摘要
Even with native aluminum oxide (Al2O3) passive film, the aluminum (Al) current collector is susceptible to pitting corrosion and anodic dissolution under high voltage (>4.0 V vs. Li+/Li). Herein, a corrosion-inhibiting binder (named as CSAP) with an ion-hydrogen bond synergistic network is developed for 5 V-class LiNi0.5Mn1.5O4 (LNMO) batteries, the abundant carboxylate (─COO−) on the backbone plays a key role in coordinating with Al2O3, resulting in a stable organic–inorganic hybrid interphase that effectively resists the attack of corrosive species generated from lithium salt. Minor current response is exhibited from the CSAP-treated Al current collector compared with the poly(vinylidene fluoride) (PVDF) counterpart during 36 h chronoamperometry test, directly indicating the suppressed corrosion reactions. A similar conclusion can be arrived at from the lower content of corrosion mass loss in finite element analysis. Furthermore, the suppression of transition-metal ion dissolution endowed by CSAP is verified through the structural retention observed in scanning transmission electron microscopy (STEM). Benefiting from these merits, a discharge capacity of 139.4 mAh g−1 is maintained in the LNMO/CSAP battery after 600 cycles at 1 C, compare with 109.7 mAh g−1 of the PVDF counterpart. More encouragingly, a discharge capacity of 108.1 mAh g−1 is exhibited for the LNMO/CSAP battery at 12 C.
| 源语言 | 英语 |
|---|---|
| 期刊论文编号 | e76724 |
| 期刊 | Advanced Functional Materials |
| 卷 | 36 |
| 期 | 59 |
| DOI | |
| 出版状态 | 已出版 - 23 7月 2026 |
| 已对外发布 | 是 |
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