动力学
空位缺陷
阴极
扩散
离子
镁
材料科学
氧气
超短脉冲
无机化学
化学工程
化学物理
化学
物理化学
结晶学
冶金
热力学
物理
激光器
有机化学
量子力学
光学
工程类
作者
Jie Xu,Yuqi Hong,Shuming Dou,Junhan Wu,Jingchao Zhang,Qingmeng Wang,Tiantian Wen,Yang Song,Wei‐Di Liu,Jianrong Zeng,Guangsheng Huang,Chaohe Xu,Yanan Chen,Jili Yue,Jingfeng Wang,Fusheng Pan
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-01-03
标识
DOI:10.1021/acs.nanolett.4c04908
摘要
Rechargeable magnesium ion batteries (RMBs) have drawn extensive attention due to their high theoretical volumetric capacity and low safety hazards. However, divalent Mg ions suffer sluggish mobility in cathodes owing to the high charge density and slow insertion/extraction kinetics. Herein, it is shown that an ultrafast nonequilibrium high-temperature shock (HTS) method with a high heating/quenching rate can instantly introduce oxygen vacancies into the olivine-structured MgFeSiO4 cathode (MgFeSiO4-HTS) in seconds. As a proof of concept, the MgFeSiO4-HTS exhibits a higher electrochemical property and fast insertion/extraction kinetics in comparison to those prepared from the conventional sintering method. The MgFeSiO4-HTS displays remarkable long-term cycling lifespan properties with a reversible capacity of 85.65 and 54.43 mAh g–1 over 500 and 1600 cycles at 2 and 5 C, respectively. Additionally, by combining the electrochemical experiments and density functional theory calculations, oxygen vacancies can weaken the interaction and energy barrier between the Mg2+ ions and the cathode, enhancing the Mg2+ diffusion kinetics.
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