阳极
X射线光电子能谱
氧化还原
电化学
电池(电)
金属有机骨架
锂(药物)
部分
锂离子电池
电流密度
氧化态
化学工程
无机化学
化学
金属
电极
吸附
有机化学
物理
物理化学
功率(物理)
内分泌学
工程类
医学
量子力学
作者
Sandipan Maiti,Atin Pramanik,Unnikrishnan Manju,Sourindra Mahanty
标识
DOI:10.1016/j.micromeso.2016.02.011
摘要
Versatility and diversity in the nature of bonding between metal ions and polyfunctional organic molecules render metal organic frameworks (MOFs) as interesting materials for a variety of applications. In this work, we have examined the electrochemical properties of solvothermally synthesized Cu-1,3,5-benzenetricarboxylate MOF as a novel anode material for lithium-ion battery (LIB). At a current density of 96 mAg−1, reversible capacity of 740 mAhg−1 is achieved, the highest ever reported for a MOF. Even at a high current density of 383 mAg−1, specific capacity of 474 mAhg−1 is observed with no apparent fading up to 50 cycles. Ex-situ studies on the electrode material in the charged and discharged state by X-ray diffraction, Fourier transformed infra-red spectroscopy and X-ray photoelectron spectroscopy suggest that Li storage in Cu3(BTC)2 MOF might not be fully explained by the conventional conversion mechanism that involves reduction into corresponding metal and subsequent oxidation. Rather, redox participation of the organic moiety is indicated. The present results would help in designing new MOFs for LIB applications.
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