Olga Naboka

Conductivity-Dependent Strain Response of Carbon Nanotube Treated Bacterial Nanocellulose

This paper reports the strain sensitivity of flexible, electrically conductive, and nanostructured cellulose which was prepared by modification of bacterial cellulose with double-walled carbon nanotubes (DWCNTs) and multiwalled carbon nanotubes (MWCNTs). The electrical conductivity depends on the modifying agent and its dispersion process. The conductivity of the samples obtained from bacterial cellulose (BNC) pellicles modified with DWCNT was in the range from 0.034 S·cm−1 to 0.39 S·cm−1, and for BNC pellicles modified with MWCNTs it was from 0.12 S·cm−1 to 1.6 S·cm−1. The strain-induced electromechanical response, resistance versus strain, was monitored during the application of tensile force in order to study the sensitivity of the modified nanocellulose. A maximum gauge factor of 252 was found from the highest conductive sample treated by MWCNT. It has been observed that the sensitivity of the sample depends on the conductivity of the modified cellulose.

Cobalt (II) chloride promoted formation of honeycomb patterned cellulose acetate films

CoCl(2) containing honeycomb patterned films were prepared from cellulose acetate (CA)/CoCl(2)/acetone solutions by the breath figure method in a wide range of humidities. Size and pore regularity depend on the CA/CoCl(2) molar ratio and humidity. When replacing CoCl(2) with Co(NO(3))(2) or CoBr(2), no formation of ordered porosity in the cellulose acetate films is observed. According to data from scanning electron microscopy (SEM), Energy Dispersive X-ray Microanalysis (EDX), X-ray Diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy, the key role in the formation of honeycomb structures can be attributed to the physical and chemical properties of CoCl(2) - hygroscopicity, low interaction with CA, and extraction from CA/CoCl(2)/acetone solution by water droplets condensed on the surface of the CA/CoCl(2) solution. Obtained films are prospective for using in catalysis, hydrogen fuel cells, and optical sensing materials.

Cellulose-derived carbon nanofibers/graphene composite electrodes for powerful compact supercapacitors

Herein, we demonstrate a unique supercapacitor composite electrode material that is originated from a sustainable cellulosic precursor via simultaneous one-step carbonization/reduction of cellulose/graphene oxide mats at 800 °C. The resulting freestanding material consists of mechanically stable carbon nanofibrous (CNF, fiber diameter 50–500 nm) scaffolds tightly intertwined with highly conductive reduced graphene oxide (rGO) sheets with a thickness of 1–3 nm. The material is mesoporous and has electrical conductivity of 49 S cm−1, attributed to the well-interconnected graphene layers. The electrochemical evaluation of the CNF/graphene composite electrodes in a supercapacitor device shows very promising volumetric values of capacitance, energy and power density (up to 46 F cm−3, 1.46 W h L−1 and 1.09 kW L−1, respectively). Moreover, the composite electrodes retain an impressive 97% of the initial capacitance over 4000 cycles. With these superior properties, the produced composite electrodes should be the “looked-for” components in compact supercapacitors used for increasingly popular portable electronics and hybrid vehicles.