Dual-metal hydroxide@oxide heterojunction catalyst constructed via corrosion engineering for large-current oxygen evolution reaction

Current OER electrocatalysts are hardly applicable for industrial use, which demands high current density (≥ 1000 mA cm-2) at low overpotential (≤ 300 mV) with long-term stability (≥ 100 h). Herein self-supported heterojunction catalyst, NiCo-OH@NixFeyO4 on Fe foam (FF), is in situ synthesized using...

Full description

Saved in:
Bibliographic Details
Main Authors: Li, Zhong, Zhang, Xinglin, Zhang, Zheye, Chen, Peng, Zhang, Yizhou, Dong, Xiaochen
Other Authors: School of Chemistry, Chemical Engineering and Biotechnology
Format: Article
Language:English
Published: 2023
Subjects:
Online Access:https://hdl.handle.net/10356/169002
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-169002
record_format dspace
spelling sg-ntu-dr.10356-1690022023-06-26T07:53:23Z Dual-metal hydroxide@oxide heterojunction catalyst constructed via corrosion engineering for large-current oxygen evolution reaction Li, Zhong Zhang, Xinglin Zhang, Zheye Chen, Peng Zhang, Yizhou Dong, Xiaochen School of Chemistry, Chemical Engineering and Biotechnology Science::Chemistry Heterojunction Catalysts Corrosion Engineering Current OER electrocatalysts are hardly applicable for industrial use, which demands high current density (≥ 1000 mA cm-2) at low overpotential (≤ 300 mV) with long-term stability (≥ 100 h). Herein self-supported heterojunction catalyst, NiCo-OH@NixFeyO4 on Fe foam (FF), is in situ synthesized using two-step corrosion engineering. It only requires an overpotential 275 mV to drive the current density of 1000 mA cm-2 with good long-term stability. Theoretical calculations reveal that such good performance is attributable to electron transfer from NiCo-OH to NixFeyO4 which weakens the adsorption energy of reaction intermediate (OOH*) to promote the release of O2 and lowers the free energy barriers for the reaction. Furthermore, a water splitting cell with NiCo-OH@NixFeyO4/FF as anode and CoP@FeP/FF as cathode demonstrates its potential for industrial application. The study presents a general strategy for in situ synthesis of heterojunction catalysts on metal foams using controlled corrosion engineering for various catalytic applications. We would like to thank financial support by The International Postdoctoral Exchange Fellowship Program (No. PC2021035). 2023-06-26T07:53:23Z 2023-06-26T07:53:23Z 2023 Journal Article Li, Z., Zhang, X., Zhang, Z., Chen, P., Zhang, Y. & Dong, X. (2023). Dual-metal hydroxide@oxide heterojunction catalyst constructed via corrosion engineering for large-current oxygen evolution reaction. Applied Catalysis B: Environmental, 325, 122311-. https://dx.doi.org/10.1016/j.apcatb.2022.122311 0926-3373 https://hdl.handle.net/10356/169002 10.1016/j.apcatb.2022.122311 2-s2.0-85145303081 325 122311 en Applied Catalysis B: Environmental © 2022 Elsevier B.V. All rights reserved.
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Chemistry
Heterojunction Catalysts
Corrosion Engineering
spellingShingle Science::Chemistry
Heterojunction Catalysts
Corrosion Engineering
Li, Zhong
Zhang, Xinglin
Zhang, Zheye
Chen, Peng
Zhang, Yizhou
Dong, Xiaochen
Dual-metal hydroxide@oxide heterojunction catalyst constructed via corrosion engineering for large-current oxygen evolution reaction
description Current OER electrocatalysts are hardly applicable for industrial use, which demands high current density (≥ 1000 mA cm-2) at low overpotential (≤ 300 mV) with long-term stability (≥ 100 h). Herein self-supported heterojunction catalyst, NiCo-OH@NixFeyO4 on Fe foam (FF), is in situ synthesized using two-step corrosion engineering. It only requires an overpotential 275 mV to drive the current density of 1000 mA cm-2 with good long-term stability. Theoretical calculations reveal that such good performance is attributable to electron transfer from NiCo-OH to NixFeyO4 which weakens the adsorption energy of reaction intermediate (OOH*) to promote the release of O2 and lowers the free energy barriers for the reaction. Furthermore, a water splitting cell with NiCo-OH@NixFeyO4/FF as anode and CoP@FeP/FF as cathode demonstrates its potential for industrial application. The study presents a general strategy for in situ synthesis of heterojunction catalysts on metal foams using controlled corrosion engineering for various catalytic applications.
author2 School of Chemistry, Chemical Engineering and Biotechnology
author_facet School of Chemistry, Chemical Engineering and Biotechnology
Li, Zhong
Zhang, Xinglin
Zhang, Zheye
Chen, Peng
Zhang, Yizhou
Dong, Xiaochen
format Article
author Li, Zhong
Zhang, Xinglin
Zhang, Zheye
Chen, Peng
Zhang, Yizhou
Dong, Xiaochen
author_sort Li, Zhong
title Dual-metal hydroxide@oxide heterojunction catalyst constructed via corrosion engineering for large-current oxygen evolution reaction
title_short Dual-metal hydroxide@oxide heterojunction catalyst constructed via corrosion engineering for large-current oxygen evolution reaction
title_full Dual-metal hydroxide@oxide heterojunction catalyst constructed via corrosion engineering for large-current oxygen evolution reaction
title_fullStr Dual-metal hydroxide@oxide heterojunction catalyst constructed via corrosion engineering for large-current oxygen evolution reaction
title_full_unstemmed Dual-metal hydroxide@oxide heterojunction catalyst constructed via corrosion engineering for large-current oxygen evolution reaction
title_sort dual-metal hydroxide@oxide heterojunction catalyst constructed via corrosion engineering for large-current oxygen evolution reaction
publishDate 2023
url https://hdl.handle.net/10356/169002
_version_ 1772825572478550016