Mukai Kazuhiko, Yamada Ikuya
Toyota Central Research and Development Laboratories, Inc., 41-1 Yokomichi, Nagakute, Aichi 480-1192, Japan.
Department of Materials Science, Graduate School of Engineering, Osaka Prefecture University, 1-2 Gakuen-cho, Sakai, Osaka 599-8570, Japan.
ACS Omega. 2020 Apr 20;5(17):10115-10122. doi: 10.1021/acsomega.0c00728. eCollection 2020 May 5.
The demand for eco-friendly materials for secondary batteries has stimulated the exploration of a wide variety of Fe oxides, but their potential as electrode materials remains unknown. In this contribution, ϵ-FeOOH was synthesized using a high-pressure/high-temperature method and examined for the first time in nonaqueous Li and Na cells. Under a pressure of 8 GPa, α-FeOOH transformed into ϵ-FeOOH at 400 °C and then decomposed into α-FeO and HO above 500 °C. Here, FeO octahedra form [2 × 1] tunnels in α-FeOOH or [1 × 1] tunnels in ϵ-FeOOH. The ϵ-FeOOH/Li cell exhibited a rechargeable capacity ( ) of ∼700 mA h·g at 0.02-3.0 V, whereas the ϵ-FeOOH/Na cell indicated a of less than 30 mA h·g at 0.02-2.7 V. The discharge and charge profiles of ϵ-FeOOH and α-FeOOH were similar, but the rate capability of ϵ-FeOOH was superior to that of α-FeOOH.
对二次电池环保材料的需求激发了对多种铁氧化物的探索,但它们作为电极材料的潜力仍不为人知。在本研究中,采用高压/高温法合成了ε-FeOOH,并首次在非水锂和钠电池中进行了研究。在8 GPa的压力下,α-FeOOH在400 °C时转变为ε-FeOOH,然后在500 °C以上分解为α-FeO和HO。在此,FeO八面体在α-FeOOH中形成[2×1]隧道,或在ε-FeOOH中形成[1×1]隧道。ε-FeOOH/Li电池在0.02-3.0 V时表现出约700 mA h·g的可充电容量( ),而ε-FeOOH/Na电池在0.02-2.7 V时的 小于30 mA h·g。ε-FeOOH和α-FeOOH的充放电曲线相似,但ε-FeOOH的倍率性能优于α-FeOOH。