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Research Article | Open Access

HsGDY on Ni Foam for Loading MoS2/Ni3S2 to Enhance the Performance on Lithium–Sulfur Batteries

Jiao XiangYuanduo QuYanxin ZengSenyu HuHuiling XuHong XiaMuwei Ji( )Lianfeng Duan( )Fushen Lu( )
College of Chemistry and Chemical Engineering, Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province, Shantou University, Shantou, Guangdong 515063, P. R. China

†These authors contributed equally to this work.

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Abstract

Lithium–sulfur batteries are considered important devices for the power of movable equipment, but there are still some challenges that limit their applications, such as how to obtain a cathode for high sulfide adsorption and rapid conversion. Here, a new strategy is proposed to enhance the performance of lithium–sulfur batteries by growing 3-dimensional hydrogen-substituted graphdiyne (HsGDY) layers on Ni foam via Glaser cross-coupling reaction to anchor MoS2/Ni3S2, enhancing the conductivity of host material of S. The results show that the 3-dimensional HsGDY framework enables the fast adsorption of lithium polysulfides and the Ni3S2/MoS2 performs as the reaction center with a low charge transfer resistance. The charge capacity of Ni@HsGDY/MoS2/Ni3S2 cell is up to 1,234.7 mAh·g−1 at the first circle, and the specific capacity keeps 486 mAh·g−1 after 500 cycles at a current density of 2 C. The incorporation of HsGDY into the cathode promotes the adsorption and the conversion of polysulfides, paving a path to obtain lithium–sulfur batteries with high energy density.

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Energy Material Advances
Article number: 0054

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Cite this article:
Xiang J, Qu Y, Zeng Y, et al. HsGDY on Ni Foam for Loading MoS2/Ni3S2 to Enhance the Performance on Lithium–Sulfur Batteries. Energy Material Advances, 2023, 4: 0054. https://doi.org/10.34133/energymatadv.0054

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Received: 29 May 2023
Accepted: 25 August 2023
Published: 26 September 2023
© 2023 Jiao Xiang et al. Exclusive licensee Beijing Institute of Technology Press. No claim to original U.S. Government Works.

Distributed under a Creative Commons Attribution License 4.0 (CC BY 4.0).