煅烧
催化作用
电催化剂
成核
纳米棒
活动站点
纳米颗粒
化学
兴奋剂
氮气
无机化学
化学工程
材料科学
纳米技术
电化学
电极
物理化学
有机化学
工程类
光电子学
作者
Chao Feng,Yuan Guo,Shanshan Qiao,Yuehong Xie,Li Zhang,Liugen Zhang,Wei Wang,Jide Wang
标识
DOI:10.1016/j.apsusc.2020.147481
摘要
The development of controllable doping strategies is essential to obtain highly active electrocatalytic materials. Transition metal atoms with corresponding nitrogen coordination have been widely proposed as active centers for electrocatalytic oxygen reduction (ORR) in [email protected] ([email protected]) electrocatalysts. In this paper, an effective competitive coordination strategy and high-temperature calcination were used to construct a novel complex Fe/[email protected] electrocatalyst. The synthesized catalyst, Fe-MIL-101-2-MI, was using 2-methylimidazole as a nitrogen source and a competitive ligand, which affects the nucleation and growth of the crystal. The morphology of the Fe-MIL-101-2-MI is nanorod, which is conducive to electron transport. Moreover, the competitive coordination of 2-methylimidazole promoted the generation of FeN active sites and greatly improved its ORR electrocatalytic performance. A series of Fe/[email protected] electrocatalytic samples was synthesized by controlling the doping amount of 2-methylimidazole and different calcining temperatures. Fe/[email protected] composites exhibit high levels of doped N, even-distribution of Fe nanoparticles, and abundant FeN active sites. It is noteworthy that the half-wave potential of Fe/[email protected] in the electrocatalytic ORR reaction is 0.813 V (vs. RHE), the initial potential is 0.873 V (vs. RHE), and the limit current density impressively reached 6.04 mA/cm2. In comparison to commercial Pt/C, the synthesized catalyst showed superior electrocatalytic performance.
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