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 (TiCT/CNF-PEDOT:PSS, TC-P) hybrid film by a simple in-situ polymerization and vacuum filtration process.

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).

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

Herein, we propose a carbon/TiO/CoO (CTC) composite carbon aerogel with a 3D porous conductive network structure derived from sodium carboxymethylcellulose (CMC)/Mxene (TiCT)/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. TiCT acts as the conductive agent and dispersant for ZIF-67, exposing more reactive sites while constructing fast conductive channels to enhance electrochemical performance.

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.

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 (TiCT/CMC/CNT) hybrid membrane.

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 -NH 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.