Robust MOF-253-derived N-doped carbon confinement of Pt single nanocrystal electrocatalysts for oxygen evolution reaction

被引:41
|
作者
Monestel, Hellen Gabriela Rivera [1 ]
Amiinu, Ibrahim Saana [1 ]
Gonzalez, Andres Alvarado [2 ]
Pu, Zonghua [1 ]
Mousavi, BibiMaryam [2 ]
Mu, Shichun [1 ]
机构
[1] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Hubei, Peoples R China
[2] Wuhan Univ Technol, Sch Chem Chem Engn & Life Sci, Wuhan 430070, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Pt; MOF-253; Carbon confinement; Oxygen evolution reaction; Electrocatalyst; ORGANIC FRAMEWORKS; GRAPHENE; REDUCTION; NITROGEN; CATALYSTS;
D O I
10.1016/S1872-2067(19)63488-1
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Although carbon-supported platinum (Pt/C) is still considered the most active electrocatalyst for hydrogen evolution reaction (HER) and oxygen reduction reaction (ORR), its applications in metal-air batteries as a cathode catalyst, or for oxygen generation via water splitting electrolysis as an anode catalyst is mainly constrained by the insufficient kinetic activity and stability in the oxygen evolution reaction (OER). Here, MOF-253-derived nitrogen-doped carbon (N/C)-confined Pt single nanocrystals (Pt@N/C) have been synthesized and shown to be efficient catalysts for the OER. Even with low Pt mass loading of 6.1 wt% (Pt@N/C-10), the catalyst exhibits greatly improved activity and long-time stability as an efficient OER catalyst. Such high catalytic performance is attributed to the core-shell structure relationship, in which the active N-doped-C shell not only provides a protective shield to avoid rapid Pt nanocrystal oxidation at high potentials and inhibits the Pt migration and agglomeration, but also improves the conductivity and charge transfer kinetics. (C) 2020, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:839 / 846
页数:8
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