Facile design of structurally robust, highly conductive and well-flexible hybrid film based on MXene, cellulose nanofiber and poly (3,4-ethylenedioxythiphoenes):polystyrene sulfonate for supercapacitors.

Robust, conductive and flexible electrode materials have been the focus of attention in portable, wearable electronics. However, it is still a significant challenge to achieve synergistic development of multiple properties simultaneously. Herein, we propose a combination of microscale design and nanostructures strategy to prepare MXene/cellulose nanofiber-poly (3,4-ethylenedioxythiphoenes):polystyrene sulfonate (Ti3C2Tx/CNF-PEDOT:PSS, TC-P) hybrid film by a simple in-situ polymerization and vacuum filtration process. CNF serves as the supporting skeleton of PEDOT:PSS, effectively mitigating its self-aggregation and structural deformation due to the expansion/contraction of the polymer network. And the CNF-PEDOT:PSS composite is capable to open up the interlayer space of Ti3C2Tx, which reduces the self-stacking of Ti3C2Tx nanosheets. The strong interactions among the three components enable the hybrid film electrode to possess both flexibility and high electrochemical properties. As a result, the film electrode exhibits a remarkable tensile strength of 77.4 MPa and an excellent conductivity of 162.5 S cm-1, as well as an outstanding areal specific capacitance of 896 mF cm-2 at 4 mA cm-2. Moreover, the assembled symmetric supercapacitor (SSC) device displays a large areal energy density of 62 µWh cm-2 at a power density of 800 µW cm-2 and demonstrates a long cycle life with 85.1 % capacitance retention after 10,000 GCD cycles. This study provides an effective strategy to balance mechanical flexibility and electrochemical properties, providing an inspiration to prepare flexible electrodes that are widely applied in a new generation of portable, wearable electronics.

High stretchable and tough xylan-g-gelatin hydrogel via the synergy of chemical cross-linking and salting out for strain sensors.

Stretchable and tough hydrogels have been extensively used in tissue engineering scaffolds and flexible electronics. However, it is still a significant challenge to prepare hydrogels with both tensile strength and toughness by utilizing xylan, which is abundant in nature. Herein, we present a novel hydrogel of carboxymethyl xylan(CMX) graft gelatin (G) and doped with conductive hydroxyl carbon nanotubes (OCNT). CMX and G are combined through amide bonding as well as intermolecular hydrogen bonding to form a semi-interpenetrating hydrogel network. The hydrogel was further subjected to salting-out treatment, which induced the aggregation of the CMX-g-G molecular chain and the formation of chain bundles to toughen the hydrogel, the tensile strain, tensile stress, and toughness of CMX-g-G hydrogels were 1.547 MPa, 324 %, and 2.31 MJ m-3, respectively. In addition, OCNT was used as a conductive filler to impart electrical conductivity and further improve the mechanical properties of CMX-g-G/OCNT hydrogel, and a tensile strength of 1.62 MPa was obtained. Thus, the synthesized CMX-g-G/OCNT hydrogel can be used as a reliable and sensitive strain sensor for monitoring human activity. This study opens up new horizons for the preparation of xylan-based high-performance hydrogels.

Sodium carboxymethylcellulose/MXene/zeolite imidazolium framework-67-derived 3D porous carbon aerogel for high-performance asymmetric supercapacitors.

Herein, we propose a carbon/TiO2/Co3O4 (CTC) composite carbon aerogel with a 3D porous conductive network structure derived from sodium carboxymethylcellulose (CMC)/Mxene (Ti3C2Tx)/zeolite imidazolium framework-67 (ZIF-67). Among them, CMC is used as the carbon skeleton, which can reduce the powdering caused by volume change and improve the cycle stability. Ti3C2Tx acts as the conductive agent and dispersant for ZIF-67, exposing more reactive sites while constructing fast conductive channels to enhance electrochemical performance. The microstructure of the CTC carbon aerogel is modulated by controlling the mass ratio of Ti3C2Tx to ZIF-67, and the carbon aerogel with a mass ratio of 2:3 (CTC-2:3) is experimentally demonstrated to have the best electrochemical performance. The CTC-2:3 electrode exhibits a high specific capacitance of 481.7 F g-1 at 1 A g-1 and possesses a rate performance of 78.9 % at 10 A g-1. The assembled asymmetric supercapacitor (ASC, CTC-2:3//Ti3C2Tx) delivers an energy density of 48.4 Wh kg-1 at a power density of 699.8 W kg-1. Moreover, the ASC device maintains 85.3 % initial capacitance and 99.1 % coulombic efficiency after 10,000 GCD cycles, indicating good cycling stability. This facile design pathway provides a new insight for the development of high-performance electrode materials.

Carboxymethylcellulose/poly(3,4-ethylenedioxythiophene):polystyrene sulfonate membrane after dimethyl sulfoxide treatment for flexible and high electrochemical performance asymmetric supercapacitors.

As the requirements for wearable electronic devices continue to increase, the development of bendable and foldable supercapacitors is becoming critical. However, it is still challenging to design free-standing electrodes with flexibility and high electrical conductivity. Herein, using carboxymethylcellulose (CMC) as the biological template and poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) as the electroactive material, a flexible CMC/PEDOT:PSS membrane with a cross-linked mesh structure was firstly synthesized by a facile in-situ polymerization and vacuum filtration process. Subsequently, the CMC/PEDOT:PSS membrane was further treated with dimethyl sulfoxide (DMSO) to remove the excess PSS, thereby enhancing their electrochemical performance. The results showed that the best performing hybrid membrane had good mechanical properties (tensile strength of 48.1 MPa) and high electrical conductivity (45.1 S cm-1). The assembled asymmetric supercapacitor (ASC) is capable of delivering an energy density of 181.9 µW h cm-2 at a power density of 750 µW cm-2 and maintains an initial capacitance of 93.4 % and a coulombic efficiency of 100 % after 10,000 GCD cycles, demonstrating an ultra-long cycle life. Moreover, good electrochemical properties can be retained even in the bent and folded state. Therefore, the hybrid membrane electrode with both flexibility and high electrochemical performance has great potential for application in wearable electronics.

Flexible and alternately layered high electrochemical active electrode based on MXene, carboxymethylcellulose, and carbon nanotube for asymmetric micro-supercapacitors.

Recent studies have shown that Ti-based MXene has great potential for electrochemical energy storage applications, including Li-ion batteries and micro-supercapacitors. However, self-stacking and weak interlayer interactions lead to poor electrochemical properties. Herein, a simple one-step vacuum filtration method was used to prepare a MXene/carboxymethylcellulose/carbon nanotube (Ti3C2Tx/CMC/CNT) hybrid membrane. Due to the unique adhesion and flexibility of CMC, it can be interwoven with CNT to form an interconnected mesh structure, which on the one hand mitigates the self-aggregation of CNT, and on the other hand, the CNT entangled on the surface of CMC imparts its electrical conductivity. Moreover, the -OH of CMC can form hydrogen bonds with the reactive terminal groups (-O, -OH, -F) of Ti3C2Tx, resulting in the tight anchoring of CMC and CNT to Ti3C2Tx nanosheet layers and bridging adjacent Ti3C2Tx nanosheets to form a complete conductive pathway. As a result, the mechanical property test indicates that the Ti3C2Tx/CMC/CNT hybrid film could achieve a maximum tensile strength of 64.9 MPa. Furthermore, an asymmetric micro-supercapacitor (MSC) using Ti3C2Tx/CMC/CNT as the cathode and reduced graphene oxide/carboxymethylcellulose/polypyrrole (RGO/CMC/PPy) as the anode was fabricated, which exhibited a high energy density of 258.8 µWh cm-2 at a power density of 750 µW cm-2, and an ultra-long cycle life (93.2% capacitance retention after 15,000 GCD cycles). The simple and scalable preparation process makes this MSC device very promising for commercial electronics applications.

Free-standing reduced graphene oxide/carboxymethylcellulose-polyaniline (RGO/CMC-PANI) hybrid film electrode for high-performance asymmetric supercapacitor device.

This work demonstrates a facile and effective strategy for the preparation of a reduced graphene oxide/carboxymethylcellulose-polyaniline (RGO/CMC-PANI) hybrid film electrode. Specifically, through the hydrogen bonding interaction between -OH of CMC molecules and -NH2 of aniline monomer, PANI grows in an ordered manner on the surface of CMC, which effectively alleviates the structural collapse of PANI during the continuous charge/discharge process. After compounding with RGO, CMC-PANI bridges adjacent RGO sheets to form a complete conductive path, and opens the gap between RGO sheet layers to obtain fast ion channels. As a result, the RGO/CMC-PANI electrode exhibits excellent electrochemical performance. Moreover, an asymmetric supercapacitor was fabricated using RGO/CMC-PANI as the anode and Ti3C2Tx as the cathode. The results show that the device has a large specific capacitance of 450 mF cm-2 (81.8 F g-1) at 1 mA cm-2 and a high energy density of 140.6 µWh cm-2 at a power density of 749.9 µW cm-2. Besides, 87.3 % initial capacitance and 100 % good coulombic efficiency can be maintained even after 20,000 GCD cycles. Therefore, the device has a broad application prospect in the field of new-generation microelectronic energy storage.

Carboxymethylcellulose-polyaniline/carbon nanotube (CMC-PANI/CNT) film as flexible and highly electrochemical active electrode for supercapacitors.

Herein, we demonstrate a flexible, structural robust and highly electrochemical active film electrode based on evenly distributed carboxymethylcellulose-polyaniline/carbon nanotube (CMC-PANI/CNT) for supercapacitors. In this process, vertically aligned PANI nanoparticles grow in an orderly manner on CMC fibers. The highly dispersed CNT nanomaterials are then introduced by simple layer-by-layer assembly, eventually forming an interwoven network structure. Mechanical tests have shown that the obtained CMC-PANI/CNT film exhibit excellent robustness and flexibility, and can be used directly as electrodes without any conductive additives and binders. The CMC-PANI/CNT electrode with optimal CMC, PANI and CNT contents demonstrates an excellent area specific capacitance of 3106.3 mF cm-2 at 5 mA cm-2 and a gravimetric specific capacitance of 348.8 F g-1 at 0.5 A g-1. Furthermore, the symmetric supercapacitor (SSC) assembled with CMC-PANI/CNT exhibits a high energy density of 99.89 µW h cm-2 at a power density of 400.02 µW cm-2, and a good cycling stability (with capacitance retention of 89.2 % after 5000 cycles). The cost-effective and eco-friendly preparation method of free-standing CMC-PANI/CNT film electrodes provide a novel insight for developing flexible energy storage devices.

LVRT capability enhancement of DFIG based wind turbine with coordination control of dynamic voltage restorer and inductive fault current limiter.

According to the coordination control of a dynamic voltage restorer (DVR) and an inductive fault current limiter (FCL), this paper proposes an efficient low-voltage ride-through (LVRT) scheme for a doubly fed induction generator (DFIG) based wind turbine. The DVR is located to the DFIG's stator circuit for stabilizing the terminal voltage and decreasing the generator current. The inductive FCL is connected to the DFIG's rotor circuit for suppressing the rotor overcurrent and protecting the converter. Theoretical discussions on structure, principle and scale criterion of the combined DVR-FCL are conducted, and simulation analyses of the proposed approach to handle symmetrical and asymmetrical faults are done in MATLAB/Simulink. In this study, the dynamic characteristics of the DFIG during the faults are analyzed from multiple aspects, and a detailed comparison of the proposed approach and the single action of DVR or FCL is carried out. From the simulation results, the effectiveness and superiority of the proposed approach are well demonstrated.