4.7 Article

Toward fast zinc-ion storage of MoS2 by tunable pseudocapacitance

期刊

JOURNAL OF ALLOYS AND COMPOUNDS
卷 871, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2021.159541

关键词

MoS2; Zinc ion batteries; Phase transition; Graphene; Pseudocapacitance

资金

  1. Science and Technology Plan of Guangzhou [201904010406]

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A hierarchical hybrid of MoS2 nanosheets with 86% of 1T phase grown on reduced graphene oxide scaffolds is proposed as a superior cathode material for aqueous rechargeable zinc ion batteries. The incorporation of reduced graphene oxide effectively stabilizes the 1T phase and reduces electron transfer resistance, resulting in high discharge capacity and excellent cycling performance. This study sheds light on the rational design of MoS2 nanoscale architecture for superior cathode materials in divalent/multivalent aqueous batteries.
While aqueous rechargeable zinc ion batteries (ARZIBs) are one of the promising energy storage devices, it is still a challenge to develop satisfactory cathode materials. Here, a hierarchical hybrid where MoS2 nanosheets with 86% of 1T phase are grown in-situ on reduced graphene oxide scaffolds is proposed to be a superior cathode of ARZIBs. The microstructure of as-prepared hybrid is correlated with its zinc storage performance by electrochemical and spectroscopic characterizations coupled with electron microscopy analysis. They reveal the incorporation of reduced graphene oxide scaffolds effectively stabilizes the 1T phase, exempting, to the maximum, the phase transition associated with the zinc insertion/extraction, reduces the electron transfer resistance and keeps the hierarchical morphology of the nanoscale MoS2 that shortens the zinc ion diffusion path length. All these together develop the pseudocapacitive property of MoS2. As a result, this hybrid electrode delivers a high discharge capacity of 108.3 mAh g(-1) at 5.0 A g(-1) and retains 88% initial capacity after 1000 cycles. Our strategy sheds some lights on the rational design of MoS2 nanoscale architecture towards superior cathode material of divalent/multivalent aqueous batteries. (C) 2021 Elsevier B.V. All rights reserved.

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