4.8 Article

Boosting fast energy storage by synergistic engineering of carbon and deficiency

期刊

NATURE COMMUNICATIONS
卷 11, 期 1, 页码 -

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-019-13945-1

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资金

  1. National Natural Science Foundation of China [51772272, 51728204]
  2. National youth talent support program of China
  3. Natural Science Funds for Distinguished Young Scholar of Zhejiang Province [LR20E020001]
  4. Fundamental Research Funds for the Central Universities [2018QNA4011]
  5. Qianjiang Talents Plan D [QJD1602029]
  6. Startup Foundation for Hundred-Talent Program of Zhejiang University
  7. Key Research and Development Program of Hainan Province [ZDYF2017166]
  8. project of Fundamental Investigation of Phase Transformative Materials for Energy Application [9610399]
  9. City University of Hong Kong
  10. Shenzhen Science and Technology Innovation Committee [R-IND14701]
  11. DOE Office of Science [DE-AC02-06CH11357]

向作者/读者索取更多资源

Exploring advanced battery materials with fast charging/discharging capability is of great significance to the development of modern electric transportation. Herein we report a powerful synergistic engineering of carbon and deficiency to construct high-quality three/two-dimensional cross-linked Ti2Nb10O29-x@C composites at primary grain level with conformal and thickness-adjustable boundary carbon. Such exquisite boundary architecture is demonstrated to be capable of regulating the mechanical stress and concentration of oxygen deficiency for desired performance. Consequently, significantly improved electronic conductivity and enlarged lithium ion diffusion path, shortened activation process and better structural stability are realized in the designed Ti2Nb10O29-x@C composites. The optimized Ti2Nb10O29-x@C composite electrode shows fast charging/discharging capability with a high capacity of 197 mA h g(-1) at 20C (similar to 3 min) and excellent long-term durability with 98.7% electron and Li capacity retention over 500 cycles. Most importantly, the greatest applicability of our approach has been demonstrated by various other metal oxides, with tunable morphology, structure and composition.

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