4.6 Article

Synthesis and performance evaluation of nanostructured NaFexCr1-X(SO4)2 cathode materials in sodium ion batteries (SIBs)

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RSC ADVANCES
卷 8, 期 57, 页码 32985-32991

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ra06583g

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  1. Center for Advanced Materials (CAM), Qatar University, Doha, Qatar

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This research work focuses on the synthesis and performance evaluation of NaFexCr1-X(SO4)(2) (X = 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 NaFe0(.8)Cr(0.2)(SO4)(2) when compared to NaFe(SO4)(2) and NaCr(SO4)(2). Galvanostatic charge/discharge analysis indicates that the intercalation/de-intercalation of a sodium ion (Na+) into/from NaFe(SO4)(2) ensues at about 3.2 V due to the Fe2+/Fe3+ active redox couple. Moreover, ex situ 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 NaFe0.8Cr0.2(SO4)(2)which has not been reported earlier. The galvanostatic measurements and X-ray photoelectron spectroscopy (XPS) analysis confirm that the Cr2+/Cr3+ redox couple is inactive in NaFexCr1-X(SO4)(2) (X = 0, 0.8) and thus does not contribute to capacity augmentation. However, suitable carbon coating may lead to activation of the Cr2+/Cr3+ redox couple in these inactive materials.

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