ABSTRACT
An amorphous SiO2 (a-SiO2) thin film was developed as an artificial passivation layer to stabilize Li metal anodes during electrochemical reactions. The thin film was prepared using an electron cyclotron resonance-chemical vapor deposition apparatus. The obtained passivation layer has a hierarchical structure, which is composed of lithium silicide, lithiated silicon oxide, and a-SiO2. The thickness of the a-SiO2 passivation layer could be varied by changing the processing time, whereas that of the lithium silicide and lithiated silicon oxide layers was almost constant. During cycling, the surface of the a-SiO2 passivation layer is converted into lithium silicate (Li4SiO4), and the portion of Li4SiO4 depends on the thickness of a-SiO2. A minimum overpotential of 21.7 mV was observed at the Li metal electrode at a current density of 3 mA cm-2 with flat voltage profiles, when an a-SiO2 passivation layer of 92.5 nm was used. The Li metal with this optimized thin passivation layer also showed the lowest charge-transfer resistance (3.948 Ω cm) and the highest Li ion diffusivity (7.06 × 10-14 cm2 s-1) after cycling in a Li-S battery. The existence of the Li4SiO4 artificial passivation layer prevents the corrosion of Li metal by suppressing Li dendritic growth and improving the ionic conductivity, which contribute to the low charge-transfer resistance and high Li ion diffusivity of the electrode.
ABSTRACT
The hybrid composite electrode comprising CuO and Cu2O micronanoparticles in a highly graphitized porous C matrix (CuO/Cu2O-GPC) has a rational design and is a favorable approach to increasing the rate capability and reversible capacity of metal oxide negative materials for Li- and Na-ion batteries. CuO/Cu2O-GPC is synthesized through a Cu-based metal-organic framework via a one-step thermal transformation process. The electrochemical performances of the CuO/Cu2O-GPC negative electrode in Li- and Na-ion batteries are systematically studied and exhibit excellent capacities of 887.3 mAh g(-1) at 60 mA g(-1) after 200 cycles in a Li-ion battery and 302.9 mAh g(-1) at 50 mA g(-1) after 200 cycles in a Na-ion battery. The high electrochemical stability was obtained via the rational strategy, mainly owing to the synergy effect of the CuO and Cu2O micronanoparticles and highly graphitized porous C formed by catalytic graphitization of Cu nanoparticles. Owing to the simple one-step thermal transformation process and resulting high electrochemical performance, CuO/Cu2O-GPC is one of the prospective negative active materials for rechargeable Li- and Na-ion batteries.
ABSTRACT
Dental gels and rinses for caries prophylactic contain fluoride at concentrations ranging from 0.1 to 1%. In addition, many types of fluoride-releasing materials have been used in dental applications. The purpose of the study was to investigate the addition effect of fluoride into artificial saliva on the corrosion resistance of pure titanium and titanium-silver alloys. Titanium and titanium-silver alloys were arc melted, homogenized at 950 degrees C for 72 h, hot rolled, and solution heat treated and quenched. In order to investigate the effect of the fluoride ions on the corrosion resistance, potentiodynamic polarization testing, potentiostatic testing, and open-circuit potential measurements were performed in plain artificial saliva and 0.1 and 1% NaF-added artificial saliva. The passive current densities of titanium and titanium-silver alloys increased with increasing fluoride-ion concentration. Ti2.0Ag and Ti3.0Ag exhibited a low current density relatively and showed a stable behavior compared to titanium. The open-circuit potential of titanium decreased and current density at 250 mV (SCE) potentiostatic testing reacted sensitively with increasing fluoride concentration. On the other hand, the open-circuit potential of titanium-silver alloys with a high silver content (3.0-4.0 at %) reacted less sensitively to the fluoride-ion concentration. Among titanium-silver alloys, Ti3.0Ag alloy had a higher resistance against the attack of fluoride ions and showed a more stable open-circuit potential and current density than titanium in the fluoride-containing solution. It is concluded that they are electrochemically stable and maintained good corrosion resistance in fluoride-containing artificial saliva.
