Search

A hierarchical spheroidal MnO@C heterogeneous interface as a cathode material for AZIBs and synthesized through a MOF, which exhibits the excellent cycling stability. [Display omitted] Aqueous zinc-ion batteries (AZIBs) have shown great potential as energy storage devices owing to their high energy density, low cost, and low toxicity. Typically, high performance AZIBs incorporate manganese-based cathode materials. Despite their advantages, these cathodes are limited by significant capacity fading and poor rate performance due to the dissolution and disproportionation of manganese. Herein, hierarchical spheroidal MnO@C structures were synthesized from Mn-based metal–organic frameworks, which benefit from a protective carbon layer to prevent manganese dissolution. The spheroidal MnO@C structures were incorporated onto a heterogeneous interface to act as a cathode material for AZIBs, which exhibited excellent cycling stability (160 mAh g−1 after 1000 cycles at 3.0 A g−1), good rate capability (165.9 mAh g−1 at 3.0 A g−1), and appreciable specific capacity (412.4 mAh g−1 at 0.1 A g−1) for AZIBs. Moreover, the Zn2+ storage mechanism in MnO@C was comprehensively investigated using ex-situ XRD and XPS studies. These results demonstrate that hierarchical spheroidal MnO@C is a potential cathode material for high-performing AZIBs. [ABSTRACT FROM AUTHOR]

Aqueous zinc-ion batteries is considered as a promising system for large scale electrochemical energy storage system owing to their intrinsic safety, and low cost. Nevertheless, the industrialization process is slow due to the constraints of high-performance cathode materials. Adjusting the layered structure of V 2 O 5 through metal ion or polymer intercalation can effectively improve low electron conductivity, vanadium dissolution, and slow ion transport kinetics. Herein, the conductive polymer polypyrrole-intercalated V 2 O 5 ·H 2 O (PVOH) was successfully prepared via simple hydrothermal method and following interface polymerization reaction. Getting benefit from the insertion of polypyrrole, the prepared PVOH composite material achieves a V 2 O 5 cathode with a more open structure, rich active sites, and greater stability, allowing for an expanded crystal plane spacing of 14.5 Å. Therefore, the PVOH electrode demonstrates a discharge capacity of 475 mAh g−1 and a cycling stability of 95 % capacity retention after 2000 cycles. The intercalating conductive polymers strategy can become a new approach to improve the electrochemical behavior of vanadium oxide cathodes. [Display omitted] • The conductive polymer polypyrrole-intercalated PVOH was successfully prepared. • The PVOH has a more open structure, rich active sites, and an expanded crystal plane spacing of 14.5 Å. • The PVOH electrode demonstrates a discharge capacity of 475 mAh g−1 at 0.1 A g−1. • A detailed investigation is conducted on the co-insertion mechanism of Zn2+/H+ by the different ex-situ characterization. [ABSTRACT FROM AUTHOR]

[Display omitted] • The functionalized graphene/polyaniline composite cathode showed high specific capacity and excellent rate performance. • A large conductive network was assembled by functionalized graphene and polyaniline. • The formation of -N-Zn-O- structure efficiently enhanced the Zn2+ storage behavior during discharging process. • A novel H+ and Zn2+ insertion mechanism was presented in this work. Polyaniline (PANI) as a typical conductive polymer has been widely applied in cathode materials of aqueous zinc ion battery (AZIB), owing to the features of high electronic conductivity and simple synthesized methods. However, the cycling instability caused of spontaneous deprotonation still limited the extensive application of PANI cathode materials. In this work, a functionalized commercial graphene (MEG) and PANI composite (MGP-1) was successfully assembled by a facile two-step method. When the MGP-1 acted as cathode material in AZIB, it demonstrated a high capacity of 184.5 mAh/g (0.2 A/g) and excellent rate performance of 137.6 mAh/g (3 A/g) compared to the PANI cathode. The corresponding analysis revealed that the boosted electrochemical behavior of MGP-1 was attributed to the large conductive network fabricated by the MEG and PANI, and the formations of -N-Zn-O- structures during discharging process. Moreover, based on the conventional H+ insertion mechanism, this work furtherly provided a H+ and Zn2+ insertion mechanism. In addition, the utilization of cheap and abundant commercial graphene would allow the graphene/polyaniline composite to be a promising cathode material applied in AZIB. [ABSTRACT FROM AUTHOR]