4.8 Article

Boosting Sodium Storage Performance of Hard Carbon Anodes by Pore Architecture Engineering

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 40, 页码 47671-47683

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c14738

关键词

pore engineering; hard carbon; initial Coulombic efficiency; rate performance; sodium-ion batteries

资金

  1. National Natural Science Foundation of China [21975026]
  2. Science and Technology Program of Guangdong Province [2020B0909030004]

向作者/读者索取更多资源

Porous hard carbon anodes with cross-coupled macropore architecture show enhanced Na storage performances, including increased initial Coulombic efficiency, reversible capacity, rate performance, and cycling stability compared to pristine hard carbon with negligible pores. The use of a binder can further optimize the initial Coulombic efficiency. This work provides valuable insights for optimizing the performance of hard carbon anodes through pore engineering, with potential applications in other electrode materials.
Hard carbon (HC) displays great potential for high-performance sodium-ion batteries (SIBs) due to its cost-effective, simple fabrication and most likely to be commercialized. However, the complicated microstructures of HC lead to difficulties in deeply understanding the structure-performance correlation. Particularly, evaluation of influence of pore structure on Na storage performances is still causing disputes and rational strategies of designing pore architecture of HC are still necessary. In this work, the skillful and controllable phase-inversion method is applied to construct porous HC with abundantly interconnected and permeable tunnel-like pores, which can promote ionic diffusion and improve electrode-electrolyte interfacial affinity. Structure-performance investigation reveals that porous HC with cross-coupled macropore architecture can boost Na storage performances comprehensively. Compared to pristine HC with negligible pores, well-regulated porous HC anodes show an obvious enhancement on initial Coulombic efficiency (ICE) of 68.3% (only 51.5% for pristine HC), reversible capacity of 332.7 mAh g(-1) at 0.05 A g(-1), rate performance with 67.4% capacity retention at 2 A g(-1) (46.5% for pristine HC), and cycling stability with 95% capacity maintained for 90 cycles (86.4% for pristine HC). Additionally, the ICE can be optimized up to 76% by using sodium carboxymethyl cellulose as a binder. This work provides an important view of optimizing Na storage performances of HC anodes by pore engineering, which can be broadened into other electrode materials.

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