Co@Co 3 O 4 core–shell particle encapsulated N-doped mesoporous carbon cage hybrids as active and durable oxygen-evolving catalysts

• Published in: Dalton transactions : an international journal of inorganic chemistry Vol. 45; no. 13; pp. 5575 - 5582
• Main Authors: Li, Xinzhe, Fang, Yiyun, Wen, Lixin, Li, Feng, Yin, Guanlin, Chen, Wanmin, An, Xingcai, Jin, Jun, Ma, Jiantai
• Format: Journal Article
• Language: English
• Published: 2016
• ISSN: 1477-9226; 1477-9234
• DOI: 10.1039/C6DT00102E

Cobalt-based nanomaterials are promising candidates as efficient, affordable, and sustainable alternative electrocatalysts for the oxygen evolution reaction (OER). However, the catalytic efficiency of traditional nanomaterials is still far below what is expected, because of their low stability in basic solutions and poor active site exposure yield. Here a unique hybrid nanomaterial comprising Co@Co 3 O 4 core–shell nanoparticle (NP) encapsulated N-doped mesoporous carbon cages on reduced graphene oxide (denoted as Co@Co 3 O 4 @NMCC/rGO) is successfully synthesized via a carbonization and subsequent oxidation strategy of a graphene oxide (GO)-based metal–organic framework (MOF). Impressively, the special carbon cage structure is very important for not only leading to a large active surface area, enhanced mass/charge transport capability, and easy release of gas bubbles, but also preventing Co@Co 3 O 4 NPs from aggregation and peeling off during prolonged electrochemical reactions. As a result, in alkaline media, the resulting hybrid materials catalyze the OER with a low onset potential of ∼1.50 V ( vs. RHE) and an over-potential of only 340 mV to achieve a stable current density of 10 mA cm −2 for at least 25 h. In addition, metallic Co cores in Co@Co 3 O 4 provide an alternative way for electron transport and accelerate the OER rate.