Login / Signup

Inhibiting Mn Migration by Sb-Pinning Transition Metal Layers in Lithium-Rich Cathode Material for Stable High-Capacity Properties.

Fei CaoWeihao ZengJiawei ZhuJinsheng XiaoZilan LiMing LiRui QinTingting WangJunxin ChenXiaoli YiJiexi WangShichun Mu
Published in: Small (Weinheim an der Bergstrasse, Germany) (2022)
Owing to the interacted anion and cation redox dynamics in Li 2 MnO 3 , the high energy density can be obtained for lithium-rich manganese-based layered transition metal (TM) oxide [Li 1.2 Ni 0.2 Mn 0.6 O 2 , LNMO]. However, irreversible migration of Mn ions and oxygen release during highly de-lithiation can destroy its layered structure, leading to voltage and capacity decline. Herein, non-TM antimony (Sb) is pinned to the TM layer of LNMO by a facile sol-gel method. High-resolution ex and in situ characterization technologies manifest that the introduction of trace Sb inhibits the migration of Mn ions, forming a more stable structure. Sb can impressively adjust the Mn-O interaction between anions and cations, beneficial to decrease the energy level of Mn 3d and O 2p orbitals and expand their band gap according to the  theoretical calculation results. As a result, the discharge specific capacity and the energy density for SbLi 1.2 [Ni 0.2 Mn 0.6 ]O 2 (SLNMO) reaches as high as 301 mAh g -1 and 1019.6 Wh kg -1 at 0.1 C, respectively. Moreover, the voltage decay is reduced by 419.8 mV compared with LNMO. The regulative interaction between Mn 3d and isolated O 2p bands provides an accurate guidance for solving electrochemical performance deficiencies of lithium-rich manganese-based cathode oxide.
Keyphrases
  • transition metal
  • ionic liquid
  • ion batteries
  • high resolution
  • solid state
  • quantum dots
  • gold nanoparticles
  • metal organic framework
  • mass spectrometry
  • room temperature
  • hyaluronic acid
  • high speed