4.8 Article

TinO2n-1/MXene Hierarchical Bifunctional Catalyst Anchored on Graphene Aerogel toward Flexible and High-Energy Li-S Batteries

期刊

ACS NANO
卷 16, 期 11, 页码 19133-19144

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.2c08246

关键词

flexible lithium-sulfur batteries; high-energy density; catalytic conversion; graphene aerogel; high safety; gel polymer electrolyte

资金

  1. National Key Research and Development Program of China [2019YFA0705700]
  2. National Natural Science Foundation of China [51774017, 51904016, 52072205]
  3. Beijing Natural Science Foundation [2214084]
  4. Key Program of Equipment Pre-Research Foundation of China [6140721020103]
  5. Shenzhen Stabilization Support Program [WDZC20200824091903001]
  6. Shiyanjia Lab

向作者/读者索取更多资源

In this study, a metallic 1T MoS2 and rich oxygen vacancies TinO2n-1/MXene hierarchical bifunctional catalyst (Mo-Ti/Mx) anchored on a reduced graphene oxide-cellulose nanofiber host (Mo-Ti/Mx-GN) was proposed to address the poor cycling stability and flexibility of lithium-sulfur batteries. The electrode demonstrated improved electrochemical properties and reversible energy storage and output over a wide temperature range.
The development of lithium-sulfur (Li-S) batteries with high-energy density, flexibility, and safety is very appealing for emerging implantable devices, biomonitoring, and roll-up displays. Nevertheless, the poor cycling stability and flexibility of the existing sulfur cathodes, flammable liquid electrolytes, and extremely reactive lithium anodes raise serious battery performance degradation and safety issues. Herein, a metallic 1T MoS2 and rich oxygen vacancies TinO2n-1/MXene hierarchical bifunctional catalyst (Mo-Ti/Mx) anchored on a reduced graphene oxide-cellulose nanofiber (GN) host (Mo-Ti/Mx-GN) was proposed to address the above challenges. By applying a directional freezing process, the hierarchical architecture of a flexible GN scaffold composed of waved multiarch morphology with long-range alignment is achieved. The synergetic effects of 1T MoS2 and TinO2n-1/MXene are beneficial to suppress the shuttling behavior of lithium polysulfides (LiPSs), expedite the redox kinetics of sulfur species, and promote the electrocatalytic reduction of LiPSs to Li2S. The electrode demonstrates improved electrochemical properties with high sulfur-mass loading (8.4 mgs cm-2) and lean electrolyte (7.6 mu L mgs-1) operation. We also explored the feasibility of producing pouch cells with such flexible electrodes, gel polymer electrolytes, and a robust lithium anode, which exhibited reversible energy storage and output, wide temperature adaptability, and good safety against rigorous strikes, implying the potential for practical applications.

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