插层(化学)
材料科学
电极
电化学
电池(电)
水溶液
阴极
无机化学
锌
化学工程
化学
冶金
功率(物理)
物理化学
工程类
物理
量子力学
作者
Hailun Yang,Pengge Ning,Junwu Chen,Yuping Li,Hongyan He,Hongbin Cao
标识
DOI:10.1021/acsami.1c23995
摘要
The development of high capacity and stable cathodes is the key to the successful commercialization of aqueous zinc-ion batteries. However, significant solvation penalties limit the choice of available positive electrodes. Herein, hydrated intercalation is proposed to promote reversible (de)intercalation within host materials by rationally designing a matching electrode. In contrast to previously reported works, the as-prepared electrode (NHVO@CC) can achieve fast and reversible intercalation of hydrated zinc ions in the interlayer gap, leading to a high capacity of 517 mAh g-1 at 0.1 A g-1 and excellent electrode stability for long-term cycling. Besides, as a consequence of the flexibility of the NHVO@CC electrode, a quasi-solid-state battery was achieved with equally advantageous electrochemical behavior under various bending states. The proposed hydrated cation direct insertion/extraction sets up an efficient way of developing high-performance positive electrodes for aqueous batteries.
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