Wang Lulu, Huang Kuo-Wei, Chen Jitao, Zheng Junrong
College of Chemistry and Molecular Engineering, Beijing National Laboratory for Molecular Sciences, Peking University, Beijing 100871, China.
KAUST Catalysis Center and Division of Physical Science and Engineering, King Abdullah University of Science and Technology, Thuwal 23955-6900, Saudi Arabia.
Sci Adv. 2019 Oct 4;5(10):eaax4279. doi: 10.1126/sciadv.aax4279. eCollection 2019 Oct.
Rechargeable aqueous zinc-ion batteries are promising candidates for large-scale energy storage but are plagued by the lack of cathode materials with both excellent rate capability and adequate cycle life span. We overcome this barrier by designing a novel hierarchically porous structure of Zn-vanadium oxide material. This ZnVO·1.5HO cathode delivers a high specific capacity of 426 mA·h g at 0.2 A g and exhibits an unprecedented superlong-term cyclic stability with a capacity retention of 96% over 20,000 cycles at 10 A g. Its electrochemical mechanism is elucidated. The lattice contraction induced by zinc intercalation and the expansion caused by hydronium intercalation cancel each other and allow the lattice to remain constant during charge/discharge, favoring cyclic stability. The hierarchically porous structure provides abundant contact with electrolyte, shortens ion diffusion path, and provides cushion for relieving strain generated during electrochemical processes, facilitating both fast kinetics and long-term stability.
可充电水系锌离子电池是大规模储能的有前途的候选者,但因缺乏兼具优异倍率性能和足够循环寿命的正极材料而受到困扰。我们通过设计一种新型的分级多孔结构的锌钒氧化物材料克服了这一障碍。这种ZnVO·1.5HO正极在0.2 A g下具有426 mA·h g的高比容量,并在10 A g下经过20000次循环后展现出前所未有的超长循环稳定性,容量保持率为96%。阐明了其电化学机理。锌嵌入引起的晶格收缩和水合氢离子嵌入导致的膨胀相互抵消,使晶格在充放电过程中保持恒定,有利于循环稳定性。分级多孔结构提供了与电解质的丰富接触,缩短了离子扩散路径,并为缓解电化学过程中产生的应变提供了缓冲,促进了快速动力学和长期稳定性。