Spontaneous migration induced Co nanokarstcave encapsulated in N-doped carbon hybrids for efficient oxygen electrocatalyst

被引:0
|
作者
Wang, Xuemin [1 ,2 ]
Liu, Ming [1 ,2 ]
Zhang, Hang [1 ,2 ]
Yan, Sihao [1 ,2 ]
Zhang, Cui [1 ,2 ]
Liu, Shuangxi [1 ,2 ,3 ,4 ]
机构
[1] Nankai Univ, Inst New Catalyt Mat Sci, Sch Mat Sci & Engn, Tianjin 300350, Peoples R China
[2] Nankai Univ, Natl Inst Adv Mat, Tianjin 300350, Peoples R China
[3] Nankai Univ, Minist Educ, Key Lab Adv Energy Mat Chem, Tianjin 300071, Peoples R China
[4] Collaborat Innovat Ctr Chem Sci & Engn, Tianjin 300072, Peoples R China
关键词
size effect; spontaneous migration; Co nanokarstcave; oxygen electrocatalyst; multicomponent synergy; METAL-ORGANIC FRAMEWORK; HYDROGEN EVOLUTION; REDUCTION REACTION; NITROGEN; GRAPHENE; POLYHEDRON; STORAGE; SITES;
D O I
10.1007/s12274-021-3375-2
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
Despite the extensive application of porous nanostructures as oxygen electrocatalysts, it is challenging to synthesize single-metal state materials with porous structures, especially the ultrasmall ones due to the uniform diffusion of the same metal. Herein, we pioneer demonstrate a new size effect-based controllable synthesis strategy for the homogeneous Co nanokarstcaves assisted by Co-CN hybrids (CCHs). The preferential migration of cobalt atoms on the surface of small size zeolitic imidazolate framework (ZIF) with high surface energy during pyrolysis is the key factor for the formation of nanokarstcave structure. Furthermore, graphene can act as a diffusion barrier to prevent the agglomeration of nanoparticles in the synthesis process, which also plays an important role in the formation of porous nanostructures. In alkali media, CCHs achieve overpotential of 287 mV (@10 mA.cm(-2)) for oxygen evolution reaction (OER) and a half wave potential of 0.86 V (vs. RHE) for oxygen reduction reaction (ORR).
引用
收藏
页码:4569 / 4576
页数:8
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