Feng Jian, Luo Shao-Hua, Zhan Yang, Yan Sheng-Xue, Li Peng-Wei, Zhang Lin, Wang Qing, Zhang Ya-Hui, Liu Xin
School of Materials Science and Engineering, Northeastern University, Shenyang 110819, PR China.
School of Materials Science and Engineering and State Key Laboratory of Rolling and Automation, Northeastern University, Shenyang 110819, PR China.
ACS Appl Mater Interfaces. 2021 Nov 3;13(43):51095-51106. doi: 10.1021/acsami.1c16957. Epub 2021 Oct 21.
Thanks to their high conductivity and theoretical capacity, transition metal selenides have demanded significant research attention as prospective anodes for sodium-ion batteries. Nevertheless, their practical applications are hindered by finite cycle life and inferior rate performance because of large volume expansion, polyselenide dissolution, and sluggish dynamics. Herein, the nitrogen-doped carbon (NC)-coated FeSe nanoparticles encapsulated in NC nanoboxes (termed FeSe@NDC NBs) are fabricated through the facile thermal selenization of polydopamine-wrapped Prussian blue precursors. In this composite, the existing nitrogen-doped dual carbon layer improves the intrinsic conductivity and structural integrity, while the unique porous yolk-shell architecture significantly mitigates the volume swelling during the sodium/desodium process. Moreover, the derived Fe-N-C bonds can effectively capture polyselenide, as well as promote Na transportation and good reversible conversion reaction. As expected, the FeSe@NDC NBs deliver remarkable rate performance (374.9 mA h g at 10.0 A g) and long-cycling stability (403.3 mA h g over 2000 loops at 5.0 A g). When further coupled with a self-made NaV(PO)@C cathode in sodium-ion full cells, FeSe@NDC NBs also exhibit considerably high and stable sodium-storage performance.
由于具有高导电性和理论容量,过渡金属硒化物作为钠离子电池的潜在负极受到了广泛的研究关注。然而,由于体积膨胀大、多硒化物溶解和动力学迟缓,它们的实际应用受到有限循环寿命和较差倍率性能的阻碍。在此,通过对聚多巴胺包裹的普鲁士蓝前驱体进行简便的热硒化,制备了封装在氮掺杂碳(NC)纳米盒中的氮掺杂碳(NC)包覆的FeSe纳米颗粒(称为FeSe@NDC NB)。在这种复合材料中,现有的氮掺杂双碳层提高了本征导电性和结构完整性,而独特的多孔蛋黄壳结构显著减轻了钠/脱钠过程中的体积膨胀。此外,衍生的Fe-N-C键可以有效地捕获多硒化物,同时促进钠的传输和良好的可逆转化反应。正如预期的那样,FeSe@NDC NB具有出色的倍率性能(在10.0 A g下为374.9 mA h g)和长循环稳定性(在5.0 A g下2000次循环后为403.3 mA h g)。当与自制的NaV(PO)@C正极在钠离子全电池中进一步耦合时,FeSe@NDC NB也表现出相当高且稳定的储钠性能。