氟
煅烧
结构精修
镍
锂(药物)
兴奋剂
分析化学(期刊)
晶格常数
氧化镍
化学
材料科学
结晶学
无机化学
晶体结构
衍射
冶金
医学
光电子学
内分泌学
生物化学
物理
色谱法
光学
催化作用
作者
Ning Zhang,Jamie E. Stark,Hongyang Li,Aaron Liu,Ying Li,Ines Hamam,J. R. Dahn
标识
DOI:10.1149/1945-7111/ab8b00
摘要
Three fluorine-doped lithium nickel oxide samples series (LiNiO 2−x F x , LiNi 1−x Mg x O 2−x F x ; Li 1+x/2 Ni 1−x/2 O 2−x F x ) were prepared and investigated. It is suggested that fluorine was introduced into the lattice structure during the calcination. As fluorine is introduced into LiNiO 2−x F x and LiNi 1−x Mg x O 2−x F x the percentage of Ni (or Ni and Mg) in the Li layer increases for x > 0.05. However, adding excess Li in Li 1+x/2 Ni 1−x/2 O 2−x F x sucessfully balances the charge differential introduced by fluorine doping therefore very little Ni 2+ was created and the lithium layers remain “uncontaminated” by other metals. Data from Li/LiNiO 2−x F x , Li/LiNi 1−x Mg x O 2−x F x and Li/Li 1+x/2 Ni 1−x/2 O 2−x F x cells mirror the percent of cation mixing as determined by X-ray diffraction (XRD) and Rietveld refinement in each case. In situ XRD of Li 1.1−x Ni 0.9 O 1.8 F 0.2 shows no multipule phase transitions which further suggests fluorine was successfully doped into the lattice. Acclelerating rate calorimetry (ARC) experiments show a potential safety advantage brought by fluorine doping. pH titration was used to explore if residual LiF (if any) at the surface converted to other lithium compounds (LiOH, Li 2 O or Li 2 CO 3 ). No evidence of residual LiF was found.
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