Oxalic acid-assisted preparation of LTO-carbon composite anode material for lithium-ion batteries.

This study presents an oxalic acid-assisted method for synthesizing spinel-structured lithium titanate (Li4Ti5O12; LTO)/carbon composite materials. The Ag-doped LTO nanoparticles (NPs) are synthesized via flame spray pyrolysis (FSP). The synthesized material is used as a precursor for synthesizing the LTO-NP/C composite material with chitosan as a carbon source and oxalic acid as an additive. Oxalic acid improves the dissolution of chitosan in water as well as changes the composition and physical and chemical properties of the synthesized LTO-NP/C composite material. The oxalic acid/chitosan ratio can be optimized to improve the electrochemical performance of the LTO-NP/C composite material, and the electrode synthesized with a high mass loading ratio (5.44 mg cm-2) exhibits specific discharge capacities of 156.5 and 136 mAh g-1at 0.05 C- and 10 C-rate currents, respectively. Moreover, the synthesized composite LTO-NP/C composite material exhibits good cycling stability, and only 1.7% decrease in its specific capacity was observed after 200 charging-discharging cycles at 10 C-rate discharging current.

Influence of induction-annealing temperature on the morphology of barley-straw-derived Si@C and SiC@graphite for potential application in Li-ion batteries.

Silicon, a material with high theoretical energy density, holds great promise as a candidate material for anodes in lithium-ion batteries. However, due to an alloying mechanism the material undergoes volume expansion of up to 300%, which results in rapid capacity fading. The coating of silicon with carbon is done by using a biomass-based carbon precursor. The effects of annealing temperature on the morphology of the silicon-carbon structures is presented herein. The mechanically and chemically treated barley straw is mixed with silicon particles and induction annealed in argon atmosphere under different temperatures. The material transformation from carbon-coated silicon (Si@C) to graphite-coated silicon carbide (SiC@graphite) is studied. The Si@C displayed initial specific capacity of 1200 mAh g-1 at 0.1 A g-1, while the capacity retention analysis of Si@C revealed improved cycling stability compared to bare silicon.

Natural cellulose ionogels for soft artificial muscles.

Rapid development of soft micromanipulation techniques for human friendly electronics has raised the demand for the devices to be able to carry out mechanical work on a micro- and macroscale. The natural cellulose-based ionogels (CEL-iGEL) hold a great potential for soft artificial muscle application, due to its flexibility, low driving voltage and biocompatibility. The CEL-iGEL composites undergo reversible bending already at ±500mV step-voltage values. A fast response to the voltage applied and high ionic conductivity of membranous actuator is achieved by a complete dissolution of cellulose in 1-ethyl-3-methylimidazolium acetate [EMIm][OAc]. The CEL-iGEL supported cellulose actuator films were cast out of cellulose-[EMIm][OAc] solution via phase inversion in H2O. The facile preparation method ensured uniform morphology along the layers and stand for the high ionic-liquid loading in a porous cellulose scaffold. During the electromechanical characterization, the CEL-iGEL actuators showed exponential dependence to the voltage applied with the max strain difference values reaching up to 0.6% at 2 V. Electrochemical analysis confirmed the good stability of CEL-iGEL actuators and determined the safe working voltage value to be below 2.5V. To predict and estimate the deformation for various step input voltages, a mathematical model was proposed.