Ice-interface assisted large-scale preparation of polypyrrole/graphene oxide films for all-solid-state supercapacitors

In this paper, large-scale, self-standing polypyrrole/graphene oxide (PPy/GO) nanocomposite films were prepared by an environmentally friendly and easy-to-operate confined polymerization method, and were also assembled as electrode materials for symmetric all-solid-state supercapacitors. In this paper, large-scale, self-standing polypyrrole/graphene oxide (PPy/GO) nanocomposite films were prepared by an environmentally friendly and easy-to-operate confined polymerization method, and were also assembled as electrode materials for symmetric all-solid-state supercapacitors. The morphology, chemical structure and electrochemical property were characterized by field emission scanning electron microscope (FESEM), Fourier transform infrared spectroscopy (FTIR), cyclic voltammetry (CV), galvanostatic charge–discharge (GCD), and electrochemical impedance spectroscopy (EIS), respectively. The lamellar structure of GO and both strong interaction with ice and pyrrole could promote polymerization of pyrrole and improve the compactness of the film. With the aid of GO, the conjugation length of PPy increased, the resistance of the material decreased, and the electrochemical energy storage of the composite film was significantly enhanced. In the case of 2.5 wt% GO, the prepared PPy/GO nanocomposite supercapacitor exhibited a high area specific capacitance of 97.3 mF cm⁻² at 1 mA cm⁻². Furthermore, the PPy/GO film supercapacitor also showed excellent cycling stability and good flexibility.

A confirned polymerization method was employed to fabricate self-standing PPy/GO film for all-solid-state supercapacitor.     

Removal of fluoride ions using a polypyrrole magnetic nanocomposite influenced by a rotating magnetic field

The impact of a varying rotating magnetic field in stimulating adsorption of fluoride ions onto a polypyrrole magnetic nanocomposite synthesized via in situ a polymerization process was evaluated. Under the effect of a rotating magnetic field, improved removal of adsorbate (10 mg L⁻¹) from aqueous solution using the polypyrrole magnetic nanocomposite was observed, with a maximum removal of 78.2% observed at a magnetic field intensity of 0.019 T. Particle aggregation resulting from the force owing to the gradient on the particles as the magnetic field was increased resulted in improved fluoride removal. This aggregation of particles leads to an improved chain collision and expanse of particle interaction with the fluoride solution. The process of adsorption of fluoride by the PPy/Fe₃O₄ nanocomposite followed both the Freudlich isotherm and the Temkin isotherm. Interestingly, under the effect of the rotating magnetic field, the adsorption process was best described by the Freundlich isotherm.

The impact of a varying rotating magnetic field in stimulating adsorption of fluoride ions onto a polypyrrole magnetic nanocomposite synthesized via in situ a polymerization process was evaluated.     

A simple strategy to prepare a layer-by-layer assembled composite of Ni–Co LDHs on polypyrrole/rGO for a high specific capacitance supercapacitor

A facile and novel electrode material of nickel–cobalt layered double hydroxides (Ni–Co LDHs) layered on polypyrrole/reduced graphene oxide (PPy/rGO) is fabricated for a symmetrical supercapacitor via chemical polymerization, hydrothermal and vacuum filtration. This conscientiously layered composition is free from any binder or surfactants which is highly favorable for supercapacitors. The PPy/rGO serves as an ideal backbone for Ni–Co LDHs to form a free-standing electrode for a high-performance supercapacitor and enhanced the overall structural stability of the film. The well-designed layered nanostructures and high electrochemical activity from the hexagonal-flakes like Ni–Co LDHs provide large electroactive sites for the charge storage process. The specific capacitance (1018 F g⁻¹ at 10 mV s⁻¹) and specific energy (46.5 W h kg⁻¹ at 464.9 W kg⁻¹) obtained for the PPy/rGO|Ni–Co LDHs symmetrical electrode in the current study are the best reported for the two-electrode system for PPy- and LDHs-based composites. The outstanding performance in the prepared LBL film is a result of the LBL architecture of the film and the combined effect of redox reaction and electrical double layer capacitance.

A facile and novel electrode material of nickel–cobalt layered double hydroxides (Ni–Co LDHs) layered on polypyrrole/reduced graphene oxide (PPy/rGO) is fabricated for a symmetrical supercapacitor via chemical polymerization, hydrothermal and vacuum filtration.     

Nanocellulose/polypyrrole aerogel electrodes with higher conductivity via adding vapor grown nano-carbon fibers as conducting networks for supercapacitor application

Nanocellulose-based conductive materials have been widely used as supercapacitor electrodes. Herein, electrode materials with higher conductivity were prepared by in situ polymerization of polypyrrole (PPy) on cellulose nanofibrils (CNF) and vapor grown carbon fiber (VGCF) hybrid aerogels. With increase in VGCF content, the conductivities of CNF/VGCF aerogel films and CNF/VGCF/PPy aerogel films increased. The CNF/VGCF₂/PPy aerogel films exhibited a maximum value of 11.25 S cm⁻¹, which is beneficial for electron transfer and to reduce interior resistance. In addition, the capacitance of the electrode materials was improved because of synergistic effects between the double-layer capacitance of VGCF and pseudocapacitance of PPy in the CNF/VGCF/PPy aerogels. Therefore, the CNF/VGCF/PPy aerogel electrode showed capacitances of 8.61 F cm⁻² at 1 mV s⁻¹ (specific area capacitance) and 678.66 F g⁻¹ at 1.875 mA cm⁻² (specific gravimetric capacitance) and retained 91.38% of its initial capacitance after 2000 cycles. Furthermore, an all-solid-state supercapacitor fabricated by the above electrode materials exhibited maximum energy and power densities of 15.08 W h Kg⁻¹, respectively. These electrochemical properties provide great potential for supercapacitors or other electronic devices with good electrochemical properties.

The electrochemical performances of nanocellulose-based electrode materials were improved via building nano-carbon conducting networks.     

Palladium supported on a novel ordered mesoporous polypyrrole/carbon nanocomposite as a powerful heterogeneous catalyst for the aerobic oxidation of alcohols to carboxylic acids and ketones on water

Preparation of an ordered mesoporous polypyrrole/carbon (PPy/OMC) composite has been described through a two-step nanocasting process using KIT-6 as a template. Characterization of the PPy/OMC nanocomposite by various analysis methods such as TEM, XRD, TGA, SEM and N₂ sorption confirmed the preparation of a material with ordered mesoporous structure, uniform pore size distribution, high surface area and high stability. This nanocomposite was then used for the immobilization of palladium nanoparticles. The nanoparticles were almost uniformly distributed on the support with a narrow particle size of 20–25 nm, confirmed by various analysis methods. Performance of the Pd@PPy/OMC catalyst was evaluated in the aerobic oxidation of various primary and secondary alcohols on water as a green solvent, giving the corresponding carboxylic acids and ketones in high yields and excellent selectivity. The catalyst could also be reused for at least 10 reaction runs without losing its catalytic activity and selectivity. High catalytic efficiency of the catalyst can be attributed to a strong synergism between the PPy/OMC and that of supported Pd nanoparticles.

Aerobic oxidation of alcohols to carboxylic acids and ketones in water using palladium species supported on an ordered mesoporous polypyrrole/carbon nanocomposite.     

Facile preparation of a polypyrrole modified Chinese yam peel-based adsorbent: characterization,performance, and application in removal of Congo red dye

In this study, Chinese yam peel (CYP) was modified with polypyrrole via an in situ polymerization method to remove Congo red from aqueous media. The prepared CYP–polypyrrole (CYP–PPy) composite was characterized using FTIR, SEM, TEM, XRD, TG and BET analysis. The performance of CYP–PPy towards the adsorption of Congo red (CR) was explored in batch mode. The removal efficiency of CR was found to be 86% at the initial concentration of 100 mg L⁻¹, contact time of 120 min, and the adsorbent dosage of 10 g L⁻¹. At equilibrium time (20 h), the removal efficiency was significantly acceptable (98.9%). The adsorption kinetics data were most consistent with the pseudo-second-order kinetic model. The adsorption equilibrium data could be described well by the Langmuir isotherm model with the maximum adsorption capacity of 86.66 mg g⁻¹. In view of thermodynamics, the adsorption process was endothermic and more favorable for CR removal at 45 °C. A reusability study indicated that CYP–PPy could be reused effectively for up to three successive cycles of ad-/de-sorption. Hence, this work provides an alternative scheme for the targeted exploitation of agricultural waste to control dye pollution.

In this study, Chinese yam peel (CYP) was modified with polypyrrole via an in situ polymerization method to remove Congo red from aqueous media.     

Facile construction of a polypyrrole–cobalt sulfide counter electrode for low-cost dye-sensitized solar cells

A polypyrrole–cobalt sulfide composite counter electrode (CE) was prepared in this work. Firstly, polypyrrole (PPy) nanorods were prepared by an in situ polymerization method on FTO, then cobalt sulfide (CoS) nanoparticles were coated on PPy nanorods by the electrodeposition method. The DSSC with PPy–CoS CE exhibits superior photoelectric conversion efficiency than that based on platinum (Pt, one of common counter electrodes), which is 7.52%, improving more than 20% compared to Pt CE (6.19%). In addition, cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) measurements demonstrated that the PPy–CoS CE exhibited excellent catalytic performance for I₃⁻/I⁻ solution.

A facile two-step strategy to construct a polypyrrole–cobalt sulfide counter electrode for low-cost dye-sensitized solar cells.     

Construction of a graphene/polypyrrole composite electrode as an electrochemically controlled release system

A new class of stimuli responsive drug delivery systems is emerging to establish new paradigms for enhancing therapeutic efficacy. To date, most electro-responsive systems rely on noble metal electrodes that likely cause the limitations for implantation applications. Herein, a graphene/polypyrrole composite electrode (GN–PPy–FL) was fabricated based on two-dimensional (2D) graphene (GN) film and conductive and biocompatible polypyrrole (PPy) nanoparticles loaded with a negative drug model of fluorescein sodium (FL) via chemical oxidation polymerization. The conductive composite electrode was utilized as a drug carrier to realize the electrically controlled release of the FL. The release rate from conductive nanoparticles can be controlled by the applied voltages. The study provides a multi-stimuli responsive drug release system, demonstrating the potential applications of the controlled release of various drugs, peptides or proteins.

A biocompatible conductive composite electrode GN–PPy–FL can realize controlled release of a drug model triggered by low voltages.     

High-efficiency solid-phase microextraction performance of polypyrrole enhanced titania nanoparticles for sensitive determination of polar chlorophenols and triclosan in environmental water samples

In this work, a polypyrrole (PPy)/TiO₂ nanocomposite coating was fabricated by the direct electropolymerization of pyrrole on annealed TiO₂ nanoparticles and evaluated as a novel direct immersion solid phase microextraction (DI-SPME) fiber coating for extraction of trace amounts of pollutants in environmental water samples. The functionalized fiber is mechanically and chemically stable, and can be easily prepared in a highly reproducible manner. The effects of the pyrrole monomer concentration, polymerization voltage and polymerization time on the fiber were discussed. Surface morphological and compositional analyses revealed that the composite coating of nano polypyrrole and titanium dioxide nanoparticles (TiO₂NP_s) uniformly doped the Ti substrate. The as-fabricated fiber exhibited good extraction capability for phenolic compounds in combination with high performance liquid chromatography-UV detection (HPLC-UV). At the optimum SPME conditions, the calibration curves were linear (R² ≥ 0.9965). LODs and LOQs of less than 0.026 μg L⁻¹ and 0.09 μg L⁻¹ , respectively, were achieved, and RSDs were in the range 3.5–7.2%. The results obtained in this work suggest that PPy/TiO₂ is a promising coating material for future applications of SPME and related sample preparation techniques.

A PPy/TiO₂ nanocomposite coating was fabricated by direct electropolymerization of pyrrole on annealed TiO₂ nanoparticles and evaluated as a novel direct immersion solid phase microextraction fiber coating for the extraction of trace pollutants in water.     

Investigation on the role of different conductive polymers in supercapacitors based on a zinc sulfide/reduced graphene oxide/conductive polymer ternary composite electrode

Conductive polymers, such as polyaniline (PANI), polypyrrole (PPy), polythiophene (PTh) and poly 3,4-ethylenedioxythiophene (PEDOT), play an important role in the application of pseudocapacitors. It is necessary to explore the effects of different conductive polymers in electrode composites. Herein, we prepare zinc sulfide/reduced graphene oxide (ZnS/RGO) by the hydrothermal method, and conductive polymers (PANI, PPy, PTh and PEDOT) doped with the same mass ratio (polymer to 70 wt%) via in situ polymerization on the surface of ZnS/RGO composite. For the supercapacitor application, the ZnS/RGO/PANI ternary electrode composite possesses the best capacitance performance and cycle stability out of all of the polymer-coated ZnS/RGO composites. In the three-electrode system, the discharge specific capacitance and cycle stability of ZnS/RGO/PANI are 1045.3 F g⁻¹ and 160% at 1 A g⁻¹ after 1000 loops. In a two-electrode symmetric system, the discharge specific capacitance and cycle stability of ZnS/RGO/PANI are 722.0 F g⁻¹ and 76.1% at 1 A g⁻¹ after 1000 loops, and the greatest energy and power density of the ZnS/RGO/PANI electrode are 349.7 W h kg⁻¹ and 18.0 kW kg⁻¹. In addition, conductive polymers can effectively improve the voltage range of the electrode composites in 6 M KOH electrolyte for the two-electrode system. The discharge voltage ∼1.6 V makes them promising electrode materials for supercapacitors.

Conductive polymers, such as polyaniline (PANI), polypyrrole (PPy), polythiophene (PTh) and poly 3,4-ethylenedioxythiophene (PEDOT), play an important role in the application of pseudocapacitors.     

Photo-assisted synthesis of coaxial-structured polypyrrole/electrochemically hydrogenated TiO2 nanotube arrays as a high performance supercapacitor electrode

An organic–inorganic coaxial-structured hybrid of PPy/EH-TNTAs electrode with outstanding supercapacitive performance was developed by incorporating electroactive polypyrrole (PPy) into a highly-conductive TiO₂ substrate, namely, electrochemically hydrogenated TiO₂ nanotube arrays (EH-TNTAs) through a photo-assisted potentiodynamic electrodeposition route. The as-fabricated PPy/EH-TNTAs hybrid electrode achieves a specific capacitance of up to 614.7 F g⁻¹ at 1.0 A g⁻¹ with 87.4% of the initial capacitance remaining after 5000 cycles at 10 A g⁻¹, outperforming other fabricated PPy-TNTAs hybrid electrodes. The photoelectrodeposited and electrodeposited hybrid samples as well as the EH-TNTAs-based and air–TNTAs-based hybrid samples were fully compared from electropolymerization process, morphology, structural feature and electrochemical perspectives. The results indicate that the synergy of remarkably improved conductivity and electrochemical properties of the TiO₂ substrate induced by intentionally introduced Ti³⁺ (O-vacancies) as well as the homogenous and integrated deposition of PPy triggered by light illumination enabled the outstanding supercapacitive performance of the PPy/EH-TNTAs hybrid electrode. A symmetric supercapacitor device was assembled using the PPy/EH-TNTAs hybrid as both a positive and negative electrode, respectively. It displays a high energy density of 17.7 W h kg⁻¹ at a power density of 1257 W kg⁻¹. This organic–inorganic coaxial-structured PPy/EH-TNTAs electrode will be a competitive and promising candidate for application in future energy storage devices.

An organic–inorganic coaxial-structured hybrid of PPy/EH-TNTAs electrode was developed and applied for high performance supercapacitors.     

Facile one-pot method of AuNPs/PEDOT/CNT composites for simultaneous detection of dopamine with a high concentration of ascorbic acid and uric acid

In this research, a facile one-pot method was used to synthesize gold/poly-3,4-ethylene-dioxythiophene/carbon nanotube (AuNPs/PEDOT/CNTs) composite material. The composite material was investigated by Fourier Transform Infrared spectroscopy (FTIR), X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM). Then the synthesized nanocomposite material was dropped on a bare glassy carbon electrode (GCE) to improve the detection performance of dopamine with a high concentration of ascorbic acid and uric acid. The electrochemical behavior of AuNPs/PEDOT/CNTs/GCE was studied by Cyclic Voltammetry (CV), Differential Pulse Voltammetry (DPV) and electrochemical impedance spectroscopy (EIS). Under optimum conditions, AuNPs/PEDOT/CNTs/GCE showed a good linear response in the concentration range from 9.14 to 29.704 μM with a detection limit (LOD) and sensitivity of 0.283 μM and 1.557 μA μM⁻¹, respectively. This sensor was applied to detect practical samples with good average recovery. It also exhibited good reproducibility and stability.

A facile one-pot method was used to synthesize ternary composite material. This modified electrode exhibited good ability of detecting dopamine. It also exhibited excellent anti-interference ability and stability.      

PPy nanoneedle based nanoplatform capable of overcoming biological barriers for synergistic chemo-photothermal therapy

The biological barriers in vivo have limited the site-specific bioavailability and impeded therapeutic efficacy. To tackle these issues, nonspherical particles with a shape effect have attracted wide attention to affect the in vivo translocation of a drug delivery system. Herein, we constructed a nanoplatform based on polypyrrole (PPy) nanoneedles by hyaluronic acid (HA) modification and doxorubicin (DOX) loading. The PPy-HA@DOX nanoneedles with high aspect ratios could enhance the extravasation through the fenestrated vasculature of tumors, transport across tumor cell membrane via an endocytosis mechanism or even penetrated the membrane directly, and ultimately enter the nucleus easily via the nuclear pore complex by passive diffusion. With the ability of overcoming biological barriers, the PPy nanoneedle based nanoplatform would deliver drugs into the organelles more effectively. Under near infrared (NIR) laser irradiation, PPy as the photothermal agent could lead to tumor cellular structure damage for photothermal therapy (PTT). Therefore, PPy-HA@DOX developed here would exploit the merits of synergistic combination of chemo-photothermal therapy, which would pave the way toward more effective nanotherapeutics.

PPy nanoneedles based nanoplatform was capable of overcoming biological barriers for synergistic chemo-photothermal therapy.     

Tremella-like NiO microspheres embedded with fish-scale-like polypyrrole for high-performance asymmetric supercapacitor

Tremella-like NiO microspheres embedded with fish-scale-like polypyrrole (PPy) were synthesized by polymerizing pyrrole (Py) onto uniform NiO nanosheets. PPy has a fish-scale-like appearance with a thickness of approximately 10 nm, and is connected to the NiO nanosheet surface. NiO/PPy microspheres (diameter of ∼4 μm) were applied as the electrode material in a supercapacitor. The NiO/PPy-6 obtained under a NiO : Py molar ratio of 6 shows a high specific capacitance of 3648.6 F g⁻¹ at 3 A g⁻¹ and good rate capability (1783 F g⁻¹ at a high current density of 30 A g⁻¹). An asymmetric supercapacitor (ASC) was fabricated using NiO/PPy-6 and activated carbon (AC) as the positive electrode and the negative electrode, respectively. NiO/PPy-6//AC can achieve a high specific capacitance of 937.5 F g⁻¹ at 3 A g⁻¹ and a high energy density of 333.3 W h kg⁻¹ at a power density of 2399.99 W kg⁻¹. The excellent supercapacitor performance is assigned to the combined contribution of both components and the unique heterostructure in NiO/PPy-6.

Tremella-like NiO/fish-scale-like PPy was fabricated via a solvothermal process coupled with in situ polymerization. The NiO/PPy-6//AC asymmetric supercapacitor can achieve a high specific capacitance and maintain a specific capacitance at 88.2% after 10 000 cycles.     

Free-standing polypyrrole/polyaniline composite film fabricated by interfacial polymerization at the vapor/liquid interface for enhanced hexavalent chromium adsorption

Interfacial polymerization is an innovative technique for the fabrication of polymeric films. However, the majority of studies on interfacial polymerization has focused on liquid/liquid interfaces, and little work has been done on vapor/liquid interfaces. In this paper, we present the fabrication of free-standing polypyrrole/polyaniline (PPy/PANI) composite films by interfacial polymerization at a vapor/liquid interface using FeCl₃ as an oxidant. The obtained PPy/PANI composite films were characterized using Fourier transform infrared spectroscopy, X-ray diffractometry, and scanning electron microscopy. It was found that the PPy/PANI composite films consist of PANI particles evenly distributed on porous PPy film. The influence of FeCl₃ concentration on the morphology of the resulting composite films was investigated. The PPy/PANI composite films show an excellent Cr(vi) adsorption capacity of 256.41 mg g⁻¹, much higher than that of PPy-based absorbents prepared from chemical and electrochemical polymerization routes. This work thus suggests a new route for the fabrication of PPy/PANI films with highly enhanced Cr(vi) adsorption capacity for practical applications.

Free-standing polypyrrole/polyaniline composite film fabricated by interfacial polymerization at vapor/liquid interface.     

Optimization of the electrodeposition process of a polypyrrole/multi-walled carbon nanotube fiber electrode for a flexible supercapacitor

In the large-scale production of flexible supercapacitors, given the poor interface stability and the low mass loading of functional films on the fiber electrode, cyclic voltammetry (CV) and constant current (CC) electrodeposition methods were adopted to prepare polypyrrole/multi-walled carbon nanotubes (PPy/MWCNTs) on the surface of polyacrylonitrile (PAN) carbon cloth to explore the optimization process. The surface morphology and structural properties of the flexible electrode were characterized, and the electrical and electrochemical properties were studied. The research indicated that the PPy/MWCNTs were uniformly distributed on the fiber surface in the form of a linear structure and were amorphous and rich in carbon, nitrogen, and oxygen functional groups. A higher deposition current density helped improve the degree of coating of the MWCNTs with PPy and the number of oxygen-containing functional groups. The electrical and electrochemical properties of the flexible electrode prepared using the CC method were excellent; the electrochemical properties of the samples in the bent state were not significantly different from those in the straightened state. Using CC and CV methods, the conductivities of the samples were 32.4 S cm⁻¹ and 24.1 S cm⁻¹, the area-specific capacitance values were C 96.24 mF cm⁻² and 46.18 mF cm⁻² at a scan rate of 100 mV s⁻¹, the equivalent series resistance R_s values were 2.74 Ω and 4.67 Ω, the specific capacitance retention rates were 94.4% and 88.3% after 1000 cycles, and the capacitance retention rates were 89.7% and 80.6% after 5000 cycles, respectively. The differences in the performances of the flexible electrodes using the same preparation solvent and different preparation processes were due to the higher deposition current density of the CC method compared with that of CV. The former enhanced the polymerization degree of the PPy/MWCNT flexible electrode and improved the electrochemical performance. The presented research results are significant for the optimization of large-scale production processes.

The difference between the electrical and electrochemical properties of PPy/MWCNTs flexible electrodes was found to be due to the constant current method having a higher deposition current density, leading to a higher degree of polymerization.     

Incorporating Ni-MOF structure with polypyrrole: enhanced capacitive behavior as electrode material for supercapacitor

Herein, Ni-MOF sheet incorporated with polypyrrole is fabricated via a simple wet-chemical approach, and the obtained PPy-MOF composite is investigated as an electrode material for supercapacitors. The composite is systematically investigated by a series of characterization studies including X-ray diffraction, scanning electron microscopy, and X-ray photoelectron spectroscopy. Besides that, the electrochemical capacitive behaviors of the products are examined by electrochemical measurements. Electrochemical results show varying the ingredient ratio can lead to different electrocapacitive behavior, and PPy-MOF-0.2 is proved to possess the best performance in the investigated recipes. Furthermore, an asymmetric supercapacitor employing PPy-MOF and activated carbon as positive and negative electrodes is also assembled, which exhibits high energy density.

PPy is incorporated with a Ni-MOF sheet to achieve a significant enhancement of electro-capacitive performance for supercapacitor application.     

Influence of electrochemical co-deposition of bimetallic Pt–Pd nanoclusters on polypyrrole modified ITO for enhanced oxidation of 4-(hydroxymethyl) pyridine

Bimetallic Pt–Pd nanoparticles were dispersed on polypyrrole coated indium-tin oxide coated polyethylene terephthalate sheets (ITO-PET sheets). The excellent filming property of pyrrole gives a high porous uniform active area for the proper adsorption of bimetallic transition metal nanoparticles. Electrochemical behavior of the modified electrodes was determined using cyclic voltammetry and impedance studies. The physicochemical properties of the modified electrodes were analyzed by scanning electron microscopy, X-ray diffraction spectroscopy, X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. To study the electrochemical oxidation of 4-(hydroxymethyl) pyridine in the presence of sodium nitrate in aqueous acidic medium, the modified electrode was used. It is evident from the study that the modified electrode shows better electrochemical activity towards the oxidation of 4-(hydroxymethyl) pyridine.

Bimetallic Pt–Pd nanoparticles were dispersed on polypyrrole coated indium–tin oxide coated polyethylene terephthalate sheets (ITO-PET sheets).     

Polypyrrole nanoparticles-based soft actuator for artificial muscle applications

Currently, a straightforward fabrication technique for the development of soft actuators to explore their potential in robotic applications using environmentally compatible raw materials represents an important challenge. A conventional conducting polymer, such as polypyrrole (PPy), shows promising conductivity for such applications. This study presents the synthesis of PPy/polyvinyl alcohol (PPy/PVA)-based ion exchange polymer films containing PEDOT:PSS/SWNT/IL electrodes that undergo conformational changes in response to the applied voltage. Four types of ionic polymer actuator films with different sizes of PPy nanoparticles were fabricated to investigate the size-dependent electromechanical actuation performance. The aim of this study is to design and develop a stable, flexible, and reliable film actuator for robotic applications. Scanning electron microscopy and transmittance electron microscopy were performed to observe the surface morphology and detailed structure of the fabricated actuator films. The current density and ionic conductivity are demonstrated by the cyclic voltammogram and linear sweep voltammogram, respectively. The enhanced values of the water uptake, ion exchange capacity and ionic conductivity of the PPy/PVA polymer composite films enhanced the electrical properties and the tip deflection performance as compared to those of the other reported expensive perfluorinated polymer-based membrane actuators. A two finger-based micro gripping device was also developed, in which both the fingers were made up of the O-PPy/PVA/EL-based ion exchange polymer films. This mechanically stable and flexible film actuator fabricated via a synergistic combination of PPy/PVA composition containing PEDOT:PSS/SWNT/IL electrode surfaces possesses a substantial potential as an actuator material for micro robotic applications.

Currently, a straightforward fabrication technique for the development of soft actuators to explore their potential in robotic applications using environmentally compatible raw materials represents an important challenge.     

Fabrication of superwetting,antimicrobial and conductive fibrous membranes for removing/collecting oil contaminants

In order to remove/collect organic contaminants from polluted water, polypyrrole/silver nanoparticles (PPy/Ag NPs) have been loaded onto spandex fabric using the method of in situ redox-oxidation polymerization to achieve a specific membrane. Observations showed that the original hydrophobic fabric became superhydrophilic and superoleophobic underwater (with an underwater oil contact angle (OCA) of 160°). The as-prepared specimen could effectively remove the oil from an oil-in-water emulsion. After further hydrophobic modification, the specimen was transformed into a fabric that possessed durable superhydrophobicity and superlipophilicity (with a water contact angle (WCA) of 159°), which could collect the oil from a water-in-oil emulsion. Apparently, the two types of fibrous membranes completely satisfied the conditions for removing/collecting organic contaminants from opposite types of water/oil mixtures. The durable evaluation results exhibited the outstanding resistance of both fibrous membranes to friction and acidic and basic scouring agents. Additionally, the multifunctional fabric membrane also possessed excellent electrical conductivity and antibacterial activities towards S. aureus, B. subtilis, and E. coli, which will greatly promote developments in the textile industry and provide a bright future for fabric-based materials.

In order to remove/collect organic contaminants from polluted water, polypyrrole/silver nanoparticles (PPy/Ag NPs) have been loaded onto spandex fabric using the method of in situ redox-oxidation polymerization to achieve a specific membrane.