دورية أكاديمية

Manipulating Oxygen Vacancies to Spur Ion Kinetics in V2O5 Structures for Superior Aqueous Zinc‐Ion Batteries.

التفاصيل البيبلوغرافية
العنوان: Manipulating Oxygen Vacancies to Spur Ion Kinetics in V2O5 Structures for Superior Aqueous Zinc‐Ion Batteries.
المؤلفون: Ye, Jia‐Jia, Li, Pei‐Hua, Zhang, Hao‐Ran, Song, Zong‐Yin, Fan, Tianju, Zhang, Wanqun, Tian, Jie, Huang, Tao, Qian, Yitai, Hou, Zhiguo, Shpigel, Netanel, Chen, Li‐Feng, Dou, Shi Xue
المصدر: Advanced Functional Materials; 11/9/2023, Vol. 33 Issue 46, p1-10, 10p
مصطلحات موضوعية: ELECTRON paramagnetic resonance spectroscopy, ELECTRON paramagnetic resonance, DIFFUSION barriers, DENSITY functional theory, ZINC ions, OXYGEN
مستخلص: Vanadium‐based intercalation materials have attracted considerable attention for aqueous zinc‐ion batteries (ZIBs). However, the sluggish interlaminar diffusion of zinc ions due to the strong electrostatic interaction, severely restricts their practical application. Herein, oxygen vacancy‐enriched V2O5 structures (Zn0.125V2O5·0.95H2O nanoflowers, Ov‐ZVO) with expanded interlamellar space and excellent structural stability are prepared for superior ZIBs. In situ electron paramagnetic resonance (EPR) and X‐ray diffraction (XRD) characterization revealed that numerous oxygen vacancies are generated at a relatively low reaction temperature because of partially escaped lattice water. In situ spectroscopy and density functional theory (DFT) calculations unraveled that the existence of oxygen vacancies lowered Zn2+ diffusion barriers in Ov‐ZVO and weakened the interaction between Zn and O atoms, thus contributing to excellent electrochemical performance. The Zn||Ov‐ZVO battery displayed a remarkable capacity of 402 mAh g−1 at 0.1 A g−1 and impressive energy output of 193 Wh kg−1 at 2673 W kg−1. As a proof of concept, the Zn||Ov‐ZVO pouch cell can reach a high capacity of 350 mAh g−1 at 0.5 A g−1, demonstrating its enormous potential for practical application. This study provides fundamental insights into formation of oxygen‐vacant nanostructures and generated oxygen vacancies improving electrochemical performance, directing new pathways toward defect‐functionalized advanced materials. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:1616301X
DOI:10.1002/adfm.202305659