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液态合金 Na-K 阳极的阴极依赖性。

Cathode Dependence of Liquid-Alloy Na-K Anodes.

机构信息

Materials Science and Engineering Program and Texas Materials Institute , The University of Texas at Austin , Austin , Texas 78712 , United States.

出版信息

J Am Chem Soc. 2018 Mar 7;140(9):3292-3298. doi: 10.1021/jacs.7b12267. Epub 2018 Feb 21.

Abstract

Alkali ions can be plated dendrite-free into a liquid alkali-metal anode. Commercialized Na-S battery technology operates above 300 °C. A low-cost Na-K alloy is liquid at 25 °C from 9.2 to 58.2 wt% of sodium; sodium and/or potassium can be plated dendrite-free in the liquid range at room temperature. The co-existence of two alkali metals in an anode raises a question: whether the liquid Na-K alloy acts as a Na or a K anode. Here we show the alkali-metal that is stripped from the liquid Na-K anode is dependent on the preference of the cathode host. It acts as the anode of a sodium rechargeable cell if the cathode host structure selectively accepts only Na ions; as the anode of a potassium rechargeable cell if the cathode accepts K ions in preference to Na ions. This dual-anode behavior means the liquid Na-K alkali-alloy can be applied as a dendrite-free anode in Na-metal batteries as well as K-metal batteries.

摘要

碱金属离子可以无枝晶地镀到液态碱金属阳极上。商业化的 Na-S 电池技术在 300°C 以上运行。一种低成本的 Na-K 合金在 25°C 时的钠含量为 9.2 至 58.2wt%;钠和/或钾可以在室温下在液态范围内无枝晶沉积。在阳极中存在两种碱金属会引发一个问题:液态 Na-K 合金是充当 Na 阳极还是 K 阳极。在这里,我们表明从液态 Na-K 阳极剥离的碱金属取决于阴极主体的偏好。如果阴极主体结构选择性地仅接受 Na 离子,则它作为钠可再充电电池的阳极;如果阴极优先接受 K 离子而不是 Na 离子,则它作为钾可再充电电池的阳极。这种双阳极行为意味着液态 Na-K 碱合金可以用作无枝晶的 Na 金属电池和 K 金属电池的阳极。

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