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Sulfur-Rich Graphene Nanoboxes with Ultra-High Potassiation Capacity at Fast Charge: Storage Mechanisms and Device Performance

机译:富含硫的石墨烯纳米氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧皂组在快速充电中有超高型电容:储存机构和设备性能

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摘要

It is a major challenge to achieve fast charging and high reversible capacity in potassium ion storing carbons. Here, we synthesized sulfur-rich graphene nanoboxes (SGNs) by one-step chemical vapor deposition to deliver exceptional rate and cyclability performance as potassium ion battery and potassium ion capacitor (PIC) anodes. The SGN electrode exhibits a record reversible capacity of 516 mAh g(-1) at 0.05 A g(-1), record fast charge capacity of 223 mA h g(-1) at 1 A g(-1), and exceptional stability with 89% capacity retention after 1000 cycles. Additionally, the SGN-based PIC displays highly favorable Ragone chart characteristics: 112 Wh kg(-1) at 505 W kg(-1) and 28 Wh kg(-1) at 14618 W kg(-1) with 92% capacity retention after 6000 cycles. X-ray photoelectron spectroscopy analysis illustrates a charge storage sequence based primarily on reversible ion binding at the structural-chemical defects in the carbon and the reversible formation of K-S-C and K2S compounds. Transmission electron microscopy analysis demonstrates reversible dilation of graphene due to ion intercalation, which is a secondary source of capacity at low voltage. This intercalation mechanism is shown to be stable even at cycle 1000. Galvanostatic intermittent titration technique analysis yields diffusion coefficients from 10(-10) to 10(-12) cm(2) s(-1), an order of magnitude higher than S-free carbons. The direct electroanalytic/analytic comparison indicates that chemically bound sulfur increases the number of reversible ion bonding sites, promotes reaction-controlled over diffusion-controlled kinetics, and stabilizes the solid electrolyte interphase. It is also demonstrated that the initial Coulombic efficiency can be significantly improved by switching from a standard carbonate-based electrolyte to an ether-based one.
机译:在钾离子储存碳中实现快速充电和高可逆容量是一个重大挑战。在这里,我们通过一步化学气相沉积法合成了富硫石墨烯纳米盒(SGN),以提供作为钾离子电池和钾离子电容器(PIC)阳极的优异速率和可循环性能。SGN电极在0.05 a g(-1)下的可逆容量为516 mAh g(-1),在1 a g(-1)下的快速充电容量为223 mAh g(-1),并且在1000次循环后保持了89%的容量,具有非凡的稳定性。此外,基于SGN的PIC显示出非常有利的拉贡图特征:505 W kg(-1)时为112 Wh kg(-1),14618 W kg(-1)时为28 Wh kg(-1),6000次循环后容量保持率为92%。X射线光电子能谱分析表明,电荷存储序列主要基于碳中结构化学缺陷处的可逆离子结合,以及K-S-C和K2S化合物的可逆形成。透射电子显微镜分析表明,由于离子插层,石墨烯发生可逆膨胀,这是低压下容量的第二来源。这种插层机制即使在循环1000时也保持稳定。恒电流间歇滴定技术分析得出的扩散系数为10(-10)至10(-12)cm(2)s(-1),比无硫碳高一个数量级。直接电分析/分析比较表明,化学结合硫增加了可逆离子键合位点的数量,促进了反应控制的扩散控制动力学,并稳定了固体电解质界面。研究还表明,从标准碳酸盐基电解液切换到乙醚基电解液可以显著提高初始库仑效率。

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