Suppr超能文献

通过调节阳离子排列来调谐富锂锰基层状氧化物正极中的氧氧化还原化学。

Tuning Oxygen Redox Chemistry in Li-Rich Mn-Based Layered Oxide Cathodes by Modulating Cation Arrangement.

机构信息

Key Laboratory of Advanced Energy Materials Chemistry, College of Chemistry, Nankai University, Tianjin, 300071, China.

Renewable Energy Conversion and Storage Center, Nankai University, Tianjin, 300071, China.

出版信息

Adv Mater. 2019 Oct;31(42):e1901808. doi: 10.1002/adma.201901808. Epub 2019 Sep 2.

Abstract

Li-rich Mn-based oxides (LRMO) are promising cathode materials to build next-generation lithium-ion batteries with high energy density exceeding 400 W h kg . However, due to a lack of in-depth understanding of oxygen redox chemistry in LRMO, voltage decay is not resolved thoroughly. Here, it is demonstrated that the oxygen redox chemistry could be tuned by modulating cation arrangement. It declares that the materials with Li/Ni disorder and Li vacancies can inhibit the formation of OO dimers. Because of the high chemical activity, OO dimers could accelerate lattice oxygen release and NiO/spinel formation. The samples without forming OO dimers show improved performance in suppressing oxygen overoxidation and mitigating cation dissolution. As a result, the optimized cathode exhibits a high capacity over 280 mA h g at 0.1 C and a high plateau voltage of 3.58 V with a very low voltage decay of 1.6% after 150 cycles at 1 C. This study opens an attractive path in designing Li-rich electrodes with stabilized redox chemistry.

摘要

富锂锰基氧化物 (LRMO) 是一种很有前途的正极材料,可用于构建能量密度超过 400 Wh kg 的下一代锂离子电池。然而,由于对 LRMO 中氧氧化还原化学的深入了解不足,电压衰减问题仍未得到彻底解决。本研究表明,通过调节阳离子排列可以调节氧氧化还原化学。研究表明,具有 Li/Ni 无序和 Li 空位的材料可以抑制 OO 二聚体的形成。由于高化学活性,OO 二聚体可以加速晶格氧的释放和 NiO/尖晶石的形成。不形成 OO 二聚体的样品在抑制过氧氧化和减轻阳离子溶解方面表现出更好的性能。结果,优化后的正极在 0.1 C 时表现出超过 280 mA h g 的高容量和 3.58 V 的高平台电压,在 1 C 下循环 150 次后,电压衰减率仅为 1.6%。这项研究为设计具有稳定氧化还原化学的富锂电极开辟了一条有吸引力的途径。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验