阳极
钴
钾离子电池
钾
金属有机骨架
氧烷
无机化学
氧化还原
金属
材料科学
化学
电极
化学工程
电池(电)
冶金
光谱学
磷酸钒锂电池
有机化学
功率(物理)
吸附
物理化学
工程类
物理
量子力学
作者
Chao Li,Xiaoshi Hu,Bingwen Hu
标识
DOI:10.1016/j.electacta.2017.09.090
摘要
Abstract Metal-organic frameworks (MOFs) are promising electrical storage materials due to their abundant electroactive components and large ion diffusion tunnels, however, there is no report on the employment of MOFs as electrodes for potassium-ion batteries (PIBs) hitherto. Here in this work, we firstly develop a cobalt(II) terephthalate-based layered MOF (referred as ‘L-Co2(OH)2BDC’, BDC = 1,4-benzenedicarboxylate) as an anode material for PIBs. The exceptional potassium storage performance of L-Co2(OH)2BDC is demonstrated with a high reversible capacity of 188 mAh g−1 after 600 prolonged cycles at 1 A g−1, revealing the considerable foreground of MOFs as superior potassium storage anodes. Moreover, the redox chemistry investigation of L-Co2(OH)2BDC based on X-ray absorption near edge structure (XANES) and soft X-ray spectroscopy (sXAS) techniques substantiate that both Co centers and organic ligands participate in the potassium storage, and the coordination between oxygen ions and cobalt significantly ensures the reversibility of potassiation and depotassiation processes. This work represents a significant step forward for the intensive application of MOFs in rechargeable metal batteries.
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