Chen Ming, Jing Qiang-Shan, Sun Hai-Bin, Xu Jun-Qi, Yuan Zhong-Yong, Ren Jin-Tao, Ding Ai-Xiang, Huang Zhong-Yuan, Dong Meng-Yang
Department of Biomedical Engineering , Case Western Reserve University , Cleveland , Ohio 44106 , United States.
Department of Chemistry , Xavier University of Louisiana , New Orleans , Louisiana 700125 , United States.
Langmuir. 2019 May 14;35(19):6321-6332. doi: 10.1021/acs.langmuir.9b00558. Epub 2019 Apr 30.
A new strategy has been innovatively proposed for wrapping the Ni-incorporated and N-doped carbon nanotube arrays (Ni-NCNTs) on porous Si with robust Ni-Si interfacial bonding to form the core-shell-structured NCNTs-NiSi@Si. The hierarchical porous silicon core was first fabricated via a novel self-templating synthesis route based on two crucial strategies: in situ thermal evaporation of crystal water from the perlite for producing porous SiO and subsequent magnesiothermic reduction of porous SiO into porous Si. Ni-NCNTs were subsequently constructed based on the Ni-catalyzed tip-growth mechanism and were further engineered to fully wrap the porous Si microparticles by forming the NiSi alloy at the heterojunction interface. When the prepared NCNTs-NiSi@Si was evaluated as the anode material for Li-ion batteries, the hierarchical porous system in the Si core and the rich void spaces in carbon nanotube arrays contributed to the remarkable accommodation of volume expansion of Si as well as the significant increase of Li diffusion and Si utilization. Moreover, the NiSi alloy, which chemically linked the Ni-NCNTs and porous Si, not only provided good electronic contact between the Si core and carbon shell but also effectively prevented the CNTs' detachment from the Si core during cycling. The multifunctional structural design rendered the whole electrode highly stable and active in Li storage, and the electrochemically active NCNTs-NiSi@Si electrode delivered a high reversible capacity of 1547 mAh g and excellent cycling stability (85% capacity retention after 600 discharge-charge cycles) at a current density of 358 mA g (0.1 C) as well as good rate performance (778 mAh g at 2 C), showing great potential as an efficient and stable anode for high energy density Li-ion batteries.
一种创新策略被提出,用于在多孔硅上包裹镍掺杂和氮掺杂的碳纳米管阵列(Ni-NCNTs),形成具有坚固Ni-Si界面键合的核壳结构NCNTs-NiSi@Si。首先通过一种基于两种关键策略的新型自模板合成路线制备分层多孔硅核:通过珍珠岩中结晶水的原位热蒸发制备多孔SiO,随后将多孔SiO进行镁热还原为多孔硅。随后基于Ni催化的尖端生长机制构建Ni-NCNTs,并通过在异质结界面形成NiSi合金进一步设计使其完全包裹多孔硅微粒。当将制备的NCNTs-NiSi@Si作为锂离子电池的负极材料进行评估时,硅核中的分层多孔体系以及碳纳米管阵列中的丰富空隙有助于显著容纳硅的体积膨胀,以及显著增加锂扩散和硅利用率。此外,化学连接Ni-NCNTs和多孔硅的NiSi合金不仅在硅核和碳壳之间提供了良好的电子接触,而且在循环过程中有效地防止了碳纳米管与硅核分离。这种多功能结构设计使整个电极在锂存储方面具有高度稳定性和活性,在358 mA g(0.1 C)的电流密度下,电化学活性的NCNTs-NiSi@Si电极具有1547 mAh g的高可逆容量和优异的循环稳定性(600次充放电循环后容量保持率为85%)以及良好的倍率性能(2 C时为778 mAh g),显示出作为高能量密度锂离子电池高效稳定负极的巨大潜力。