4.6 Article

Mg,Ti-base surface integrated layer and bulk doping to suppress lattice oxygen evolution of Ni-rich cathode material at a high cut-off voltage

期刊

JOURNAL OF ENERGY CHEMISTRY
卷 71, 期 -, 页码 434-444

出版社

ELSEVIER
DOI: 10.1016/j.jechem.2022.03.0532095-4956

关键词

Ni-rich layered oxide; Mg; Ti -base surface integrated layer; Bulk doping; Lattice oxygen evolution

资金

  1. National Natural Science Foundation of China [51902108, 51762006, 51964013]
  2. Special Projects for Central Government [GUIKE ZY20198008]
  3. Guangxi Innovation-Driven Development Subject [GUIKE AA19182020, GUIKE AA19254004]
  4. Guangxi Technology Base and Talent Subject [GUIKE AD18126001, GUIKE AD20999012, GUIKE AD20297086]
  5. Special Fund for Guangxi Distinguished Expert

向作者/读者索取更多资源

The simultaneous construction of a Mg, Ti-based surface integrated layer and bulk doping through Mg, Ti surface treatment can suppress the lattice oxygen evolution and improve the stability and capacity retention of nickel-rich layered cathode materials during high-voltage cycling.
The Nickel-rich layered cathode materials charged to 4.5 V can obtain a specific capacity of more than 200 mAh g-1. However, the nickel-rich layered cathode materials suffer from the severe capacity fade during high-voltage cycling, which is related to the phase transformation and the surface sides reactions caused by the lattice oxygen evolution. Here, the simultaneous construction of a Mg, Ti-based surface integrated layer and bulk doping through Mg, Ti surface treatment could suppress the lattice oxygen evolution of Nirich material at deep charging. More importantly, Mg and Ti are co-doped into the particles surface to form an Mg2TiO4 and Mg0.5-xTi2-y(PO4)3 outer layer with Mg and Ti vacancies. In the constructed surface integrated layer, the reverse electric field in the Mg2TiO4 effectively suppressed the outward migration of the lattice oxygen anions, while Mg0.5-xTi2-y(PO4)3 outer layer with high electronic conductivity and good lithium ion conductor could effectively maintained the stability of the reaction interface during highvoltage cycling. Meanwhile, bulk Mg and Ti co-doping can mitigate the migration of Ni ions in the bulk to keep the stability of transition metal-oxygen (M-O) bond at deep charging. As a result, the NCM@MTP cathode shows excellent long cycle stability at high-voltage charging, which keep high capacity retention of 89.3% and 84.3% at 1C after 200 and 100 cycles under room and elevated temperature of 25 and 55 degrees C, respectively. This work provides new insights for manipulating the surface chemistry of electrode materials to suppress the lattice oxygen evolution at high charging voltage. (c) 2022 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.

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