High-defect hydrophilic carbon cuboids anchored with Co/CoO nanoparticles as highly efficient and ultra-stable lithium-ion battery anodes

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Xiaolei Sun - , Leibniz Institute for Solid State and Materials Research Dresden, Chemnitz University of Technology (Author)
  • Guang Ping Hao - , Chair of Inorganic Chemistry I (Author)
  • Xueyi Lu - , Leibniz Institute for Solid State and Materials Research Dresden (Author)
  • Lixia Xi - , Leibniz Institute for Solid State and Materials Research Dresden (Author)
  • Bo Liu - , Chair of Molecular Biotechnology (Author)
  • Wenping Si - , Leibniz Institute for Solid State and Materials Research Dresden (Author)
  • Chuansheng Ma - , Xi'an Jiaotong University (Author)
  • Qiming Liu - , Saitama University (Author)
  • Qiang Zhang - , Tsinghua University (Author)
  • Stefan Kaskel - , Chair of Inorganic Chemistry I (Author)
  • Oliver G. Schmidt - , Leibniz Institute for Solid State and Materials Research Dresden, Chemnitz University of Technology (Author)

Abstract

We propose an effective strategy to engineer a unique kind of porous carbon cuboid with tightly anchored cobalt/cobalt oxide nanoparticles (PCC-CoOx) that exhibit outstanding electrochemical performance for many key aspects of lithium-ion battery electrodes. The host carbon cuboid features an ultra-polar surface reflected by its high hydrophilicity and rich surface defects due to high heteroatom doping (N-/O-doping both higher than 10 atom%) as well as hierarchical pore systems. We loaded the porous carbon cuboid with cobalt/cobalt oxide nanoparticles through an impregnation process followed by calcination treatment. The resulting PCC-CoOx anode exhibits superior rate capability (195 mA h g-1 at 20 A g-1) and excellent cycling stability (580 mA h g-1 after 2000 cycles at 1 A g-1 with only 0.0067% capacity loss per cycle). Impressively, even after an ultra-long cycle life exceeding 10 000 cycles at 5 A g-1, the battery can recover to 1050 mA h g-1 at 0.1 A g-1, perhaps the best performance demonstrated so far for lithium storage in cobalt oxide-based electrodes. This study provides a new perspective to engineer long-life, high-power metal oxide-based electrodes for lithium-ion batteries through controlling the surface chemistry of carbon host materials.

Details

Original languageEnglish
Pages (from-to)10166-10173
Number of pages8
JournalJournal of Materials Chemistry. A, Materials for energy and sustainability
Volume4
Issue number26
Publication statusPublished - 6 Jun 2016
Peer-reviewedYes