材料科学
过电位
阳极
成核
电镀(地质)
纳米-
化学工程
纳米技术
剥离(纤维)
复合材料
电化学
电极
化学
有机化学
物理化学
工程类
地质学
地球物理学
作者
Syam Kandula,Eunji Kim,Chi Won Ahn,Jinwoo Lee,Bongjun Yeom,Seung Woo Lee,Jinhan Cho,Hyung‐Kyu Lim,Yonghee Lee,Jeong Gon Son
标识
DOI:10.1016/j.ensm.2023.103024
摘要
Anode-free sodium-metal batteries are considered one of the most promising alternatives for developing high-end batteries due to their high theoretical capacity, low cost, and high natural abundance. However, they have severe drawbacks in the form of inferior long-term cyclic stability. We engineered mechanically resilient MXene/CNT nano-accordion frameworks (NAFs) to host significant Na without dendrite development, even at high currents. The microcellular structures of MXene/CNT-NAFs possess numerous micro-sized pores and sodium nucleation sites. The synergetic effects of strong adhesion and charge transfer between MXene and CNT reduce overpotential during plating/stripping and facilitate uniform Na deposition. Resilient nano-accordion structures are compressed by capillary of Na nucleation during plating and expand during stripping, allowing long-term plating/stripping with little volume change. These benefits allow the MXene/CNT-NAFs/Na asymmetric cell to maintain its average CE at 99.7% with capacities of 1.0 mAh⋅cm−2 at 1.0 mA⋅cm−2 for 900 h. Furthermore, MXene/CNT-NAFs symmetric cell exhibits a very low overpotential of 12.0 mV after 1,500 h with a capacity of 3.0 mAh⋅cm−2 at 3.0 mA⋅cm−2 and stores high capacities of 20.0 mAh⋅cm−2 at 5.0 mA⋅cm−2 for 1,200 h. The anode-free MXene/CNT-NAFs//Na3V2(PO4)3@C full-cell demonstrates exceptional long-term cyclic stability over 5,000 cycles at 5.0 C and 10.0 C without cell failure.
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