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The cellulose derived carbon/graphene/ZnO aerogel composite was prepared as an electrode in order to investigate the electrochemical properties. Carbon aerogel was synthesized using paper as an available cellulose source, and the composite was obtained through a new and simple preparation method including the immersion of monolithic carbon aerogel in graphene oxide/Zn2+ suspension and subsequent chemical reduction and freeze drying. The morphology, functional groups and crystalline structure of the samples were studied with Scanning Electron Microscopy (SEM), Fourier Transform Infrared Spectroscopy (FTIR) and X-ray Diffraction Spectroscopy (XRD), respectively. Electrochemical performance of the prepared binder free electrodes was examined using Cyclic Voltammetry (CV), Galvanostatic Charge-Discharge (GCD) and Electrochemical Impedance Spectroscopy (EIS). The data revealed that flexible carbon/graphene/ZnO composite resulted in a low density (0.035 g cm−3) electrode with the capacitance of 900 mF cm−2 at a high current density of 10 mA cm−2, lower IR drop and high cyclic stability (capacitance retention of 96%) after 1000 cycles, at 10 mA cm−2. These features were due to the presence of 3D porous conductive network, highly reduced graphene oxide, and the formation of ZnO nanoparticles on graphene sheets. Moreover, polyaniline (PANI) was introduced to carbon/graphene/ZnO composite electrode using electro-oxidation method at different reaction time and aniline concentration in order to achieve remarkably improved capacitance of 2500 mF cm−2 (at 10 mA cm−2) and low charge transfer resistance. Also, after the supercapacitor device assembly, the capacitance was retained. Based on the results, the synthesized composite is a promising material for new generation of lightweight freestanding electrodes with the high electrochemical performance.

Two-step growth of ZnO nanowires (NWs) on carbon fiber (CF) surface via hydrothermal synthesis was studied and their application in the preparation of paper-based friction materials by wet-forming process was also investigated. SEM and EDS results showed a dense and uniform ZnO NWs layer with vertical alignment was well established on surface of CFs. UV–vis spectra and XRD characterization further confirmed the formation of ZnO NWs on CFs surface. In comparison with control sample (paper-based friction material containing pristine CFs), the modified sample (paper-based friction material containing modified CFs) exhibited higher and more stable dynamic friction coefficient and greater wear resistance. It was concluded that the CFs@ZnO NWs had excellent tribological properties and was highly promising for wet paper-based friction material.

In this work, a robust and flexible bilayered MXene/cellulose paper sheet with superhigh electrical conductivity was prepared via vacuum-assisted filtration and a subsequent hot-pressing process for electromagnetic interference (EMI) shielding applications. By tightly assembling few-layered MXene (f-Ti3C2Tx) on the cellulose substrate via hydrogen bonds, an effective and interconnected conductive network was constructed in the paper sheet, resulting in a high electrical conductivity of 774.6–5935.4 S m−1 at various f-Ti3C2Tx loadings. The highly conductive MXene layer can promptly reflect a great amount of incident EM waves, a process which preceded the transmission of EM waves in the cellulose matrix. Owing to the highly efficient reflection-dominated EMI shielding mechanism, the resultant bilayered MXene/cellulose paper sheets exhibit excellent EMI shielding effectiveness of 34.9–60.1 dB and specific EMI shielding efficiency of 290.6–600.7 dB mm−1. Moreover, the MXene/cellulose paper sheets demonstrated improved mechanical strength (up to 25.7 MPa) and flexibility due to the mechanical frame effect acted by the cellulose substrate. Consequently, the robust and flexible bilayered MXene/cellulose paper sheet is a promising candidate for application in next-generation electric devices.

The paper describes the structure and properties of preceramic paper-derived Ti3Al(Si)C2-based composites fabricated by spark plasma sintering. The effect of sintering temperature and pressure on microstructure and mechanical properties of the composites was studied. The microstructure and phase composition were analyzed by scanning electron microscopy (SEM) and X-ray diffraction (XRD), respectively. It was found that at 1150 °C the sintering of materials with the MAX-phase content above 84 vol% leads to nearly dense composites. The partial decomposition of the Ti3Al(Si)C2 phase becomes stronger with the temperature increase from 1150 to 1350 °C. In this case, composite materials with more than 20 vol% of TiC were obtained. The paper-derived Ti3Al(Si)C2-based composites with the flexural strength > 900 MPa and fracture toughness of >5 MPa m1/2 were sintered at 1150 °C. The high values of flexural strength were attributed to fine microstructure and strengthening effect by secondary TiC and Al2O3 phases. The flexural strength and fracture toughness decrease with increase of the sintering temperature that is caused by phase composition and porosity of the composites. The hardness of composites increases from ~9.7 GPa (at 1150 °C) to ~11.2 GPa (at 1350 °C) due to higher content of TiC and Al2O3 phases.

Traditional slurry-based electrodes consist of heavy current collectors and electroactive materials with a low weight percentage, which inevitably increase the total weight and cost of lithium-ion batteries (LIBs). Consequently, the development of low-cost, lightweight, flexible and binder-free electrodes for LIBs is highly desirable but also greatly challenging. In this work, we report the synthesis of small ZnO nanoparticles uniformly embedded in N-doped carbon (NC) nanoplate arrays (NPAs) tightly grown on a N-doped carbon paper (NCP) substrate (ZnO/NC NPAs@NCP) through a facile metal-organic framework-engaged strategy. This electrode design not only avoids the utilisation of insulating polymer binders but also offers other advantages, including large electrode/electrolyte contact areas, abundant electroactive sites, good wettability of the electrolyte, fast electron/ion transport and efficient volume accommodation. Notably, the freestanding ZnO/NC NPAs@NCP electrode displays a high reversible capacity of 610 mA h g−1 (based on the mass of entire electrode) at a current density of 100 mA g−1 for 50 cycles and excellent long-term cycling stability (363 mA h g−1 at 500 mA g−1 for 200 cycles). Furthermore, a full cell employing ZnO/NC NPAs@NCP as the anode and commercial LiFePO4 as the cathode is constructed, indicating the feasibility for practical application. Moreover, an analysis of the electrode kinetics confirms the favourable lithium-ion storage kinetics within the ZnO/NC NPAs@NCP electrode. The present work could provide a new approach to develop low-cost, lightweight and flexible electrodes for advanced energy storage.

Carbon materials with layered structure and high conductivity are promising electrode candidates for dual-ion batteries (DIBs). However, the size mismatch of electrolyte ions and interlayer spacing of carbon materials limits the overall performance of DIBs. Thus, finding an effective strategy to adjust the interlayer spacing of carbon materials is of great importance. Here, we describe an efficient electrochemical strategy combining ion pre-intercalation and gas evolution reaction treatment to expand the interlayer spacing and modify graphene layers of carbon fiber papers. Furthermore, through the theoretical calculation we have demonstrated that the anion adsorption energy is reduced and kinetics is accelerated by the introduction of functional groups on the graphene layer. After the electrochemical modification, the discharge capacity of CFP increases more than 50%, the transfer resistance reduces even more than 40% and the capacity retains 94% after 1000 cycles in an ionic liquid electrolyte. These promising results demonstrate an effective and convenient method to solve the size mismatch issue, and therefore, arouse the potentials of carbon materials and other materials with layered structure for high performance DIBs.

Porous layers of paper-derived titanium silicon carbide (Ti3SiC2), with a thickness ranging from 300 to 700 µm, were obtained by the heat treatment of preceramic papers containing Ti3SiC2 as filler particles. The tearing strength of the preceramic papers was provided by cellulose fibers obtained from wood by the kraft pulping process, also described as pulp fibers, and ionic starches. Short pulp fibers with an average length of 657 µm were derived from short fibered hardwood (eucalyptus), while long pulp fibers with an average length of 1665 µm were derived from long fibered softwood (spruce, pine and larch). The fiber length of pulp fibers in the preceramic papers also influenced the microstructure and the properties of the paper-derived Ti3SiC2. Preceramic papers fabricated with short pulp fibers exclusively led to an average porosity of 18.6 vol% for the paper-derived Ti3SiC2, whereas the paper-derived Ti3SiC2 had an average porosity of 45.3 vol% when preceramic papers with long pulp fibers only were used. The density of the paper-derived Ti3SiC2 also affected the flexural strength, as could be shown by densifying preceramic papers using a calender. Thereby, the flexural strength of paper-derived Ti3SiC2 could be increased by more than five times, from 13 MPa to 83 MPa. The purity of the paper-derived Ti3SiC2 was found to be dependent on the purity of the raw materials and the process cycle, with TiCx and Al2O3 impurities present in the ceramics.

Al 2 O 3 /Cu-O composites were fabricated from the paper-derived alumina matrix infiltrated with a Cu-3.2 wt% O alloy. Paper-derived alumina preforms with an open porosity ranging from ∼ 14 to ∼ 25 vol% were prepared by sintering of alumina-loaded preceramic papers at 1600 °C for 4 h. Pressureless infiltration at 1320 °C for 4 h of the preforms with Cu–O alloy resulted in the nearly dense materials with good mechanical and electrical properties, e.g. fracture toughness up to 6 MPa m 0.5 , four-point-bending strength up to 342 MPa, Young's modulus up to 281 GPa and electrical conductivity up to 2 MS/m depending on the volume fraction of copper alloy in the composites. The technological capability of this approach was demonstrated using prototypes in various engineering fields fabricated by lamination, corrugating and Laminated Object Manufacturing (LOM) methods.