Reversible High-Voltage N-Redox Chemistry in Metal–Organic Frameworks for High-Rate Anion-Intercalation Batteries
Source abstract
Abstract
Because of the capacity limitation in traditional transition-metal oxide cathodes, the design of novel cathodes is vital for the performance enhancement in lithium-ion batteries. In this work, we propose a new anion-intercalation strategy for the design of metal–organic frameworks that can be used as high-voltage cathodes in lithium-ion batteries. A novel pcu-topology [Zn4O2(DAnT)3(DMF)4]·(DMF)6 MOF is synthesized with enriched nitrogen active sites and porous cage structure. When applied as cathode with LiPF6 based electrolyte, this MOF reaches the theoretical capacity of ∼60 mAh g–1 at a current density of 100 mA g–1 within high working voltage of 2.5–4.0 V versus Li/Li+. Even at a high current density of 1000 mA g–1 (∼16C), half capacity can still be obtained. The reversible conversion of N/N+ and adsorption/desorption of PF6– were also examined by a series of ex situ characterizations including XPS, XRD, and FTIR, which clearly validates our strategy that permits good electrochemical performance at relatively high working potential.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Metal-Organic Frameworks: Synthesis and Applications · Chemical Synthesis and Characterization
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Shanghai Key Laboratory of Magnetic Resonance, School of Physics and Materials Science, East China Normal University, Shanghai 200062, China
Funding
National Natural Science Foundation of China
References (31)
Show source-provided references
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