碳化
材料科学
细菌纤维素
纳米纤维
化学工程
成核
掺杂剂
纤维素
比表面积
碳纳米纤维
碳纤维
多孔性
纳米技术
催化作用
兴奋剂
复合材料
扫描电子显微镜
化学
复合数
有机化学
碳纳米管
光电子学
工程类
作者
Yang Huang,Kaiyuan Tang,Fanshu Yuan,Weiwei Zhang,Bengang Li,Farzad Seidi,Huining Xiao,Dongping Sun
出处
期刊:Carbon
[Elsevier]
日期:2020-06-26
卷期号:168: 12-21
被引量:71
标识
DOI:10.1016/j.carbon.2020.06.052
摘要
Abstract A nanofiber-directed templating strategy has been employed in this work to fabricate reticulated composites by decorating metal organic framework (MOF) onto a biomass scaffold of bacterial cellulose (BC). The abundant oxygen-containing groups on BC facilitate the highly dispersed nucleation of ZIF-8 (a typical MOF) and thus direct these nanocrystals assembly and growth along BC nanofibers homogeneously. The as-prepared ZIF-8@BC composites are converted into hierarchically porous carbon nanofibers with high intensity of N-dopants (N-PC@CBC) by a convenient carbonization process. In comparison with the bulk N-doping porous carbon (N-PC) by direct carbonization of pristine ZIF-8, N-PC@CBC exhibits more pronounced specific surface area and pore volume. As a result, N-PC@CBC shows outstanding oxygen reduction reaction catalytic performance approaching or even surpassing the commercial Pt/C catalyst. Additionally, the robust architecture of highly interweaved N-PC@CBC nanofibers as well as the sufficient N-dopants is also favorable for the enhancement of sodium-ion storage capability. After assembling the sodium-ion half-cells, the free-standing N-PC@CBC anodes display relatively high specific capacity, superior rate capability, and excellent cycling stability. The present work sheds light on a promising avenue to develop high-performance MOF-derived electrodes with cost-effective cellulose skeleton.
科研通智能强力驱动
Strongly Powered by AbleSci AI