Molybdenum‐Incorporated O3‐type Sodium Layered Oxide Cathodes for High‐Performance Sodium‐Ion Batteries

阴极 电化学 材料科学 氧化物 介电谱 电解质 电池(电) 钠离子电池 热稳定性 化学工程 无机化学 电极 化学 冶金 物理化学 法拉第效率 功率(物理) 工程类 物理 量子力学
作者
Buzaina Moossa,Jeffin James Abraham,Ranasinghe Arachchige Harindi Gayara,Abdul Moiz Ahmed,Rana Faisal Shahzad,Ramazan Kahraman,Siham Y. Al-Qaradawi,Shahid Rasul,Abdul Shakoor
出处
期刊:Energy technology [Wiley]
卷期号:11 (12) 被引量:13
标识
DOI:10.1002/ente.202300437
摘要

Transition metal layered oxide materials with a general formula Na x MO 2 (M = Ni, Mn, Co, Fe) are widely researched with various possible electrode configurations. Herein, O3‐type NaNi (1− x )/2 Mn (1− x )/2 Mo x O 2 ( x = 0, 0.05,0.1) layered oxide cathode materials are synthesized by solid‐state reaction method, and its structural, thermal, and electrochemical performance in sodium ion battery is investigated. The structural analysis reveals that a single phase highly crystalline O3‐type cathode material with an irregular particle shape is formed. The introduction of molybdenum improves the thermal stability of cathode materials, which can be attributed to the improved TMO 2 layers that provide stability to the material. The addition of Mo to Na‐layered oxide cathode materials enhances electrochemical performance. The developed cathode materials, the NaNi 0.475 Mn 0.475 Mo 0.05 O 2 , exhibit excellent specific discharge capacity (≈154 mAh g −1 ) at C/20 rate, (an increase of ≈20% when compared to the NaNi 0.5 Mn 0.5 O 2 ) which can be attributed to the increased capacitance effect by the addition of Mo. The electrochemical impedance spectroscopy study reveals that the diffusion of Na+ into/from the host structure is rapid during the first cycle and then gradually reduces with subsequent cycling due to the formation of the solid electrolyte interface layer, which hinders Na+ migration. This has a potential effect on the improved electrochemical performance of the material.
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