电催化剂
金属有机骨架
纳米复合材料
钴
催化作用
材料科学
X射线光电子能谱
热解
掺杂剂
碳纳米管
碳纤维
化学工程
无机化学
电化学
化学
纳米技术
兴奋剂
电极
有机化学
吸附
复合数
冶金
复合材料
光电子学
物理化学
工程类
作者
Yudong Xue,Yunting Wang,Zhenhua Pan,Chunhui Zhang
标识
DOI:10.1016/j.jpowsour.2020.227747
摘要
In this study, metal-organic frameworks (MOFs) derived cobalt encapsulated in porous nitrogen-doped carbon (Co/N–C) nanocomposite electrocatalyst is developed towards the highly efficient and durable oxygen reduction reaction (ORR) via pyrolysis of core-shell MOFs precursor. Electrochemical characterization results indicate that the as-prepared Co/N–C nanocomposite shows superior ORR selectivity through a four-electron pathway and extraordinary long-term stability. The uniform nitrogen dopants on the surface of the polyhedron are determined and deconvoluted by the X-ray photoelectron spectroscopy (XPS). We contribute this superior catalytic activity to the characteristic attributes of Co/N–C nanocomposite, which could be stemmed from its exquisite catalyst design: (i) the existence of Co/N-doped carbon nanotubes nanostructure on the catalyst surface and (ii) the proper nitrogen content on the N-doped carbon (N–C) layer. Moreover, Co/N–C nanocomposite presents favorable long-term catalytic stability for 60 h, owning to the protective effect of the porous N–C layer. The present work demonstrates that the MOFs-derived nanomaterial can be transformed into high-value functional transition metal/N-doped carbon nanocomposite electrocatalysts. From both the stability and activity prospects, our work opens a new avenue to strategically design highly active and stable-oriented electrocatalysts.
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