1. Effect of 3D Metal on Electrochemical Properties of Sodium Intercalation Cathode P2-NaxMe1/3Mn2/3O2 (M = Co, Ni, or Fe)
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Trang Thi Thu Nguyen, Akhil Ranjan Garg, Xujian Cui, Nguyen Le Thanh Huynh, Man Van Tran, Dieu Thi Ngoc Nguyen, Nam Pham Phuong Le, Hoang Van Nguyen, Phung My Loan Le, and An Le Bao Phan
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Article Subject ,Coprecipitation ,Inorganic chemistry ,Intercalation (chemistry) ,Oxide ,02 engineering and technology ,General Chemistry ,010402 general chemistry ,021001 nanoscience & nanotechnology ,Electrochemistry ,01 natural sciences ,Redox ,0104 chemical sciences ,law.invention ,Metal ,Chemistry ,chemistry.chemical_compound ,chemistry ,law ,visual_art ,visual_art.visual_art_medium ,Calcination ,0210 nano-technology ,QD1-999 ,Solid solution - Abstract
This research aims to evaluate the influence of different 3D metals (Fe, Co, and Ni) substituted to Mn on the electrochemical performance of P2-NaxMe1/3Mn2/3O2 material, which was synthesized by the coprecipitation process followed by calcination at high temperature. X-ray diffraction (XRD) results revealed that the synthesized Mn-rich materials possessed a P2-type structure with a negligible amount of oxide impurities. The materials possessed their typical cyclic voltammogram and charge-discharge profiles; indeed, a high reversible redox reaction was obtained by NaxCo1/3Mn2/3O2 sample. Both NaxCo1/3Mn2/3O2 and NaxFe1/3Mn2/3O2 provided a high specific capacity of above 140 mAh·g−1; however, the former showed better cycling performance with 83% capacity retention after 50 cycles at C/10 and high rate capability. Meanwhile, the Ni-sub NaxNi1/3Mn2/3O2 exhibited excellent cycling stability but a low specific capacity of 110 mAh·g−1 and inferior rate capability. The diffusion coefficient of Na+ ions into the structure tended to decrease with a depth of discharge; those values were in the range of 10−10–10−9 cm2·s−1 and 10−11–10−10 cm2·s−1 in the solid solution region and biphasic region, respectively.
- Published
- 2021
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