Mengluan Gao, Zhe Cui, Jinqi Zhu, Rujia Zou, Wenqing Wang, Ye Chen and Huifang Chen
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Secondly, the optimized Se-doped MoS<small><sub>3</sub></small> inside the CNF structure is formed after the initial discharge/charge cycles, and can prevent detrimental interfacial side reactions, decrease the Li<small><sup>+</sup></small> diffusion barriers, increase electronic conductivity, and limit the dissolution of polysulfides or polyselenides in the electrolyte. Finally, the N-doped flexible porous carbon nanofiber accommodates the volume expansion, and prevents the aggregation issues of MoS<small><sub>3</sub></small> and irreversible decomposition of Li<small><sub>2</sub></small>S or Li<small><sub>2</sub></small>Se into the electrolyte, which can greatly benefit reaction kinetics and structural stability for improved lithium storage performance. 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引用次数: 0
摘要
过渡金属硫族化合物(TMCs)由于其高比容量的特性,作为锂离子电池(LIBs)的负极材料得到了广泛的研究。然而,不稳定的反应中间体聚硫锂的溶解和团聚不可避免地导致活性成分的大量损失和反应可逆性的降低,导致寿命缩短。在此,我们成功地构建了嵌入柔性多孔碳纳米纤维(MoSSe/CNFs)的多层超薄MoSSe纳米片。首先,MoSSe/CNFs不仅通过大孔隙网络赋予碳纤维优越的柔韧性和完整性,而且还增强了快速电子传递能力。其次,优化后的CNFs结构内部掺杂硒的MoS3在第一次充放电循环后形成,可以防止有害的界面副反应,降低Li+扩散势垒,提高电子电导率,并限制多硫化物或多硒化物在电解质中的溶解。最后,n掺杂的柔性多孔碳纳米纤维适应了体积膨胀,防止了MoS3的聚集问题和Li2S或Li2Se在电解质中的不可逆分解,这大大有利于反应动力学和结构稳定性,从而提高锂的存储性能。由于这些改进,自立型MoSSe/CNFs电极在0.5 a g-1和5 a g-1下的稳定容量分别为738 mAh g-1和578 mAh g-1,在950次循环中容量保持几乎100%。
Anchoring intermediate phases via few-layer MoSSe nanosheets in flexible porous carbon fiber for stable lithium ion storage†
Transition metal chalcogenides (TMCs) have been widely studied as anode materials for lithium-ion batteries (LIBs) due to their high specific capacity properties. However, the dissolution and agglomeration of the unstable reaction intermediate lithium polysulfide inevitably leads to a significant loss of the active ingredient and a reduction in the reversibility of the reaction, resulting in a shortened lifetime. Herein, we successfully constructed few-layered ultrathin MoSSe nanosheets embedded in flexible porous carbon nanofibers (MoSSe/CNFs). Firstly, MoSSe/CNFs not only confer superior flexibility and integrity to the carbon fibers through a network of large pores but also enhance the fast electron transport capability. Secondly, the optimized Se-doped MoS3 inside the CNF structure is formed after the initial discharge/charge cycles, and can prevent detrimental interfacial side reactions, decrease the Li+ diffusion barriers, increase electronic conductivity, and limit the dissolution of polysulfides or polyselenides in the electrolyte. Finally, the N-doped flexible porous carbon nanofiber accommodates the volume expansion, and prevents the aggregation issues of MoS3 and irreversible decomposition of Li2S or Li2Se into the electrolyte, which can greatly benefit reaction kinetics and structural stability for improved lithium storage performance. As a result of these improvements, the self-standing MoSSe/CNFs electrodes show a stable capacity of 738 mA h g−1 at 0.5 A g−1 and 578 mA h g−1 at 5 A g−1 with a capacity retention of almost 100% over 950 cycles.
期刊介绍:
The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.