合理设计
催化作用
材料科学
电化学
钴
吸附
化学工程
纳米颗粒
蚀刻(微加工)
分离器(采油)
纳米技术
熔盐
氧化还原
电极
无机化学
过渡金属
盐(化学)
硫黄
氮气
作者
Zhengran Wang,Fangbing Dong,Liwen Tan,Shenglin Xiong,Jinkui Feng
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-12-03
卷期号:25 (50): 17308-17316
被引量:3
标识
DOI:10.1021/acs.nanolett.5c04418
摘要
Designing electrocatalysts with high catalytic activity and strong adsorption capacity is crucial for overcoming the key challenges in lithium-sulfur batteries. In this paper, a nitrogen-functionalized MXene loaded with cobalt nanoparticles is prepared via a fluoride-free molten salt etching method. The N-functional groups were introduced via an in situ substitution strategy, while maintaining the layered character of MXene. The resulting cobalt nanoparticles from the etching process were retained in the composite, synergizing with nitrogen to enhance the chemical anchoring of polysulfides and accelerate the redox reaction kinetics. Electrochemical tests demonstrate that Co/N-MX exhibits outstanding catalytic ability and adsorption capacity. Benefiting from the synergistic effect, lithium-sulfur batteries with a Co/N-MX modified separator exhibit improved electrochemical performance. Importantly, this strategy can be extended to other metals such as Cu, Fe, and Ni, with nitrogen functional groups simultaneously introduced onto the MXene surface, demonstrating its versatility and broad applicability.
科研通智能强力驱动
Strongly Powered by AbleSci AI