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Bifunctional mesoporous CoO/nitrogen-incorporated graphene electrocatalysts for high-power and long-term stability of rechargeable zinc-air batteriesopen access

Authors
Park, Tae HoYeon, Jeong SeokSivakumar, PeriyasamyKim, YoungkwonPark, Ho Seok
Issue Date
Apr-2021
Publisher
WILEY
Keywords
bifunctional catalysts; cobalt monoxide; mesoporous structure; nitrogen doping; zinc‐ air batteries
Citation
INTERNATIONAL JOURNAL OF ENERGY RESEARCH, v.45, no.5, pp 6698 - 6707
Pages
10
Indexed
SCIE
SCOPUS
Journal Title
INTERNATIONAL JOURNAL OF ENERGY RESEARCH
Volume
45
Number
5
Start Page
6698
End Page
6707
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/5129
DOI
10.1002/er.6263
ISSN
0363-907X
1099-114X
Abstract
Despite high energy density, low-cost, and ecofriendly, rechargeable Zinc-air batteries (ZABs) suffer from sluggish kinetics stability during oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) at the cathode. Herein, we demonstrate CoO nanoparticles anchored on N-doped reduced graphene oxide (CoO/N-rGO) with an excellent bifunctional catalytic activity and stability and facile redox kinetics of ORR and OER for high-performance rechargeable ZABs. The CoO/N-rGO catalysts are featured with the abundant active sites, a large accessible area, and high electrochemical conductivity, which are associated with increased oxygen vacancy surface, reduced valence, and mesoporous architecture. The half-wave potential (E-1/2) and electron transfer number for ORR are 0.79 V and 3.72 at 0.40 V (vs RHE), respectively, while OER potential at 10 mA cm(-2) (E-j = 10) is 1.61 V (vs RHE). Remarkably, the ZAB cell with CoO/N-rGO achieves high specific capacity of 545 mAh g(zn)(-1), power density of 41 mW cm(-2), and cyclic stabilities with high energy efficiency of 64.44% at 2 mA cm(-2). In addition, postmortem analysis validates that the oxidation and aggregation of CoO/N-rGO catalyst is mitigated while the inactivation of Zn anode is inhibited.
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