Abstract
Single-crystal Ni-rich cathodes offer promising prospects in mitigating intergranular microcracks and side reaction issues commonly encountered in conventional polycrystalline cathodes. However, the utilization of micrometer-sized single-crystal particles has raised concerns about sluggish Li+ diffusion kinetics and unfavorable structural degradation, particularly in high Ni content cathodes. Herein, we present an innovative in situ doping strategy to regulate the dominant growth of characteristic planes in the single-crystal precursor, leading to enhanced mechanical properties and effectively tackling the challenges posed by ultrahigh-nickel layered cathodes. Compared with the traditional dry-doping method, our in situ doping approach possesses a more homogeneous and consistent modifying effect from the inside out, ensuring the uniform distribution of doping ions with large radius (Nb, Zr, W, etc). This mitigates the generally unsatisfactory substitution effect, thereby minimizing undesirable coating layers induced by different solubilities during the calcination process. Additionally, the uniformly dispersed ions from this in situ doping are beneficial for alleviating the two-phase coexistence of H2/H3 and optimizing the Li+ concentration gradient during cycling, thus inhibiting the formation of intragranular cracks and interfacial deterioration. Consequently, the in situ doped cathodes demonstrate exceptional cycle retention and rate performance under various harsh testing conditions. Our optimized in situ doping strategy not only expands the application prospects of elemental doping but also offers a promising research direction for developing high-energy-density single-crystal cathodes with extended lifetime.
Original language | English |
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Pages (from-to) | 8002-8016 |
Number of pages | 15 |
Journal | ACS Nano |
Volume | 18 |
Issue number | 11 |
DOIs | |
State | Published - Mar 19 2024 |
Externally published | Yes |
Funding
This work was supported by National Natural Science Foundation of China (52070194, 52073309), Natural Science Foundation of Hunan Province (2022JJ20069) and Fundamental Research Funds for Central Universities of the Central South University (2023ZZTS0782). This work gratefully acknowledges support from the U.S. Department of Energy (DOE), Office of Energy Efficiency and Renewable Energy, Vehicle Technologies Office. Work performed at the Center for Nanoscale Materials, a U.S. Department of Energy Office of Science User Facility, was supported by the U.S. DOE, Office of Basic Energy Sciences, Argonne National Laboratory is operated for DOE Office of Science by UChicago Argonne, LLC, under contract number DE-AC02-06CH11357.
Funders | Funder number |
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Office of Energy Efficiency and Renewable Energy, Vehicle Technologies Office | |
Basic Energy Sciences | |
U.S. Department of Energy | |
Office of Science | |
National Natural Science Foundation of China | 52073309, 52070194 |
Fundamental Research Funds for Central Universities of the Central South University | 2023ZZTS0782 |
Argonne National Laboratory | DE-AC02-06CH11357 |
Natural Science Foundation of Hunan Province | 2022JJ20069 |
Keywords
- improved Li diffusion kinetics
- precursors engineering
- single-crystal
- ultrahigh-nickel layered cathodes
- uniform in situ doping