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通过揭示和减轻表面降解实现稳定、高能、部分无序的富锰尖晶石阴极

Toward Stable, High-Energy, Partially Disordered Mn-Rich Spinel Cathodes by Revealing and Mitigating Surface Degradation.

作者信息

Xia Dawei, Yao Junyi, Shi Chenguang, Wang Qian, Seok Changgyu, Olayiwola Afolabi, Huang Weibo, Nordlund Dennis, Chen Si Athena, Sun Cheng-Jun, Li Luxi, Hou Dewen, Quan Lina, Liu Yuzi, Xiong Hui, Lin Feng

机构信息

Department of Chemistry, Virginia Tech, Blacksburg, VA, 24061, USA.

Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, Menlo Park, CA, 94025, USA.

出版信息

Adv Mater. 2025 Aug;37(34):e2501352. doi: 10.1002/adma.202501352. Epub 2025 Jun 18.

DOI:10.1002/adma.202501352
PMID:40531600
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12392868/
Abstract

Mn-rich cathodes balance performance and sustainability but suffer from limited cyclability due to Mn dissolution and cathode-to-anode crosstalk. The Jahn-Teller (J-T) effect of Mn is often linked to the above phenomena, such as in spinel LiMnO. However, in typical voltage ranges, significant Mn only appears near the end of discharge, highlighting the need to reassess its role in driving Mn dissolution, structural degradation, and battery performance. Here, the spinel cathode's degree of disorder is tailored to expand the Mn redox range, enabling segmentation into J-T active and less active voltage ranges. Cycling at segmented voltage windows reveals surface degradation mechanisms with and without the major J-T effect. Despite a stronger J-T effect below 3.6 V vs. Li/Li, Mn dissolution is less significant than above 3.6 V. Expanding the cycling window to 2.0-4.3 V causes severe degradation as the J-T active range induces a tetragonal phase and Mn-rich surface, driving Mn dissolution and consuming Li-ion inventory in full cells. Reducing electrolyte acidity minimizes Mn disproportionation, enabling a stable dopant-free Mn-only cathode with a 250 mAh g specific capacity. These findings demonstrate that full cells using Mn-rich cathodes have the potential to avoid the notorious crosstalk problem through electrolyte engineering.

摘要

富锰阴极在性能和可持续性之间取得了平衡,但由于锰溶解和阴极与阳极之间的串扰,其循环稳定性有限。锰的 Jahn-Teller(J-T)效应通常与上述现象有关,例如在尖晶石 LiMnO 中。然而,在典型的电压范围内,大量的锰仅在放电末期出现,这凸显了重新评估其在驱动锰溶解、结构退化和电池性能方面作用的必要性。在这里,尖晶石阴极的无序度被调整以扩大锰的氧化还原范围,从而能够将其分为 J-T 活性和活性较低的电压范围。在分段电压窗口下循环揭示了有无主要 J-T 效应时的表面退化机制。尽管相对于 Li/Li,在 3.6 V 以下 J-T 效应更强,但锰的溶解在 3.6 V 以上时更为显著。将循环窗口扩大到 2.0 - 4.3 V 会导致严重退化,因为 J-T 活性范围会诱导四方相和富锰表面,驱动锰溶解并消耗全电池中的锂离子库存。降低电解质酸度可最大限度地减少锰的歧化反应,从而实现具有 250 mAh g 比容量的稳定无掺杂纯锰阴极。这些发现表明,使用富锰阴极的全电池有潜力通过电解质工程避免臭名昭著的串扰问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eff/12392868/e2d5bce9bfbc/ADMA-37-2501352-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eff/12392868/f95effcd9a1e/ADMA-37-2501352-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eff/12392868/98f42a5f0618/ADMA-37-2501352-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eff/12392868/01a05c287a2c/ADMA-37-2501352-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eff/12392868/e254e9b06995/ADMA-37-2501352-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eff/12392868/ba283f7cacfa/ADMA-37-2501352-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eff/12392868/e2d5bce9bfbc/ADMA-37-2501352-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eff/12392868/f95effcd9a1e/ADMA-37-2501352-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eff/12392868/98f42a5f0618/ADMA-37-2501352-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eff/12392868/01a05c287a2c/ADMA-37-2501352-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eff/12392868/e254e9b06995/ADMA-37-2501352-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eff/12392868/ba283f7cacfa/ADMA-37-2501352-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eff/12392868/e2d5bce9bfbc/ADMA-37-2501352-g007.jpg

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