硒化物
阳极
铋
拓扑绝缘体
材料科学
电化学
钠
电解质
电极
纳米技术
化学工程
冶金
化学
物理化学
硒
凝聚态物理
物理
工程类
作者
Wanjie Gao,Yuhan Lu,Junlun Cao,Shuanglong Xu,Yinxu Lu,Xi Liu,Dan Liú,Yuping Wu,Jiarui He
出处
期刊:Small
[Wiley]
日期:2025-08-30
卷期号:21 (42): e06772-e06772
被引量:3
标识
DOI:10.1002/smll.202506772
摘要
Abstract Metallic sodium (Na) is an attractive anode material for sodium metal batteries (SMBs) due to its high theoretical capacity and natural abundance. However, the unstable electrolyte/electrode interface and uncontrollable Na dendrite growth arising from the inhomogeneous Na + transfer have significantly restricted its practical feasibility. Herein, the topological insulator of bismuth selenide (Bi 2 Se 3 ), which has protected conducting states on its surface, is selected as a regulator to guide uniform Na + transfer. An in situ conversion/alloying reaction between Bi 2 Se 3 and Na can construct a multifunctional heterogeneous interlayer composed of sodium bismuth alloy (Na 3 Bi) and sodium selenide (Na 2 Se). Such a heterogeneous interlayer with excellent sodiophilic capability and superior ionic conductivity can facilitate rapid Na + diffusion and guide uniform Na deposition. Consequently, the Bi 2 Se 3 ‐Na symmetric cell achieves an ultralong cycling lifespan over 2100 h at 1 mA cm −2 /1 mA h cm −2 with extremely low voltage hysteresis of 14 mV. In addition, the Bi 2 Se 3 ‐Na||Na 3 V 2 (PO 4 ) 3 (NVP) full cell exhibits a high‐capacity retention of 93.7% after 1500 cycles at a high current density of 20 C. More impressively, the constructed anode‐free Bi 2 Se 3 ‐Cu||NVP cell demonstrates excellent cycling stability (75.1 mA h g −1 at 1 C after 100 cycles).
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