Yuxin Tian , Jiankang Chen , Guofeng Wang , Bing Sun , Alan Meng , Lei Wang , Guicun Li , Jianfeng Huang , Shiqi Ding , Zhenjiang Li
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引用次数: 0
Abstract
Rechargeable magnesium batteries (RMBs) hold promise for offering higher volumetric energy density and safety features, attracting increasing research interest as the next post lithium-ion batteries. Developing high performance cathode material by inducing multi-electron reaction process as well as maintaining structural stability is the key to the development and application of RMBs. Herein, multi-electron reaction occurred in VS4 by simple W doping strategy. W doping induces valence of partial V as V2+ and V3+ in VS4 structure, and then stimulates electrochemical reaction involving multi-electrons in 0.5% W-V-S. The flower-like microsphere morphology as well as rich S vacancies is also modulated by W doping to neutralize structure change in such multi-electron reaction process. The fabricated 0.5% W-V-S delivers higher specific capacity (149.3 mA h g−1 at 50 mA g−1, which is 1.6 times higher than that of VS4), superior rate capability (76 mA h g−1 at 1000 mA g−1), and stable cycling performance (1500 cycles with capacity retention ratio of 93.8%). Besides that, pesudocapaticance-like contribution analysis as well as galvanostatic intermittent titration technique (GITT) further confirms the enhanced Mg2+ storage kinetics during such multi-electron involved electrochemical reaction process. Such discovery provides new insights into the designing of multi-electron reaction process in cathode as well as neutralizing structural change during such reaction for realizing superior electrochemical performance in energy storage devices.
可充电镁电池(RMBs)有望提供更高的体积能量密度和安全性,作为下一个锂离子电池,吸引了越来越多的研究兴趣。通过诱导多电子反应过程和保持结构稳定性来开发高性能正极材料是阴极材料发展和应用的关键。通过简单的W掺杂策略,在VS4中发生了多电子反应。W掺杂在VS4结构中诱导部分V的价态为V2+和V3+,在0.5% W-V- s中激发多电子的电化学反应。在多电子反应过程中,W掺杂还可以调制花状微球形态和丰富的S空位,以中和结构变化。制备的0.5% W-V-S具有更高的比容量(50 mA g - 1时为149.3 mA h g - 1,是VS4的1.6倍),优越的倍率能力(1000 mA g - 1时为76 mA h g - 1)和稳定的循环性能(1500次循环,容量保持率为93.8%)。此外,准电容样贡献分析和恒流间歇滴定技术(git)进一步证实了这种多电子参与的电化学反应过程中Mg2+的储存动力学增强。这一发现为阴极多电子反应过程的设计以及中和反应过程中的结构变化,实现储能器件优异的电化学性能提供了新的思路。