Wang Yuesheng, Feng Zimin, Cui Peixin, Zhu Wen, Gong Yue, Girard Marc-André, Lajoie Gilles, Trottier Julie, Zhang Qinghua, Gu Lin, Wang Yan, Zuo Wenhua, Yang Yong, Goodenough John B, Zaghib Karim
Center of Excellence in Transportation Electrification and Energy Storage, Hydro Québec, 1800 Boulevard Lionel-Boulet, Varennes, Québec, J3X 1S1, Canada.
Key Laboratory of Soil Environment and Pollution Remediation, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, Jiangsu, 210008, China.
Nat Commun. 2021 Jan 4;12(1):13. doi: 10.1038/s41467-020-20169-1.
Energy storage with high energy density and low cost has been the subject of a decades-long pursuit. Sodium-ion batteries are well expected because they utilize abundant resources. However, the lack of competent cathodes with both large capacities and long cycle lives prevents the commercialization of sodium-ion batteries. Conventional cathodes with hexagonal-P2-type structures suffer from structural degradations when the sodium content falls below 33%, or when the integral anions participate in gas evolution reactions. Here, we show a "pillar-beam" structure for sodium-ion battery cathodes where a few inert potassium ions uphold the layer-structured framework, while the working sodium ions could diffuse freely. The thus-created unorthodox orthogonal-P2 K[NiMn]O cathode delivers a capacity of 194 mAh/g at 0.1 C, a rate capacity of 84% at 1 C, and an 86% capacity retention after 500 cycles at 1 C. The addition of the potassium ions boosts simultaneously the energy density and the cycle life.
具有高能量密度和低成本的能量存储一直是长达数十年的追求目标。钠离子电池备受期待,因为它们利用的资源丰富。然而,缺乏兼具大容量和长循环寿命的合格阴极阻碍了钠离子电池的商业化。当钠含量低于33%,或者当整体阴离子参与析气反应时,具有六方-P2型结构的传统阴极会发生结构退化。在此,我们展示了一种用于钠离子电池阴极的“柱-梁”结构,其中一些惰性钾离子支撑着层状结构框架,而工作钠离子可以自由扩散。由此产生的非传统正交-P2 K[NiMn]O阴极在0.1 C时的容量为194 mAh/g,在1 C时的倍率容量为84%,在1 C下循环500次后的容量保持率为86%。钾离子的加入同时提高了能量密度和循环寿命。