钒化合物作为钒电池电极材料的稳定性及电化学行为研究
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作者单位:

1.武汉科技大学 资源与环境工程学院, 湖北 武汉 430081 ;2.国家环境保护矿冶资源利用与污染控制重点实验室, 湖北 武汉 430081 ;3.战略钒资源利用省部共建协同创新中心, 湖北 武汉 430081 ;4.湖北省页岩钒资源高效清洁利用工程技术研究中心, 湖北 武汉 430081 ;5.六盘水师范学院 矿业与机械工程学院, 贵州 六盘水 553004

作者简介:

潘东(1989—),男,贵州安顺市人,博士研究生,主要研究方向为钒化合物及其储能利用。

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中图分类号:

TM912;TF841.3;TF801

基金项目:

国家自然科学基金资助项目(51774216);湖北省科技创新专项资助项目(2017ACA185)


Stability and electrochemical behaviour of vanadium compounds as electrode materials for vanadium batteries
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1.School of Resources and Environmental Engineering, Wuhan University of Science and Technology, Wuhan 430081 , China ;2.State Environmental Protection Key Laboratory of Mineral Metallurgical Resources Utilization and Pollution Control, Wuhan 430081 , China ;3.Collaborative Innovation Center of Strategic Vanadium Resources Utilization, Wuhan 430081 , China ;4.Hubei Provincial Engineering Technology Research Center of High Efficient Cleaning Utilization for Shale Vanadium Resource, Wuhan 430081 , China ;5.School of Mining and Mechanical Engineering, Liupanshui Normal University, Liupanshui, 553004 , China

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    摘要:

    钒化合物具有较好电化学活性,有望用于提升钒电池电极电化学活性,但目前对于钒化合物在电解液中的稳定性及电化学行为的研究有待开展。因此,本文利用E-pH图、开路电位法、循环伏安法等方法,研究了V2O5、VO2、V2O3、NaV2O5、VN等钒化合物在酸性电解液中的稳定性及电化学行为。在稳定性方面,结合钒化合物的E-pH图、溶解试验以及开路电位分析,VO2、NaV2O5在钒电池电解液中不稳定,会发生快速溶解;V2O5在钒电池电解液中相对稳定,会发生缓慢溶解;V2O3和VN在钒电池电解液中较稳定,仅发生少量溶解。在电化学行为方面,结合钒化合物在2.0mol·L-1 H2SO4、0.1mol·L-1 V3++2.0mol·L-1 H2SO4、0.1mol·L-1 V4++2.0mol·L-1 H2SO4电解液中的循环伏安曲线分析,V2O5、V2O3、VN会在电势0.4~1.5V发生显著的氧化还原反应,在电势-0.8~-0.2V不会发生明显的氧化还原反应;VN对V5+/V4+、V3+/V2+电对反应具有较好的催化作用,V2O3的催化作用次之,V2O5的催化作用最弱。因此,V2O3、VN可作为V3+/V2+电对反应催化材料用于提高钒电池负极电化学活性,实现钒电池性能的提升。

    Abstract:

    Vanadium compounds have good electrochemical activity and are expected to be used to enhance the electrochemical activity of vanadium battery electrodes, but the stability and electrochemical behavior of vanadium compounds in electrolytes have not been investigated yet. Therefore, the stability and electrochemical behavior of vanadium compounds such as V2O5 VO2, V2O3, NaV2O5 and VN in acidic electrolytes have been investigated using E-pH diagram, open circuit potential method and cyclic voltammetry in this paper. In terms of stability, the E-pH diagram, dissolution tests and open circuit potential analysis of vanadium compounds show that VO2 and Na V2O5 are unstable in vanadium battery electrolytes and undergo rapid dissolution; V2O5 is relatively stable in vanadium battery electrolytes and undergoes slow dissolution; V2O3 and VN are more stable in vanadium battery electrolytes and undergo small amounts of dissolution. In terms of electrochemical behavior, combined with cyclic voltametric analysis of vanadium compounds in 2.0mol·L-1 H2SO4, 0.1mol·L-1 V3++2.0mol·L-1 H2SO4, and 0.1mol·L-1 V4++2.0mol·L-1 H2SO4 electrolytes, V2O5, V2O3 and VN undergo significant redox reactions at 0.4 to 1.5V and no significant redox reactions at -0.8 to -0.2V; VN has better catalytic effect on the V5+/V4+ and V3+/V2+ electro pair reactions, with V2O3 being the next most catalytic and V2O5 the weakest. Therefore, V2O3 and VN can be used as catalytic materials for V3+/V2+ electro pair reactions to improve the electrochemical activity of vanadium battery anodes to achieve improved performance of vanadium batteries.

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潘东,刘涛,张一敏,等.钒化合物作为钒电池电极材料的稳定性及电化学行为研究[J]. 中国有色冶金, 2023, 52(5): 51-59.

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  • 收稿日期:2023-03-08
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  • 在线发布日期: 2025-12-23
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