异质结
阳极
法拉第效率
电场
材料科学
工作职能
锡
光电子学
扩散
储能
工作(物理)
纳米技术
电容
体积热力学
双金属片
电子转移
扩散阻挡层
电荷(物理)
领域(数学)
化学物理
带隙
半导体
工程物理
硫化物
电子
电流密度
动力学
作者
Tengfei Wang,Zhaoyu Tang,Chen Wang,Mao Xu,Zhikang Qin,Guoqing Tong,Yang Jiang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-03-13
卷期号:26 (11): 3830-3837
标识
DOI:10.1021/acs.nanolett.5c06515
摘要
Tin sulfide exhibits promise as a high-capacity anode for sodium-ion batteries but suffers from substantial volume expansion and sluggish kinetics. We constructed a hydrangea-like Bi/SnS heterojunction to address these challenges. Theoretical calculations reveal that the work function difference between metallic Bi and semiconducting SnS drives electron transfer from Bi to SnS, generating a built-in electric field (BIEF) at the interface. This field significantly enhances charge transfer kinetics while reducing the Na+ diffusion barrier to 0.12 eV and buffering volume variations. Consequently, the Bi/SnS anode demonstrates exceptional performance with an initial Coulombic efficiency of 92%, delivering 901 mAh g–1 at 0.1 A g–1 and maintaining 400 mAh g–1 at 20 A g–1. It exhibits remarkable cycling stability with 79.21% capacity retention after 3000 cycles at 10 A g–1, providing fundamental insights for heterointerface engineering in energy storage applications.
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