Author
Listed:
- Yu-Jie Guo
(Institute of Chemistry, Chinese Academy of Sciences (CAS)
University of Chinese Academy of Sciences)
- Peng-Fei Wang
(Institute of Chemistry, Chinese Academy of Sciences (CAS)
University of Chinese Academy of Sciences)
- Yu-Bin Niu
(Institute of Chemistry, Chinese Academy of Sciences (CAS)
University of Chinese Academy of Sciences)
- Xu-Dong Zhang
(Institute of Chemistry, Chinese Academy of Sciences (CAS)
University of Chinese Academy of Sciences)
- Qinghao Li
(University of Chinese Academy of Sciences
Institute of Physics, CAS)
- Xiqian Yu
(University of Chinese Academy of Sciences
Institute of Physics, CAS)
- Min Fan
(Institute of Chemistry, Chinese Academy of Sciences (CAS)
University of Chinese Academy of Sciences)
- Wan-Ping Chen
(Institute of Chemistry, Chinese Academy of Sciences (CAS)
University of Chinese Academy of Sciences)
- Yang Yu
(University of Chinese Academy of Sciences)
- Xiangfeng Liu
(University of Chinese Academy of Sciences)
- Qinghai Meng
(Institute of Chemistry, Chinese Academy of Sciences (CAS)
University of Chinese Academy of Sciences)
- Sen Xin
(Institute of Chemistry, Chinese Academy of Sciences (CAS)
University of Chinese Academy of Sciences)
- Ya-Xia Yin
(Institute of Chemistry, Chinese Academy of Sciences (CAS)
University of Chinese Academy of Sciences)
- Yu-Guo Guo
(Institute of Chemistry, Chinese Academy of Sciences (CAS)
University of Chinese Academy of Sciences)
Abstract
Na-ion cathode materials operating at high voltage with a stable cycling behavior are needed to develop future high-energy Na-ion cells. However, the irreversible oxygen redox reaction at the high-voltage region in sodium layered cathode materials generates structural instability and poor capacity retention upon cycling. Here, we report a doping strategy by incorporating light-weight boron into the cathode active material lattice to decrease the irreversible oxygen oxidation at high voltages (i.e., >4.0 V vs. Na+/Na). The presence of covalent B–O bonds and the negative charges of the oxygen atoms ensures a robust ligand framework for the NaLi1/9Ni2/9Fe2/9Mn4/9O2 cathode material while mitigating the excessive oxidation of oxygen for charge compensation and avoiding irreversible structural changes during cell operation. The B-doped cathode material promotes reversible transition metal redox reaction enabling a room-temperature capacity of 160.5 mAh g−1 at 25 mA g−1 and capacity retention of 82.8% after 200 cycles at 250 mA g−1. A 71.28 mAh single-coated lab-scale Na-ion pouch cell comprising a pre-sodiated hard carbon-based anode and B-doped cathode material is also reported as proof of concept.
Suggested Citation
Yu-Jie Guo & Peng-Fei Wang & Yu-Bin Niu & Xu-Dong Zhang & Qinghao Li & Xiqian Yu & Min Fan & Wan-Ping Chen & Yang Yu & Xiangfeng Liu & Qinghai Meng & Sen Xin & Ya-Xia Yin & Yu-Guo Guo, 2021.
"Boron-doped sodium layered oxide for reversible oxygen redox reaction in Na-ion battery cathodes,"
Nature Communications, Nature, vol. 12(1), pages 1-11, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-25610-7
DOI: 10.1038/s41467-021-25610-7
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Citations
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Cited by:
- Gupta, Yamini & Siwatch, Poonam & Karwasra, Reetika & Sharma, Kriti & Tripathi, S.K., 2024.
"Recent progress of layered structured P2- and O3- type transition metal oxides as cathode material for sodium-ion batteries,"
Renewable and Sustainable Energy Reviews, Elsevier, vol. 192(C).
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