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Interfacial built-in electric field and crosslinking pathways enabling WS2/Ti3C2T heterojunction with robust sodium storage at low temperature

异质结 材料科学 电场 离子 动力学 电化学 电子 光电子学 储能 纳米技术 扩散 化学物理 化学工程 化学 电极 物理化学 热力学 物理 工程类 功率(物理) 量子力学 有机化学
作者
Jiabao Li,Shaocong Tang,Jingjing Hao,Quan Yuan,Tianyi Wang,Likun Pan,Jinliang Li,Shenbo Yang,Chengyin Wang
出处
期刊:Journal of Energy Chemistry [Elsevier]
卷期号:89: 635-645 被引量:12
标识
DOI:10.1016/j.jechem.2023.10.037
摘要

Developing efficient energy storage for sodium-ion batteries (SIBs) by creating high-performance heterojunctions and understanding their interfacial interaction at the atomic/molecular level holds promise but is also challenging. Besides, sluggish reaction kinetics at low temperatures restrict the operation of SIBs in cold climates. Herein, cross-linking nanoarchitectonics of WS2/Ti3C2Tx heterojunction, featuring built-in electric field (BIEF), have been developed, employing as a model to reveal the positive effect of heterojunction design and BIEF for modifying the reaction kinetics and electrochemical activity. Particularly, the theoretical analysis manifests the discrepancy in work functions leads to the electronic flow from the electron-rich Ti3C2Tx to layered WS2, spontaneously forming the BIEF and "ion reservoir" at the heterogeneous interface. Besides, the generation of cross-linking pathways further promotes the transportation of electrons/ions, which guarantees rapid diffusion kinetics and excellent structure coupling. Consequently, superior sodium storage performance is obtained for the WS2/Ti3C2Tx heterojunction, with only 0.2% decay per cycle at 5.0 A g−1 (25 °C) up to 1000 cycles and a high capacity of 293.5 mA h g−1 (0.1 A g−1 after 100 cycles) even at −20 °C. Importantly, the spontaneously formed BIEF, accompanied by "ion reservoir", in heterojunction provides deep understandings of the correlation between structure fabricated and performance obtained.
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