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Defect-Rich Soft Carbon Porous Nanosheets for Fast and High-Capacity Sodium-Ion Storage

机译:用于快速和高容量钠离子储存的缺陷富含软碳多孔纳米片

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摘要

Soft carbon has attracted tremendous attention as an anode in rocking-chair batteries owing to its exceptional properties including low-cost, tunable interlayer distance, and favorable electronic conductivity. However, it fails to exhibit decent performance for sodium-ion storage owing to difficulties in the formation of sodium intercalation compounds. Here, microporous soft carbon nanosheets are developed via a microwave induced exfoliation strategy from a conventional soft carbon compound obtained by pyrolysis of 3,4,9,10-perylene tetracarboxylic dianhydride. The micropores and defects at the edges synergistically leads to enhanced kinetics and extra sodium-ion storage sites, which contribute to the capacity increase from 134 to 232 mAh g(-1) and a superior rate capability of 103 mAh g(-1) at 1000 mA g(-1) for sodium-ion storage. In addition, the capacitance-dominated sodium-ion storage mechanism is identified through the kinetics analysis. The in situ X-ray diffraction analyses are used to reveal that sodium ions intercalate into graphitic layers for the first time. Furthermore, the as-prepared nanosheets can also function as an outstanding anode for potassium-ion storage (reversible capacity of 291 mAh g(-1)) and dual-ion full cell (cell-level capacity of 61 mAh g(-1) and average working voltage of 4.2 V). These properties represent the potential of soft carbon for achieving high-energy, high-rate, and low-cost energy storage systems.
机译:由于其具有低成本,可调谐层间距离和有利的电子电导率,软碳在摇椅电池中吸引了巨大的关注。然而,由于肝脏酸钠化合物的困难,它未能表现出钠离子储存的体面性能。这里,通过微波诱导的剥离策略从通过热解3,4,9,10-鲍缩四羧酸二酐得到的常规软碳化合物进行微孔诱导的剥离策略。边缘的微孔和缺陷协同导致增强的动力学和额外的钠离子储存位点,这有助于从134到232mAhg(-1)增加到103mAhg(-1)的高速速率能力1000 mA g(-1)用于钠离子储存。此外,通过动力学分析识别电容束缚的钠离子储存机构。原位X射线衍射分析用于揭示钠离子首次嵌入石墨层中。此外,制备的纳米片也可以用作钾离子储存的优异阳极(可逆容量为291mAh(-1))和双离子全细胞(电池级容量为61mAhg(-1)和平均工作电压为4.2 V)。这些性质代表了用于实现高能,高速率和低成本储能系统的软碳的潜力。

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