Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/123618
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: Unraveling oxygen evolution reaction on carbon-based electrocatalysts: effect of oxygen doping on adsorption of oxygenated intermediates
Author: Li, L.
Yang, H.
Miao, J.
Zhang, L.
Wang, H.-Y.
Zeng, Z.
Huang, W.
Dong, X.
Liu, B.
Citation: ACS Energy Letters, 2017; 2(2):294-300
Publisher: American Chemical Society
Issue Date: 2017
ISSN: 2380-8195
2380-8195
Statement of
Responsibility: 
Laiquan Li, Hongbin Yang, Jianwei Miao, Liping Zhang, Hsin-Yi Wang, Zhiping Zeng, Wei Huang, Xiaochen Dong, and Bin Liu
Abstract: Carbon-based nanomaterials have been widely studied as promising electrocatalysts for energy conversion and storage. Understanding the oxygen evolution and reduction reactions on carbon-based nanomaterials is of critical importance for development of highly active metal-free electrocatalysts. Here, the adsorption of oxygenated intermediates during oxygen evolution reaction (OER) on carbon nanotubes (CNTs) was examined by ex-situ X-ray photoelectron spectroscopy and in situ electrochemical impedance spectroscopy. The results demonstrate that the carbon atoms on CNTs near the C═O functional groups are active for OER. On the basis of this result, we further revealed the origin of the enhanced intermediate adsorption on surface-oxidized CNTs and the relationship between surface groups and apparent activation energy. Our study gained new understanding of OER on oxygen-doped carbon nanomaterials and provided an effective approach for investigating electrocatalysis on heteroatom-doped carbon electrocatalysts.
Description: Published: January 5, 2017
Rights: © 2017 American Chemical Society
DOI: 10.1021/acsenergylett.6b00681
Grant ID: RG10/16
RG111/15
Published version: http://dx.doi.org/10.1021/acsenergylett.6b00681
Appears in Collections:Aurora harvest 3
Chemical Engineering publications

Files in This Item:
File Description SizeFormat 
hdl_123618.pdfAccepted version2.92 MBAdobe PDFView/Open


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