Core-shell Co-NC@NC nanomaterial for efficient oxygen reduction reaction

被引:0
|
作者
Xi, Wenjie
Liu, Wei
Yu, Ao [1 ]
Mu, Mingying [1 ]
Gu, Wenling [2 ]
Shi, Le [1 ]
机构
[1] Xian Jiaotong Univ XJTU, Ctr Nanomat Renewable Energy CNRE, Sch Elect Engn, State Key Lab Elect Insulat & Power Equipment, Xian, Peoples R China
[2] Cent China Normal Univ, Coll Chem, Wuhan, Peoples R China
基金
中国国家自然科学基金;
关键词
Core -shell structure; Oxygen reduction reaction; Co nanoparticle; Long-term durability; DOPED CARBON NANOTUBES; COBALT NANOPARTICLES; FACILE SYNTHESIS; GRAPHENE OXIDE; POROUS CARBON; ACTIVE-SITES; ELECTROCATALYSTS; NANOFIBERS; PYROLYSIS; EVOLUTION;
D O I
10.1016/j.ijhydene.2024.05.358
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Transition metal and nitrogen doped carbons (M-N-C) catalysts present significant potential as substitutes for platinum-carbon (Pt/C) in catalyzing oxygen reduction reaction (ORR). Hence, we employ an epitaxial growth strategy to prepare Zn/Co-ZIF@ZIF-8 crystals with core-shell structure. Subsequent pyrolysis and acid etching produce highly porous cobalt-doped nitrogen materials for ORR investigation. The resulting Co-NC@NC catalyst demonstrates a graded porous structure alongside remarkable conductivity, possessing a specific surface area measuring 623 m2 g-1. It showcases heightened ORR activity with a half-wave potential (E1/2) of 0.886 V, superior kinetic performance (illustrated by an extremely low Tafel slope measuring 45.98 mV/dec), and strengthened stability (with mere 25 mV day after 40,000 cycles) when contrast with Pt/C catalysts in 0.1 M KOH. Additionally, it exhibits notable activity and stability in acidic environments. These remarkable attributes are attributable to the graded structure, which facilitates rapid mass transfer, a high electrochemically active area that exposes highly dispersed active sites, and a conductive carbon skeleton network that promotes electron transfer.
引用
收藏
页码:141 / 148
页数:8
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