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超薄锰基金属有机框架纳米片:具有金属和配体氧化还原活性共存的低成本、高能量密度锂离子存储负极。

Ultrathin Manganese-Based Metal-Organic Framework Nanosheets: Low-Cost and Energy-Dense Lithium Storage Anodes with the Coexistence of Metal and Ligand Redox Activities.

机构信息

State Key Laboratory of Precision Spectroscopy, Shanghai Key Laboratory of Magnetic Resonance, Institute of Functional Materials, School of Physics and Materials Science, East China Normal University , Shanghai 200062, P.R. China.

Anhui Key Laboratory of Condensed Matter Physics at Extreme Conditions, High Magnetic Field Laboratory, Chinese Academy of Sciences , Hefei 230031, P.R. China.

出版信息

ACS Appl Mater Interfaces. 2017 Sep 6;9(35):29829-29838. doi: 10.1021/acsami.7b09363. Epub 2017 Aug 25.

DOI:10.1021/acsami.7b09363
PMID:28812873
Abstract

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 at 100 mA g for 100 cycles), excellent rate capability (701 mAh g even at 2 A g), rapid Li diffusion coefficient (2.48 × 10 cm s), 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 Mn centers participate in lithium storage.

摘要

我们在此通过一种简便且通用的超声方法展示了具有相同配位模式的 Mn 和 Ni 基超薄金属有机骨架纳米片的制备(分别称为“Mn-UMOFNs”和“Ni-UMOFNs”),并首次研究了它们作为可充电锂电池阳极材料的电化学性能。与 Ni-UMOFNs 相比,所获得的具有结构优势的 Mn-UMOFNs(更薄的纳米片、更小的金属离子半径、更高的比表面积)表现出高可逆容量(100 mA g 下 100 个循环时为 1187 mAh g)、优异的倍率性能(即使在 2 A g 时仍为 701 mAh g)、快速的 Li 扩散系数(2.48×10 cm s)以及具有低平均工作电位(0.4 V)的合理充放电曲线。鉴于 Mn 金属和对苯二甲酸配体的低成本和环境友好性,我们的 Mn-UMOFNs 有望成为未来 LIB 用低成本高能量阳极材料。此外,通过磁测量、电子顺磁共振和基于同步加速器的软 X 射线光谱(O K 边和 Mn L 边)实验的结合,明确研究了 Mn-UMOFNs 的嵌锂-脱锂化学,结果表明,芳族螯合配体和 Mn 中心都参与了锂存储。

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