阳极
材料科学
金属有机骨架
介孔材料
扫描电子显微镜
X射线光电子能谱
傅里叶变换红外光谱
锰
锂(药物)
电极
部分
化学工程
纳米技术
吸附
有机化学
化学
催化作用
物理化学
复合材料
医学
工程类
冶金
内分泌学
作者
Sandipan Maiti,Atin Pramanik,Unnikrishnan Manju,Sourindra Mahanty
标识
DOI:10.1021/acsami.5b03414
摘要
Metal organic frameworks (MOFs) with diverse structural chemistry are being projected as futuristic electrode materials for Li-ion batteries. In this work, we report synthesis of Mn-1,3,5-benzenetricarboxylate MOF by a simple solvothermal method and its application as an anode material for the first time. Scanning electron microscopy of the synthesized MOF shows a bar shaped morphology where these bars, about 1 μm wide and of varied lengths between 2 and 20 μm, are made of porous sheets containing mesoporous walls and macroporous channels. The MOF anode, when examined in the potential window of 0.01-2.0 V versus Li/Li(+), shows high specific capacities of 694 and 400 mAh g(-1) at current densities of 0.1 and 1.0 A g(-1) along with good cyclability, retention of capacity, and sustenance of the MOF network. Ex situ X-ray diffraction, Fourier transform infrared, and X-ray photoelectron spectroscopy studies on the electrode material at different states of charge suggest that the usual conversion reaction for Li storage might not be applicable in this case. Conjugated carboxylates being weakly electron withdrawing ligands with a stronger π-π interaction, a probable alternative Li storage mechanism has been proposed that involves the organic moiety. The present results show promise for applying Mn-1,3,5-benzenetricarboxylate MOF as high performance <2 V anode.
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