2021
DOI: 10.1016/j.electacta.2020.137476
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Enhanced interfacial reaction interface stability of Ni-rich cathode materials by fabricating dual-modified layer coating for lithium-ion batteries

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Cited by 39 publications
(19 citation statements)
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“…The pristine LNCM electrode in Figure S4a,b shows extensive cracking and severe particle destruction after the 60°C storage test. These changes may allow the penetration of the electrolyte into the exposed surface and accelerate the side reaction, leading to a decrease in the capacity, which is consistent with the result in Figure 7A 57,58 . In contrast, the 1 wt% LNO‐LNCM electrode in Figures S4c,d showed significantly suppressed cracks and particle morphology.…”
Section: Results and Disscussionsupporting
confidence: 83%
See 1 more Smart Citation
“…The pristine LNCM electrode in Figure S4a,b shows extensive cracking and severe particle destruction after the 60°C storage test. These changes may allow the penetration of the electrolyte into the exposed surface and accelerate the side reaction, leading to a decrease in the capacity, which is consistent with the result in Figure 7A 57,58 . In contrast, the 1 wt% LNO‐LNCM electrode in Figures S4c,d showed significantly suppressed cracks and particle morphology.…”
Section: Results and Disscussionsupporting
confidence: 83%
“…These changes may allow the penetration of the electrolyte into the exposed surface and accelerate the side reaction, leading to a decrease in the capacity, which is consistent with the result in Figure 7A. 57,58 In contrast, the 1 wt% LNO-LNCM electrode in Figures S4c,d showed significantly suppressed cracks and particle morphology. This suggests that the LNO coating acts as a physical barrier that inhibits the side reaction and provides structural stability, resulting in excellent electrochemical performance even after harsh conditions such as high-temperature storage.…”
Section: Electrochemical Measurementssupporting
confidence: 82%
“…16,[19][20][21][22] In addition, the formed alkaline lithium impurities will hinder the lithium ion transmission, leading to the improvement of the interface impedance and serious degradation of the cathode structure. [22][23][24] Overall, the existence of residual lithium is a major threat to the industrialization of nickel-rich materials.…”
Section: Introductionmentioning
confidence: 99%
“…The popularity of consumer electronics and the rapid development of electric vehicles have put forward higher energy density and longer service life requirements for lithium-ion batteries (LIBs), which are mainly limited by cathode materials. Among the various promising cathode materials, the nickel-rich layered oxides (LiNi x Co y Mn z O 2 , x ≥ 0.6, x + y + z = 1) attract widespread attention due to their extremely high reversible capacity that can even exceed 200 mAh g –1 when the charging voltage exceeds 4.5 V. Except for the contribution of cations, additional capacity is achieved by the redox reaction of anionic oxygen (O 2– /O 2 n – , where 1 < n < 2) during a high charging voltage. , However, Ni-rich materials suffer from severe phase transformation and surface side reactions that cause the capacity and voltage to fade during high-voltage cycling. Therefore, many surface protectors, such as oxides (e.g., Al 2 O 3 , ZrO 2 , TiO 2 ), phosphates (Li 3 PO 4 , FePO 4 , LiFePO 4 ), and fluorides (AlF 3 , LiF, MgF 2 ), were designed to mechanically restrain unwanted structural transformations and inhibit surface side reactions by avoiding direct contact between the cathode materials and the electrolyte.…”
Section: Introductionmentioning
confidence: 99%