| Literature DB >> 30740881 |
Man Huang1, Baojuan Xi1, Zhenyu Feng1, Fangfang Wu1, Denghu Wei2, Jing Liu3, Jinkui Feng4, Yitai Qian1, Shenglin Xiong1,5.
Abstract
The significant issues with alkali metal batteries arise from their poor electrochemical properties and safety problems, limiting their applications. Herein, TiO2 nanoparticles embedded into N-doped porous carbon truncated ocatahedra (TiO2 ⊂NPCTO) are engineered as a cathode material with different metal anodes, including solid Na or K and liquid Na-K alloy. Electrochemical performance and kinetics are systematically analyzed, with the aim to determine detailed electrochemistry. By using a galvanostatic intermittent titration technique, TiO2 ⊂NPCTO/NaK shows faster diffusion of metal ions in insertion and extraction processes than that of Na-ions and K-ions in solid Na and K. The lower reaction resistance of liquid Na-K alloy electrode is also examined. The higher b-value of TiO2 ⊂NPCTO/NaK confirms that the reaction kinetics are promoted by the surface-induced capacitive behavior, favorable for high rate performance. This superiority highly pertains to the distinct liquid-liquid junction between the electrolyte and electrode, and the prohibition of metal dendrite growth, substantiated by symmetric cell testing, which provides a robust and homogeneous interface more stable than the traditional solid-liquid one. Hence, the liquid Na-K alloy-based battery exhibits to better cyclablity with higher capacity, rate capability, and initial coulombic efficiency than solid Na and K batteries.Entities:
Keywords: N-doped porous carbon; Na-K liquid alloy anode; alkali metal batteries; dendrite growth; liquid−liquid interface
Year: 2019 PMID: 30740881 DOI: 10.1002/smll.201804916
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281