Kim Taewhan, Kim Kyoung Ho, Kim Hansol, Lee Wontae, Choi Woosung, Yoon Jaesang, Song Lianghao, Kim Ki Jae, Bulakhe Ravindra N, Yoon Won-Sub, Kim Ji Man
Convergence Research Center for Energy and Environmental Sciences, Sungkyunkwan University, Suwon, 16419, South Korea.
Department of Energy Science, Sungkyunkwan University, Suwon, 16419, South Korea.
Small. 2025 Feb;21(5):e2406243. doi: 10.1002/smll.202406243. Epub 2024 Oct 4.
Anode materials storing large-scale lithium ions gradually decrease electrochemical performance due to severe volume changes during cycling. Therefore, there is an urgent need to develop anode materials with high electrochemical capacity and durability, without deterioration arising due to the volume changes during the electrochemical processes. To date, mesoporous materials have received attention as anode materials due to their ability to mitigate volume expansion, offer a short pathway for Li transport, and exhibit anomalous high capacity. However, the nano-frameworks of transition metal oxide collapse during conversion reactions, demanding an improvement in nano-framework structure stability. In this study, ordered mesoporous nickel manganese oxide (m-NMO) is designed as an anode material with a highly durable nanostructure. Interestingly, m-NMO showed better cycle performance and higher electrochemical capacity than those of nickel oxide and manganese oxide. Operando small-angle X-ray scattering and ex situ transmission electron microscopic results confirmed that the binary m-NMO sustained a highly durable nanostructure upon cycling, unlike the single metal oxide electrodes where the mesostructures collapsed. Ex situ X-ray absorption spectroscopy proved that nickel and manganese showed different electrochemical reaction voltages, and thus undergoes sequential conversion reactions. As a result, both elements can act as complementary nano-propping buffers to maintain stable mesostructure.
存储大量锂离子的阳极材料由于在循环过程中发生严重的体积变化,其电化学性能会逐渐下降。因此,迫切需要开发具有高电化学容量和耐久性的阳极材料,且不会因电化学过程中的体积变化而导致性能恶化。迄今为止,介孔材料因其能够减轻体积膨胀、为锂传输提供短路径并展现出异常高的容量而受到关注,被用作阳极材料。然而,过渡金属氧化物的纳米框架在转化反应过程中会坍塌,这就需要提高纳米框架结构的稳定性。在本研究中,有序介孔镍锰氧化物(m-NMO)被设计为一种具有高度耐用纳米结构的阳极材料。有趣的是,m-NMO表现出比氧化镍和氧化锰更好的循环性能和更高的电化学容量。原位小角X射线散射和非原位透射电子显微镜结果证实,与介孔结构会坍塌的单一金属氧化物电极不同,二元m-NMO在循环过程中维持了高度耐用的纳米结构。非原位X射线吸收光谱证明镍和锰表现出不同的电化学反应电压,因此会经历顺序转化反应。结果,两种元素都可以作为互补的纳米支撑缓冲剂来维持稳定的介孔结构。