The effect of the thermal reduction on the kinetics of low temperature 4He sorption and the structural characteristics of graphene oxide

TL;DR

This study investigates how thermal reduction affects helium sorption kinetics and structural properties of graphene oxide, revealing changes in diffusion mechanisms and activation energies with different annealing temperatures.

Contribution

It provides new insights into how thermal treatment modifies helium sorption kinetics and structural defects in graphene oxide, especially regarding diffusion mechanisms and activation energy variations.

Findings

Lower activation energy in TRGO-200 compared to GtO.

Transition from thermally activated diffusion to tunneling at low temperatures.

Structural recovery and defect generation influence activation energy dependence.

Abstract

The kinetics of the sorption and the subsequent desorption of 4He by the starting graphite oxide (GtO) and the thermally reduced graphene oxide samples (TRGO, Treduction = 200, 300, 500, 700 and 900 C) have been investigated in the temperature interval 1.5 - 20 K. The effect of the annealing temperature on the structural characteristics of the samples was examined by the X-ray diffraction (XRD) technique. On lowering the temperature from 20 K to 11-12 K, the time of 4He sorption increased for all the samples, which is typically observed under the condition of thermally activated diffusion. Below 5 K the characteristic times of 4He sorption by the GtO and TRGO-200 samples were only weakly dependent on temperature, suggesting the dominance of the tunnel mechanism. In the same region (T<5 K) the characteristic times of the TRGOs reduced at higher temperatures (300, 500, 700 and 900 C) were growing with lowering temperature, presumably due to the defects generated in the carbon planes on removing the oxygen functional groups (oFGs). The estimates of the activation energy (Ea) of 4He diffusion show that in the TRGO-200 sample the Ea value is 2.9 times lower as compared to the parent GtO, which is accounted for by GtO exfoliation due to evaporation of the water intercalated in the interlayer space of carbon. The nonmonotonic dependences Ea vs T for the GtO samples treated above 200 C are determined by a competition between two processes - the recovery of the graphite carbon structure, which increases the activation energy, and the generation of defects, which decreases the activation energy by opening additional surface areas and ways for sorption. The dependence of the activation energy on treatment temperature correlates well with the contents of the crystalline phase in GtO varying with a rise of the annealing temperature.