二硫化钼
硫氰酸盐
钼
硫氰酸铵
离子
铵
无机化学
二硫键
化学
材料科学
有机化学
冶金
生物化学
作者
Hang Li,Ruohan Yu,Haibo Chen,Jing Hu,Jianli Zhang,Guangya Hou,Qiang Chen,Jun Lü,Yiping Tang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-12-16
卷期号:: 168-176
标识
DOI:10.1021/acsenergylett.4c02712
摘要
Aqueous ammonium ion storage utilizes the intercalation and coordination diffusion mechanisms of NH4+ within the host material, resulting in a low-cost, high-safety energy storage device. However, the capacity of the NH4+ storage hosts, represented by layered materials, is mainly limited by the limited interlayer size and coordination sites. Here, a strategy is proposed to enhance NH4+ storage by utilizing nonmetallic ions with long-chain structures to regulate the interlayer spacing and coordination activity of MoS2. Atomic-level electron microscopy, chemical reactions, and theoretical simulations revealed that SCN– was successfully intercalated into MoS2 and coordinated with S atoms to construct an interlayer network. The intercalation of SCN– provides sufficient space and abundant hydrogen-bonding sites. This work effectively solves the dilemma of traditional layered materials in NH4+ storage and demonstrates the broad prospects of interlayer coordination engineering strategies for energy storage devices.
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