Wang Rui, Sun Bingxin, Dong Yan, Zhang Wang, Wu Qianhui, Guo Fang, Li Chunsheng, Li Wenting, Chen Ming
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, PR China.
i-Lab & CAS Key Laboratory of Nanophotonic Materials and Devices, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215123, PR China.
J Colloid Interface Sci. 2025 Apr;683(Pt 1):499-508. doi: 10.1016/j.jcis.2024.12.080. Epub 2024 Dec 12.
Conversion-type selenium cathodes are considered a highly promising alternative to sulfur cathodes due to their high conductivity and similar theoretical capacity. However, stress-diffusion and shuttle effects during the conversion process remain significant challenges that urgently need to be addressed. Herein, a composite matrix of MoSe anchored on the surface of N-doped hollow mesoporous carbon nanospheres (NHMCNS) was designed as a Se host to construct Se/C cathodes (Se/MoSe@NHMCNS). Anchored MoSe successfully mitigated selenium loss by enhancing the chemisorption of polyselenides within the matrix. Meanwhile, polyselenides adsorbed on the Se/C cathode surface exhibit lower diffusion barriers and more negative Gibbs free energy during the conversion from chain polyselenides to NaSe. MoSe accelerated the catalytic conversion of polyselenides to the final discharge products from both kinetic and thermodynamic perspectives. The huge stress induced by structural transformation during the conversion process is mitigated by MoSe synergistic carbon walls, which effectively maintain the structural stability of the cathode. Based on this three-in-one strategy, the sodium-selenium battery assembled with Se/MoSe@NHMCNS exhibits stable cycling performance (400.6 mAh g at 2C after 500 cycles), and the pouch battery also demonstrates good practical performance.
由于具有高导电性和相似的理论容量,转换型硒阴极被认为是硫阴极极具前景的替代品。然而,转换过程中的应力扩散和穿梭效应仍然是亟待解决的重大挑战。在此,设计了一种锚定在氮掺杂中空介孔碳纳米球(NHMCNS)表面的MoSe复合基质作为硒宿主,以构建硒/碳阴极(Se/MoSe@NHMCNS)。锚定的MoSe通过增强基质内多硒化物的化学吸附成功减轻了硒的损失。同时,吸附在硒/碳阴极表面的多硒化物在从链状多硒化物转化为NaSe的过程中表现出较低的扩散势垒和更负的吉布斯自由能。MoSe从动力学和热力学角度加速了多硒化物向最终放电产物的催化转化。MoSe协同碳壁减轻了转换过程中结构转变引起的巨大应力,有效地保持了阴极的结构稳定性。基于这种三合一策略,采用Se/MoSe@NHMCNS组装的钠硒电池表现出稳定的循环性能(500次循环后在2C下为400.6 mAh g),软包电池也展示出良好的实际性能。