材料科学
阳极
锂(药物)
电化学
锰
氧化还原
金属
金属有机骨架
化学工程
过渡金属
电池(电)
无机化学
纳米技术
物理化学
电极
化学
有机化学
冶金
功率(物理)
催化作用
物理
吸附
医学
量子力学
内分泌学
工程类
作者
Chao Li,Xiaoshi Hu,Wei Tong,Wensheng Yan,Xiaobing Lou,Ming Shen,Bingwen Hu
标识
DOI:10.1021/acsami.7b09363
摘要
We herein demonstrate the fabrication of Mn- and Ni-based ultrathin metal-organic framework nanosheets with the same coordination mode (termed "Mn-UMOFNs" and "Ni-UMOFNs", respectively) through an expedient and versatile ultrasonic approach and scrutinize their electrochemical properties as anode materials for rechargeable lithium batteries for the first time. The obtained Mn-UMOFNs with structure advantages over Ni-UMOFNs (thinner nanosheets, smaller metal-ion radius, higher specific surface area) exhibit high reversible capacity (1187 mAh g-1 at 100 mA g-1 for 100 cycles), excellent rate capability (701 mAh g-1 even at 2 A g-1), rapid Li+ diffusion coefficient (2.48 × 10-9 cm2 s-1), and a reasonable charge-discharge profile with low average operating potential at 0.4 V. On the grounds of the low-cost and environmental benignity of Mn metals and terephthalic acid linkers, our Mn-UMOFNs show alluring promise as a low-cost high-energy anode material for future LIBs. Furthermore, the lithiation-delithiation chemistry of Mn-UMOFNs was unequivocally studied by a combination of magnetic measurements, electron paramagnetic resonance, and synchrotron-based soft X-ray spectroscopy (O K-edge and Mn L-edge) experiments, the results of which substantiate that both the aromatic chelating ligands and the Mn2+ centers participate in lithium storage.
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