4.8 Article

Bimetallic nickel cobalt sulfides with hierarchical coralliform architecture for ultrafast and stable Na-ion storage

期刊

NANO RESEARCH
卷 14, 期 11, 页码 4014-4024

出版社

TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-021-3328-9

关键词

nickel cobalt sulfides; hierarchical coralliform architecture; sodium-ion batteries; anode materials; pseudocapacitive behavior

资金

  1. Shandong Provincial Natural Science Foundation [ZR2020QB123, ZR2020QB108, ZR2019MEM030]
  2. National Natural Science Foundation of China [51972180, 22071135, 51572134]
  3. Academy of Sciences large apparatus United Fund of China [U1832187]
  4. Key Research AMP
  5. Development Project of Shandong Province [2019GGX102070]
  6. Program for Scientific Research Innovation Team in Colleges and Universities of Jinan [2018GXRC006]

向作者/读者索取更多资源

A series of bimetallic nickel cobalt sulfides with hierarchical micro/nano architectures were successfully fabricated using a facile synthesis strategy, displaying excellent performance in sodium-ion storage. The enhanced conductivity by bimetallic components, the unique coral-like micro/nanostructure, and fast sodium ion diffusion were key factors contributing to the remarkable electrochemical properties observed during charging and discharging cycles.
A series of bimetallic nickel cobalt sulfides with hierarchical micro/nano architectures were fabricated via a facile synthesis strategy of bimetallic micro/nano structure precursor construction-anion exchange via solvothermal method. Among the nickel cobalt sulfides with different Ni/Co contents, the coral-like Ni1.01Co1.99S4 (Ni/Co, 1/2) delivers ultrafast and stable Na-ion storage performance (350 mAh.g(-1) after 1,000 cycles at 1 A.g(-1) and 355 mAh.g(-1) at 5 A.g(-1)). The remarkable electrochemical properties can be attributed to the enhanced conductivity by co-existence of bimetallic components, the unique coral-like micro/nanostructure, which could prevent structural collapse and self-aggregation of nanoparticles, and the easily accessibility of electrolyte, and fast Na+ diffusion upon cycling. Detailed kinetics studies by a galvanostatic intermittent titration technique (GITT) reveal the dynamic change of Na+ diffusion upon cycling, and quantitative kinetic analysis indicates the high contribution of pseudocapacitive behavior during charge-discharge processes. Moreover, the ex-situ characterization analysis results further verify the Na-ion storage mechanism based on conversion reaction. This study is expected to provide a feasible design strategy for the bimetallic sulfides materials toward high performance sodium-ion batteries.

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