organic materials is crucial for the advancement of various fields, such as optoelectronics, energy storage, sensing, and biomedicine. In this context, we successfully prepared a stable ambipolar perfluoroporphyrin-based polymeric film by electrochemical synthesis. Our strategy involved the synthesis of a novel tetra-pentafluorophenyl porphyrin covalently linked to four 3,4-ethylenedioxythiophene (EDOT) moieties. The resulting monomer, EDOT-TPPF16, was obtained through a straightforward synthetic approach with a good overall yield. The unique molecular structure of EDOT-TPPF16 serves a dual function, with EDOT moieties allowing electropolymerization for polymeric film formation, while the electron-acceptor porphyrin core enables electrochemical reduction and electron transport. The electrochemical polymerization permits the polymer (PEDOT-TPPF16) synthesis and film formation in a reproducible and controllable manner in one step at room temperature. Spectroelectrochemical experiments confirmed that the porphyrin retained its optoelectronic properties within the polymeric matrix after the electrochemical polymerization. The obtained polymeric material exhibited stable redox capabilities. Current charge-discharge cycles and electrochemical impedance spectroscopy of the electrochemically generated organic film demonstrated that the polymer could be applied as a promising active material in the development of supercapacitor energy storage devices.

Layer-by-layer Fabrication of Gold Nanoparticles/Polyaniline Modified Gold Electrodes for Direct Non-enzymatic Oxidation of Glucose

Background: Non-enzymatic direct glucose biofuel cell is a promising technology to harness sustainable renewable energy. Furthermore, monitoring glucose levels is essential for human lives with age. Thus, there is an increasing need to develop highly efficient and stable modified electrodes. Methods: This study reported the manufacture of gold nanoparticles/polyaniline/modified gold electrodes (Au NPs/PANI/Au electrode) based on the electrochemical polymerization method followed by the deposition of gold nanoparticles. The shapes and chemical constitution of the electrodes were examined by using different techniques including SEM, FTIR, XRD, EDS, and Raman spectroscopy techniques. The electrocatalytic efficiency of the present electrodes toward direct glucose oxidation was evaluated by applying cyclic voltammetry, linear sweep voltammetry, and square wave voltammetry techniques. objective: fabrication of stable modified electrodes uses of the modified electrodes for renewable energy Results: The results exhibited high electrocatalytic performance for direct glucose electrooxidation in alkaline media. The modified electrodes show the ability to electrooxidation of various glucose concentrations (1 μM ̶ 100 μM) with a limit of detection and limit of quantitation of 140 nM and 424 nM, respectively. Furthermore, the Au NPs/PANI/Au electrode showed higher durability, sensitivity, and selectivity toward glucose oxidation than the Au NPs/ Au electrode, which confirmed the role of the PANI layer in enhancing the stability of the modified electrode. Conclusion: Moreover, the molar fraction of glucose to KOH has a crucial role in the output current. Hence, the modified electrodes are great candidates for direct glucose biofuel cell application. result: The electrocatalytic efficiency of the present electrodes toward direct glucose oxidation was evaluated by applying the cyclic voltammetry technique. The results exhibited high electrocatalytic performance for direct glucose electrooxidation in alkaline media. The modified electrodes show the ability to electrooxidation of various glucose concentrations (0.125M-2M). Furthermore, the Au NPs/PANI/Au electrode showed higher durability toward glucose oxidation than the Au NPs/ Au electrode, which confirmed the role of the PANI layer in enhancing the stability of the modified electrode. Moreover, the molar fraction of glucose to KOH has a crucial role in the output current.

Electrochemical polymerization of PEDOT:PSS with graphene oxide and silver nanoparticles for antibacterial coating and SERS detection

This study involved the use of electrochemical polymerization to coat poly(3,4-ethylenedioxythiophene) (PEDOT), polystyrene sulfonate (PSS) and graphene oxide (GO) onto SUS316L stainless steel substrates, aiming to produce PEDOT:PSS and GO@PEDOT:PSS films. Following this, Ag@PEDOT:PSS and GO/Ag@PEDOT:PSS films were developed through the electrochemical deposition of silver nitrate. Electrochemical impedance spectroscopy (EIS) indicated that adding GO increased the impedance of film, while AgNPs deposition decreased it, thereby enhancing conductivity. Films with AgNPs showed surface enhanced Raman scattering (SERS) effects, as assessed using malachite green (MG). Compared to films without GO, the GO/Ag@PEDOT:PSS films exhibit enhanced conductivity and SERS detection performance due to the negatively charged functional groups on the GO surface forming a continuous layer of AgNPs. Moreover, antibacterial capabilities were evaluated through bacterial attachment and inhibition zone assays. Both Ag@PEDOT:PSS and GO/Ag@PEDOT:PSS films were effective in inhibiting bacterial adhesion, achieving up to 99.4 % and 99.0 % inhibition, respectively. In the inhibition zone assays, the GO/Ag@PEDOT:PSS film showed a 1.33 times increase in antibacterial efficacy compared to Ag@PEDOT:PSS. Furthermore, the effectiveness of electrodepositing antibiotics on these substrates was investigated, confirming optimal antibacterial performance. This efficacy is attributed to the synergistic interaction between silver nanoparticles and antibiotics, potentially reducing the need for antibiotics. The findings of this study highlight its significant potential for applications in antibacterial treatments and biomedical detection.

Tunable optoelectronic performances of fluorinated benzene-EDOT based hybrid electrochromic polymers

Due to its high electronegativity and small atomic radius without undesirable steric hindrance, the incorporation of fluorine atoms into the benzene unit which started from the commercially available compounds is a feasible way to tune the energy levels of polymers, and its electrochromic application is expected to achieve a new breakthrough. Herein, in this paper, benzene units with different fluorine atom numbers were selected as the core and 3,4-ethylenedioxythiophene (EDOT) as the terminal unit, three fluorinated electrochromic precursors (FPh-EDOT, 2FPh-EDOT, and 4FPh-EDOT) were designed and synthesized by Stille coupling reaction, and the corresponding fluorinated π-conjugated electrochromic polymers (P(FPh-EDOT), P(2Ph-EDOT), and P(4FPh-EDOT)) were prepared by electrochemical polymerization method. The effects of different fluorinated benzene units on the photophysics, electrochemistry, and electrochromic properties of precursors and polymers were systematically investigated, and the structure-property relationship was further revealed. All of them have low initial oxidation potentials {FPh-EDOT (0.65 V), 2FPh-EDOT (0.72 V), and 4FPh-EDOT (0.70 V)}, which makes it easy to obtain high-quality new fluorinated polymers at low polymerization potential. With the increase of the number of F atoms, the UV–vis absorption spectra and emission spectra of fluorinated monomer firstly red-shifted and then blue-shifted. The corresponding fluorinated polymers have good electrochemical activity and stability (the P(2Ph-EDOT) activity remained 82.7% after 500 cycles), making it possible to realize their electrochromic devices. All these three fluorinated polymers show obvious color change from the neutral state to the fully oxidized state (P(FPh-EDOT) changes from brown to grayish blue, P(2FPh-EDOT) changes from brown to gray, and P(4FPh-EDOT) changes from dark blue to light blue). The kinetic study further shows that all of them have distinguish electrochromic properties with good optical stability, very short response time (0.9 s for P(2FPh-EDOT) at 700 nm), and favorable coloration efficiency (130.7 cm2 C−1 for P(FPh-EDOT) at 503 nm). Overall, all these three fluorinated polymers have low optical band gap, good redox stability and electrochromic properties, are very promising electrochromic materials, which is worthy for the further research and development.

Microenvironment regulation of electropolymerized Thiophene-Based conductive polymers for enhanced electrocatalyzed hydrogen evolutions and oxygen reductions

Herein, a series of thiophene-based conductive polymers were prepared through electrochemical polymerization processes, and their microenvironments were modulated by introducing triazine/benzene linkers and co-polymerizing with various hydrophilic thiophene derivatives. Importantly, the rationally designed polythiophene G-3TT-COOCH3 with electron-withdrawing triazine unit and most satisfied hydrophilic surface exhibits the satisfied electrochemically catalyzed hydrogen evolutions and selective oxygen reduction properties to H2O2 which are better than most of organic catalysts.

Properties and corrosion protection of polypyrrole prepared by electrochemical polymerization on aluminum

AbstractIn a one‐step procedure that did not require any surface preparation, polypyrrole (PPy) films doped with 3‐nitrosalicylic acid (3Nisa) became effectively electropolymerized on the aluminum substrate in aqueous solutions. Fourier transform infrared, scanning electron microscopy, and thermal gravimetric analysis were used to analyze the properties of PPy‐based films. Open circuit potential (OCP), electrochemical impedance spectroscopy, Tafel polarization, and salt spray tests were used to study the corrosion‐resistant efficiency of the coatings. The as‐prepared PPy films performed corrosion resistance on aluminum in the 3% NaCl solution. However, the PPy films prepared in the 0.01 m solution of 3Nisa showed the best protection ability on aluminum. The self‐healing characteristic of the PPy films was recorded by varying the potential in the OCP measurement. The findings indicate the potential of using 3‐nitrosalicylic acid‐doped PPy films for applications as anti‐corrosion coatings for aluminum.

A Portable Polymer‐based Sensor Platform for the Detection of Atrazine

AbstractDespite being banned by the European Union (EU), Atrazine, a synthetic herbicide, was found in Europe's coastal waters. Given the widespread ban on atrazine in many countries, it is imperative to perform screenings to detect its presence in food and water samples, as it poses significant risks to both human health and aquatic ecosystems. This study presents the development of an innovative, simple, and cost‐effective electrochemical sensing platform that comprises a portable system equipped with a poly‐8‐Amino‐1‐naphthol‐3,6‐disulfonic acid (8‐ANDSA) customized carbon paste electrode (CPE). The poly‐8 ANDSA/CPE was acquired using the process of electrochemical polymerization, utilizing cyclic voltammetry (CV) over the potential domain of −0.8 V to 1.8 V for 25 sweep cycles. The poly‐8‐ANDSA/CPE exhibited a linear relationship between the square wave voltammetric (SWV) peak current amplitude and ATZ concentration within 0.1–100 μM. The limit of detection for ATZ was determined to be 30 nM. Spiked recovery results of 97.71 % to 102.73 % with RSD (%) values less than 5 % validated the method‘s applicability for atrazine detection from water samples. The favorable outcomes indicated that the portable system performs exceptionally well and validates the practicality of ATZ detection, facilitating on‐site detection in actual water samples.

Self-Powered UV Photodetector Construction of the P(EDOS-TTh) Copolymer-Modified ZnO Nanoarray.

To solve the problem that zinc oxide nanorods (ZnO NRs)-based self-powered ultraviolet (UV) photodetectors cannot obtain both higher responsiveness and shorter response time, P(EDOS-TTh) was prepared using 3,4-ethylenedioxyselenphene (EDOS) and terthiophene (TTh) as copolymers, which modify the ZnO NRs surface, and the ZnO/P(EDOS-TTh) P-N junction self-powered UV device is assembled. The effect of the number of electrochemical polymerization cycles on the UV photodetection performance of ZnO/P(EDOS-TTh) P-N heterojunction was studied by adjusting the number of electrochemical polymerization cycles at the monomer molar ratio of 1:1. Benefiting from the enhanced built-in electric field of the ZnO/P(EDOS-TTh) interface, balancing photogenerated carriers, and charge separation and transport. The results show that the contact between N-type ZnO NRs and P-type P(EDOS-TTh) is best when the number of polymerization cycles is 3, due to the fact that EDOS-TTh and ZnO NRs form excellent P-N heterojunctions with strong internal electric fields, and the devices show good pyroelectric effect and UV photodetection performance. Under 0 V bias and 0.32 mW/cm2 UV irradiation, the responsivity (R) of ZnO/P(EDOS-TTh) reaches 3.31 mA/W, the detectivity (D*) is 7.25 × 1010 Jones, and the response time is significantly shortened. The rise time is 0.086 s, which exhibited excellent photoelectric properties and stability. UV photodetection performance with high sensitivity and fast response time is achieved.

Ultra-Stable High-Capacity Polythiophene Derivative for Wide-Potential-Window Supercapacitors.

Conducting polymer (CP)-based supercapacitors show great promise for applications in the field of wearable and portable electronics. However, these supercapacitors face persistent challenges, notably low energy density and inadequate stability. In this study, we introduce a polythiophene derivative, designated as poly(EPE), synthesized via the electrochemical polymerization of 8-bis(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)-3,3-dimethyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine (EPE). The resulting poly(EPE) polymer exhibits an exemplary 3D porous network-like structure, significantly enhancing its capacitance performance. When employed as the electrode material, the symmetric supercapacitor demonstrates an exceptionally high specific capacitance of 1342 F g-1 at a current density of 4.0 A g-1, along with impressive energy and power densities of 119.3 W h kg-1 and 38.83 kW kg-1, respectively. These capacitance values surpass those of previously reported pristine CP-based supercapacitors. Notably, the supercapacitor showcases outstanding stability, maintaining a retention rate of 92.5% even after 50,000 charge-discharge cycles. These findings underscore the substantial potential of poly(EPE) as an electrode material for the advancement of the supercapacitor technology.

Electrochemical Formation of Ionic Porous Organic Polymers Based on Viologen for Electrochromic Applications.

The systematic study of two ionic porous organic polymers (iPOPs) based on viologens and their first applications in the electrochromic field are reported. The viologen-based iPOPs were synthesized by electrochemical polymerization with cyano groups, providing a simple and controllable method for iPOPs which solves the film preparation problems common to viologens. After characterisation of these iPOPs a detailed study of their electrochromic properties was conducted. The iPOPs films based on viologens structure exhibit excellent electrochromic properties. In addition, the resulting iPOPs films show highly sensitivity to electrolyte ions of different sizes in the redox process. Electrochemical and electrochromic data of the iPOPs explain this phenomenon in detail. These results demonstrate that iPOPs of this type are ideal candidates as electrochromic materials due to their inherent porous structures and ion-rich properties. This article is protected by copyright. All rights reserved.

Smart polyurethane endosponges for endoluminal vacuum therapy: Integration of a bacteria sensor

The development of smart biomedical devices as efficient tools in early diagnosis and therapy monitoring has recently witnessed unprecedented growth, becoming an emerging field in biomedical engineering. Sponges for endoluminal vacuum therapy, which are intended for transmitting negative pressure as trigger for tissue regeneration and for draining infections in anastomotic leakages, are massively used implants with very complex geometry and high risk of infection. In this work, commercial polyurethane (PU) sponges have been converted into smart biomedical devices by incorporating an electrochemical sensor to monitor the growth of bacteria. Such innovative approach, which allows to track the tissue healing process avoiding further infection development, has been performed applying a three-step process: 1) activation of PU using low pressure oxygen plasma; 2) incorporation of conducting polymer (CP) nanoparticles (NPs) at the surface of the activated PU by chemical oxidative polymerization; and 3) formation of a homogeneous electroactive coating using the CP NPs obtained in 2), as growth nuclei in an electrochemical polymerization. The functionalized PU sponge is able to monitor the bacteria growth in the surrounding media by detecting the concentration of nicotinamide adenine dinucleotide (NADH) from respiration reactions in the cytosol (i.e. bacteria do not have mitochondria). Conversely, respiration in normal eukaryotic cells takes place in the mitochondria, whose double membrane is not permeable to NADH. The sensing performance of the CP-coated PU sponges (limit of detection: 0.06 mM; sensitivity: 1.21 mA/cm2) has been determined in the lab using NADH solutions, while a proof of concept have been conducted using Escherichia coli bacteria cultures.

Biphasic nanocomposite films of polypyrrole and poly(3,4-ethylene dioxythiophene) using a surface-tethered dopant strategy

Using a newly invented surface-tethered dopant approach for the electrochemical polymerization growth of conductive polymer films, nanocomposites are created consisting of two distinct phases of polypyrrole (PPy) and Poly(3,4-ethylene dioxythiophene) (PEDOT). The growth of the conductive nanocomposite films takes advantage of the unique way in which a conductive polymer film forms when grown using a surface-tethered dopant, starting out as a highly nanoporous film that gradually becomes more and more solid as additional polymer deposition occurs preferentially within the nanopores rather than at the films outer surface. Nanocomposite films can thus be fabricated simply and controllably by first growing one nanoporous conductive polymer film followed by the deposition of a second conductive polymer within the nanopores of the first. This study investigates the morphological and electrochemical properties of nanocomposite films grown using a surface-tethered dopant and how these properties are affected by simple changes in electrochemical polymerization parameters.

An ionic liquid-modified PEDOT/Ti3C2TX based molecularly imprinted electrochemical sensor for pico-molar sensitive detection of L-Tryptophan in milk

L-Tryptophan (L-Trp) is essential for the human body and can only be obtained externally. It is important to develop a method to efficiently detect L-Trp in food. In this work, ionic liquid (IL) modified poly(3,4-ethylendioxythiophene)/ Titanium carbide (PEDOT/Ti3C2TX) was used as a substrate material to improve detection sensitivity. Molecular imprinted polymers (MIP) film for specific recognition of L-Trp was fabricated on the surface of modified electrodes using electrochemical polymerization. The monitoring results showed that the molecularly imprinted electrochemical sensors (MIECS) exhibited good linearity ranges (10−6 - 0.1 μM and 0.1–100 μM) with a low detection limit (LOD) of 2.09 × 10−7 μM. In addition, the MIECS exhibited remarkable stability, reproducibility, and immunity to interference. A good recovery (93.54–99.59%) was demonstrated in the detection of milk. The sensor was expected to be developed as a highly selective and sensitive portable assay, and applied to the detection of L-Trp in food.

A novel molecularly imprinted electrochemical sensor from poly (3, 4-ethylenedioxythiophene)/chitosan for selective and sensitive detection of levofloxacin

The improper usage of levofloxacin (LEV) endangers both environmental safety and human public health. Therefore, trace analysis and detection of LEV have extraordinary significance. In this paper, a novel molecularly imprinted polymer (MIP) electrochemical sensor was developed for the specific determination of LEV by electrochemical polymerization of o-phenylenediamine (o-PD) using poly(3,4-ethylenedioxythiophene)/chitosan (PEDOT/CS) with a porous structure and rich functional groups as a carrier and LEV as a template molecule. The morphology, structure and properties of the modified materials were analyzed and studied. The result showed that the electron transfer rate and the electroactive strength of the electrode surface are greatly improved by the interconnection of PEDOT and CS. Meanwhile, PEDOT/CS was assembled by imprinting with o-PD through non-covalent bonding, which offered more specific recognition sites and a larger surface area for the detection of LEV and effectively attracted LEV through intermolecular association. Under the optimized conditions, MIP/PEDOT/CS/GCE showed good detection performance for LEV in a wide linear range of 0.0019– 1000 μM, with a limit of detection (LOD, S/N = 3) of 0.4 nM. Furthermore, the sensor has good stability and selectivity, and exhibits excellent capabilities in the microanalysis of various real samples.

Introducing electrolytic electrochemical polymerization for constructing protective layers on Ni-rich cathodes of Li-ion batteries

Introducing electrolytic electrochemical polymerization for constructing protective layers on Ni-rich cathodes of Li-ion batteries

Different donors' effect on the electrochemical behavior and electrochromic performances of the D-A type chlorinated polymers

Chlorination has proved to be an efficient method in tuning energy levels and optoelectronic properties of organic semiconducting materials with cheaper synthesis and low-cost raw materials when compared with the fluorinated analogues. Herein, in this work, 5-chlorobenzo[c][1,2,5]thiadizole (Cl-BT) unit was chosen as a new acceptor unit to design two new D-A type electrochromic conjugated polymer: P(Cl-T) and P(Cl-EDOT). The electrochemical behavior and electrochromic performances of above-mentioned chlorinated polymers were studied by electrochemical polymerization techniques and spectroelectrochemistry. Thanks to the strong electron-withdrawing ability of Cl-BT unit and the strong electron-donating properties of EDOT unit, the resultant Cl-EDOT precursor could electropolymerize into high quality hybrid polymer films at lower potential (0.71 V vs. Ag/AgCl) with favorable redox activity and better redox stability. Spectroelectrochemistry shown that as-formed lower band gaps P(Cl-EDOT) exhibits reversible color-changing nature from pale blue to gray accompanied with the moderate optical contrast (13.9%), fast response time (0.6 s), and favorable coloration efficiency (126.4 cm2 C−1) in the NIR region that was measured from the kinetic studies. By optimizing the tested electrolyte and solution, its electrochromic performance is further improved (optical contrast: 25.6%, response time: 0.25 s, coloration efficiency: 275.9 C−1 cm2). The favorable redox stability and electrochromic performance of P(Cl-EDOT) make it a good candidate to construct electrochromic device, and Cl-BT unit should be a promising building block in designing high performance near infrared electrochromic materials.

Stimuli-responsive thin film composites of conducting polymers and cellulose nanocrystals for tissue engineering

Thin composite films comprising two primary representatives of conducting polymers, poly(3, 4-ethylenedioxythiophene) (PEDOT) and polypyrrole (PPy), with eco-friendly cellulose nanocrystals (CNC) were prepared through electrochemical polymerization. The combination of CNC and PEDOT (or PPy) results in the formation of films with highly different surface topography and thickness. Intriguingly, different surface conductivity of PEDOT and PPy was revealed by atomic force microscopy albeit that the electrochemical properties were rather similar. The biological properties of the composites in contact with prospective human induced pluripotent stem cells (hiPSC) and cardiomyocytes derived from hiPSC demonstrated good cytocompatibility of both composites and their potential in engineering of electro-sensitive tissues. The as-prepared conducting, eco-friendly and cytocompatible composites are thus promising candidates for biomedical applications where stimuli-responsivity is a crucial cell-instructive property.

Electrochemical synthesis of donor-acceptor triazine based polymers with halochromic and electrochromic properties

Two triazine monomers substituted with aromatic α,β unsaturated ketones (chalcones) as connecting arms, holding triphenylamine or carbazole ending groups, were by the first time synthesized using commercial and inexpensive starting materials in just two steps. Triphenylamine and carbazole groups were strategically introduced in order to allow electrochemical polymerization and redox activity of the obtained films. The chalcone, together with the triphenylamine or carbazole outer groups, give rise to the formation of a donor-acceptor systems, allowing the generation of photoinduced intramolecular charge transfer (ICT) electronic transitions and providing basic sites for protonation. Because of the star-like chemical structure of the used triazine, electrochemical polymerization of these monomers conducted to the formation of hyperbranched structures. The polymeric materials exhibited not only electrochromic properties but also showed a halochromic behavior. Spectroelectrochemical studies of the films showed different colorations in the three redox states (neutral, semioxidized and fully oxidized). The color changes are fast and easily detected by the naked eye. Electrochemical parameters such as optical contrast, coloration efficiency, optical memory, and long-term stability for both films were obtained and compared. A quasi-solid window-type electrochromic device was assembled using the electrogenerated polymer with the best electrochromic performance and stability. Moreover, the triphenylamine based polymer showed reversible color changes upon acid-base vapor exposure cycles, demonstrating that this polymer can be used not only in electrochromic devices but also in acid vapor sensors.

An Electrochemical Sensor Based on Simple Nano-Modification for Sensitive Detection of Ofloxacin Residue in Animal Derived Food

The residue of ofloxacin in animal derived food would seriously affect human health. This study reports an inexpensive, fast, and simple electrochemical sensor for the sensitive detection of OFL in animal derived food samples. A poly-L-glutamic acid/poly(sulfobutyl-β-cyclodextrin) CdTe quantum dot-modified electrode P(L-Glu)/SEB-β-CD@CdTeQDs/GCE was prepared by an electrochemical polymerization reaction. We investigated the electrochemical behavior of OFL on the sensing electrode by cyclic voltammetry and square wave voltammetry. The results showed that the sensitivity of the sensor was significantly improved under the synergistic effect of L-glutamic acid, sulfobutyl-β-cyclodextrin, and CdTe quantum dots. In addition, the electrochemical reaction process of OFL on the sensing electrode was investigated and the results showed that the transfers of two protons and two electrons were involved in the reaction. Subsequently, the electrochemical sensing method based on P(L-Glu)/SEB-β-CD@CdTeQDs/GCE was developed and validated for the determination of OFL, showing a good linear response in the range of 0.07 ∼ 1 μg·ml−1 with a detection limit of 3.4 ng·ml−1, and the precision and accuracy were high enough. Compared with the conventional HPLC method, the established electrochemical sensing method shows the merits of being eco-friendly, shorter detection time and being much more simple, sensitive, and convenient.

Porphyrin-Thiophene Based Conjugated Polymer Cathode with High Capacity for Lithium-Organic Batteries.

Organic electrode materials are promising for next-generation energy storage materials due to their environmental friendliness and sustainable renewability. However, problems such as their high solubility in electrolytes and low intrinsic conductivity have always plagued their further application. Polymerization to form conjugated organic polymers can not only inhibit the dissolution of organic electrodes in the electrolyte, but also enhance the intrinsic conductivity of organic molecules. Herein, we synthesized a new conjugated organic polymer (COPs) COP500-CuT2TP (poly [5,10,15,20-tetra(2,2'-bithiophen-5-yl) porphyrinato] copper (II)) by electrochemical polymerization method. Due to the self-exfoliation behavior, the porphyrin cathode exhibited a reversible discharge capacity of 420 mAh g-1, and a high specific energy of 900 Wh Kg-1 with a first coulombic efficiency of 96 % at 100 mA g-1. Excellent cycling stability up to 8000 cycles without capacity loss was achieved even at a high current density of 5 A g-1. This highly conjugated structure promotes COP500-CuT2TP combined high energy density, high power density, and good cycling stability, which would open new opportunity for the designable and versatile organic electrodes for electrochemical energy storage.