{"title":"用于高性能锂氧电池的磁场和光子共同增强 S 型 MXene/In2S3/CoFe2O4 异质结。","authors":"Na Xiao , Ping Han , Zhaoqi Chen , Qiuling Chen","doi":"10.1016/j.jcis.2024.11.062","DOIUrl":null,"url":null,"abstract":"<div><div>Under the spotlight for their potential to reduce over-potential, photo-assisted Li–O<sub>2</sub> batteries still face a key challenge: the rapid recombination of photo-generated electron-hole pairs, which limits their efficiency. In this study, we address this limitation by designing a Li–O<sub>2</sub> battery that integrates both photo and magnetic field assistance, using an S-scheme MXene/In<sub>2</sub>S<sub>3</sub>/CoFe<sub>2</sub>O<sub>4</sub> heterojunction photocathode. This unique combination enhances visible light absorption and generates a strong built-in electric field, facilitating effective charge separation and boosting photocatalytic activity. During discharge, photo-generated electrons participate in the oxygen reduction reaction, while photo-induced holes contribute to the decomposition of discharge products during charging. Furthermore, the introduction of a magnetic field, confirmed through vibrating sample magnetometer, Mössbauer spectroscopy, X-ray absorption near edge structure, and cyclic voltammetry analyses, enhances electron-hole separation via Lorentz forces and spin–orbit coupling, accelerating the formation and decomposition of Li<sub>2</sub>O<sub>2</sub>. With this synergistic approach, the battery achieves a high specific capacity of 26,500 mAh g<sup>−1</sup>, ultra-low oxygen reduction/evolution reaction over-potentials of 0.08 V/0.17 V, and a long cycle life of 2000 cycles with energy efficiency of 98.11 %. This work demonstrates the promising potential of combining photo and magnetic field effects to improve the electrochemical performance of Li–O<sub>2</sub> batteries, opening new avenues for high-performance energy storage systems.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"680 ","pages":"Pages 911-927"},"PeriodicalIF":9.4000,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Magnetic field and photon co-enhanced S-scheme MXene/In2S3/CoFe2O4 heterojunction for high-performance lithium-oxygen batteries\",\"authors\":\"Na Xiao , Ping Han , Zhaoqi Chen , Qiuling Chen\",\"doi\":\"10.1016/j.jcis.2024.11.062\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Under the spotlight for their potential to reduce over-potential, photo-assisted Li–O<sub>2</sub> batteries still face a key challenge: the rapid recombination of photo-generated electron-hole pairs, which limits their efficiency. In this study, we address this limitation by designing a Li–O<sub>2</sub> battery that integrates both photo and magnetic field assistance, using an S-scheme MXene/In<sub>2</sub>S<sub>3</sub>/CoFe<sub>2</sub>O<sub>4</sub> heterojunction photocathode. This unique combination enhances visible light absorption and generates a strong built-in electric field, facilitating effective charge separation and boosting photocatalytic activity. During discharge, photo-generated electrons participate in the oxygen reduction reaction, while photo-induced holes contribute to the decomposition of discharge products during charging. Furthermore, the introduction of a magnetic field, confirmed through vibrating sample magnetometer, Mössbauer spectroscopy, X-ray absorption near edge structure, and cyclic voltammetry analyses, enhances electron-hole separation via Lorentz forces and spin–orbit coupling, accelerating the formation and decomposition of Li<sub>2</sub>O<sub>2</sub>. With this synergistic approach, the battery achieves a high specific capacity of 26,500 mAh g<sup>−1</sup>, ultra-low oxygen reduction/evolution reaction over-potentials of 0.08 V/0.17 V, and a long cycle life of 2000 cycles with energy efficiency of 98.11 %. This work demonstrates the promising potential of combining photo and magnetic field effects to improve the electrochemical performance of Li–O<sub>2</sub> batteries, opening new avenues for high-performance energy storage systems.</div></div>\",\"PeriodicalId\":351,\"journal\":{\"name\":\"Journal of Colloid and Interface Science\",\"volume\":\"680 \",\"pages\":\"Pages 911-927\"},\"PeriodicalIF\":9.4000,\"publicationDate\":\"2024-11-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Colloid and Interface Science\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0021979724026389\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Colloid and Interface Science","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0021979724026389","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
光辅助锂-O2 电池因其降低过电位的潜力而备受关注,但它仍然面临着一个关键挑战:光产生的电子-空穴对的快速重组限制了其效率。在本研究中,我们利用 S 型 MXene/In2S3/CoFe2O4 异质结光电阴极,设计了一种集成了光辅助和磁场辅助的二氧化锰锂电池,从而解决了这一限制。这种独特的组合增强了对可见光的吸收,并产生了强大的内置电场,促进了有效的电荷分离,提高了光催化活性。在放电过程中,光产生的电子参与氧还原反应,而光诱导的空穴则在充电过程中促进放电产物的分解。此外,通过振动样品磁力计、莫斯鲍尔光谱学、X 射线吸收近边缘结构和循环伏安法分析证实,磁场的引入通过洛伦兹力和自旋轨道耦合增强了电子-空穴分离,加速了 Li2O2 的形成和分解。通过这种协同方法,电池实现了 26,500 mAh g-1 的高比容量、0.08 V/0.17 V 的超低氧还原/进化反应过电位,以及 2000 次循环的长循环寿命和 98.11 % 的能量效率。这项研究表明,结合光场和磁场效应来改善锂-O2 电池的电化学性能具有广阔的前景,为高性能储能系统开辟了新的途径。
Magnetic field and photon co-enhanced S-scheme MXene/In2S3/CoFe2O4 heterojunction for high-performance lithium-oxygen batteries
Under the spotlight for their potential to reduce over-potential, photo-assisted Li–O2 batteries still face a key challenge: the rapid recombination of photo-generated electron-hole pairs, which limits their efficiency. In this study, we address this limitation by designing a Li–O2 battery that integrates both photo and magnetic field assistance, using an S-scheme MXene/In2S3/CoFe2O4 heterojunction photocathode. This unique combination enhances visible light absorption and generates a strong built-in electric field, facilitating effective charge separation and boosting photocatalytic activity. During discharge, photo-generated electrons participate in the oxygen reduction reaction, while photo-induced holes contribute to the decomposition of discharge products during charging. Furthermore, the introduction of a magnetic field, confirmed through vibrating sample magnetometer, Mössbauer spectroscopy, X-ray absorption near edge structure, and cyclic voltammetry analyses, enhances electron-hole separation via Lorentz forces and spin–orbit coupling, accelerating the formation and decomposition of Li2O2. With this synergistic approach, the battery achieves a high specific capacity of 26,500 mAh g−1, ultra-low oxygen reduction/evolution reaction over-potentials of 0.08 V/0.17 V, and a long cycle life of 2000 cycles with energy efficiency of 98.11 %. This work demonstrates the promising potential of combining photo and magnetic field effects to improve the electrochemical performance of Li–O2 batteries, opening new avenues for high-performance energy storage systems.
期刊介绍:
The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality.
Emphasis:
The journal emphasizes fundamental scientific innovation within the following categories:
A.Colloidal Materials and Nanomaterials
B.Soft Colloidal and Self-Assembly Systems
C.Adsorption, Catalysis, and Electrochemistry
D.Interfacial Processes, Capillarity, and Wetting
E.Biomaterials and Nanomedicine
F.Energy Conversion and Storage, and Environmental Technologies