X射线吸收光谱法
阳极
X射线光电子能谱
拉曼光谱
电化学
材料科学
电池(电)
阴极
分析化学(期刊)
碳纤维
化学工程
电极
吸收光谱法
化学
物理化学
复合材料
量子力学
复合数
光学
物理
工程类
功率(物理)
色谱法
作者
Sebahat Altundağ,Emine Altin,S. Altın,Mehmet Nurullah Ateş,Xiaobo Ji,Sevda Sahinbay
标识
DOI:10.1016/j.electacta.2023.143183
摘要
Na-ion batteries have gained significant attention as a cost-effective and efficient energy storage option for large scale applications, serving as an alternative to the Li-ion batteries. However, commercialization of these batteries is still many steps away since most cathode materials suffer from significant capacity loss and more full-cell studies are required. In this work, we report the electrochemical properties of half- and full-cells of P2-type Na0.67Mn0.85Cu0.15O2 synthesized by solid state technique. X-ray diffraction, FT-IR, and Raman spectroscopy, scanning electron microscopy, and energy-dispersive X-ray spectroscopy techniques are used to determine the structural properties. Surface properties are studied by X-ray photoelectron spectroscopy and Brunauer–Emmett–Teller techniques. Half cells and full cells were constructed with Na-metal and hard carbon, respectively. Na-ion diffusion kinetics at 10 °C, room temperature, and 50 °C were determined experimentally. Galvanostatic cycling tests on half-cells show capacity values of 165/124 mAh/g for the 1./100. cycles with 24.8 % capacity fade. Operando x-ray absorption spectroscopy measurements were utilized to study local structural modification around transition metal ions during charge/discharge. In the full-cell studies, electrode mass ratio (p/n) and parameters for presodiation of hard carbon were optimized. Using 30 mA/g current density, the unprocessed and the pre-sodiated full-cells reach capacity values of 48 mAh/g (p/n = 2.5) and 150 mAh/g (p/n = 0.75 and 1.15), respectively.
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