TY - JOUR
T1 - Revisiting Cationic Doping Impacts in Ni-Rich Cathodes
AU - Hou, Xueyan
AU - Katsumata, Takuya
AU - Kimura, Yuta
AU - Tamenori, Yusuke
AU - Nitta, Kiyofumi
AU - Yamagishi, Hirona
AU - Amezawa, Koji
AU - Nakamura, Takashi
N1 - Funding Information:
The synchrotron radiation experiments were performed at BL27SU of SPring-8 with the approval of JASRI (Proposals 2020A0749, 2021A1343, 2021B1660, and 2022A1424) and the SR-Center of Ritsumeikan University (Proposal No. S20015). This work was financially supported by JSPS KAKENHI Grants JP18K05288 and JP19H05814, the JACI Prize for Encouraging Young Researcher, the Research Foundation for the Electrotechnology of Chubu, and the Tokuyama Science Foundation.
Funding Information:
This work was financially supported by JSPS KAKENHI Grants JP18K05288 and JP19H05814, the JACI Prize for Encouraging Young Researcher, the Research Foundation for the Electrotechnology of Chubu, and the Tokuyama Science Foundation.
Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023/2/13
Y1 - 2023/2/13
N2 - As a promising cathode material for high-energy-density Li-ion batteries, Ni-rich layered oxide cathode active materials deliver high specific capacity. However, their electrochemical performance degrades rapidly upon charge/discharge cycles probably due to electrochemical/thermochemical instabilities. While cationic doping in the transition-metal site has been regarded as an effective strategy to enhance the electrochemical performance, the true impact of cation doping is not well understood. To quantitatively assess the impact of cationic doping, in this work, the electrochemical performance and lattice oxygen stability of LiNi0.82Co0.18O2, isovalent Al3+-doped LiNi0.82Co0.15Al0.03O2, and high-valent Ti4+-doped LiNi0.82Co0.15Ti0.03O2 were investigated. Despite significant improvements in electrochemical performance by Al3+ and Ti4+ doping, it was revealed that these cation dopings had no discernible effect on the lattice oxygen stability. Such information suggests that the electrochemical enhancement by Al3+/Ti4+ doping is not attributed to the stabilization of lattice oxygen. This work highlights the importance of independent and quantitative experimental evaluations on kinetic electrochemical properties and thermodynamic stability of lattice oxygen to establish rational guidelines for doping strategy toward high-energy-density and reliable cathode-active materials.
AB - As a promising cathode material for high-energy-density Li-ion batteries, Ni-rich layered oxide cathode active materials deliver high specific capacity. However, their electrochemical performance degrades rapidly upon charge/discharge cycles probably due to electrochemical/thermochemical instabilities. While cationic doping in the transition-metal site has been regarded as an effective strategy to enhance the electrochemical performance, the true impact of cation doping is not well understood. To quantitatively assess the impact of cationic doping, in this work, the electrochemical performance and lattice oxygen stability of LiNi0.82Co0.18O2, isovalent Al3+-doped LiNi0.82Co0.15Al0.03O2, and high-valent Ti4+-doped LiNi0.82Co0.15Ti0.03O2 were investigated. Despite significant improvements in electrochemical performance by Al3+ and Ti4+ doping, it was revealed that these cation dopings had no discernible effect on the lattice oxygen stability. Such information suggests that the electrochemical enhancement by Al3+/Ti4+ doping is not attributed to the stabilization of lattice oxygen. This work highlights the importance of independent and quantitative experimental evaluations on kinetic electrochemical properties and thermodynamic stability of lattice oxygen to establish rational guidelines for doping strategy toward high-energy-density and reliable cathode-active materials.
KW - Li-ion battery
KW - Ni-rich cathode
KW - cationic doping
KW - electrochemistry
KW - lattice oxygen stability
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U2 - 10.1021/acsaem.2c04141
DO - 10.1021/acsaem.2c04141
M3 - Article
AN - SCOPUS:85147265969
SN - 2574-0962
VL - 6
SP - 2072
EP - 2080
JO - ACS Applied Energy Materials
JF - ACS Applied Energy Materials
IS - 3
ER -