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In Situ Neutron Powder Diffraction Using Custom-made Lithium-ion Batteries
Published on: November 10, 2014
Insights into the lithium diffusion process in a defect-containing porous crystalline POM@MOF anode material
Peipei Zhu1, Xiya Yang, Xiao Li
1Shandong Key Laboratory of Inorganic Chemistry, Department of Chemistry and Chemical Engineering, Jining University, Qufu, Shandong, PR China. shajq2002@126.com.
Abstract:
Rechargeable lithium-ion batteries (LIBs) for potentially low-cost and high-energy-density storage have been intensively researched to meet ever-growing demands. Achieving higher storages and understanding the transporting and storing diffusion process of Li ions are still great challenges. Herein, a porous crystalline polyoxometalate-based metal-organic framework (POM@MOF), H2[Cu(Htrz)5(H2O)2][MoCuO26]0.5·3H2O, with defect sites as a LIB electrode material is reported. The Li-ion diffusion process in the material was investigated using ex situ X-ray photoelectron spectroscopy (XPS) and off-line powder X-ray diffraction (PXRD), indicating that O atoms of POM nano-clusters can be regarded as Li-ion acceptors (storage sites); meanwhile the defect sites (uncoordinated N atoms or -N-H groups) in the crystalline material also participate in the Li-ion storage. The reported porous crystalline POM@MOF material with defects delivers a remarkable Li-ion storage capacity of ca. 700 mA h g-1 in 200 cycles at a current density of 100 mA g-1.

