4.8 Article

Spindle Single-Crystalline Rutile TiO2 with Excellent Cyclability for Low-Cost Li-Storage Materials

Journal

ACS MATERIALS LETTERS
Volume 3, Issue 4, Pages 372-378

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsmaterialslett.1c00135

Keywords

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Funding

  1. Japan Society for the Promotion of Science (JSPS) KAKENHI [19H02817, 19K05649, 20H00399]
  2. Japan Association for Chemical Innovation (JACI)
  3. Advanced Characterization Nanotechnology Platform, Nanotechnology Platform Program of the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan at the Research Center for Ultra-High Voltage Electron Microscopy at Osaka University [A-20-OS0001, A-19-OS-0001]

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The study found that increasing the degree of single-crystal formation can improve the charge-discharge capacity and initial Coulombic efficiency of lithium storage materials, with the structural integrity of spindle TiO2 particles maintained during charge-discharge reactions. Doping Nb can further enhance the anode performance, suggesting that single-crystalline rutile TiO2 particles have the potential to be low-cost, high-performance lithium storage materials.
We investigated the Li storage properties of spindle single-crystalline rutile TiO2 fine particles synthesized by a large-scale sulfate process. Their anode properties were compared with those of polycrystalline rutile TiO2 particles. An increase in the degree of single-crystal formation improved the charge-discharge capacity and initial Coulombic efficiency. In situ X-ray diffraction and transmission electron microscopic observation demonstrated the structural integrity of the spindle particles during the charge-discharge reactions. These results concluded that the degree is a critical parameter determining the anode performance of rutile TiO2. The anode performance was further enhanced by doping Nb into the spindle TiO2 particles. These findings suggest that single-crystalline rutile TiO2 particles are very promising low-cost and high-performance Li storage materials.

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