Zhaowei Sun, Ronghou Yao, Yingshan Huang, Jin Wu, Caiju Li, Jianhong Yi, Shizhao Xiong, Hongying Hou, Hengxing Ji
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引用次数: 0
Abstract
Sodium (Na) metal anode is the essential component of low-cost and high-performance Na metal batteries, yet its application is hampered by the unstable anode/electrolyte interface and inevitable growth of Na dendrites. In this work, a hierarchically porous artificial surface layer with sodiophilic silver (Ag) nanoparticles decorating the bottom surface (HPFA) is reported, which can regulate the uniform deposition of Na and eliminate the local overgrowth of dendrites on the surface of Na substrate. The dependence of Na deposition behavior on the hierarchical structure of surface layers is revealed by operando optical microscopy and multiphysics simulation, indicating the multifunction of the HPFA layer in stabilizing the Na anode during the electrochemical plating/stripping process. The as-fabricated HPFA/Na anode depicts prolonged life-span and improved stability in both ether and carbonate electrolytes, while the symmetric cell shows no sign of short-circuit even after 1200 h of repeated charging/discharging at 2 mA cm−2 with a high area capacity of 4 mAh cm−2. Besides, when the HPFA/Na anode is paired with Na3V2(PO4)3 cathode and ether electrolyte, the full cell exhibits a low decay rate of ≈0.28% with a stable coulombic Efficiency value of ≈99.88% at 2 C rate.
金属钠(Na)阳极是低成本、高性能钠金属电池的重要组成部分,但其应用受到阳极/电解质界面不稳定和Na枝晶不可避免生长的制约。本文报道了一种由亲钠银(Ag)纳米粒子装饰底表面的分层多孔人工表面层(HPFA),它可以调节Na的均匀沉积并消除Na衬底表面局部枝晶的过度生长。通过光学显微镜和多物理场模拟,揭示了表面层的分层结构对Na沉积行为的依赖性,表明HPFA层在电化学镀/剥离过程中稳定Na阳极的多功能。制备的HPFA/Na阳极在乙醚和碳酸盐电解质中均表现出延长的寿命和提高的稳定性,而对称电池即使在以2 mA cm - 2的高面积容量达到4 mAh cm - 2的情况下重复充放电1200小时后也没有短路的迹象。此外,当HPFA/Na阳极与Na3V2(PO4)3阴极和醚电解质配对时,整个电池在2℃速率下的衰减率约为0.28%,库仑效率稳定为约99.88%。
期刊介绍:
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