Mesoporous carbon layer encapsulated SnSe nanosheets via covalent bonds for high-performance sodium ion batteries

Mengfei Wang , Liang Yang , Maocheng Liu
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Abstract

Sodium ion batteries (SIBs) have been widely studied because of their low cost, low standard redox potential, and abundant sodium availability. However, the structural rupture during the Na+ insertion/extraction processes and the poor conductivity of the anode material limit its cycling stability and rate capability. Herein, SnSe@C was prepared by high-temperature annealing with dopamine hydrochloride as the carbon source, while SnSe was prepared by a protein reduction method. The carbon layer not only works as a protective layer to limit the volume expansion of SnSe and reduce the dissolution of Na2Se and poly-selenides generated during the discharge process in the electrolyte, but also as a conductive matrix to expedite electron transfer, thereby boosting the cycling stability and rate capability of SnSe@C. Benefiting from the above advantages, SnSe@C exhibits a specific capacity of 211.3 mAh g−1 at 0.1 A g−1 after 110 cycles and outstanging rate capability (210.1 mAh g−1 at 5.0 A g−1 and capacity retention rate of 63.2% from 0.1 to 1.0 A g−1). This study not only proposes an idea for promoting the cycling stability and rate capability of SnSe, but also paves the way for providing anodic materials with a stable structure for SIBs.

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用于高性能钠离子电池的共价键介孔碳层包覆SnSe纳米片
钠离子电池(SIBs)由于其低成本、低标准氧化还原电位和丰富的钠可用性而被广泛研究。然而,在Na+插入/提取过程中的结构断裂和阳极材料的不良导电性限制了其循环稳定性和倍率能力。在此SnSe@C以盐酸多巴胺为碳源,通过高温退火制备SnSe。碳层不仅起到保护层的作用,以限制SnSe的体积膨胀,减少放电过程中产生的Na2Se和聚硒化物在电解质中的溶解,而且还起到导电基体的作用,加快电子转移,从而提高SnSe@C.得益于上述优点,SnSe@C110次循环后,在0.1 a g−1时表现出211.3 mAh g−1的比容量和突出速率能力(在5.0 a g−2时表现出210.1 mAh g–1,从0.1到1.0 a g−的容量保持率为63.2%)。本研究不仅为提高SnSe的循环稳定性和倍率性能提出了思路,而且为为SIBs提供具有稳定结构的阳极材料铺平了道路。
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