Xu Shuzheng, Guo Meng, Fang Zhenchun, Wang Yinan, Li Hongda, Chang Haixin, Zhou Guowei, Gu Shaonan
Key Laboratory of Fine Chemicals in Universities of Shandong, Jinan Engineering Laboratory for Multi-Scale Functional Materials, School of Chemistry and Chemical Engineering, Qilu University of Technology (Shandong Academy of Sciences), Jinan, 250353, China.
Liuzhou Key Laboratory for New Energy Vehicle Power Lithium Battery, School of Microelectronics and Materials Engineering, Guangxi University of Science and Technology, Liuzhou, 545006, China.
Small. 2024 Jan;20(1):e2304618. doi: 10.1002/smll.202304618. Epub 2023 Aug 27.
The development of lithium-sulfur (Li-S) batteries is very promising and yet faces the issues of hindered polysulfides conversion and Li dendrite growth. Different from using different materials strategies to overcome these two types of problems, here multifunctional catalytic hierarchical interfaces of Ni P -Ni P porous nanosheets formed by Ni P partially in situ converted from Ni P are proposed. The unique electronic structure in the interface endows Ni P -Ni P effective electrocatalysis effect toward both sulfides' reduction and oxidation through reducing Gibbs free energies, indicating a bidirectional conversion acceleration. Importantly, Ni P -Ni P porous nanosheets with hierarchical interfaces also reduced the Li nucleation energy barrier, and a dendrite-free Li deposition is realized during the overall Li deposition and stripping steps. To this end, Ni P -Ni P decorated carbon nanotube/S cathode showing a high capacity of over 1500 mAh g , and a high rate capability of 8 C. Moreover, the coin full cell delivered a high capacity of 1345 mAh g at 0.2 C and the pouch full cell delivered a high capacity of 1114 mAh g at 0.2 C with high electrochemical stability during 180° bending. This work inspires the exploration of hierarchical structures of 2D materials with catalytically active interfaces to improve the electrochemistry of Li-S full battery.
锂硫(Li-S)电池的发展前景广阔,但面临多硫化物转化受阻和锂枝晶生长的问题。与采用不同材料策略来克服这两类问题不同,本文提出了由部分原位从NiP转化而来的NiP形成的NiP-NiP多孔纳米片的多功能催化分级界面。界面中独特的电子结构赋予NiP-NiP通过降低吉布斯自由能对硫化物的还原和氧化均具有有效的电催化作用,表明双向转化加速。重要的是,具有分级界面的NiP-NiP多孔纳米片还降低了锂成核能垒,并在整个锂沉积和剥离步骤中实现了无枝晶锂沉积。为此,NiP-NiP修饰的碳纳米管/S阴极显示出超过1500 mAh g的高容量和8 C的高倍率性能。此外,并型全电池在0.2 C时具有1345 mAh g的高容量,软包全电池在0.2 C时具有1114 mAh g的高容量,并且在180°弯曲过程中具有高电化学稳定性。这项工作激发了对具有催化活性界面的二维材料分级结构的探索,以改善锂硫全电池的电化学性能。