Electrocatalysis of Co/CoxOy nanofilms supported by synchronously nitrogen-doped Ketjenblack carbon towards oxygen reduction reaction

被引:0
|
作者
Liu, Yong [1 ]
Chen, Yumei [1 ]
Li, Qing [1 ]
Shi, Jianchao [1 ]
Liu, Baozhong [1 ,2 ]
机构
[1] Henan Polytech Univ, Coll Chem & Chem Engn, Jiaozuo 454000, Peoples R China
[2] State Collaborat Innovat Ctr Coal Work Safety & Cl, Jiaozuo 454003, Peoples R China
基金
中国国家自然科学基金;
关键词
Co/CoxOy nanofilms; Oxygen reduction reaction; Non-precious metal catalyst; Nitrogen doping; Structural regulation; ONE-POT SYNTHESIS; EFFICIENT; NANOPARTICLES; GRAPHENE; CATALYSTS; DESIGN; ORR;
D O I
10.1016/j.jcis.2024.09.235
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
Developing a highly active and stable non-precious metal catalyst for oxygen reduction reaction (ORR) is of great practical significance for advancing fuel cell technology. In this work, a continuous two-step hydrothermal reaction followed by high temperature pyrolysis were employed to achieve in situ N-doping preferentially into Ketjenblack carbon (KB-N) and composite of KB-N and Co/CoxOy nanofilms (Co/CoxOy-NFs) as Co/CoxOy-NFs@KB-N. The N-doped state strongly affects the ORR activity of catalyst. All prepared Co/CoxOy-NFs@KB-N catalysts exhibit observably improved ORR activity compared with the basal KB-N and N-doped Co/CoxOy-NFs, in which the optimal Co/CoxOy-NFs@KB-N catalyst demonstrate the positive E-onset (0.864 V) and E-1/2 (0.788 V) vs. RHE, the low Tafel slope (69.27 mV dec(-1)), implying quick ORR kinetics. And, the Co/CoxOy-NFs@KB-N catalyst exhibits highly electrochemical durability. The KB-N substrate can purify Co valence in CoO component, promote amorphization of CoO crystalline structure and enhance the interaction between Co/CoxOy-NFs and KB-N in Co/CoxOy-NFs@KB-N catalyst. Thus electronic effect, structural effect and synergistic effect can strengthen O-2 adsorption, provide enough adsorbed sites and accelerate electron transfer, resulting in prominent ORR performance of Co/CoxOy-NFs@KB-N catalyst.
引用
收藏
页码:253 / 261
页数:9
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