材料科学
氧化物
阳极
微观结构
化学工程
电化学
衍射
水溶液
相(物质)
化学
电极
复合材料
冶金
光学
有机化学
物理
工程类
物理化学
作者
Caroline Piffet,Bénédicte Vertruyen,Frédéric Hatert,Rudi Cloots,Frèdéric Boschini,Abdelfattah Mahmoud
标识
DOI:10.1016/j.jechem.2021.05.050
摘要
Na2Ti3O7 has attracted much attention in the field of anode materials for Na-ion batteries thanks to its non-toxicity and very low working potential of 0.3 V vs Na0/Na+. Building a clearer picture of its formation from cheap Na2CO3 and TiO2 starting materials is therefore of obvious interest. Here, we report new insights from an in-situ high temperature X-ray diffraction study conducted from room temperature to 800 °C, complemented by ex-situ characterizations. We were thereby able to position the previously reported Na4Ti5O12 and Na2Ti6O13 intermediate phases in a reaction scheme involving three successive steps and temperature ranges. Shifts and/or broadening of a subset of the Na2Ti6O13 reflections suggested a combination of intra-layer disorder with the well-established ordering of successive layers. This in-situ study was carried out on reproducible mixtures of Na2CO3 and TiO2 in 1:3 molar ratio prepared by spray-drying of mixed aqueous suspensions. Single-phase Na2Ti3O7 was obtained after only 8 h at 800 °C in air, instead of a minimum of 20 h for a conventional solid-state route using the same precursors. Microstructure analysis revealed ~ 15 µm diameter granules made up from rectangular rods of a few-µm length presenting electrochemical properties in line with expectations. In the absence of grinding or formation of intimate composites with conductive carbon, the specific capacity of 137 mAh/g at C/5 decreased at higher rates.
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