Scalable cellulose-sponsored functionalized carbon nanorods induced by cobalt for efficient overall water splitting

被引:58
作者
Amiinu, Ibrahim Saana [1 ]
Pu, Zonghua [1 ]
He, Daping [2 ]
Monestel, Hellen Gabriela Rivera [1 ]
Mu, Shichun [1 ]
机构
[1] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Peoples R China
[2] Wuhan Univ Technol, Sch Sci, Hubei Engn Res Ctr RF Microwave Technol & Applica, Wuhan 430070, Peoples R China
关键词
Cellulose fibers; Structural evolution; DFT calculations; Overall water splitting; Large scale; N-DOPED CARBON; HYDROGEN EVOLUTION; OXYGEN REDUCTION; BIFUNCTIONAL ELECTROCATALYST; TRANSFORMING WASTE; GRAPHENE; NITROGEN; OXIDE; NANOPARTICLES; NANOTUBES;
D O I
10.1016/j.carbon.2018.05.025
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
A balanced design of cheaper, durable, and highly active electrocatalysts for large scale and sustainable hydrogen production is crucial for the emerging hydrogen economy. Herein, a scalable method is implemented to design a very active heteroatom cofunctionalized carbon nanorods with bifunctional electrocatalytic activity via structural transformation of the cellulose fibers from waste tissue paper. Cobalt (Co) is used as both a promoter-catalyst to induce structural evolution of the nanorods, and a self-doped catalyst moiety by coupling with sulfur and nitrogen to enhance the electrocatalytic properties. The obtained catalyst (Co9S8@Co-N/C nanorods) displays high hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) activity, resulting in a small overall water splitting potential of 1.61 V@10mA cm(-2) and high electrochemical stability for over 70 h. This synthesis approach is further demonstrated to be very suitable for implementation toward large-scale application and can reproduce consistent catalytic properties, which are highly desirable for mass hydrogen production. (c) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:274 / 281
页数:8
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