No abstract

No abstract

No abstract

No abstract

While the soft chemistry of layered alkali metal oxides is adequately understood, the effect of the post-synthesis thermal treatment on their structure, composition, and properties has been underexplored. In this article, we thoroughly investigated the bulk and surface modifications of KMTiO (M = Ni, Cu, Zn) lepidocrocite titanate thermally treated within 200 °C above its synthetic temperature under air. This practice was typically employed in e.g., specimen fabrication for physical property measurements. We observed the expansion of the interlayer distance (b/2) accompanied by a reduction in layer charge density. These findings can be explained by the deintercalation of interlayer K ions and the loss of intralayer Ti, M, and O species. Meanwhile, the enrichment of potassium and carbonate on the surfaces was evident. The slight differences in dielectric properties of the pellets thermally treated at different temperatures were attributed to the combination of bulk and surface modifications. At 10 Hz and RT-250 °C, the maximum dielectric constants ε' of ∼10 with the dielectric loss (tan δ) ∼0.9-1.5 were obtained for KZnTiO.

No abstract

A novel concept to simultaneously modify the electric responses of the grain and grain boundaries of CaCu3Ti4O12 ceramics was proposed, involving doping with F− anions to improve the giant dielectric properties.

Although manganese oxide- and graphene-based supercapacitors have been widely studied, their charge storage mechanisms are not yet fully investigated. In this work, we have studied the charge storage mechanisms of K-birnassite MnO2 nanosheets and N-doped reduced graphene oxide aerogel (N-rGOae) using an in situ X-ray absorption spectroscopy (XAS) and an electrochemical quart crystal microbalance (EQCM). The oxidation number of Mn at the MnO2 electrode is +3.01 at 0 V vs. SCE for the charging process and gets oxidized to +3.12 at +0.8 V vs. SCE and then reduced back to +3.01 at 0 V vs. SCE for the discharging process. The mass change of solvated ions, inserted to the layers of MnO2 during the charging process is 7.4 μg cm−2. Whilst, the mass change of the solvated ions at the N-rGOae electrode is 8.4 μg cm−2. An asymmetric supercapacitor of MnO2//N-rGOae (CR2016) provides a maximum specific capacitance of ca. 467 F g−1 at 1 A g−1, a maximum specific power of 39 kW kg−1 and a specific energy of 40 Wh kg−1 with a wide working potential of 1.6 V and 93.2% capacity retention after 7,500 cycles. The MnO2//N-rGOae supercapacitor may be practically used in high power and energy applications.