聚丙烯腈
材料科学
化学工程
沸石咪唑盐骨架
碳纳米纤维
咪唑酯
碳纤维
金属有机骨架
催化作用
掺杂剂
纳米纤维
硼
多孔性
纳米技术
无机化学
兴奋剂
复合材料
化学
碳纳米管
有机化学
吸附
复合数
聚合物
光电子学
工程类
作者
Bipeen Dahal,Su-Hyeong Chae,Alagan Muthurasu,Tanka Mukhiya,Jagadis Gautam,Kisan Chhetri,Subhangi Subedi,Gunendra Prasad Ojha,Arjun Prasad Tiwari,Joong Hee Lee,Hak Yong Kim
标识
DOI:10.1016/j.jpowsour.2020.227883
摘要
In this work, polyacrylonitrile (PAN) and metal-organic framework (MOF)-derived 3D B and N codoped core-shell carbon nanofibers (CNFs) with multiscale carbon layers derived from continuous zeolitic imidazolate frameworks (ZIF-8 and ZIF-67) are synthesized via dual-functional ZnO and Co3O4 nanostructures. Here, ZnO and Co3O4 act as a metal-ion source for the MOF formation and as pore creating agents. Further, dual-function NaBH4 reduces metallic ions into respective metals as well as providing three-dimensionality to the conventional two dimensional CNF mat. Additionally, B and N doping can be achieved by treatment with a single dopant, NH4HB4O7·3H2O. The resulting core-shell multiscale-3D CNFs with hierarchical pores ([email protected]) deliver exceptional onset (0.94 V vs RHE) and half wave potential (0.86 V vs RHE)) with excellent cyclic stability toward the oxygen reduction reaction (ORR). Moreover, the electrode maintained a remarkably high current retention of 97.2%, even after 25 000 s, which is better than that of a commercial Pt/C catalyst (89.6%). The superior catalytic activity and stability of the CNF-based catalyst are attributed to the synergistic effect of the structure and codoping of B and N with highly porous 3D hierarchical core-shell nanoarchitecture.
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