Li Yilin, Yuan Zeyu, Li Dongdong, Li Junzhi, Zhang Yuming, Wang Mingrui, Li Guangshe, Wang Lili, Han Wei
College of Physics, State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, International Center of Future Science, Jilin University, Changchun 130012, P.R. China.
State Key Laboratory for Superlattices and Microstructures, Institute of Semiconductors, Chinese Academy of Sciences & Center of Materials Science and Optoelectronic Engineering, University of Chinese Academy of Sciences, Beijing 100083, P.R. China.
ACS Nano. 2024 Feb 13;18(6):4733-4745. doi: 10.1021/acsnano.3c07977. Epub 2024 Jan 30.
Sodium-ion batteries (SIBs) have great potential as electrochemical energy storage systems; however, their commercial viability is limited by the lack of anode materials with fast charge/discharge rates and long lifetimes. These challenges were addressed by developing a multi-interface design strategy using FCSe (FeSe/CoSe) nanoparticles on VCT MXene nanosheets as conductive substrates. The heterogeneous interface created between the two materials provided high-speed transport of sodium ions, suppressed the chalking-off of nanoparticles, and improved the cycling stability. Additionally, the Fe-Co bonds generated at the interface effectively relieved mechanical stress, further enhancing the electrode durability. The C@FCSe@VC electrode exhibited high-speed charging and discharging characteristics, and maintained a high specific capacity of 260.5 mAh g even after 15,000 cycles at 10 A g, with a capacity retention rate of 50.2% at an ultrahigh current density of 20 A g. Furthermore, the composite displayed a good cycling capability in the fast discharge and slow charge mode. This demonstrates its promising commercial potential. This multi-interface design strategy provides insights and guidance for solving the reversibility and cycling problems of transformed selenide anode materials.
钠离子电池(SIBs)作为电化学储能系统具有巨大潜力;然而,其商业可行性受到缺乏具有快速充放电速率和长寿命的负极材料的限制。通过在VCT MXene纳米片上使用FCSe(FeSe/CoSe)纳米颗粒作为导电基底开发一种多界面设计策略,解决了这些挑战。两种材料之间形成的异质界面提供了钠离子的高速传输,抑制了纳米颗粒的粉化,并提高了循环稳定性。此外,界面处产生的Fe-Co键有效地缓解了机械应力,进一步提高了电极耐久性。C@FCSe@VC电极表现出高速充放电特性,即使在10 A g下循环15000次后仍保持260.5 mAh g的高比容量,在20 A g的超高电流密度下容量保持率为50.2%。此外,该复合材料在快速放电和慢速充电模式下表现出良好的循环性能。这证明了其具有广阔的商业潜力。这种多界面设计策略为解决转化硒化物负极材料的可逆性和循环问题提供了见解和指导。