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Developing electrode materials with high specific capacitance and excellent stability for energy storage is necessary to solve energy shortage issues. In this work, we prepare ZnCo2O4@CoMoO4 core–shell structures on nickel foam by a simple hydrothermal approach. The as-synthesized products show excellent electrochemical performances. It reveals that the secondary growth of CoMoO4 nanosheets induces many active sites and facilitates rapid ion and electron transmission. In addition, the as-assembled device delivers high energy density, indicating that the as-obtained samples are excellent candidates for future energy storage applications. [ABSTRACT FROM AUTHOR]

Recently, carboxylate metal‐organic framework (MOF) materials were reported to perform well as anode materials for lithium‐ion batteries (LIBs); however, the presumed lithium storage mechanism of MOFs is controversial. To gain insight into the mechanism of MOFs as anode materials for LIBs, a self‐supported Cu‐TCNQ (TCNQ: 7,7,8,8‐tetracyanoquinodimethane) film was fabricated via an in situ redox routine, and directly used as electrode for LIBs. The first discharge and charge specific capacities of the self‐supported Cu‐TCNQ electrode are 373.4 and 219.4 mAh g−1, respectively. After 500 cycles, the reversible specific capacity of Cu‐TCNQ reaches 280.9 mAh g−1 at a current density of 100 mA g−1. Mutually validated data reveal that the high capacity is ascribed to the multiple‐electron redox conversion of both metal ions and ligands, as well as the reversible insertion and desertion of Li+ ions into the benzene rings of ligands. This work raises the expectation for MOFs as electrode materials of LIBs by utilizing multiple active sites and provides new clues for designing improved electrode materials for LIBs. [ABSTRACT FROM AUTHOR]

Developing electrode materials with high specific capacitance and excellent stability for energy storage is necessary to solve energy shortage issues. In this work, we prepare ZnCo2O4@CoMoO4 core-shell structures on nickel foam by a simple hydrothermal approach. The as-synthesized products show excellent electrochemical performances. It reveals that the secondary growth of CoMoO4 nanosheets induces many active sites and facilitates rapid ion and electron transmission. In addition, the as-assembled device delivers high energy density, indicating that the as-obtained samples are excellent candidates for future energy storage applications.

Recently, carboxylate metal-organic framework (MOF) materials were reported to perform well as anode materials for lithium-ion batteries (LIBs); however, the presumed lithium storage mechanism of MOFs is controversial. To gain insight into the mechanism of MOFs as anode materials for LIBs, a self-supported Cu-TCNQ (TCNQ: 7,7,8,8-tetracyanoquinodimethane) film was fabricated via an in situ redox routine, and directly used as electrode for LIBs. The first discharge and charge specific capacities of the self-supported Cu-TCNQ electrode are 373.4 and 219.4 mAh g -1 , respectively. After 500 cycles, the reversible specific capacity of Cu-TCNQ reaches 280.9 mAh g -1 at a current density of 100 mA g -1 . Mutually validated data reveal that the high capacity is ascribed to the multiple-electron redox conversion of both metal ions and ligands, as well as the reversible insertion and desertion of Li + ions into the benzene rings of ligands. This work raises the expectation for MOFs as electrode materials of LIBs by utilizing multiple active sites and provides new clues for designing improved electrode materials for LIBs., (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)