Active
Sites Implanted Carbon Cages in Core–Shell
Architecture: Highly Active and Durable Electrocatalyst for Hydrogen
Evolution Reaction
Version 2 2016-02-11, 16:27Version 2 2016-02-11, 16:27
Version 1 2016-02-11, 16:27Version 1 2016-02-11, 16:27
Posted on 2016-01-26 - 00:00
Low
efficiency and poor stability are two major challenges we encounter
in the exploration of non-noble metal electrocatalysts for the hydrogen
evolution reaction (HER) in both acidic and alkaline environment.
Herein, the hybrid of cobalt encapsulated by N, B codoped ultrathin
carbon cages (Co@BCN) is first introduced as a highly active and durable
nonprecious metal electrocatalysts for HER, which is constructed by
a bottom-up approach using metal organic frameworks (MOFs) as precursor
and self-sacrificing template. The optimized catalyst exhibited remarkable
electrocatalytic performance for hydrogen production from both both
acidic and alkaline media. Stability investigation reveals the overcoating
of carbon cages can effectively avoid the corrosion and oxidation
of the catalyst under extreme acidic and alkaline environment. Electrochemical
active surface area (EASA) evaluation and density functional theory
(DFT) calculations revealed that the synergetic effect between the
encapsulated cobalt nanoparticle and the N, B codoped carbon shell
played the fundamental role in the superior HER catalytic performance.
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Zhang, Huabin; Ma, Zuju; Duan, Jingjing; Liu, Huimin; Liu, Guigao; Wang, Tao; et al. (2016). Active
Sites Implanted Carbon Cages in Core–Shell
Architecture: Highly Active and Durable Electrocatalyst for Hydrogen
Evolution Reaction. ACS Publications. Collection. https://doi.org/10.1021/acsnano.5b05728