She Kaihang, Huang Ying, Fan Wanqing, Yu Meng, Zhang Jiaxin, Chen Chen
MOE Key Laboratory of Material Physics and Chemistry Under Extraordinary Conditions, School of Chemistry and Chemical Engineering, Northwestern Polytechnical University, Xi'an 710072, China.
MOE Key Laboratory of Material Physics and Chemistry Under Extraordinary Conditions, School of Chemistry and Chemical Engineering, Northwestern Polytechnical University, Xi'an 710072, China.
J Colloid Interface Sci. 2024 Feb 15;656:270-279. doi: 10.1016/j.jcis.2023.11.108. Epub 2023 Nov 19.
Constructing an anode with fast electron transport and high cycling stability is important but challenging for large-scale applications of sodium-ion batteries (SIB). In this study, hierarchical flower-like MXene structures were synthesized using poly (methyl methacrylate) (PMMA) microsphere as templates. Subsequently, a straightforward hydrothermal reaction was utilized to anchor small-sized MoS nanosheets. The resulting MXene@MoS heterostructure exhibits a distinctive three-dimensional (3D) porous hollow architecture. This structure effectively addresses challenges related to self-aggregation of MoS nanosheets and volume expansion of the electrode material during Na insertion/extraction processes. Furthermore, the robust hetero-interface supports fast and stable electron transfer, thereby enhancing electrochemical reaction kinetics. The prepared MXene@MoS electrode demonstrates the specific capacity of 682.1 mA h g at 0.2 A/g and the reversible capacity of 494.4 mA h g after 1000 cycles at 5 A/g. It is noteworthy that the full battery assembled with the composite material as the anode can still maintain the capacity of 456.2 mA h g after 80 cycles at 0.5 A/g. This outstanding reversible capacity and sustained stability over numerous cycles highlights its potential for a wide range of applications.
构建具有快速电子传输和高循环稳定性的阳极对于钠离子电池(SIB)的大规模应用而言至关重要但具有挑战性。在本研究中,以聚甲基丙烯酸甲酯(PMMA)微球为模板合成了分级花状MXene结构。随后,利用简单的水热反应来锚定小尺寸的MoS纳米片。所得的MXene@MoS异质结构呈现出独特的三维(3D)多孔中空结构。这种结构有效解决了与MoS纳米片自聚集以及在钠嵌入/脱出过程中电极材料体积膨胀相关的挑战。此外,坚固的异质界面支持快速且稳定的电子转移,从而增强电化学反应动力学。制备的MXene@MoS电极在0.2 A/g时展现出682.1 mA h g的比容量,在5 A/g下循环1000次后可逆容量为494.4 mA h g。值得注意的是,以该复合材料作为阳极组装的全电池在0.5 A/g下循环80次后仍可保持456.2 mA h g的容量。这种出色的可逆容量以及在众多循环中的持续稳定性凸显了其在广泛应用中的潜力。