Alveolate porous carbon aerogels supported Co9S8 derived from a novel hybrid hydrogel for bifunctional oxygen electrocatalysis

被引:184
作者
Hu, Xuejiao [1 ]
Chen, Yifan [1 ]
Zhang, Mengru [1 ]
Fu, Gengtao [2 ]
Sun, Dongmei [1 ]
Lee, Jong-Min [2 ]
Tang, Yawen [1 ]
机构
[1] Nanjing Normal Univ, Sch Chem & Mat Sci, Jiangsu Collaborat Innovat Ctr Biomed Funct Mat, Jiangsu Key Lab New Power Batteries, Nanjing 210023, Jiangsu, Peoples R China
[2] Nanyang Technol Univ, Maritime Inst, Sch Chem & Biomed Engn, Singapore 637459, Singapore
基金
中国国家自然科学基金;
关键词
NITROGEN-DOPED GRAPHENE; EFFICIENT ELECTROCATALYST; SYNERGISTIC CATALYST; COBALT OXIDE; IRON NITRIDE; EVOLUTION; REDUCTION; NANOPARTICLES; NANOCRYSTALS; FRAMEWORKS;
D O I
10.1016/j.carbon.2018.12.099
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
Incorporation of transition-metal dopants into carbon aerogels is a powerful way to develop highly-active and robust bifunctional oxygen electrocatalysts. Herein, we develop a novel hybrid hydrogel method for the preparation of Co9S8-doped alveolate carbon aerogels. The hydrogel formation depends on a simple sol-gel polymerization of chitosan, sodium tripolyphosphate and polyhexamethyleneguanidine phosphate. The repeating units of polymer contain a binding site (-NH2) for Co2+ ions, after pyrolysis which ensures a uniform anchor of Co9S8 particles within the carbon aerogels. The newly developed catalyst exhibits excellent bifunctional activity and robust stability for both the oxygen reduction reaction and oxygen evolution reaction, resulting from the significant synergy between Co9S8 and 3D porous N, P-codoped carbon aerogels. Moreover, we also demonstrate that Co9S8 material is more active to OER than to ORR through the density functional theory (DFT) theoretical computation. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:557 / 566
页数:10
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