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Unveiling yavapaiite-type KxFe(SO4)(2) as a new Fe-based cathode with outstanding electrochemical performance for potassium-ion batteries

机译:揭开亚比塔钛矿型KXFE(SO4)(2)作为新的Fe基阴极,具有耐受电化学性能的耐钾离子电池

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We report KFe(SO4)(2) as a novel cathode material for potassium-ion batteries. The synthesis of phase-pure KFe(SO4)(2) is confirmed through Rietveld refinement of X-ray diffraction data, and the ion diffusion path and possible positions of K+ ions in the crystal structure are verified using bond-valence sum analysis. In addition, the theoretical average voltage, ion diffusion paths, and associated activation barrier energies obtained by first-principles calculations predict feasibility of the KFe(SO4)(2) as a robust cathode for potassium-ion batteries. . Experimentally, the average working voltage of KFe(SO4)(2) is approximately 3.3 V (vs. K+/K) assisted by Fe3+/2+ redox pair, and the resulting specific capacity (94 mAh g(-1)) obtained at C/20 approaches to the theoretical capacity, 94 mAh g(-1). In addition, the capacity retention of KFe(SO4)(2) at 2C was approximately 80% of the initial capacity after 300 cycles, with a Coulombic efficiency of over 99%. X-ray absorption near-edge structure and operando synchrotron X-ray diffraction analyses reveals the reversible change of the crystal structure with a minimal volume difference (1.83%) by occurrence of Fe3+/2+ redox reaction during dis/charge. The demonstrated excellent structural stability of KFe(SO4)(2) endorses feasibility of the KFe(SO4)(2) as a sustainable cathode for potassium-ion batteries.
机译:我们将KFE(SO4)(2)报告为钾离子电池的新型阴极材料。通过X射线衍射数据的RIETVELD细化确认相纯KFE(SO4)(2)的合成,并且使用键合价分析验证晶体结构中的k +离子的离子扩散路径和k +离子的可能位置。另外,通过第一原理计算获得的理论平均电压,离子扩散路径和相关的激活屏障能量将KFE(SO4)(2)的可行性预测为耐钾离子电池的鲁棒阴极。 。实验地,KFE(SO4)(2)的平均工作电压约为Fe3 + / 2 +氧化还原对辅助的3.3V(与k + / k),并获得所得的特定容量(94mAhg(-1)) C / 20对理论能力的方法,94mAhg(-1)。此外,在300次循环后,2C的KFE(SO4)(2)的容量保持约为初始容量的80%,水库效率超过99%。 X射线吸收近边缘结构和Operando同步调节X射线衍射分析显示在DIS /电荷期间通过发生Fe3 + / 2 +氧化还原反应的最小体积差(1.83%)的晶体结构的可逆变化。 kFe(SO4)(2)的优异结构稳定性认可了KFE(SO4)(2)作为钾离子电池的可持续阴极的可行性。

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