Nisar Umair, Gulied Mona Hersi, Shakoor R A, Essehli Rachid, Ahmad Zubair, Alashraf Abdullah, Kahraman Ramazan, Al-Qaradawi Siham, Soliman Ahmed
Center for Advanced Materials (CAM), Qatar University P. O. Box 2713 Doha Qatar
Department of Chemical Engineering, College of Engineering, Qatar University P. O. Box 2713 Doha Qatar.
RSC Adv. 2018 Sep 24;8(57):32985-32991. doi: 10.1039/c8ra06583g. eCollection 2018 Sep 18.
This research work focuses on the synthesis and performance evaluation of NaFe Cr (SO) ( = 0, 0.8 and 1.0) cathode materials in sodium ion batteries (SIBs). The novel materials having a primary particle size of around 100-200 nm were synthesized through a sol-gel process by reacting stoichiometric amounts of the precursor materials. The structural analysis confirms the formation of crystalline, phase pure materials that adopt a monoclinic crystal structure. Thermal analysis indicates the superior thermal stability of NaFe0Cr(SO) when compared to NaFe(SO) and NaCr(SO). Galvanostatic charge/discharge analysis indicates that the intercalation/de-intercalation of a sodium ion (Na) into/from NaFe(SO) ensues at about 3.2 V due to the Fe/Fe active redox couple. Moreover, XRD analysis confirms that the insertion/de-insertion of sodium into/from the host structure during charging/discharging is accompanied by a reversible single-phase reaction rather than a biphasic reaction. A similar sodium intercalation/de-intercalation mechanism has been noticed in NaFeCr(SO)which has not been reported earlier. The galvanostatic measurements and X-ray photoelectron spectroscopy (XPS) analysis confirm that the Cr/Cr redox couple is inactive in NaFe Cr (SO) ( = 0, 0.8) and thus does not contribute to capacity augmentation. However, suitable carbon coating may lead to activation of the Cr/Cr redox couple in these inactive materials.
本研究工作聚焦于钠离子电池(SIBs)中NaFeₓCr₁₋ₓ(SO₄)₂(x = 0、0.8和1.0)正极材料的合成与性能评估。通过使化学计量的前驱体材料反应,采用溶胶 - 凝胶法合成了初级粒径约为100 - 200 nm的新型材料。结构分析证实形成了具有单斜晶体结构的结晶、相纯材料。热分析表明,与NaFe(SO₄)₂和NaCr(SO₄)₂相比,NaFe₀Cr₁(SO₄)₂具有优异的热稳定性。恒电流充放电分析表明,由于Fe³⁺/Fe²⁺活性氧化还原对,钠离子(Na⁺)在约3.2 V时嵌入/脱嵌NaFe(SO₄)₂。此外,XRD分析证实,充电/放电过程中钠离子在主体结构中的嵌入/脱嵌伴随着可逆的单相反应而非双相反应。在NaFeₓCr₁₋ₓ(SO₄)₂中也观察到了类似的钠离子嵌入/脱嵌机制,这在之前尚未见报道。恒电流测量和X射线光电子能谱(XPS)分析证实,在NaFeₓCr₁₋ₓ(SO₄)₂(x = 0、0.8)中Cr³⁺/Cr²⁺氧化还原对不活跃,因此对容量增加没有贡献。然而,合适的碳涂层可能会使这些不活跃材料中的Cr³⁺/Cr²⁺氧化还原对活化。