{"title":"Ultrafast Synthesis of Oxygen Vacancy-Rich MgFeSiO4 Cathode to Boost Diffusion Kinetics for Rechargeable Magnesium-Ion Batteries","authors":"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","doi":"10.1021/acs.nanolett.4c04908","DOIUrl":null,"url":null,"abstract":"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 MgFeSiO<sub>4</sub> cathode (MgFeSiO<sub>4</sub>-HTS) in seconds. As a proof of concept, the MgFeSiO<sub>4</sub>-HTS exhibits a higher electrochemical property and fast insertion/extraction kinetics in comparison to those prepared from the conventional sintering method. The MgFeSiO<sub>4</sub>-HTS displays remarkable long-term cycling lifespan properties with a reversible capacity of 85.65 and 54.43 mAh g<sup>–1</sup> 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 Mg<sup>2+</sup> ions and the cathode, enhancing the Mg<sup>2+</sup> diffusion kinetics.","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"73 1","pages":""},"PeriodicalIF":9.1000,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nano Letters","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acs.nanolett.4c04908","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
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.
可充电镁离子电池因其理论容量大、安全隐患小而受到广泛关注。然而,由于高电荷密度和缓慢的插入/提取动力学,二价Mg离子在阴极中迁移缓慢。研究表明,采用高加热/猝灭速率的超快非平衡高温冲击(HTS)方法可以在数秒内将氧空位引入橄榄石结构的MgFeSiO4阴极(MgFeSiO4-HTS)。作为概念证明,与传统烧结方法制备的MgFeSiO4-HTS相比,MgFeSiO4-HTS具有更高的电化学性能和快速的插入/提取动力学。MgFeSiO4-HTS具有良好的长期循环寿命,在2℃和5℃下循环500次和1600次,可逆容量分别为85.65和54.43 mAh g-1。此外,结合电化学实验和密度泛函理论计算,氧空位可以减弱Mg2+离子与阴极之间的相互作用和能垒,增强Mg2+扩散动力学。
期刊介绍:
Nano Letters serves as a dynamic platform for promptly disseminating original results in fundamental, applied, and emerging research across all facets of nanoscience and nanotechnology. A pivotal criterion for inclusion within Nano Letters is the convergence of at least two different areas or disciplines, ensuring a rich interdisciplinary scope. The journal is dedicated to fostering exploration in diverse areas, including:
- Experimental and theoretical findings on physical, chemical, and biological phenomena at the nanoscale
- Synthesis, characterization, and processing of organic, inorganic, polymer, and hybrid nanomaterials through physical, chemical, and biological methodologies
- Modeling and simulation of synthetic, assembly, and interaction processes
- Realization of integrated nanostructures and nano-engineered devices exhibiting advanced performance
- Applications of nanoscale materials in living and environmental systems
Nano Letters is committed to advancing and showcasing groundbreaking research that intersects various domains, fostering innovation and collaboration in the ever-evolving field of nanoscience and nanotechnology.