File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Template-free synthesis of non-noble metal single-atom electrocatalyst with N-doped holey carbon matrix for highly efficient oxygen reduction reaction in zinc-air batteries

Author(s)
Zhang, SuyuanYang, WeiguangLiang, YulinYang, XueCao, MinnaCao, Rong
Issued Date
2021-05
DOI
10.1016/j.apcatb.2020.119780
URI
https://scholarworks.unist.ac.kr/handle/201301/52529
Fulltext
https://www.sciencedirect.com/science/article/pii/S0926337320311978?via%3Dihub
Citation
APPLIED CATALYSIS B-ENVIRONMENTAL, v.285, pp.119780
Abstract
M-N-C single-atom electrocatalysts recently have received significant attention because of high catalytic activity and maximal atom utilization. Here, it is firstly reported that macrocycle cucurbit[6]uril (CB[6]) self-assembly was employed as precursor to fabricate M-N-C single-atom electrocatalysts for the Zn-air battery (ZAB). This template-free method using CB[6] self-assembly acquires the holey N-doped matrixes with hierarchical micro/mesoporous structure. The Fe loaded N-doped holey carbon single-atom electrocatalyst (Fe-NHC) exhibited high activity with the half-wave potential (E-1/2) of 0.89 V) versus reversible hydrogen electrode (RHE) for oxygen reduction reaction (ORR) in alkaline condition, which was better than those of Co or Ni loaded catalyst and commercial Pt/C (E-1/2 = 0.83 V). Moreover, the ZAB employing Fe-NHC catalyst achieved higher power and energy density with longer-term stability than those of Pt/C + Ir/C catalyst. This work provided a promising strategy to design stable and highly efficient catalyst for long-life electrochemical storage devices.
Publisher
ELSEVIER
ISSN
0926-3373
Keyword (Author)
Oxygen reductionSingle-atom catalystCucurbit[6]urilHoley matrixZn-air battery

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.