Electrochemical performances of polyvanadate plate-like crystals

被引:1
|
作者
Nefzi, H. [1 ]
Sediri, F. [1 ,2 ]
机构
[1] Univ Tunis, Unite Rech Mat & Environm UR15ES01, IPEIT, 2 Rue Jawaher Lel Nahru, Tunis 1089, Tunisia
[2] Univ Tunis El Manar, Fac Sci Tunis, Tunis 2092, Tunisia
关键词
Batteries; Charging/discharging; Electrochemical characterizations; Intercalation compounds; COMPOSITE CATHODE MATERIALS; VANADIUM-OXIDE; ENERGY-STORAGE; HYDROTHERMAL SYNTHESIS; CARBON NANOTUBES; V2O5; ELECTRODES; HYBRID; PSEUDOCAPACITANCE; MICROSPHERES;
D O I
10.1007/s11581-020-03898-7
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Layered hybrid compounds (H3N(CH2)(3)NH3)[V4O10] and (H3N(CH2)(4)NH3)[V6O14] have been synthesized via the hydrothermal method. Compounds were analyzed through X-ray powder diffraction, scanning electron microscopy, and X-ray photoelectron spectroscopy. The electrochemical performance of electrode materials was evaluated by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). CV curves show only one electron transfer reaction, which is in accordance with insertion/extraction of the Li+ ion into/out from the material electrode. Furthermore, the kinetics of electrode reaction is controlled by charge transfer and diffusion processes. EIS measurements illustrate the lower charge transfer, which makes Li+ ion transfer quicker. In addition, values of lithium ion diffusion coefficient into these intercalation materials were found to be 0.1 x 10(-10) and 0.21 x 10(-11) cm(2) s(-1) for (H3N(CH2)(3)NH3)[V4O10] and (H3N(CH2)(4)NH3)[V6O14], respectively, after the 50th cycle.
引用
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页码:1297 / 1305
页数:9
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