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用于可充电金属电池的拉丝金属。

Brushed Metals for Rechargeable Metal Batteries.

作者信息

Chen Weiyin, Salvatierra Rodrigo V, Li John T, Luong Duy X, Beckham Jacob L, Li Victor D, La Nghi, Xu Jianan, Tour James M

机构信息

Chemistry Department, Rice University, 6100 Main St, Houston, TX, 77005, USA.

Applied Physics Program, Rice University, 6100 Main St, Houston, TX, 77005, USA.

出版信息

Adv Mater. 2022 Aug;34(31):e2202668. doi: 10.1002/adma.202202668. Epub 2022 Jul 5.

Abstract

Battery designs are swiftly changing from metal-ion to rechargeable metal batteries. Theoretically, metals can deliver maximum anode capacity and enable cells with improved energy density. In practice, these advantages are only possible if the parasitic surface reactions associated with metal anodes are controlled. These undesirable surface reactions are responsible for many troublesome issues, like dendrite formation and accelerated consumption of active materials, which leads to anodes with low cycle life or even battery runaway. Here, a facile and solvent-free brushing method is reported to convert powders into films atop Li and Na metal foils. Benefiting from the reactivity of Li metal with these powder films, surface energy can be effectively tuned, thereby preventing parasitic reaction. In-operando study of P S -modified Li anodes in liquid electrolyte cells reveals a smoother electrode contour and more uniform metal electrodeposition and dissolution behavior. The P S -modified Li anodes sustain ultralow polarization in symmetric cell for >4000 h, ≈8× longer than bare Li anodes. The capacity retention is ≈70% higher when P S -modified Li anodes are paired with a practical LiFePO cathode (≈3.2 mAh cm ) after 340 cycles. Brush coating opens a promising avenue to fabricate large-scale artificial solid-electrolyte-interphase directly on metals without the need for organic solvent.

摘要

电池设计正在迅速从金属离子电池转向可充电金属电池。从理论上讲,金属可以提供最大的阳极容量,并使电池具有更高的能量密度。实际上,只有当与金属阳极相关的寄生表面反应得到控制时,这些优势才有可能实现。这些不良的表面反应会导致许多麻烦问题,如枝晶形成和活性材料的加速消耗,从而导致阳极的循环寿命较低,甚至引发电池失控。在此,报道了一种简便且无溶剂的刷涂方法,可将粉末转化为锂和钠金属箔上的薄膜。受益于锂金属与这些粉末薄膜的反应性,可以有效地调节表面能,从而防止寄生反应。对液体电解质电池中PS改性锂阳极的原位研究表明,电极轮廓更平滑,金属电沉积和溶解行为更均匀。PS改性锂阳极在对称电池中可保持超低极化超过4000小时,比裸锂阳极长约8倍。当PS改性锂阳极与实用的磷酸铁锂阴极(≈3.2 mAh cm)配对时,经过340次循环后,容量保持率高出约70%。刷涂为直接在金属上大规模制备人造固体电解质界面开辟了一条有前景的途径,而无需有机溶剂。

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