The Remarkable Role of Indium in Synergistically Optimizing Carrier Concentration and Phase Distribution of AgCuTe-Based Materials.

Carrier regulation has proven to be an effective approach for optimizing the thermoelectric performance of materials. One common method to adjust the carrier concentration is through element doping. In the case of AgCuTe-based materials, it tends to form with cation vacancies, resulting in a high hole concentration and complex phase composition at low temperatures, which also hinders material stability. However, this also offers additional opportunities to manipulate the carrier concentration. In this study, the improved performance of AgCuTe through indium doping is reported, which leads to a reduction in hole concentration. In combination with a significant increase in the effective mass of the carriers, the enhanced Seebeck coefficient is also realized. Particularly, a notable improvement in power factor is observed in the hexagonal phase near room temperature. Furthermore, a lower electron thermal conductivity is achieved, contributing to an average figure of merit value of ≈1.21 (between 523 and 723 K). Additionally, the presence of indium inhibits the formation of the second phase and ensures a homogeneous phase distribution, which reduces the instability arising from phase transition. This work significantly enhances the potential of AgCuTe-based materials for low to medium-temperature applications.

Migration behavior of impurities during the purification of waste graphite powders.

Metal-laden solid wastes (e.g., waste graphite powders) have attracted great attention owing to their hazardous effects on the surrounding soil and water. Additionally, the metal-bearing impurities also hinder the reutilization of waste graphite powders. Thus, it is necessary to remove these inorganic impurities and figure out the removal mechanism of impurities in the purification process. In this study, an alkaline roasting-water washing-acid leaching (AWA) method was used to upgrade the waste graphite powders, and the migration behavior of diverse impurities has been qualitatively and quantitatively investigated. A graphite product with high impurity removal efficiencies is attained under optimal conditions. The removal of impurities mainly follows three routes: (1) V-, P-, and S-bearing impurities were complete removed (some formed soluble salts during alkaline roasting, and the remainder was dissolved in acid); (2) most Al-, K-, and Si-bearing impurities were removed by alkaline roasting, with the remainder was dissolved in the acid-leaching process; and (3) Fe-, Mg-, Ti-, Ca-, and Zn-bearing impurities were decomposed at high temperature and reacted with alkali to form hydroxides or oxides, which was subsequently dissolved in acid. In addition, the treatment of the generated wastewater is also discussed. The uncovered migration mechanisms of diverse impurities would guide the purification and reutilization process of other metal-bearing solid wastes efficiently.

The adsorption and mass-transfer process of cationic red X-GRL dye on natural zeolite.

The adsorption behavior of natural zeolite was studied in order to determine the adsorption capacity and mass-transfer process of cationic red X-GRL (C(18)H(21)BrN(6)) onto the adsorbent. The adsorption tests to determine both the uptake capacity and the mass-transfer process at equilibrium were performed under batch conditions, which showed rapid uptake in general for the initial 5 min, corresponding to 92% total removal. The equilibrium adsorption capacity value (q(e,cal)) in pseudo-second-order kinetics was 13.51 mg/g at 293 K and the whole adsorption process was governed by physical adsorption with an endothermic, endothermic spontaneous nature. Adsorption tests indicated that the zeolite has great potential as an alternative low-cost material in the treatment of X-GRL drainage. However, the mass-transfer process to determine the rate-controlling steps showed that both film diffusion and pore diffusion were important in controlling the adsorption rate. The adsorption process was governed by film diffusion while pore diffusion was poor because the X-GRL molecules could not penetrate into the zeolite easily. The X-GRL molecules were only adsorbed on the external surface of the zeolite. Hence, to improve the adsorption capacity of natural zeolite further, modification to expand its micropores is necessary.

Revealing the Multi-Electron Reaction Mechanism of Na3 V2 O2 (PO4 )2 F Towards Improved Lithium Storage.

Na3 V2 O2 (PO4 )2 F (NVOPF) as an attractive electrode material has received much attention based on the one-electron reaction of V4+ /V5+ . However, the electrochemical reactions involving lower vanadium valences were not investigated till now. Herein, a composite of graphene decorated nanosheet-assembled NVOPF microflowers (NVOPF/G) was synthesized and the multi-electron reaction of NVOPF/G was conducted by controlling the operation voltage windows. The reaction mechanism, structural changes, and vanadium valences during the insertion/extraction of Li ions (from 2 to 6) were elucidated clearly by in-situ X-ray diffraction and ex-situ X-ray photoelectron spectroscopy. Theoretical computations also revealed the Li-ion locations in the structure of NaV2 O2 (PO4 )2 F. Due to the additional redox couple of V3+ /V4+ , NVOPF/G displayed a much higher initial capacity of 183.3 mAh g-1 in the wider voltage window of 1.0-4.8 V than that of 2.5-4.8 V (129.3 mAh g-1 ). Moreover, excellent Li-storage performance of NVOPF/G at a lower voltage (≤2.5 V) with the active reaction of V2+ /V3+ /V4+ was obtained for the first time, demonstrating the high potential of NVOPF/G as an anode material for Li ion storage.