Santoro Gonzalo, Amarilla José Manuel, Tartaj Pedro, Vázquez-Santos María Beatriz
Institute of Materials Science of Madrid, ICMM-CSIC, c/ Sor Juana Inés de la Cruz 3, Cantoblanco, E-28049, Madrid, Spain.
Mater Today Energy. 2018 Dec 1;10:23-27. doi: 10.1016/j.mtener.2018.08.005. Epub 2018 Aug 24.
Na-ion batteries are nowadays receiving renewed attention because of its propitiousness for large-scale stationary applications. Although the Na storage mechanism is still not completely understood, TiO nanoparticles are very promising active anode materials in Na-ion batteries provided that a correct dispersion is achieved within the battery electrode. Whilst the structural changes, either in crystallinity or crystalline phase, that occur during operation are receiving much recent attention, the nanometric morphological evolution of the TiO nanoparticles within the electrode is yet to be thoroughly addressed, despite its implication in battery efficiency. In the present work, small-angle x-ray scattering studies on TiO/Na-ion batteries show that whereas the nanoparticle size is preserved during the discharge-charge cycles, the mean distance between nanoparticles increases. The observed morphological changes are consistent with electrode swelling and nanoparticle aggregation during operation, being one phenomenon dominant over the other depending on the applied density current; thus, depending on the differences in ion diffusion within the electrode.
由于钠离子电池在大规模固定应用方面具有优势,如今正重新受到关注。尽管钠存储机制仍未完全理解,但只要在电池电极内实现正确的分散,TiO纳米颗粒在钠离子电池中是非常有前景的活性负极材料。虽然运行过程中发生的结晶度或晶相的结构变化最近受到了很多关注,但电极内TiO纳米颗粒的纳米级形态演变尚未得到充分研究,尽管其对电池效率有影响。在本工作中,对TiO/钠离子电池的小角X射线散射研究表明,虽然纳米颗粒尺寸在充放电循环中保持不变,但纳米颗粒之间的平均距离增加。观察到的形态变化与运行过程中的电极膨胀和纳米颗粒聚集一致,根据施加的密度电流,一种现象比另一种现象更占主导;因此,取决于电极内离子扩散的差异。