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High-Performance Sodium Metal Anodes Enabled by a Bifunctional Potassium Salt

机译:通过双官能钾盐使能高性能钠金属阳极

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Developing Na metal anodes that can be deeply cycled with high efficiency for a long time is a prerequisite for rechargeable Na metal batteries to be practically useful despite their notable advantages in theoretical energy density and potential low cost. Their high chemical reactivity with the electrolyte and tendency for dendrite formation are two major issues limiting the reversibility of Na metal electrodes. In this work, we introduce for the first time potassium bis(trifluoromethylsulfonyl)imide (KTFSI) as a bifunctional electrolyte additive to stabilize Na metal electrodes, in which the TFSI- anions decompose into lithium nitride and oxynitrides to render a desirable solid electrolyte interphase layer while the K+ cations preferentially adsorb onto Na protrusions and provide electrostatic shielding to suppress dendritic deposition. Through the cooperation of the cations and anions, we have realized Na metal electrodes that can be deeply cycled at a capacity of 10mAhcm(-2) for hundreds of hours.
机译:在长期内,开发可以深入循环的Na金属阳极是可充电Na金属电池的前提,尽管它们在理论能量密度和潜在的低成本中具有显着的优点,但是尽管它们的显着优势以及潜在的低成本。它们与电解质的高化学反应性和树突式形成的趋势是限制Na金属电极可逆性的两个主要问题。在这项工作中,我们将第一时间钾二(三氟甲基磺酰基)酰亚胺(KTFSI)作为双官能电解质添加剂介绍,以稳定Na金属电极,其中TFSIION分解成氮化锂和氮氧化物,以呈现理想的固体电解质相互异位层虽然K +阳离子优先吸附在Na突起上并提供静电屏蔽以抑制树突沉积。通过阳离子和阴离子的合作,我们已经实现了Na金属电极,其能够以10mAhcm(-2)的容量深度循环数百小时。

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