化学
退火(玻璃)
结晶度
氧化剂
电化学
机械化学
相(物质)
过渡金属
化学工程
结晶学
物理化学
有机化学
催化作用
冶金
电极
材料科学
工程类
作者
Rebecca D. McAuliffe,Gabrielle E. Kamm,Matthew J. McDermott,Raphaël P. Hermann,Neyanel Vasquez-Garcia,Robert L. Sacci,Kristin A. Persson,Karena W. Chapman,Gabriel M. Veith
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2023-02-16
卷期号:62 (8): 3358-3367
被引量:11
标识
DOI:10.1021/acs.inorgchem.2c03286
摘要
To better understand polymorph control in transition metal oxides, the mechanochemical synthesis of NaFeO2 was explored. Herein, we report the direct synthesis of α-NaFeO2 through a mechanochemical process. By milling Na2O2 and γ-Fe2O3 for 5 h, α-NaFeO2 was prepared without high-temperature annealing needed in other synthesis methods. While investigating the mechanochemical synthesis, it was observed that changing the starting precursors and mass of precursors affects the resulting NaFeO2 structure. Density functional theory calculations on the phase stability of NaFeO2 phases show that the α phase is stabilized over the β phase in oxidizing environments, which is provided by the oxygen-rich reaction between Na2O2 and Fe2O3. This provides a possible route to understanding polymorph control in NaFeO2. Annealing the as-milled α-NaFeO2 at 700 °C has resulted in increased crystallinity and structural changes that improved electrochemical performance in terms of capacity over the as-milled sample.
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