A novel nanofibrous gel electrolyte was prepared via gelatin electrospinning for use as a nonaqueous electrolyte in electric double-layer capacitors (EDLCs). An electrospinning technique with a 25 wt% gelatin solution was applied to produce gelatin electrospun (GES) nanofiber electrolytes. Structural analysis of the GES products showed a clearly nanofibrous structure with fiber diameters in the 306.2–428.4 nm range and exhibiting high thermal stability, high tensile strength, and a stable form of nanofibrous structure after immersion in 1-ethyl-3-methylimidazolium tetrafluoroborate (EMImBF₄). After testing over a range of spinning times, GES electrolytes that were produced at 25 min (GES-25) had a suitable thickness for the assembly of EDLC with the optimized tensile properties and were used to fabricate EDLC test cells with EMImBF₄. These test cells were compared to those with pure EMImBF₄ and a separator as an electrolyte. The electrochemical properties of the test cells were characterized by charge-discharge testing, discharge capacitance, and alternative current (AC) impedance measurements. AC impedance measurements showed that the test cell with the GES-25/EMImBF₄ gel electrolyte showed slightly poorer contact with the electrode when compared to that with pure EMImBF₄, whereas exhibited comparable IR drop and discharge capacitance (calculated capacitance retention was 56.6%). The results demonstrated that this novel gel electrolyte can be used as a nonaqueous electrolyte in order to improve the safety in EDLCs.

Oxidized cellulose (OC) nanofiber was successfully prepared from the dry sheet of Nata De Coco (DNDC) using the mixture system of HNO₃/H₃PO₄–NaNO₂for the first time. The carboxyl content of the OC was investigated at different conditions (HNO₃/H₃PO₄ratios, reaction times, and reaction temperatures). The results revealed that the carboxyl content of the OC increased along with the reaction time, which yielded 0.6, 14.8, 17.5, 20.9, 21.0, and 21.0% after 0, 6, 12, 36, and 48 hours, respectively. The reaction yields of the OC ranged between 79% and 85% when using HNO₃/H₃PO₄ratio of 1 : 3, 1.4% wt of NaNO₂at 30°C at different reaction times. From the structural analysis, the OC products showed a nanofibrous structure with a diameter of about 58.3–65.4 nm. The Fourier transform infrared spectra suggested the formation of carboxyl groups in the OC after oxidation reaction. The crystallinity and crystalline index decreased with an increase of reaction time. The decrease of crystallinity from oxidation process agreed with the decrease of degree of polymerization from the hydrolysis ofβ-1,4-glycosidic linkages in the cellulose structure. The thermal gravimetric analysis results revealed that the OC products were less thermally stable than the raw material of DNDC. In addition, the OC products showed blood agglutinating property by dropping blood on the sample along with excellent antibacterial activity.