Caffeine derived graphene-wrapped Fe3C nanoparticles entrapped in hierarchically porous Fe-N-C nanosheets for boosting oxygen reduction reaction

被引:76
作者
Chen, Meng-Ting [1 ]
Huang, Zheng-Xiong [1 ]
Ye, Xin [1 ]
Zhang, Lu [1 ]
Feng, Jiu-Ju [1 ]
Wang, Ai-Jun [1 ]
机构
[1] Zhejiang Normal Univ, Coll Chem & Mat Sci, Coll Geog & Environm Sci, Key Lab,Minist Educ Adv Catalysis Mat, Jinhua 321004, Peoples R China
基金
中国国家自然科学基金;
关键词
Caffeine; Pyrolysis synthesis; Electrocatalysis; Oxygen reduction reaction; METAL-ORGANIC FRAMEWORKS; COBALT NANOPARTICLES; CARBON NANOTUBES; ELECTROCATALYST; CATALYSTS; NITROGEN; STRATEGIES; PROGRESS; LAYERS; OXIDE;
D O I
10.1016/j.jcis.2023.01.077
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
It is a vital requirement to explore high-efficiency and stable electrocatalysts for oxygen reduction reac-tion (ORR) to further relieve energy depletion. However, it is a critical challenge to develop low cost and high-quality carbon-based catalysts. Herein, a caffeine chelation-triggered pyrolysis approach was devel-oped to construct graphene-wrapped Fe3C nanoparticles incorporated in hierarchically porous Fe-N-C nanosheets (G-Fe3C/Fe-N-C). The present Fe salt and its content as well as the pyrolysis temperature were carefully investigated in the control groups. The G-Fe3C/Fe-N-C catalyst showed a more positive onset potential (Eonset = 1.09 V) and half-wave potential (E1/2 = 0.88 V) in a 0.1 M KOH solution, which outperformed commercial Pt/C (E1/2 = 0.83 V, Eonset = 0.95 V), showing the excellent catalytic performance for the ORR activity, coupled with remarkable stability (only 0.18 mV negative shift in E1/2 after 2000 cycles). This work provides some valuable insights for developing advanced electrocatalysts for energy storage and conversion related research.(c) 2023 Elsevier Inc. All rights reserved.
引用
收藏
页码:216 / 224
页数:9
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