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Surface Coupling between Mechanical and Electric Fields Empowering Ni‐Rich Cathodes with Superior Cyclabilities for Lithium‐Ion Batteries
Ni‐rich cathodes with high energy densities are considered as promising candidates for advanced lithium‐ion batteries, whereas their commercial application is in dilemma due to dramatic capacity decay and poor structure stability stemmed from interfacial instability, structural degradation, and stre...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218785/ https://www.ncbi.nlm.nih.gov/pubmed/35478438 http://dx.doi.org/10.1002/advs.202200622 |
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author | Dai, Zhongsheng Wang, Jianhang Zhao, Huiling Bai, Ying |
author_facet | Dai, Zhongsheng Wang, Jianhang Zhao, Huiling Bai, Ying |
author_sort | Dai, Zhongsheng |
collection | PubMed |
description | Ni‐rich cathodes with high energy densities are considered as promising candidates for advanced lithium‐ion batteries, whereas their commercial application is in dilemma due to dramatic capacity decay and poor structure stability stemmed from interfacial instability, structural degradation, and stress–strain accumulation, as well as intergranular cracks. Herein, a piezoelectric LiTaO(3) (LTO) layer is facilely deposited onto Li[Ni (x) Co(y)Mn(1−) (x) (−) (y) ]O(2) (x = 0.6, 0.8) cathodes to induce surface polarized electric fields via the intrinsic stress–strain of Ni‐rich active materials, thus modulating interfacial Li(+) kinetics upon cycling. Various characterizations indicate that the electrochemical performances of LTO‐modified cathodes are obviously enhanced even under large current density and elevated temperature. Intensive explorations from in situ X‐ray diffraction technique, finite element analysis, and first‐principle calculation manifest that the improvement mechanism of LTO decoration can be attributed to the enhanced structural stability of bulk material, suppressed stress accumulation, and regulated ion transportation. These findings provide deep insight into surface coupling strategy between mechanical and electric fields to regulate the interfacial Li(+) kinetics behavior and enhance structure stability for Ni‐rich cathodes, which will also arouse great interest from scientists and engineers in multifunctional surface engineering for electrochemical systems. |
format | Online Article Text |
id | pubmed-9218785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92187852022-06-29 Surface Coupling between Mechanical and Electric Fields Empowering Ni‐Rich Cathodes with Superior Cyclabilities for Lithium‐Ion Batteries Dai, Zhongsheng Wang, Jianhang Zhao, Huiling Bai, Ying Adv Sci (Weinh) Research Articles Ni‐rich cathodes with high energy densities are considered as promising candidates for advanced lithium‐ion batteries, whereas their commercial application is in dilemma due to dramatic capacity decay and poor structure stability stemmed from interfacial instability, structural degradation, and stress–strain accumulation, as well as intergranular cracks. Herein, a piezoelectric LiTaO(3) (LTO) layer is facilely deposited onto Li[Ni (x) Co(y)Mn(1−) (x) (−) (y) ]O(2) (x = 0.6, 0.8) cathodes to induce surface polarized electric fields via the intrinsic stress–strain of Ni‐rich active materials, thus modulating interfacial Li(+) kinetics upon cycling. Various characterizations indicate that the electrochemical performances of LTO‐modified cathodes are obviously enhanced even under large current density and elevated temperature. Intensive explorations from in situ X‐ray diffraction technique, finite element analysis, and first‐principle calculation manifest that the improvement mechanism of LTO decoration can be attributed to the enhanced structural stability of bulk material, suppressed stress accumulation, and regulated ion transportation. These findings provide deep insight into surface coupling strategy between mechanical and electric fields to regulate the interfacial Li(+) kinetics behavior and enhance structure stability for Ni‐rich cathodes, which will also arouse great interest from scientists and engineers in multifunctional surface engineering for electrochemical systems. John Wiley and Sons Inc. 2022-04-27 /pmc/articles/PMC9218785/ /pubmed/35478438 http://dx.doi.org/10.1002/advs.202200622 Text en © 2022 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Dai, Zhongsheng Wang, Jianhang Zhao, Huiling Bai, Ying Surface Coupling between Mechanical and Electric Fields Empowering Ni‐Rich Cathodes with Superior Cyclabilities for Lithium‐Ion Batteries |
title | Surface Coupling between Mechanical and Electric Fields Empowering Ni‐Rich Cathodes with Superior Cyclabilities for Lithium‐Ion Batteries |
title_full | Surface Coupling between Mechanical and Electric Fields Empowering Ni‐Rich Cathodes with Superior Cyclabilities for Lithium‐Ion Batteries |
title_fullStr | Surface Coupling between Mechanical and Electric Fields Empowering Ni‐Rich Cathodes with Superior Cyclabilities for Lithium‐Ion Batteries |
title_full_unstemmed | Surface Coupling between Mechanical and Electric Fields Empowering Ni‐Rich Cathodes with Superior Cyclabilities for Lithium‐Ion Batteries |
title_short | Surface Coupling between Mechanical and Electric Fields Empowering Ni‐Rich Cathodes with Superior Cyclabilities for Lithium‐Ion Batteries |
title_sort | surface coupling between mechanical and electric fields empowering ni‐rich cathodes with superior cyclabilities for lithium‐ion batteries |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218785/ https://www.ncbi.nlm.nih.gov/pubmed/35478438 http://dx.doi.org/10.1002/advs.202200622 |
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