No abstract

We report the effect of the Ti3C2Tx MXene flake thickness on its inherent electrochemistry and heterogeneous charge transfer characteristics. It is shown that Ti3C2Tx undergoes irreversible oxidation in a positive potential window, which strongly depends on the flake thickness and pH of the electrolyte. Few-layered Ti3C2Tx exhibits faster electron transfer kinetics (k0 = 0.09533 cm s-1) with a [Fe(CN)6]4-/3- redox mediator compared to multi-layered Ti3C2Tx (k0 = 0.00503 cm s-1). In addition, the few-layered free standing Ti3C2Tx film electrode remains intact after enduring irreversible oxidation.

The influence of bismuth (Bi) substitution on the thermoelectric properties of AgSbTe2 compounds was investigated and compared with the undoped AgSbTe2. The addition of Bi dopants not only resulted in a reduction in thermal conductivity but also markedly increased the thermopower in the Ag(Sb1−xBix)Te2 series. Additional phonon scatterings were created by Bi doping and led to a reduction of thermal conductivity. The lattice thermal conductivity is significantly reduced which could be ascribed to enhancement of phonon scattering by dopants with greater atomic weight. In addition, the thermopower was enhanced, which was attributed to the electron-filtering effects caused by the nanoscaled microstructures. Because of the extremely low thermal conductivity (0.48 Wm−1K−1) and moderate power factor of AgBi0.05Sb0.95Te2, a maximum ZT value of (1.04 ± 0.08) was reached at 570 K; yielding an enhancement of greater than 10% compared with an undoped AgSbTe2. this result shows promising thermoelectric properties in the medium temperature range.