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The Effect of Crystalline Structure and Iron Doping on the Electrochemical Behavior of Germanium Oxide Anodes in Lithium-Ion Batteries

机译:晶体结构和铁掺杂对锂离子电池氧化锗阳极电化学行为的影响

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The need for alternative anode materials for lithium-ion batteries (LIBs) is one of the decisive steps towards the electrification of our public and private transportation, since the state-of-the-art anode material graphite intrinsically limits the energy and power density of current LIBs. As a potential alternative, alloying metal-oxides such as ZnO and SnO_2 have been widely studied, mostly due to their high theoretical specific capacities of 988 mAh g~(-1) and 1494 mAh g~(-1), respectively. Nevertheless, the pure oxides reveal poor electrochemical performance as a result of the eventually irreversible formation of the Li_2O matrix and the pronounced volume variation, causing active material exfoliation. When doped with transition metals, however, the Li_2O formation turns very reversible and the theoretically possible capacities can be achieved. As an example, Co-doped ZnO offers substantially higher specific capacities than pure ZnO (i.e., 966 mAh g~(-1) vs 330 mAh g~(-1)). Recently, the class of TM-doped alloying metal oxides has been extended to Fe-doped GeO_2, offering even higher specific capacities than transition metal doped SnO_2 (theoretically 2152 mAh g~(-1)).
机译:对于锂离子电池(LIBS)的替代阳极材料的需要是朝向我们公共和私人运输电气化的决定性步骤之一,因为最先进的阳极材料石墨本质上限制了能量和功率密度目前的libs。作为潜在的替代方案,已经广泛研究了诸如ZnO和SnO_2的合金化金属氧化物,主要是由于它们的高理论特异性为988mAhg〜(-1)和1494mAhg〜(-1)。尽管如此,纯氧化物由于Li_2O基质的最终不可逆形成和发明体积变化而导致差的电化学性能呈现出差的电化学性能,导致活性物质剥离。然而,当掺​​杂过渡金属时,Li_2O形成变得非常可逆,并且理论上可以实现可能的容量。作为一个例子,共掺杂的ZnO提供比纯ZnO(即966mAhg〜(-1)与330mah g〜(-1))的更高的特定能力。最近,TM掺杂合金化金属氧化物的类已经延伸到Fe掺杂的GeO_2,比过渡金属掺杂SnO_2(理论上2152mAhg〜(-1))提供甚至更高的比物质。

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