Retracted article : nanoporous PtFe surface alloy architecture for enhanced methanol electro-oxidation

By selectively dealloying PtFeAl ternary alloy in 0.5 M NaOH solution, a novel nanoporous PtFe (npPtFe) alloy with nanorod-like morphology and inherent three-dimensional bicontinuous ligament-pore structure was successfully fabricated. X-Ray diffraction and electron microscope characterization demon...

Full description

Saved in:
Bibliographic Details
Main Authors: Qiu, Huajun, Huang, Xirong
Other Authors: School of Chemical and Biomedical Engineering
Format: Article
Language:English
Published: 2013
Subjects:
Online Access:https://hdl.handle.net/10356/96587
http://hdl.handle.net/10220/11542
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-96587
record_format dspace
spelling sg-ntu-dr.10356-965872020-03-07T11:35:37Z Retracted article : nanoporous PtFe surface alloy architecture for enhanced methanol electro-oxidation Qiu, Huajun Huang, Xirong School of Chemical and Biomedical Engineering DRNTU::Engineering::Chemical engineering By selectively dealloying PtFeAl ternary alloy in 0.5 M NaOH solution, a novel nanoporous PtFe (npPtFe) alloy with nanorod-like morphology and inherent three-dimensional bicontinuous ligament-pore structure was successfully fabricated. X-Ray diffraction and electron microscope characterization demonstrated the crystal nature of the alloy ligament with ligament size down to 3 nm. NaOH concentration plays a key role in the formation of a uniform PtFe alloy structure. Dealloying solution with a low NaOH concentration (0.5 M) is suitable for the formation of a pure PtFe alloy structure, while Fe3 O4/np-PtFe nanocomposite is obtained when using a high NaOH concentration ($2 M). The np-PtFe alloy can be facilely converted into a nanoporous near-surface alloy structure with a Pt-rich surface and PtFe alloy core by a second dealloying process in dilute HNO3 solution. Electrochemical measurements show that the nanoporous near-surface alloy has greatly enhanced catalytic activity and durability towards methanol electro-oxidation compared with the state-of-the-art Pt/C catalyst. The peak current density of methanol electro-oxidation on the nanoporous surface alloy is about five times that on Pt/C. More importantly, continuous potential cycling from 0.6 to 0.9 V (vs. RHE) in 0.5 M H2 SO4 aqueous solution demonstrates that the np-PtFe surface alloy has a better structural stability than commercial Pt/C. With evident advantages of facile preparation and enhanced electrocatalytic activity and durability, the np-PtFe surface alloy holds great potential as an anode catalyst in direct methanol fuel cells. 2013-07-16T04:42:11Z 2019-12-06T19:32:48Z 2013-07-16T04:42:11Z 2019-12-06T19:32:48Z 2012 2012 Journal Article Qiu, H., & Huang, X. (2012). Retracted article: Nanoporous PtFe surface alloy architecture for enhanced methanol electro-oxidation. Journal of Materials Chemistry, 22(15), 7602-7608. https://hdl.handle.net/10356/96587 http://hdl.handle.net/10220/11542 10.1039/c2jm16106k en Journal of materials chemistry © 2012 The Royal Society of Chemistry.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic DRNTU::Engineering::Chemical engineering
spellingShingle DRNTU::Engineering::Chemical engineering
Qiu, Huajun
Huang, Xirong
Retracted article : nanoporous PtFe surface alloy architecture for enhanced methanol electro-oxidation
description By selectively dealloying PtFeAl ternary alloy in 0.5 M NaOH solution, a novel nanoporous PtFe (npPtFe) alloy with nanorod-like morphology and inherent three-dimensional bicontinuous ligament-pore structure was successfully fabricated. X-Ray diffraction and electron microscope characterization demonstrated the crystal nature of the alloy ligament with ligament size down to 3 nm. NaOH concentration plays a key role in the formation of a uniform PtFe alloy structure. Dealloying solution with a low NaOH concentration (0.5 M) is suitable for the formation of a pure PtFe alloy structure, while Fe3 O4/np-PtFe nanocomposite is obtained when using a high NaOH concentration ($2 M). The np-PtFe alloy can be facilely converted into a nanoporous near-surface alloy structure with a Pt-rich surface and PtFe alloy core by a second dealloying process in dilute HNO3 solution. Electrochemical measurements show that the nanoporous near-surface alloy has greatly enhanced catalytic activity and durability towards methanol electro-oxidation compared with the state-of-the-art Pt/C catalyst. The peak current density of methanol electro-oxidation on the nanoporous surface alloy is about five times that on Pt/C. More importantly, continuous potential cycling from 0.6 to 0.9 V (vs. RHE) in 0.5 M H2 SO4 aqueous solution demonstrates that the np-PtFe surface alloy has a better structural stability than commercial Pt/C. With evident advantages of facile preparation and enhanced electrocatalytic activity and durability, the np-PtFe surface alloy holds great potential as an anode catalyst in direct methanol fuel cells.
author2 School of Chemical and Biomedical Engineering
author_facet School of Chemical and Biomedical Engineering
Qiu, Huajun
Huang, Xirong
format Article
author Qiu, Huajun
Huang, Xirong
author_sort Qiu, Huajun
title Retracted article : nanoporous PtFe surface alloy architecture for enhanced methanol electro-oxidation
title_short Retracted article : nanoporous PtFe surface alloy architecture for enhanced methanol electro-oxidation
title_full Retracted article : nanoporous PtFe surface alloy architecture for enhanced methanol electro-oxidation
title_fullStr Retracted article : nanoporous PtFe surface alloy architecture for enhanced methanol electro-oxidation
title_full_unstemmed Retracted article : nanoporous PtFe surface alloy architecture for enhanced methanol electro-oxidation
title_sort retracted article : nanoporous ptfe surface alloy architecture for enhanced methanol electro-oxidation
publishDate 2013
url https://hdl.handle.net/10356/96587
http://hdl.handle.net/10220/11542
_version_ 1681039924243988480